MAKITA Naomasa 蒔田直昌

Researcher Number	00312356
Other IDs
Affiliation (Current)	2025: 社会医療法人禎心会札幌禎心会病院(禎心会循環器病疾患研究所), 循環器内科, 研究員 2025: 国立研究開発法人国立循環器病研究センター, 研究所, 客員部長
Affiliation (based on the past Project Information) *help	2022 – 2023: 国立研究開発法人国立循環器病研究センター, 研究所, 客員部長 2018 – 2021: 国立研究開発法人国立循環器病研究センター, 研究所, 副所長 2014 – 2018: 長崎大学, 医歯薬学総合研究科(医学系), 教授 2014: 長崎大学, 大学院医歯薬学総合研究科, 教授 2012 – 2013: 長崎大学, 医歯(薬)学総合研究科, 教授 … More 2012: 北海道大学, 大学院・医学研究科, 准教授 2009 – 2012: Nagasaki University, 大学院・医歯薬学総合研究科, 教授 2008: 北海道大学, 大学院・医学研究科, 准教授 2006 – 2007: 北海道大学, 北海道大学病院, 講師 1999 – 2004: 北海道大学, 大学院・医学研究科, 助手 1999: 北海道大学, 医学部, 助手 Less
Review Section/Research Field	Principal Investigator Circulatory organs internal medicine / Basic Section 53020:Cardiology-related / Medium-sized Section 53:Organ-based internal medicine and related fields / Cardiovascular medicine / Circulatory organs internal medicine / Complex systems Except Principal Investigator Cardiovascular medicine / Basic Section 53020:Cardiology-related / Obstetrics and gynecology / Complex systems / Biological Sciences / Circulatory organs internal medicine / General physiology
Keywords	Principal Investigator 致死性不整脈 / 遺伝子変異 / ゲノム編集 / SCN5A / 心臓伝導障害 / 心臓突然死 / ノックインマウス / パッチクランプ / 突然死 / ブルガダ症候群 … More / コンピュータシミュレーション / イオンチャネル / GWAS / ゲノムワイド関連解析 / Na/Ca交換体 / QT短縮症候群 / 早期再分極症候群 / Na-Ca交換体 / CRISPR/Cas9 / 進行性心臓伝導障害 / Akt / Na channel / Brugada syndrome / Naチャネル / 心室細動 / Brugada症候群 / 遺伝子多型 / ギャップ結合 / エクソーム / エクソーム解析 / リスク予測 / 複雑形質 / 人種特異性 / マルチオミックス解析 / リスク層別化 / ポリジニックリスクスコア / 選択的スプライシング / 人種横断的解析 / J波症候群 / Kaplan-Meier解析 / 多遺伝子リスクスコア / 多因子疾患 / 生存曲線 / 一塩基多型 / ポリジェニックリスクスコア / COX比例ハザード解析 / 個別化予防医療 / COX回帰解析 / 単一塩基多型 / 光学マッピング / 歯骨格異常 / コネキシン / Crispr/cas9ゲノム編集 / Crispr/Cas9ゲノム編集 / 歯骨形成異常 / コネキシン４５ / 胎生致死 / コネキシン45 / コネキシン40 / 分子心臓学 / 内科 / カルモジュリン / J波 / トランスポータ / CRISPR/CAS / CRISPR/cas9 / コラーゲン / Lethal arrhythmias / phosphorylation / トランスジェニック動物 / リン酸化シグナル / リン酸化 / atrial standstill / Long QT syndrome / polymorphism / mutation / ion channel / lathal arrhythmia / 心房停止 / QT延長症候群 / Mutations / Ventricular fibrillation / Transgenic mice / 光シグナルマッピング / 不整脈 / トランスジェニックマウス / 次世代シークエンサー / SCN10A / 全エクソン解析 / 遺伝子改変動物 / プロモータ / 伝導障害 / 国際情報交換（フランス） / iPS / シミュレーション / 心拍数 / ゼブラフィッシュ / 網羅的遺伝子解析 / サルコメア / 遺伝性不整脈 / ミオシン重鎖 / MYH6 / 洞不全症候群 / 遺伝子 / ギャップジャンクション … More Except Principal Investigator 遺伝子解析 / 電子顕微鏡 / 免疫染色 / 心筋生検 / 心筋症 / QT延長症候群 / 遺伝性不整脈 / 変異 / 突然死 / ノックインマウス / 膜タンパク / 心臓突然死 / 特発性心室細動 / トランスポータ / 遺伝子変異 / 循環器 / 病理所見 / 光学顕微鏡 / 病理組織診断 / カルモジュリンキナーゼ / 心室細動ストーム / 心臓電気生理学 / 植込み型除細動器 / 電気的ストーム / 遅延ナトリウム電流 / CaMKII / トルサード・ド・ポアンツ / 心室細動 / connexin / ovariectomy / estrogen / resting membrane potential / mesenteric artery / rat / potassium channel / endothelium-derived hyperpolarizing factor / 腸間脈動脈 / カリウムチャネル / コネキシン / 卵巣摘出 / エストロゲン / 静止膜電位 / 腸間膜動脈 / ラット / カリウムチャンネル / 内皮由来過分極因子 / プラコグロビン / 心不全 / 拡張型心筋症 / 生物学 / 生物物理 / 薬物動態学 / 代謝 / 全身循環 / 薬物動態 / 不整脈 / 心臓 / 生物物理学 / 生理学 / システム生物学 / ストレス応答 / 心血管病 / 活性酸素 / 酸化ストレス / ミトコンドリア / ST上昇 / カテコラミン感受性多形心室頻拍 / SCN5A / HERG / KvLQT1 / チャネル遺伝子 / Brugada症候群 / Na チャネル / パッチクランプ / 心筋細胞 / Naチャネル / イオンチャネル / 遺伝子導入 / アデノウイルス Less

A multi-omics study to elucidate the novel molecular basis of the complex traits and ethnicity in Brugada syndromePrincipal Investigator
- Principal Investigator
  
  Makita Naomasa
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  National Cardiovascular Center Research Institute
Elucidation of molecular pathogenesis for inherited lethal arrhythmia associated with transporter abnormalities
- Principal Investigator
  
  石川泰輔
- Project Period (FY)
  2020 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  National Cardiovascular Center Research Institute
Novel pathophysiology underlying cardiac conduction defect due to mutations of gap junction genesPrincipal Investigator
- Principal Investigator
  
  Makita Naomasa
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 53:Organ-based internal medicine and related fields
- Research Institution
  National Cardiovascular Center Research Institute
  Nagasaki University
Ethnicity-oriented genomic analysis of pathogenesis underlysing sudden cardiac death of unknown causePrincipal Investigator
- Principal Investigator
  
  Makita Naomasa
- Project Period (FY)
  2018 – 2021
- Research Category
  
  Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
- Review Section
  
  Medium-sized Section 53:Organ-based internal medicine and related fields
- Research Institution
  National Cardiovascular Center Research Institute
  Nagasaki University
Novel molecular basis underlying lethal arrhythmic syndrome due to mutations in cardiac Na/Ca exchanger genePrincipal Investigator
- Principal Investigator
  
  MAKITA Naomasa
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 53020:Cardiology-related
- Research Institution
  National Cardiovascular Center Research Institute
Usefulness of histopathological evaluation for the diagnosis and prediction of clinical prognosis in patients with cardiomyopathy
- Principal Investigator
  
  KAWANO Hiroaki
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Nagasaki University
Novel molecular basis of cardriac conduction disturbance associated with a collagene gene mutationPrincipal Investigator
- Principal Investigator
  
  MAKITA Naomasa
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Nagasaki University
Elucidation of novel pathophysiology underlysing lethal arrhythmia due to mutations in cardiac ion transportersPrincipal Investigator
- Principal Investigator
  
  MAKITA Naomasa
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Nagasaki University
Usefulness of endomyocardial biopsy for the diagnosis of dilated cardiomyopathy
- Principal Investigator
  
  KAWANO Hiroaki
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Nagasaki University
Role of CaMKII in an experimental model of ventricular fibrillation storm
- Principal Investigator
  
  TSUJI Yukiomi
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Cardiovascular medicine
- Research Institution
  Nagasaki University
Identification of Novel Genes and Pathogenesis Responsible for Brugada Syndrome Using Whole Exome SequencingPrincipal Investigator
- Principal Investigator
  
  MAKITA Naomasa
- Project Period (FY)
  2012 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  Nagasaki University
Establishment of Integrative Multi-level Systems Biology and its Applications
- Principal Investigator
  
  KURACHI YOSHIHISA
- Project Period (FY)
  2010 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
- Review Section
  
  Complex systems
- Research Institution
  Osaka University
Genetic and functional basis of cardiac ion channelopathyPrincipal Investigator
- Principal Investigator
  
  MAKITA Naomasa
- Project Period (FY)
  2010 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
- Review Section
  
  Complex systems
- Research Institution
  Nagasaki University
Mutations in cardiac gap junction genes and the pathophysiology underlying progressive cardiac conduction defect.Principal Investigator
- Principal Investigator
  
  MAKITA Naomasa
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  Nagasaki University
Regulation of mitochondrial ROS signaling in the cardiovascular stress response
- Principal Investigator
  
  TSUTSUI Hiroyuki
- Project Period (FY)
  2008 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
- Review Section
  
  Biological Sciences
- Research Institution
  Hokkaido University
Akt phosphorylation and arrhythmogenic modification of the cardiac sodium channelPrincipal Investigator
- Principal Investigator
  
  MAKITA Naomasa
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  Hokkaido University
致死性不整脈発症の分子基盤に関する調査・研究
- Principal Investigator
  
  平岡昌和
- Project Period (FY)
  2003
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  Tokyo Medical and Dental University
Phamacogenomic studies for the genetic basis for lethal arrhythmiasPrincipal Investigator
- Principal Investigator
  
  MAKITA Naomasa
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  HOKKAIDO UNIVERSITY
Development and electrophysiological analysis of genetically engineered transgenic mice for Brugada syndrome.Principal Investigator
- Principal Investigator
  
  NAOMASA Makita
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  HOKKAIDO UNIVERSITY
アデノウイルスベクターを用いた心筋イオンチャネル病の病態解明
- Principal Investigator
  
  TOHSE Noritsugu
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  General physiology
- Research Institution
  Sapporo Medical University
A study forthe effects of estrogen on actions ofendothelium-derived hyperpolarizing factor
- Principal Investigator
  
  SAKUMA Ichiro
- Project Period (FY)
  1999 – 2001
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  HOKKAIDO UNIVERSITY

[Book] 週刊　医学の歩み2022
- Author(s)
  蒔田直昌石川泰輔
- Total Pages
  6
- Publisher
  医歯薬出版株式会社
- Data Source
  KAKENHI-PROJECT-21H02920
[Book] ゼロから学ぶブルガダ症候群2020
- Author(s)
  石川泰輔, 蒔田直昌
- Total Pages
  133
- Publisher
  大道学館出版部
- ISBN
  9784924391840
- Data Source
  KAKENHI-PROJECT-18KK0245
[Book] ゼロから学ぶブルガダ症候群2020
- Author(s)
  石川泰輔, 蒔田直昌
- Total Pages
  133
- Publisher
  大道学館出版部
- ISBN
  9784924391840
- Data Source
  KAKENHI-PROJECT-18K19550
[Book] ゼロから学ぶ　Burugada症候群2020
- Author(s)
  石川泰輔, 蒔田直昌
- Total Pages
  133
- Publisher
  大道学館出版部
- Data Source
  KAKENHI-PROJECT-18H02808
[Book] 標準生理学第9版2019
- Author(s)
  蒔田直昌　（本間研一　編）
- Total Pages
  1172
- Publisher
  医学書院
- ISBN
  9784260034296
- Data Source
  KAKENHI-PROJECT-15H04823
[Book] 標準生理学第9版2019
- Author(s)
  蒔田直昌　（本間研一　編）
- Total Pages
  1172
- Publisher
  医学書院
- ISBN
  9784260034296
- Data Source
  KAKENHI-PROJECT-18KK0245
[Book] 循環器科の心電図2018
- Author(s)
  石川泰輔蒔田直昌（村川　裕二編）
- Total Pages
  224
- Publisher
  南江堂
- ISBN
  9784524237913
- Data Source
  KAKENHI-PROJECT-18K19550
[Book] 循環器科の心電図: ECG for Cardiologists2018
- Author(s)
  石川泰輔蒔田直昌(村川裕二編）
- Total Pages
  215
- Publisher
  南江堂
- ISBN
  9784524237913
- Data Source
  KAKENHI-PROJECT-15H04823
[Book] 不整脈識る・診る・治す2018
- Author(s)
  辻幸臣蒔田直昌（平尾見三、小室一成編）
- Total Pages
  376
- Publisher
  中山書店
- ISBN
  9784521745855
- Data Source
  KAKENHI-PROJECT-18K19550
[Book] 循環器科の心電図: ECG for Cardiologists2018
- Author(s)
  石川泰輔、蒔田直昌　（村川裕二　編）
- Total Pages
  215
- Publisher
  南江堂
- ISBN
  9784524237913
- Data Source
  KAKENHI-PROJECT-18KK0245
[Book] 循環器内科専門医バイブル2018
- Author(s)
  辻幸臣・蒔田直昌(小室一成・平尾見三編）
- Total Pages
  376
- Publisher
  中山書店
- ISBN
  9784521745855
- Data Source
  KAKENHI-PROJECT-18KK0245
[Book] 循環器内科専門医バイブル2018
- Author(s)
  辻幸臣・蒔田直昌(小室一成・平尾見三編）
- Total Pages
  376
- Publisher
  中山書店
- ISBN
  9784521745855
- Data Source
  KAKENHI-PROJECT-15H04823
[Book] 不整脈診療クリニカルクエスチョン2002015
- Author(s)
  蒔田直昌
- Total Pages
  333
- Publisher
  診療と治療社
- Data Source
  KAKENHI-PROJECT-24390199
[Book] 不整脈症候群－遺伝子変異から不整脈治療を捉えるー2015
- Author(s)
  蒔田直昌
- Total Pages
  196
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-15H04823
[Book] 不整脈診療クリニカルクエスチョン2002015
- Author(s)
  蒔田直昌
- Total Pages
  333
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-15H04823
[Book] 不整脈症候群－遺伝子変異から不整脈治療を捉えるー2015
- Author(s)
  石川泰輔,蒔田直昌
- Total Pages
  196
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-24390199
[Book] 不整脈診療クリニカルクエスチョン2002015
- Author(s)
  蒔田直昌
- Total Pages
  333
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-15K15311
[Book] 不整脈症候群2015
- Author(s)
  蒔田直昌
- Total Pages
  196
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-15K15311
[Book] 日本心電学会30年の軌跡: 遺伝性不整脈研究の黎明期とその後の急速な展開2013
- Author(s)
  蒔田直昌
- Total Pages
  419
- Publisher
  日本心電学会
- Data Source
  KAKENHI-PLANNED-22136007
[Book] 不整脈2013:心臓伝導障害の遺伝子基盤2013
- Author(s)
  蒔田直昌
- Total Pages
  215
- Publisher
  メディカルレビュー
- Data Source
  KAKENHI-PROJECT-24390199
[Book] 日本心電学会30年の軌跡.:遺伝性不整脈研究の黎明期とその後の急速な展開.2013
- Author(s)
  蒔田直昌
- Total Pages
  419
- Publisher
  日本心電学会
- Data Source
  KAKENHI-PROJECT-24390199
[Book] 不整脈2013: 心臓伝導障害の遺伝子基盤2013
- Author(s)
  蒔田直昌
- Total Pages
  215
- Publisher
  メディカルレビュー
- Data Source
  KAKENHI-PLANNED-22136007
[Book] Genes and Cardiovascular Function. (Springer, NY)2012
- Author(s)
  Makita N.
- Publisher
  Phenotypic Overlap of Lethal Arrhythmias Associated with Cardiac Sodium Mutations. Individual-specific or mutation-specific?
- Data Source
  KAKENHI-PROJECT-21590921
[Book] Genes and Cardiovascular Function. (Springer, NY)2012
- Author(s)
  Makita N
- Publisher
  Phenotypic Overlap of Lethal Arrhythmias Associated with Cardiac Sodium Mutations. Individual-specific or mutation-specific?
- Data Source
  KAKENHI-PLANNED-22136007
[Book] Genes and Cardiovascular Function2011
- Author(s)
  Makita N
- Publisher
  Springer(In press)
- Data Source
  KAKENHI-PLANNED-22136007
[Book] Genes and Cardiovascular Function2011
- Author(s)
  Makita N
- Publisher
  Springer(In press)
- Data Source
  KAKENHI-PROJECT-21590921
[Book] Genes and Cardiovascular Function2011
- Author(s)
  Makita N
- Publisher
  Springer
- Data Source
  KAKENHI-PROJECT-21590921
[Book] 循環器病学基礎と臨床2010
- Author(s)
  蒔田直昌
- Publisher
  西村書店
- Data Source
  KAKENHI-PROJECT-21590921
[Book] 不整脈にCa拮抗薬とATPをどう使うか-基礎と臨床-2010
- Author(s)
  有田眞、蒔田直昌, 他(編集)
- Total Pages
  106
- Publisher
  株式会社ライフメディコム
- Data Source
  KAKENHI-PROJECT-21590921
[Book] 不整脈にCa拮抗薬とATPをどう使うか-基礎と臨床-2010
- Author(s)
  有田眞、蒔田直昌, 他(編集)
- Total Pages
  106
- Publisher
  株式会社ライフメディコム
- Data Source
  KAKENHI-PLANNED-22136007
[Book] 循環器病学基礎と臨床2010
- Author(s)
  蒔田直昌
- Publisher
  西村書店
- Data Source
  KAKENHI-PROJECT-21590921
[Book] Brugada症候群,2010
- Author(s)
  蒔田直昌
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-21590921
[Book] 循環器病学基礎と臨床2010
- Author(s)
  蒔田直昌
- Publisher
  西村書店
- Data Source
  KAKENHI-PLANNED-22136007
[Book] 心臓突然死2009
- Author(s)
  蒔田直昌
- Publisher
  最新医学社
- Data Source
  KAKENHI-PROJECT-21590921
[Book] Brugada症候群, Medical View2009
- Author(s)
  蒔田直昌
- Data Source
  KAKENHI-PROJECT-21590921
[Book] 失神を究める, Medical View2009
- Author(s)
  蒔田直昌
- Data Source
  KAKENHI-PROJECT-21590921
[Book] QT間隔の診かた・考え方2007
- Author(s)
  蒔田直昌
- Total Pages
  260
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-18590757
[Book] Hokkaido University Medical Library Series vol.46, 167-1732003
- Author(s)
  Makita N, Kitabatake A
- Total Pages
  183
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Book] Genetics basis of life-threatening arrhythmias. In Integrated cardiology - From benchtop to clinic.2003
- Author(s)
  Makita N, Kitabatake A
- Total Pages
  183
- Publisher
  Hokkaido University Medical Library Series vol.46,167-173
- Data Source
  KAKENHI-PROJECT-15590711
[Book] 新不整脈学 Brugada症候群と遺伝子異常2003
- Author(s)
  蒔田直昌
- Total Pages
  665
- Publisher
  南江堂
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] TAD boundary deletion causes PITX2-related cardiac electrical and structural defects2024
- Author(s)
  Barc J. Makita N.et al.
- Journal Title
  
  Nat Commun
  
  Volume: in press
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02920
[Journal Article] Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci2024
- Author(s)
  Ishikawa T, Makita N et al.
- Journal Title
  
  European Heart Journal
  
  Volume: in press Issue: 26 Pages: 2320-2332
- DOI
  10.1093/eurheartj/ehae251
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02920
[Journal Article] A Noonan‐like pediatric patient with a de novo CBL pathogenic variant and an RNF213 polymorphism p.R4810K presenting with cardiopulmonary arrest due to left main coronary artery ostial atresia2023
- Author(s)
 Chida‐Nagai Ayako、Makita Naomasa et al
- Journal Title
 
 American Journal of Medical Genetics Part A
 
 Volume: 191 Issue: 12 Pages: 2837-2842
- DOI
 10.1002/ajmg.a.63370
- Peer Reviewed / Open Access
- Data Source
 KAKENHI-PROJECT-21H02920
[Journal Article] Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry2023
- Author(s)
  Crotti L, Spazzolini C, Nyegaard M, Fukuyama M, Horie M, Wilde AAM, Wolf CM, Ackerman MJ, Schwartz PJ. et al
- Journal Title
  
  European Heart Journal
  
  Volume: 44 Issue: 35 Pages: 3357-3370
- DOI
  10.1093/eurheartj/ehad418
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K08179, KAKENHI-PROJECT-21H02920
[Journal Article] Disrupted CaV1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model2023
- Author(s)
  Kashiwa A、Makiyama T、Kohjitani H、Maurissen T L、Ishikawa T、Yamamoto Y、Wuriyanghai Y、Gao J、Huang H、Imamura T、Aizawa T、Nishikawa M、Chonabayashi K、Mishima H、Ohno S、Toyoda F、Sato S、Yoshiura K、Takahashi K、Yoshida Y、Woltjen K、Horie M、Makita N、Kimura T
- Journal Title
  
  Heart Rhythm
  
  Volume: 20 Issue: 1 Pages: 89-99
- DOI
  10.1016/j.hrthm.2022.08.021
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K06781, KAKENHI-PROJECT-21K07800, KAKENHI-PROJECT-19K17560, KAKENHI-PROJECT-21H02920
[Journal Article] Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.2023
- Author(s)
  Gao J, Makiyama T, Yamamoto Y, Kobayashi T, Aoki H, Maurissen TL, Wuriyanghai Y, Kashiwa A, Imamura T, Aizawa T, Huang H, Kohjitani H, Nishikawa M, Chonabayashi K, Fukuyama M, Manabe H, Nakau K, Wada T, Kato K, Toyoda F, Yoshida Y, Makita N, Woltjen K, Ohno S, Kurebayashi N, Murayama T, Sakurai T, Horie M, Kimura T.
- Journal Title
  
  Circulation: Arrhythmia and Electrophysiology
  
  Volume: 16 Issue: 3 Pages: 9999-9999
- DOI
  10.1161/circep.122.011387
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K11368, KAKENHI-PROJECT-21K06781, KAKENHI-PROJECT-22K08179, KAKENHI-PROJECT-20K17113, KAKENHI-PROJECT-22K06652, KAKENHI-PROJECT-21H02920
[Journal Article] Rotors anchored by refractory islands drive torsades de pointes in an experimental model of electrical storm2022
- Author(s)
  Yamazaki M, Makita N, Tsuji Y, et al.
- Journal Title
  
  Heart Rhythm
  
  Volume: 19 Issue: 2 Pages: 318-329
- DOI
  10.1016/j.hrthm.2021.10.012
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-19H04443, KAKENHI-PROJECT-20K08450, KAKENHI-PROJECT-21K19913, KAKENHI-PROJECT-21K18036, KAKENHI-PROJECT-21H04953, KAKENHI-PROJECT-21H02920
[Journal Article] European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases2022
- Author(s)
  Wilde Arthur A M、Makita N. et al
- Journal Title
  
  Europace
  
  Volume: 24 Issue: 8 Pages: 1307-1367
- DOI
  10.1093/europace/euac030
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02920
[Journal Article] European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases2022
- Author(s)
  Wilde Arthur A.M.、Makita N. et al
- Journal Title
  
  Heart Rhythm
  
  Volume: 19 Issue: 7 Pages: e1-e60
- DOI
  10.1016/j.hrthm.2022.03.1225
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02920
[Journal Article] Targeted deep sequencing analyses of long QT syndrome in a Japanese population2022
- Author(s)
  NagataY、WatanabeR、EichhornC、OhnoS、AibaT、IshikawaT、NakanoY、AizawaY、HayashiKi、MurakoshiN、NakajimaT、YagiharaN、MishimaH、SudoT、HiguchiC、TakahashiA、SekineA、MakiyamaT、TanakaY、WatanabeA、TachibanaM、MoritaH、YoshiuraK-i、TsunodaT、WatanabeH、KurabayashiM、NogamiA、KiharaY、HorieM、ShimizuW、MakitaN、TanakaT
- Journal Title
  
  PLOS ONE
  
  Volume: 17 Issue: 12 Pages: e0277242-e0277242
- DOI
  10.1371/journal.pone.0277242
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07800, KAKENHI-PROJECT-21K08028, KAKENHI-PROJECT-21K08075, KAKENHI-PROJECT-21K16985, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-20K08487, KAKENHI-PROJECT-20K08447
[Journal Article] Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian population2022
- Author(s)
  Murakami Haruka、Tanimoto Yoko、Tanimoto Kojiro、Inoue Satomi、Ishikawa Taisuke、Makita Naomasa、Yamazawa Kazuki
- Journal Title
  
  Human Genome Variation
  
  Volume: 9 Issue: 1 Pages: 28-28
- DOI
  10.1038/s41439-022-00206-9
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K19751, KAKENHI-PROJECT-20K19082, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-23K24309
[Journal Article] Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome.2021
- Author(s)
  Ishikawa T, Kimoto H, Mishima H, Yamagata K, Ogata S, Aizawa Y, Hayashi K, Morita H, Nakajima T, Nakano Y, Nagase S, Murakoshi N, Kowase S, Ohkubo K, Aiba T, Morimoto S, Ohno S, Kamakura S, Nogami A, Takagi M, Karakachoff M, Dina C, Schott JJ, Yoshiura KI, Horie M, Shimizu W, Nishimura K, Kusano K, Makita N.
- Journal Title
  
  Eur Heart J.
  
  Volume: 42(29) Issue: 29 Pages: 2854-2863
- DOI
  10.1093/eurheartj/ehab254
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09524, KAKENHI-PROJECT-18K15407, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-20H03591, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-20K08487, KAKENHI-PROJECT-21K07800, KAKENHI-PROJECT-21K08028, KAKENHI-PROJECT-21K08075, KAKENHI-PROJECT-20K08416
[Journal Article] Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants2021
- Author(s)
 Kozek K, Wada Y, Makita N, Ishikawa T, Crotti L, Kroncke BM, et al.
- Journal Title
 
 Circulation: Genomic and Precision Medicine
 
 Volume: 14 Issue: 4
- DOI
 10.1161/circgen.120.003289
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
 KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-20K08416
[Journal Article] Electrocardiographic Diagnosis of Hypertrophic Cardiomyopathy in the Pre- and Post-Diagnostic Phases in Children and Adolescents2021
- Author(s)
  Yoshinaga M, Horigome H, Yasuda K, Kogaki S, Tateno S, Ohta K, Hirono K, Hosokawa S, Takechi F, Ishikawa Y, Hata T, Ichida F, Ohno S, Makita N, Horie M, Takahashi H, Nagashima M.
- Journal Title
  
  Circ J
  
  Volume: 86 Issue: 1 Pages: 118-127
- DOI
  10.1253/circj.CJ-21-0376
- NAID
  130008132672
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2021-12-24
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-18K02505, KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-21K07765
[Journal Article] Novel electrocardiographic criteria for short QT syndrome in children and adolescents2021
- Author(s)
  Suzuki H, Horie M, Ishikawa T, Makita N, Nagashima M, et al.
- Journal Title
  
  EP Europace
  
  Volume: 23 Issue: 12 Pages: 2029-2038
- DOI
  10.1093/europace/euab097
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-20K08416
[Journal Article] Pathological Features of Lamin Cardiomyopathy2020
- Author(s)
  Kawano H., Ishimatsu T., Ishijima I., Hayashi T., Ishikawa T., Makita N., Maemura K.
- Journal Title
  
  Circulation Journal
  
  Volume: -
- NAID
  130007864268
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K19550
[Journal Article] Brugada症候群の遺伝的背景2020
- Author(s)
  蒔田直昌
- Journal Title
  
  別冊・医学のあゆみ　遺伝性心血管疾患のすべて
  
  Volume: - Pages: 87-90
- Data Source
  KAKENHI-PROJECT-18KK0245
[Journal Article] SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families2020
- Author(s)
  3.Wijeyeratne YD, Tanck MW, Mizusawa Y, Batchvarov V, Barc J, Crotti L, et al.
- Journal Title
  
  Circulation: Genomic and Precision Medicine
  
  Volume: 13 Issue: 6
- DOI
  10.1161/circgen.120.002911
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-20K08416
[Journal Article] Brugada症候群の遺伝的背景2020
- Author(s)
  石川泰輔, 蒔田直昌
- Journal Title
  
  別冊・医学のあゆみ　遺伝性心血管疾患のすべて
  
  Volume: - Pages: 87-90
- Data Source
  KAKENHI-PROJECT-18H02808
[Journal Article] Identification of transmembrane protein 168 mutation in familial Brugada syndrome.2020
- Author(s)
  Shimizu A, Zankov DP, Sato A, Komeno M, Toyoda F, Yamazaki S, Makita T, Noda T, Ikawa M, Asano Y, Miyashita Y, Takashima S, Morita H, Ishikawa T, Makita N, Hitosugi M, Matsuura H, Ohno S, Horie M, Ogita H.
- Journal Title
  
  FASEB Journal
  
  Volume: 34 Issue: 5 Pages: 6399-6417
- DOI
  10.1096/fj.201902991r
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08075, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-ORGANIZER-19H05749, KAKENHI-PROJECT-17F17418, KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K08627, KAKENHI-PROJECT-17K08657, KAKENHI-PROJECT-16H06276, KAKENHI-PROJECT-19K09408, KAKENHI-PROJECT-20K08489, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08033, KAKENHI-PROJECT-19H03652, KAKENHI-PROJECT-18K19547, KAKENHI-PROJECT-21K08119
[Journal Article] Pathological Features of Lamin Cardiomyopathy2020
- Author(s)
  Kawano H., Ishimatsu T., Ishijima I., Hayashi T., Ishikawa T., Makita N., Maemura K.
- Journal Title
  
  Circulation Journal
  
  Volume: -
- NAID
  130007864268
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18KK0245
[Journal Article] Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome2020
- Author(s)
  Lahrouchi N, Tadros R, Crotti L, Makiyama T et al.
- Journal Title
  
  Circulation
  
  Volume: 142 Issue: 4 Pages: 324-338
- DOI
  10.1161/circulationaha.120.045956
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-20K08416
[Journal Article] 遺伝性不整脈のPrecision medicine2020
- Author(s)
  石川泰輔, 蒔田直昌
- Journal Title
  
  週間　医学のあゆみ
  
  Volume: 272 Pages: 1279-1283
- Data Source
  KAKENHI-PROJECT-18KK0245
[Journal Article] Cardiac Emerinopathy2020
- Author(s)
  Ishikawa Taisuke、Ichida Fukiko、Makita Naomasa　et al
- Journal Title
  
  Circulation: Arrhythmia and Electrophysiology
  
  Volume: 13 Issue: 10 Pages: 1165-1174
- DOI
  10.1161/circep.120.008712
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-19K21724, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-20H03591, KAKENHI-PROJECT-18K07850, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-20K08416, KAKENHI-PROJECT-18H03083
[Journal Article] Brugada症候群の遺伝的背景2020
- Author(s)
  蒔田直昌
- Journal Title
  
  別冊・医学のあゆみ　遺伝性心血管疾患のすべて
  
  Volume: - Pages: 87-90
- Data Source
  KAKENHI-PROJECT-18K19550
[Journal Article] Pathological Features of Lamin Cardiomyopathy2020
- Author(s)
  Kawano H, Ishimatsu T, Kawamura K, Ishijima M, Hayashi T, Ishikawa T, Makita N, Maemura K.
- Journal Title
  
  Circ J
  
  Volume: 84 Issue: 7 Pages: 1193
- DOI
  10.1253/circj.CJ-20-0187
- NAID
  130007864268
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2020-06-25
- Language
  English
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08416
[Journal Article] Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls2020
- Author(s)
  2.Walsh R, Lahrouchi N, Tadros R, Kyndt F, Glinge C, Postema PG, et al.
- Journal Title
  
  Genetics in Medicine
  
  Volume: 23 Issue: 1 Pages: 47-58
- DOI
  10.1038/s41436-020-00946-5
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08100, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18K15407, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-20K08416
[Journal Article] Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome2020
- Author(s)
  Lahrouchi N., Ishikawa T., Makita N., Connie R. B., et al.
- Journal Title
  
  Circulation
  
  Volume: -
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Journal Article] Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome2020
- Author(s)
  Lahrouchi N., Ishikawa T., Makita N., et al.
- Journal Title
  
  Circulation
  
  Volume: -
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Journal Article] 遺伝性不整脈のPrecision medicine2020
- Author(s)
  石川泰輔, 蒔田直昌
- Journal Title
  
  週間　医学のあゆみ
  
  Volume: - Pages: 1279-1283
- Data Source
  KAKENHI-PROJECT-18H02808
[Journal Article] Desmin‐related myopathy characterized by non‐compaction cardiomyopathy, cardiac conduction defect, and coronary artery dissection2020
- Author(s)
  Tamiya R., Saito Y., Fukamachi D., Nagashima K., Aizawa Y., Ohkubo K., Hatta T., Sezai A., Tanaka M, Ishikawa T., Makita N., Sumitomo N., Okumura Y.
- Journal Title
  
  ESC Heart Failure
  
  Volume: - Issue: 3 Pages: 1338-1343
- DOI
  10.1002/ehf2.12667
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894
[Journal Article] TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway2020
- Author(s)
  Miyao N., Hata Y., Izumi H., Nagaoka R., Oku Y., Takasaki I., Ishikawa T., Takarada S., Okabe M., Nakaoka H., Ibuki K., Ozawa S., Yoshida T., Hasegawa H., Makita N., Nishida N., Mori H., Ichida F., Hirono K.
- Journal Title
  
  PLOS ONE
  
  Volume: 15 Issue: 4 Pages: 0227393-0227393
- DOI
  10.1371/journal.pone.0227393
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PUBLICLY-19H04744, KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894, KAKENHI-PROJECT-18K07365, KAKENHI-PROJECT-20H03350
[Journal Article] 遺伝性不整脈の遺伝子診断：有効性と限界2019
- Author(s)
  石川泰輔, 蒔田直昌
- Journal Title
  
  循環器病研究の進歩 Recent Advances in Cadiovascular Disease
  
  Volume: 40 Pages: 58-66
- Data Source
  KAKENHI-PROJECT-18H02808
[Journal Article] 遺伝性不整脈のPrecision medicine2019
- Author(s)
  石川泰輔, 蒔田直昌
- Journal Title
  
  週間　医学のあゆみ
  
  Volume: 272 Pages: 1279-1283
- Data Source
  KAKENHI-PROJECT-18K19550
[Journal Article] 遺伝性不整脈の遺伝子診断：有効性と限界2019
- Author(s)
  石川泰輔, 蒔田直昌
- Journal Title
  
  循環器病研究の進歩
  
  Volume: 40 Pages: 58-66
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K19550
[Journal Article] 遺伝性不整脈の遺伝子診断：有効性と限界2019
- Author(s)
  石川泰輔, 蒔田直昌
- Journal Title
  
  循環器病研究の進歩
  
  Volume: 40 Pages: 58-66
- Data Source
  KAKENHI-PROJECT-18KK0245
[Journal Article] Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients2019
- Author(s)
  Shimizu Wataru、Makimoto Hisaki、Yamagata Kenichiro、Kamakura Tsukasa、Wada Mitsuru、Miyamoto Koji、Inoue-Yamada Yuko、Okamura Hideo、Ishibashi Kohei、Noda Takashi、Nagase Satoshi、Miyazaki Aya、Sakaguchi Heima、Shiraishi Isao、Makiyama Takeru、Ohno Seiko、Itoh Hideki、et al
- Journal Title
  
  JAMA Cardiology
  
  Volume: in press Issue: 3 Pages: 246-254
- DOI
  10.1001/jamacardio.2018.4925
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09494, KAKENHI-PROJECT-18K08100, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15KK0302, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-17K09524, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08075, KAKENHI-PROJECT-19K08566, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18H02808
[Journal Article] Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry2019
- Author(s)
  Crotti Lia、Spazzolini Carla、Tester David J、Ohno Seiko、Ackerman Michael J、Schwartz Peter J, et al.
- Journal Title
  
  European Heart Journal
  
  Volume: 40 Issue: 35 Pages: 2964-2975
- DOI
  10.1093/eurheartj/ehz311
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-16H06277, KAKENHI-PROJECT-18H02808
[Journal Article] Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants2018
- Author(s)
  Gray B., Hasdemir C., Ingles J., Aiba T., Makita N., Probst V., Wilde A. A. M., Newbury-Ecob R., Sheppard M. N., Semsarian C., Sy R. W., Behr E. R.
- Journal Title
  
  Heart Rhythm
  
  Volume: 15 Issue: 7 Pages: 1051-1057
- DOI
  10.1016/j.hrthm.2018.03.015
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-18H02808
[Journal Article] 家族性心房細動の遺伝子基盤2018
- Author(s)
  蒔田直昌
- Journal Title
  
  心電図
  
  Volume: 38 Pages: 286-290
- NAID
  130007596013
- Data Source
  KAKENHI-PROJECT-18KK0245
[Journal Article] HCN4 pacemaker channels attenuate the parasympathetic response and stabilize the spontaneous firing of the sinoatrial node2018
- Author(s)
  Kozasa Yuko、Nakashima Noriyuki、Ito Masayuki、Ishikawa Taisuke、Kimoto Hiroki、Ushijima Kazuo、Makita Naomasa、Takano Makoto
- Journal Title
  
  The Journal of Physiology
  
  Volume: 596 Issue: 5 Pages: 809-825
- DOI
  10.1113/jp275303
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16H05124, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15K18967, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894
[Journal Article] HCN4 Gene Polymorphisms Are Associated With Occurrence of Tachycardia-Induced Cardiomyopathy in Patients With Atrial Fibrillation2018
- Author(s)
  Nakano Yukiko、Ochi Hidenori、Sairaku Akinori、Onohara Yuko、Tokuyama Takehito、Motoda Chikaaki、Matsumura Hiroya、Tomomori Shunsuke、Amioka Michitaka、Hironobe Naoya、Ohkubo Yousaku、Okamura Shou、Makita Naomasa、Yoshida Yukihiko、Chayama Kazuaki、Kihara Yasuki
- Journal Title
  
  Circulation: Genomic and Precision Medicine
  
  Volume: 11 Issue: 7 Pages: 1-7
- DOI
  10.1161/circgen.117.001980
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09501, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-18H02808
[Journal Article] 心臓突然死の病態解明における最新の遺伝学研究―ゲノムワイド関連解析と次世代シークエンス解析―2018
- Author(s)
  蒔田直昌
- Journal Title
  
  循環器内科
  
  Volume: 84 Pages: 699-704
- NAID
  40021757349
- Data Source
  KAKENHI-PROJECT-18KK0245
[Journal Article] Lack of genotype-phenotype correlation in Brugada syndrome and sudden arrhythmic death syndrome families with reported pathogenic SCN1B variants.2018
- Author(s)
  Gray B, Hasdem C, Ingles J, Aiba T, Makita N, Probst V, Wilde A, Newbury-Ecob R, Sheppard M, Semsarian C, Sy R, Behr E
- Journal Title
  
  Heart Rhythm
  
  Volume: in Press
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Journal Article] 進行性心臓伝導障害の病態と遺伝的背景2018
- Author(s)
  石川泰輔, 蒔田直昌
- Journal Title
  
  循環器内科
  
  Volume: 84 Pages: 721-728
- NAID
  40021757390
- Data Source
  KAKENHI-PROJECT-18KK0245
[Journal Article] Brugada症候群の遺伝的背景2018
- Author(s)
  蒔田直昌
- Journal Title
  
  医学のあゆみ
  
  Volume: 268 Pages: 771-774
- Data Source
  KAKENHI-PROJECT-18KK0245
[Journal Article] Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry2018
- Author(s)
 14.Nakajima K, Aiba T, Makiyama T, Nishiuchi S, Ohno S, Kato K, Yamamoto Y, Doi T, Shizuta S, Onoue K, Yagihara N, Ishikawa T, Watanabe I, Kawakami H, Oginosawa Y, Murakoshi N, Nogami A, Aonuma K, Saito Y, Kimura T, Yasuda S, Makita N, Shimizu W, Horie M, Kusano K.
- Journal Title
 
 Circ J
 
 Volume: 82 Issue: 11 Pages: 2707-2714
- DOI
 10.1253/circj.CJ-18-0339
- NAID
 40021697176
- ISSN
 1346-9843, 1347-4820
- Year and Date
 2018-10-25
- Language
 English
- Peer Reviewed / Open Access
- Data Source
 KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18K15847, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894
[Journal Article] Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death.2017
- Author(s)
  Oshima Y, Yamamoto T, Ishikawa T, Mishima H, Matsusue A, Umehara T, Murase T, Abe Y, Kubo SI, Yoshiura KI, Makita N, Ikematsu K.
- Journal Title
  
  J Hum Genet.
  
  Volume: 62 Issue: 11 Pages: 989-995
- DOI
  10.1038/jhg.2017.79
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16KT0112, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-16H05159, KAKENHI-PROJECT-15K08892, KAKENHI-PROJECT-15K15311
[Journal Article] A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest2017
- Author(s)
  Takahashi K, Ishikawa T, Makita N, Takefuta K, Nabeshima T, Nakayashiro M
- Journal Title
  
  HeartRhythm Case Reports
  
  Volume: 3 Issue: 1 Pages: 69-72
- DOI
  10.1016/j.hrcr.2016.09.004
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15K15311
[Journal Article] Progressive atrial conduction system defects associated with bone malformation caused by a connexin45 mutation2017
- Author(s)
  Seki A, Ishikawa T, Daumy X, Mishima H, Barc J, Sasaki R, Nishii K, Saito K, Urano M, Ohno S, Otsuki S, Kimoto H, Baruteau A, Thollet A, Fouchard S, Bonnaud S, Parent P, Shibata Y, Perrin JP, Le Marec H, Hagiwara N, Mercier S, Horie M, Probst V, Yoshiura KI, Redon R, Schott JJ, Makita N.
- Journal Title
  
  J Am Coll Cardiol
  
  Volume: 印刷中
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Journal Article] Letter to the Editor2017
- Author(s)
  Ishikawa T, Makita N, Aoki H, Saida Y
- Journal Title
  
  J Vet Intern Med
  
  Volume: 31 Issue: 4 Pages: 967-968
- DOI
  10.1111/jvim.14781
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15K15311
[Journal Article] Genotype-phenotype correlation of SCN5A mutation for clinical and electrocardiographic characteristics of probands with Brugada syndrome: Japanese Multicenter Registry.2017
- Author(s)
  Yamagata K, Horie M, et al.
- Journal Title
  
  Circulation
  
  Volume: 印刷中 Issue: 23 Pages: 0-0
- DOI
  10.1161/circulationaha.117.027983
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-26461130, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15KK0302, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15K09082, KAKENHI-PROJECT-15K09689
[Journal Article] The Phenotypic Spectrum of a Mutation Hotspot Responsible for the Short QT Syndrome2017
- Author(s)
  Hu D, Li Y, Zhang J, Pfeiffer R, Gollob MH, Healey J, Harrell DT, Makita N, Abe H, Sun Y, Guo J, Zhang L, Yan G, Mah D, Walsh EP, Leopold HB, Giustetto C, Gaita F, Zienciuk-Krajka A, Mazzanti A, Priori SG, Antzelevitch C, Barajas-Martinez H.
- Journal Title
  
  JACC: Clinical Electrophysiology
  
  Volume: 印刷中 Issue: 7 Pages: 727-743
- DOI
  10.1016/j.jacep.2016.11.013
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823
[Journal Article] Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction.2017
- Author(s)
  Ishikawa T, Horie M, et al.
- Journal Title
  
  Heart Rhythm
  
  Volume: 印刷中 Issue: 5 Pages: 717-724
- DOI
  10.1016/j.hrthm.2017.01.020
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K09680, KAKENHI-PROJECT-16KT0112, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-16H05159, KAKENHI-PROJECT-15K15311
[Journal Article] Flecainide ameliorates arrhythmogenicity through NCX flux in Andersen-Tawil syndrome-iPS cell-derived cardiomyocytes.2017
- Author(s)
  Kuroda Y, Yuasa S, Watanabe Y, Ito S, Egashira T, ・・・Horie M, Kamiya K, Fukuda K.
- Journal Title
  
  Biochemistry and Biophysics Reports
  
  Volume: 9 Pages: 245-256
- DOI
  10.1016/j.bbrep.2017.01.002
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25461051, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-16K15415, KAKENHI-PUBLICLY-15H01521, KAKENHI-PROJECT-16H02651, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-16H05304, KAKENHI-PROJECT-26293052, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K15311
[Journal Article] Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers.2017
- Author(s)
  Nishiuchi S, Makiyama T, Aiba T, Nakajima K, Hirose S, Kohjitani H, Yamamoto Y, Harita T, Hayano M, Wuriyanghai Y, Chen J, Sasaki K, Yagihara N, Ishikawa T, Onoue K, Murakoshi N, Watanabe I, Ohkubo K, Watanabe H, Ohno S, Doi T, Shizuta S, Minamino T, et.al
- Journal Title
  
  Circ Cardiovasc Genet.
  
  Volume: 6 Issue: 6
- DOI
  10.1161/circgenetics.116.001603
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09421, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PLANNED-26115008, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-17H06806, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-15K15311
[Journal Article] Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.2017
- Author(s)
  Seki A, Ishikawa T, Daumy X, Mishima H, Barc J, Sasaki R, Nishii K, Saito K, Urano M, Ohno S, Otsuki S, Kimoto H, Baruteau AE, Thollet A, Fouchard S, Bonnaud S, Parent P, Shibata Y, Perrin JP, Le Marec H, Hagiwara N, Mercier S, Horie M, Probst V, Yoshiura KI, Redon R, Schott JJ, Makita N.
- Journal Title
  
  J Am Coll Cardiol.
  
  Volume: 70 Issue: 3 Pages: 358-370
- DOI
  10.1016/j.jacc.2017.05.039
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16KT0112, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-16H05159, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-15K15311
[Journal Article] Allele-specific Ablation Rescues Electrophysiological Abnormalities in a Human iPS Cell Model of Long-QT Syndrome with a CALM2 Mutation.2017
- Author(s)
  Yamamoto Y, Horie M, et al.
- Journal Title
  
  Human Molecular Genetics
  
  Volume: 印刷中 Issue: 9 Pages: 1670-1677
- DOI
  10.1093/hmg/ddx073
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-16H05297
[Journal Article] Reply: Search for Evidence-Based Medicine for Brugada Syndrome: The Complex Network of the Brugada Syndrome2016
- Author(s)
  Nademanee K, Raju H, De Noronha S, Papadakis M, Robinson L, Rothery S, Makita N, Kowase S, Boonmee N, Vitayakritsirikul V, Ratanarapee S, Sharma S, van der Wal A. C. Christiansen M, Tan H. L, Wilde A. A, Nogami A, Sheppard M. N, Veerakul G, Behr E. R.
- Journal Title
  
  J Am Coll Cardiol
  
  Volume: 67 Issue: 13 Pages: 1658-1659
- DOI
  10.1016/j.jacc.2016.01.032
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823
[Journal Article] Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I.2016
- Author(s)
  Daumy X, Amarouch MY, Lindenbaum P, Bonnaud S, Charpentier E, Bianchi B, Nafzger S, Baron E, Fouchard S, Thollet A, Kyndt F, Barc J, Le Scouarnec S, Makita N, Le Marec H, Dina C, Gourraud JB, Probst V, Abriel H, Redon R, Schott JJ.
- Journal Title
  
  Int J Cardiol
  
  Volume: 207 Pages: 349-358
- DOI
  10.1016/j.ijcard.2016.01.052
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-24390199
[Journal Article] Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes.2016
- Author(s)
  Yagihara N,Minamino T,33名中28番
- Journal Title
  
  J Am Heart Assoc.
  
  Volume: 19 Issue: 9 Pages: 644-650
- DOI
  10.1161/jaha.116.003644
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PLANNED-26115008, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-26461130, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15K19373, KAKENHI-PROJECT-15H04823
[Journal Article] Partial IK1 blockade destabilizes spiral wave rotation center without inducing wave breakup and facilitates termination of reentrant arrhythmias in ventricles2016
- Author(s)
  Kushiyama Y, Honjo H, Niwa R, Takanari H, Yamazaki M, Takemoto Y, Sakuma I, Kodama I, Kamiya K
- Journal Title
  
  American Journal of Physiology Heart and Circulatory Physiology
  
  Volume: 311 Issue: 1 Pages: 750-758
- DOI
  10.1038/srep34198
- NAID
  120005946586
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H01801, KAKENHI-PROJECT-15H04684, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-25461051, KAKENHI-PROJECT-26461087, KAKENHI-PROJECT-15K15049, KAKENHI-PROJECT-15K09078, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-16K15415, KAKENHI-PUBLICLY-15H01521, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-16H05304, KAKENHI-PROJECT-26293052
[Journal Article] Inherited bradyarrhythmia: A diverse genetic background.2016
- Author(s)
  Ishikawa T, Tsuji Y, Makita N
- Journal Title
  
  Journal of Arrhythmia
  
  Volume: 印刷中 Issue: 5 Pages: 352-358
- DOI
  10.1016/j.joa.2015.09.009
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-24390199
[Journal Article] 遺伝性不整脈疾患に伴うelectrical storm：プルキンエ細胞の電気生理学的特殊性2015
- Author(s)
  辻　幸臣、Daniel Toshio Harrell、石川泰輔、蒔田直昌
- Journal Title
  
  心電図
  
  Volume: NA
- Data Source
  KAKENHI-PROJECT-26461074
[Journal Article] Molecular Mechanisms Underlying Urate-Induced Enhancement of Kv1.5 Channel Expression in HL-1 Atrial Myocytes2015
- Author(s)
  Maharani N, Ting YK, Cheng J, Hasegawa A, Kurata Y, Li P, Nakayama Y, Ninomiya H, Ikeda N, Morikawa K, Yamamoto K, Makita N, Yamashita T, Shirayoshi Y, Hisatome I.
- Journal Title
  
  Circ J
  
  Volume: 79 Issue: 12 Pages: 2659-2668
- DOI
  10.1253/circj.CJ-15-0416
- NAID
  130005110934
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26501003, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15K21170, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-25461109, KAKENHI-PROJECT-24390199
[Journal Article] A novel mutation in alpha-myosin heavy chain gene is associated with sick sinus syndrome2015
- Author(s)
  Ishikawa T, Jou CJ, Nogami A, Kowase S, Arrington CB, Barnett SM, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N
- Journal Title
  
  Circ Arrhythm Electrophysiol
  
  Volume: 8 Issue: 2 Pages: 400-108
- DOI
  10.1161/circep.114.002534
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-25670172, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25293181
[Journal Article] A novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.2015
- Author(s)
  Ishikawa T, Jou CJ, Nogami A, Kowase S, Arrington CB, Barnett SM, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N.
- Journal Title
  
  Circ Arrhythm Electrophysiol.
  
  Volume: in press
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.2015
- Author(s)
  Hayashi K, Konno T, Tada H, Tani S, Liu L, Fujino N, Nohara A, Hodatsu A, Tsuda T, Tanaka Y, Kawashiri MA, Ino H, Makita N, Yamagishi M.
- Journal Title
  
  Circ Arrhythm Electrophysiol.
  
  Volume: 8 Issue: 5 Pages: 1095-1104
- DOI
  10.1161/circep.114.002519
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09118, KAKENHI-PROJECT-26460670, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-25460648, KAKENHI-PROJECT-25860589, KAKENHI-PROJECT-24390199
[Journal Article] Electrical Storm Associated with Inherited Arrhythmia Syndromes : Cardiac Purkinje Fiber Arrhythmogenesis2015
- Author(s)
  辻幸臣，Harrell DT，石川泰輔，蒔田直昌
- Journal Title
  
  Japanese Journal of Electrocardiology
  
  Volume: 35 Issue: 2 Pages: 104-115
- DOI
  10.5105/jse.35.104
- NAID
  130005139469
- ISSN
  0285-1660, 1884-2437
- Language
  Japanese
- Data Source
  KAKENHI-PROJECT-26461074
[Journal Article] Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome.2015
- Author(s)
  Harrell DT, Ashihara T, Ishikawa T, et al.
- Journal Title
  
  International Journal of Cardiology.
  
  Volume: 190 Pages: 393-402
- DOI
  10.1016/j.ijcard.2015.04.090
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25461053, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-25461106, KAKENHI-PROJECT-25461113, KAKENHI-PROJECT-26670292, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-24300145, KAKENHI-PROJECT-24390199
[Journal Article] A novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.2015
- Author(s)
  Ishikawa T, Jou CJ, Nogami A, Kowase S, Arrington CB, Barnett SM, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N.
- Journal Title
  
  Circ Arrhythm Electrophysiol.
  
  Volume: in press
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome2015
- Author(s)
  Nademanee K, Raju H, de Noronha SV, Papadakis M, Robinson L, Rothery S, Makita N, Kowase S, Boonmee N, Vitayakritsirikul V, Ratanarapee S, Sharma S, van der Wal AC, Christiansen M, Tan HL, Wilde AA, Nogami A, Sheppard MN, Veerakul G, Behr ER
- Journal Title
  
  J Am Coll Cardiol
  
  Volume: 66(18) Issue: 18 Pages: 1976-1986
- DOI
  10.1016/j.jacc.2015.08.862
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-24390199
[Journal Article] Normal dose of pilsicainide showed marked negative inotropic effects in a patient who had no underlying heart disease.2014
- Author(s)
  Yoshida M, Ando S, Chishaki A,Makita N, Hasegawa Y, Narita S, Momii H, Kadokami T.
- Journal Title
  
  J Arrhythmia.
  
  Volume: 30 Pages: 68-70
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] わが国における遺伝性不整脈診断・治療の今後の展望-欧米との違いも含めて.2014
- Author(s)
  清水渉, 蒔田直昌, 堀江稔, 相庭武司.
- Journal Title
  
  Cardiac Practice.
  
  Volume: 25 Pages: 65-72
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Normal dose of pilsicainide showed marked negative inotropic effects in a patient who had no underlying heart disease2014
- Author(s)
  Yoshida M, Ando S, Chishaki A, Makita N, Hasegawa Y, Narita S, Momii H, Kadokami T.
- Journal Title
  
  Journal Arrhythmia.
  
  Volume: 30 Pages: 68-70
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] わが国における遺伝性不整脈診断・治療の今後の展望-欧米との違いも含めて.2014
- Author(s)
  清水渉, 蒔田直昌, 堀江稔, 相庭武司.
- Journal Title
  
  Cardiac Practice.
  
  Volume: 25 Pages: 65-72
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] A rare KCNE1 polymorphism, D85N, as a genetic modifier of long QT syndrome2014
- Author(s)
  Hasegawa K, Ohno S, Itoh H, Makiyama T, Aiba T, Nakano Y, Shimizu W, Matsuura H, Makita N, Horie M
- Journal Title
  
  J Arrhythmia
  
  Volume: in press Issue: 3 Pages: 161-166
- DOI
  10.1016/j.joa.2013.08.004
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25460287
[Journal Article] 遺伝性不整脈の遺伝子診断の歴史.2014
- Author(s)
  蒔田直昌.
- Journal Title
  
  呼吸と循環.
  
  Volume: 62 Pages: 827-831
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] 重症不整脈 electrical storm : 基礎研究からのアプローチ.2014
- Author(s)
  辻幸臣, 蒔田直昌.
- Journal Title
  
  長崎市医師会報
  
  Volume: 48 Pages: 7-11
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] 重症不整脈 electrical storm : 基礎研究からのアプローチ.2014
- Author(s)
  辻幸臣, 蒔田直昌.
- Journal Title
  
  長崎市医師会報
  
  Volume: 48 Pages: 7-11
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] Right bundle branch block without overt heart disease predicts higher risk of pacemaker implantation: the study of atomic-bomb survivors.2014
- Author(s)
  Kusumoto S, Kawano H, Makita N, Ichimaru S, Kaku T, Haruta D, Hida A, Sera N, Imaizumi M, Nakashima E, Maemura K, Akahoshi M.
- Journal Title
  
  Int J Cardiol.
  
  Volume: 174 Issue: 1 Pages: 77-82
- DOI
  10.1016/j.ijcard.2014.03.152
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25461113
[Journal Article] Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction2014
- Author(s)
  Ohno S, Omura M, Kawamura M, Kimura H, Itoh H, Makiyama T, Ushinohama H, Makita N, Horie M
- Journal Title
  
  Europace
  
  Volume: in press Issue: 11 Pages: 1646-1654
- DOI
  10.1093/europace/eut382
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136705, KAKENHI-PROJECT-25460406
[Journal Article] 遺伝性不整脈の遺伝子診断の歴史.2014
- Author(s)
  蒔田直昌.
- Journal Title
  
  呼吸と循環.
  
  Volume: 62 Pages: 827-831
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Molecular mechanisms of heart failure progression associated with implantable cardioverter-defibrillator shocks for ventricular tachyarrhythmias.2014
- Author(s)
  Tsuji Y, Ishikawa T, Makita N.
- Journal Title
  
  J Arrhythmia.
  
  Volume: 30 Issue: 4 Pages: 235-241
- DOI
  10.1016/j.joa.2014.04.003
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-26461074, KAKENHI-PROJECT-26860572
[Journal Article] Efficacy of bepridil to prevent ventricular fibrillation in severe form of early repolarization syndrome2014
- Author(s)
  Katsuumi G, Shimizu W, Watanabe H, Noda T, Nogami A, Ohkubo K, Makiyama T, Takehara N, Kawamura Y, Hosaka Y, Sato M, Fukae S, Chinushi M, Oda H, Okabe M, Kimura A, Maemura K, Watanabe I, Kamakura S, Horie M, Aizawa Y, Makita N, Minamino T
- Journal Title
  
  Int J Cardiol
  
  Volume: 172 Issue: 2 Pages: 519-522
- DOI
  10.1016/j.ijcard.2014.01.036
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390195, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591038, KAKENHI-PUBLICLY-25126706, KAKENHI-PROJECT-25461113, KAKENHI-PROJECT-25670382, KAKENHI-PLANNED-26115008
[Journal Article] Normal dose of pilsicainide showed marked negative inotropic effects in a patient who had no underlying heart disease.2014
- Author(s)
  Yoshida M, Ando S, Chishaki A, Makita N, Hasegawa Y, Narita S, Momii H, Kadokami T.
- Journal Title
  
  J Arrhythmia.
  
  Volume: 30 Pages: 68-70
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Novel calmodulin mutations associated with congenital arrhythmia susceptibility.2014
- Author(s)
  Makita N, Tsuji Y（39人中21番目）et al
- Journal Title
  
  Circ Cardiovasc Genet.
  
  Volume: 7 Issue: 4 Pages: 466-474
- DOI
  10.1161/circgenetics.113.000459
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591038, KAKENHI-PROJECT-24591086, KAKENHI-PUBLICLY-25110720, KAKENHI-PROJECT-25293181, KAKENHI-PROJECT-25670172, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-221S0002
[Journal Article] Normal dose of pilsicainide showed marked negative inotropic effects in a patient who had no underlying heart disease.2014
- Author(s)
  Yoshida M, Ando S, Chishaki A, Makita N, Hasegawa Y, Narita S, Momii H, Kadokami T.
- Journal Title
  
  Journal of Arrhythmia
  
  Volume: 30 Pages: 68-70
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] Sodium channelopathy underlying familial sick sinus syndrome with early onset and predominantly male characteristics.2014
- Author(s)
  Abe K, Machida T, Sumitomo N, Yamamoto H, Ohkubo K, Watanabe I, Makiyama T, Fukae S, Kohno M, Harrell DT, Ishikawa T, Tsuji Y, Nogami A, Watabe T, Oginosawa Y, Abe H, Maemura K, Motomura H, Makita N.
- Journal Title
  
  Circ Arrhythm Electrophysiol
  
  Volume: in press Issue: 3 Pages: 511-517
- DOI
  10.1161/circep.113.001340
- NAID
  120006986434
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25461054, KAKENHI-PROJECT-25461113, KAKENHI-PROJECT-26860572
[Journal Article] Variable expressivity of phenotype in a frameshift mutation of cardiac sodium channel SCN5A.2013
- Author(s)
  Kawakami H Makita N, et al
- Journal Title
  
  J. Arrhythmia
  
  Volume: (In press) Issue: 5 Pages: 291-295
- DOI
  10.1016/j.joa.2013.04.005
- Year and Date
  2013-05-24
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] Paradigm shifts in the genetics of inherited arrhythmias: Using next-generation sequencing technologies to uncover hidden etiologies2013
- Author(s)
  Makita N
- Journal Title
  
  J Arrhythmia
  
  Volume: 29 Issue: 6 Pages: 305-307
- DOI
  10.1016/j.joa.2013.09.001
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199
[Journal Article] 【イオンチャネル病のすべて】　進行性心臓伝導障害.2013
- Author(s)
  蒔田直昌
- Journal Title
  
  医学のあゆみ
  
  Volume: 245 Pages: 802-809
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] SCN5A mutation associated with ventricular fibrillation, early repolarization, and concealed myocardial abnormalities2013
- Author(s)
  Watanabe H, Ohkubo K, Watanabe I, Matsuyama TA, Ishibashi-Ueda H, Yagihara N, Shimizu W, Horie M, Minamino T, Makita N
- Journal Title
  
  Int J Cardiol.
  
  Volume: 165 Issue: 2 Pages: e21-e23
- DOI
  10.1016/j.ijcard.2012.10.074
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390195, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591038, KAKENHI-PUBLICLY-25126706, KAKENHI-PROJECT-25670382
[Journal Article] Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.2013
- Author(s)
  Bezzina CR, Makita N(63人中31番目)et al
- Journal Title
  
  Nat Genet.
  
  Volume: 45 Issue: 9 Pages: 1044-1049
- DOI
  10.1038/ng.2712
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24390195, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591038, KAKENHI-PROJECT-24591086, KAKENHI-PUBLICLY-25126706, KAKENHI-PUBLICLY-25136727, KAKENHI-PROJECT-25670382
[Journal Article] 進行性心臓伝導障害の基礎と臨床2013
- Author(s)
  蒔田直昌
- Journal Title
  
  心電図
  
  Volume: 33 (S3) Pages: 34-42
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] Novel SCN3B Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.52013
- Author(s)
  Ishikawa T, Makita N, et al
- Journal Title
  
  Circ J
  
  Volume: 77 Pages: 959-67
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] 致死性不整脈診療の最前線】致死性不整脈診療　遺伝性心臓伝導障害2013
- Author(s)
  蒔田直昌
- Journal Title
  
  最新医学
  
  Volume: 68 Pages: 1588-1596
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Variable phenotype expression with a frameshift mutation of the cardiac sodium channel gene SCN5A.2013
- Author(s)
  Kawakami H, Aiba T, Yamada T, Okayama H, Kazatani Y, Konishi K, Nakajima I, Miyamoto K, Yamada Y, Okamura H, Noda T, Satomi K, Kamakura S, Makita N, Shimizu W.
- Journal Title
  
  J Arrhythmia
  
  Volume: 29 Pages: 291-295
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] A nonsynonymous polymorphism in semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillation2013
- Author(s)
  Nakano Y, Makita N, (32人中31番目) et al
- Journal Title
  
  PLOS Genet
  
  Volume: 9 Issue: 4 Pages: e1003364-e1003364
- DOI
  10.1371/journal.pgen.1003364
- NAID
  120006985866
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591086, KAKENHI-PROJECT-24591575, KAKENHI-PUBLICLY-25136727, KAKENHI-PROJECT-25640066, KAKENHI-PROJECT-25670369
[Journal Article] Variable expressivity of phenotype in a frameshift mutation of cardiac sodium channel SCN5A.2013
- Author(s)
  Kawakami H Makita N, et al
- Journal Title
  
  J. Arrhythmia
  
  Volume: -
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] 【致死性不整脈診療の最前線】致死性不整脈診療　遺伝性心臓伝導障害2013
- Author(s)
  蒔田直昌
- Journal Title
  
  最新医学.
  
  Volume: 68 Pages: 1588-1596
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] Successful control of life-threatening polymorphic ventricular tachycardia by radiofrequency catheter ablation in an infant2013
- Author(s)
  Abe Y, Sumitomo N, Okuma H, Nakamura T, Fukuhara J, Ichikawa R, Matsumura M, Miyashita M, Kamiyama H, Ayusawa M, Watanabe M, Joo K, Makita N, Horie M
- Journal Title
  
  Heart Vessels
  
  Volume: 29 Issue: 3 Pages: 1-5
- DOI
  10.1007/s00380-013-0390-6
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199
[Journal Article] Novel SCN3B Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.52013
- Author(s)
 Ishikawa T
- Journal Title
 
 Circ J
 
 Volume: 77 Issue: 4 Pages: 959-967
- DOI
 10.1253/circj.CJ-12-0995
- NAID
 10031138998
- ISSN
 1346-9843, 1347-4820
- Language
 English
- Peer Reviewed
- Data Source
 KAKENHI-PROJECT-22390157, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-23659414, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591575
[Journal Article] 進行性心臓伝導障害の基礎と臨床2013
- Author(s)
  蒔田直昌
- Journal Title
  
  心電図
  
  Volume: 33(S3) Pages: 34-42
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] 難治性不整脈の遺伝子解析2013
- Author(s)
  蒔田直昌
- Journal Title
  
  循環器専門医
  
  Volume: 21 Pages: 3-8
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] A nonsynonymous polymorphism in Semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillation.2013
- Author(s)
  Nakano Y, Makita N, et al
- Journal Title
  
  PLOS Genet
  
  Volume: -
- NAID
  120006985866
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Editorial: 不整脈の病因研究におけるパラダイムシフト2013
- Author(s)
  蒔田直昌
- Journal Title
  
  心電図
  
  Volume: 33 Pages: 1-2
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Editorial: 不整脈の病因研究におけるパラダイムシフト2013
- Author(s)
  蒔田直昌
- Journal Title
  
  心電図
  
  Volume: 33 Pages: 1-2
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] 難治性不整脈の遺伝子解析2013
- Author(s)
  蒔田直昌
- Journal Title
  
  循環器専門医
  
  Volume: 21 Pages: 3-8
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Variable phenotype expression with a frameshift mutation of the cardiac sodium channel gene SCN5A.2013
- Author(s)
  Kawakami H, Aiba T, Yamada T, Okayama H, Kazatani Y, Konishi K, Nakajima I, Miyamoto K, Yamada Y, Okamura H, Noda T, Satomi K, Kamakura S, Makita N, Shimizu W.
- Journal Title
  
  J Arrhythmia
  
  Volume: 29 Pages: 291-295
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] 【イオンチャネル病のすべて】　進行性心臓伝導障害2013
- Author(s)
  蒔田直昌
- Journal Title
  
  医学のあゆみ
  
  Volume: 245 Pages: 802-809
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.52013
- Author(s)
  Ishikawa T, Takahashi N, Ohno S, Sakurada H, Nakamura K, On YK, Park JE, Makiyama T, Horie M, Arimura T, Makita N, Kimura A
- Journal Title
  
  Circ J
  
  Volume: 77 Pages: 959-967
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.2013
- Author(s)
  Ishikawa T, Takahashi N, Ohno S, Sakurada H, Nakamura K, On YK, Park JE, Makiyama T, Horie M, Arimura T, Makita N, Kimura A.
- Journal Title
  
  Circ J
  
  Volume: 77 Pages: 959-967
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] Response to Letter Regarding Article," Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization"2012
- Author(s)
  Watanabe H, Makita N, et al
- Journal Title
  
  Circ Arrhythm Electrophysiol
  
  Volume: 5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Electrocardiographic abnormalities and risk of complete atrioventricular block2012
- Author(s)
  Watanabe H, Makita N, et al
- Journal Title
  
  Int J Cardiol
  
  Volume: 155 Issue: 3 Pages: 462-464
- DOI
  10.1016/j.ijcard.2011.12.028
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-22790696, KAKENHI-PROJECT-24591038
[Journal Article] Clinical characteristics and risk of arrhythmia recurrences in patients with idiopathic ventricular fibrillation associated with early repolarization.2012
- Author(s)
  Watanabe H
- Journal Title
  
  Int J Cardiol.
  
  Volume: 159 Issue: 3 Pages: 238-40
- DOI
  10.1016/j.ijcard.2012.05.091
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-23591031, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591038, KAKENHI-PLANNED-22136007, KAKENHI-PLANNED-22136011
[Journal Article] ブルガタ症候群2012
- Author(s)
  蒔田　直昌
- Journal Title
  
  内科
  
  Volume: 109 Pages: 1020-1022
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] イオンチャネル研究の最先端家族性進行性心臓伝導障害(PCCD)の臨床像と分子病態2012
- Author(s)
  蒔田　直昌
- Journal Title
  
  血管
  
  Volume: 35 Pages: 25-25
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] A Connexin 40 Mutation Associated with a Malignant Variant of Progressive Familial Heart Block Type-12012
- Author(s)
  Makita N, Seki A, Sumitomo N, et al
- Journal Title
  
  Circ Arrhythm Electrophysiol
  
  Volume: 5 Pages: 163-172
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Cardiac connexins, mutations and arrhythmias.2012
- Author(s)
  Delmar M, Makita N.
- Journal Title
  
  Curr Opin Cardiol.
  
  Volume: 27 Issue: 3 Pages: 236-241
- DOI
  10.1097/hco.0b013e328352220e
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390199, KAKENHI-PLANNED-22136007
[Journal Article] Cardiac connexins, mutations and arrhythmias2012
- Author(s)
  Delmar M, Makita N
- Journal Title
  
  Curr Opin Cardiol
  
  Volume: (in press) Issue: 1 Pages: 163-172
- DOI
  10.1161/circep.111.967604
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921, KAKENHI-PLANNED-22113009, KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-22390040, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-23591091, KAKENHI-PROJECT-24591038
[Journal Article] 早期再分極とJ波症候群：オーバービュー2012
- Author(s)
  蒔田　直昌
- Journal Title
  
  心臓
  
  Volume: 44 Pages: 1226-1231
- NAID
  130003396400
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Disease characterization using LQTS-specific induced pluripotent stem cells.2012
- Author(s)
  Egashira T, Yuasa S, Suzuki T, Tohyama S, et al.
- Journal Title
  
  Cardiovasc. Res.
  
  Volume: 95 Issue: 4 Pages: 419-29
- DOI
  10.1093/cvr/cvs206
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-11J05269, KAKENHI-PROJECT-11J30002, KAKENHI-PROJECT-22590779, KAKENHI-PROJECT-22590813, KAKENHI-PROJECT-22689027, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-23590297, KAKENHI-PROJECT-23790873, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591086, KAKENHI-PLANNED-22136007, KAKENHI-PUBLICLY-23136503, KAKENHI-PUBLICLY-24117716
[Journal Article] Electrocardiographic abnormalities and risk of complete atrioventricular block2012
- Author(s)
  Watanabe H, Makita N, et al
- Journal Title
  
  Int J Cardiol
  
  Volume: 155 Pages: 462-464
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 早期再分極とJ波症候群:オーバービュー2012
- Author(s)
  蒔田直昌
- Journal Title
  
  心臓
  
  Volume: 44 Pages: 1226-1231
- NAID
  130003396400
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] 遺伝子とチャネルからみた先天性QT延長症候群2012
- Author(s)
  蒔田直昌
- Journal Title
  
  不整脈学
  
  Pages: 491-495
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] ブルガタ症候群2012
- Author(s)
  蒔田直昌
- Journal Title
  
  内科
  
  Volume: 109 Pages: 1020-1022
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] 器質的心疾患を伴わない致死性不整脈の診断と治療2012
- Author(s)
  蒔田　直昌
- Journal Title
  
  日本集中治療医学会雑誌
  
  Volume: 19 Pages: 163-163
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Response to Letter Regarding Article, "Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization"2012
- Author(s)
  Watanabe H, Makita N, et al
- Journal Title
  
  Circulation : Arrhythmia and Electrophysiology
  
  Volume: 5 Issue: 2
- DOI
  10.1161/circep.112.971507
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390199, KAKENHI-PLANNED-22136007
[Journal Article] Cardiac connexins, mutations and arrhythmias2012
- Author(s)
  Delmar M, Makita N.
- Journal Title
  
  Curr Opin Cardiol
  
  Pages: 236-241
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 遺伝子とチャネルからみた先天性QT延長症候群2012
- Author(s)
  蒔田　直昌
- Journal Title
  
  不整脈学
  
  Volume: - Pages: 491-495
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] イオンチャネル研究の最先端家族性進行性心臓伝導障害(PCCD)の臨床像と分子病態2012
- Author(s)
  蒔田直昌
- Journal Title
  
  血管
  
  Volume: 35 Pages: 25-25
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] 特発性心室細動とJ波症候群の遺伝子診断2012
- Author(s)
  蒔田直昌
- Journal Title
  
  CIRCULATION Up-to-Date
  
  Volume: 7 Pages: 20-25
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] A novel 5' splice site mutation of SCN5A associated with Brugada syndrome resulting in multiple cryptic transcripts2012
- Author(s)
  Shimada T, Makita N, et al
- Journal Title
  
  Int J Cardiol
  
  Volume: 158 Issue: 3 Pages: 441-3
- DOI
  10.1016/j.ijcard.2012.04.114
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390199, KAKENHI-PLANNED-22136007
[Journal Article] 器質的心疾患を伴わない致死性不整脈の診断と治療2012
- Author(s)
  蒔田直昌
- Journal Title
  
  日本集中治療医学会雑誌
  
  Volume: 19 Pages: 163-163
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] Similarities and differences in genetic and clinical characteristics between early repolarization syndrome and Brugada syndrome2012
- Author(s)
  Watanabe H, Makita N, et al
- Journal Title
  
  Circ Arrhythm Electrophysiol
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] 特発性心室細動とJ波症候群の遺伝子診断2012
- Author(s)
  蒔田直昌
- Journal Title
  
  CIRCULATION Up-to-Date
  
  Volume: 7 Pages: 20-25
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.52012
- Author(s)
  Ishikawa T
- Journal Title
  
  Circ Arrhythm Electrophysiol
  
  Volume: 5 Issue: 6 Pages: 1098-1107
- DOI
  10.1161/circep.111.969972
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22390157, KAKENHI-PROJECT-23591031, KAKENHI-PROJECT-23659414, KAKENHI-PROJECT-24390199, KAKENHI-PLANNED-22136007
[Journal Article] Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated with Early Repolarization2011
- Author(s)
  Watanabe H, Nogami A, Ohkubo K, Kawata H, Hayashi Y, Ishikawa T, Makiyama T, Nagao S, Yagihara N, Takehara N, Kawamura Y, Sato A, Okamura K, Hosaka Y, Sato M, Fukae S, Chinushi M, Oda H, Okabe M, Kimura A, Maemura K, Watanabe I, Kamakura S, Horie M, Aizawa Y, Shimizu W, Makita N
- Journal Title
  
  Circ Arrhythm Electrophysiol
  
  Volume: 4 Issue: 6 Pages: 874-881
- DOI
  10.1161/circep.111.963983
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390244, KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-22790696, KAKENHI-PUBLICLY-23132507, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-23659414
[Journal Article] 不整脈とイオンチャネル病2011
- Author(s)
  蒔田直昌
- Journal Title
  
  ここまで進んだ不整脈研究の最新動向
  
  Pages: 5-12
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 遺伝性心臓伝導障害の分子基盤2011
- Author(s)
  蒔田直昌
- Journal Title
  
  循環器内科
  
  Volume: 70 Pages: 460-46
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated with Early Repolarization2011
- Author(s)
  Watanabe H, Makita N, et al
- Journal Title
  
  Circ Arrhythm Electrophysiol
  
  Volume: 4 Pages: 874-881
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 後天性QT延長症候群の新しい展開2011
- Author(s)
  蒔田直昌
- Journal Title
  
  不整脈+PLUS
  
  Pages: 3-8
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 致死性不整脈の基礎と臨床-特発性心室細動-2011
- Author(s)
  蒔田直昌
- Journal Title
  
  臨床と研究
  
  Volume: 88 Pages: 127-129
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 不整脈とイオンチャネル病2011
- Author(s)
  蒔田直昌
- Journal Title
  
  別冊・医学のあゆみ
  
  Pages: 5-12
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] 不整脈とイオンチャネル病2011
- Author(s)
  蒔田直昌
- Journal Title
  
  別冊・医学のあゆみ
  
  Volume: 7 Pages: 5-12
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 不整脈とイオンチャネル病2011
- Author(s)
  蒔田直昌
- Journal Title
  
  ここまで進んだ不整脈研究の最新動向
  
  Pages: 5-12
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] 後天性QT延長症候群の新しい展開2011
- Author(s)
  蒔田直昌
- Journal Title
  
  不整脈+PLUS
  
  Pages: 3-8
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] 後天性QT延長症候群の新しい展開2011
- Author(s)
  蒔田直昌
- Journal Title
  
  不整脈+ PLUS
  
  Pages: 3-8
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 致死性不整脈の基礎と臨床-特発性心室細動-2011
- Author(s)
  蒔田直昌
- Journal Title
  
  臨床と研究
  
  Volume: 88 Pages: 127-129
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] カルシウム拮抗薬不整脈における使い方2011
- Author(s)
  蒔田直昌
- Journal Title
  
  Heart View
  
  Volume: 14 Pages: 111-115
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 遺伝性心臓伝導障害の分子基盤2010
- Author(s)
  蒔田直昌
- Journal Title
  
  循環器内科
  
  Volume: 70 Pages: 460-46
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 不整脈とイオンチャネル病2010
- Author(s)
  蒔田直昌
- Journal Title
  
  医学のあゆみ
  
  Volume: 216 Pages: 619-626
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 不整脈とイオンチャネル病2010
- Author(s)
  蒔田直昌
- Journal Title
  
  医学のあゆみ
  
  Volume: 216 Pages: 619-626
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] カルシウム拮抗薬不整脈における使い方2010
- Author(s)
  蒔田直昌
- Journal Title
  
  Heart View
  
  Volume: 14 Pages: 111-115
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] カルシウム拮抗薬不整脈における使い方2010
- Author(s)
  蒔田直昌
- Journal Title
  
  Heart View
  
  Volume: 14 Pages: 111-115
- Data Source
  KAKENHI-PLANNED-22136007
[Journal Article] 心電学マイルストーン2009
- Author(s)
  蒔田直昌
- Journal Title
  
  日本心電学会誌 29
  
  Pages: 355-355
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Phenotypic Overlap of Cardiac Sodium Channelopathies : Individual-specific or mutation-specific?2009
- Author(s)
  Makita N.
- Journal Title
  
  Circ J 73
  
  Pages: 810-7
- NAID
  10025929978
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article]2009
- Author(s)
  蒔田直昌
- Journal Title
  
  心電学マイルストーン日本心電学会誌
  
  Volume: 29 Pages: 355-355
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 難治性不整脈の遺伝子検査2009
- Author(s)
  蒔田直昌
- Journal Title
  
  Heart View 13
  
  Pages: 32-8
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Long-term Prognosis of Probands with Brugada-pattern ST-elevation in leads V1-V3. Circ Arrhythm2009
- Author(s)
  Kamakura S, Makita N, et al
- Journal Title
  
  Electrophysiol
  
  Volume: 2 Pages: 495-503
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Aborted Sudden Cardiac Death Associated with Short QT Syndrome2009
- Author(s)
  Okishige K, Makita N, et al
- Journal Title
  
  J Arrh
  
  Volume: 25 Pages: 214-218
- NAID
  10027081082
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Aborted sudden cardiac death associated with short QT syndrome.2009
- Author(s)
  Okishige K, Makita N, et al
- Journal Title
  
  J Arrhythmia 25
  
  Pages: 214-8
- NAID
  10027081082
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] 難治性不整脈の遺伝子検査2009
- Author(s)
  蒔田直昌
- Journal Title
  
  Heart View
  
  Volume: 13 Pages: 32-8
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article]2009
- Author(s)
  蒔田直昌
- Journal Title
  
  失神を究める(Medical View)
  
  Pages: 215-224
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Novel mechanisms of trafficking defect caused by KCNQ1 mutations found in long QT syndrome2009
- Author(s)
  Sato A, Makita N, et al
- Journal Title
  
  J Biol Chem
  
  Volume: 284 Pages: 122-133
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article]2009
- Author(s)
  蒔田直昌
- Journal Title
  
  Brugada症候群(Medical View)
  
  Pages: 224-233
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Novel mechanisms of trafficking defect caused by KCNQ1 mutations found in long QT syndrome.2009
- Author(s)
  Sato A, Makita N, et al
- Journal Title
  
  J Biol Chem 284
  
  Pages: 122-33
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Phenotypic Overlap of Cardiac Sodium Channelopathies : Individual-specific or mutation-specific2009
- Author(s)
  Makita N
- Journal Title
  
  Circ J
  
  Volume: 73 Pages: 810-817
- NAID
  10025929978
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article]2009
- Author(s)
  蒔田直昌
- Journal Title
  
  心臓突然死(最新医学社)
  
  Pages: 180-189
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Long-term Prognosis of Probands with Brugada-pattern ST-elevation in leads V1-V3.2009
- Author(s)
  Kamakura S, Makita N, et al
- Journal Title
  
  Circ Arrhythm Electrophysiol 2
  
  Pages: 495-503
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] SCN5A variants in Japanese patients with left ventricular noncomp action and arrhythmia.2008
- Author(s)
  Shan L, Makita N , et. al.
- Journal Title
  
  Mol Genet Metab 93
  
  Pages: 468-474
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Single common mutation in the cardiac sodium channel gene SCN5A with diverse clinical phenotypes2008
- Author(s)
  Makita N , et. al.
- Journal Title
  
  J Clin Invest (印刷中)
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] The E1784K mutation SCN5A is associated with mixed phenotype of type 3 long QT syndrome2008
- Author(s)
  Makita N, et. al.
- Journal Title
  
  J Clin Invest (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Absence of a trafficking defect in R1232W/T1620M, a double SCN5A mutant re soonsible for Brugada syndrome2008
- Author(s)
  Makita N. et.al.
- Journal Title
  
  Circ J 72
  
  Pages: 1018-1019
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-20117004
[Journal Article] The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome2008
- Author(s)
  Makita N. et.al.
- Journal Title
  
  J Clin Inves 118
  
  Pages: 2219-2229
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-20117004
[Journal Article] The E1784K mutation in SCN5Ais associated with mixed clinical phenotype oftype 3 long QT syndrome2008
- Author(s)
  Makita N, Behr E, Shimizu W, Horie M, Sunami A, Crotti L, Schulze-Bahr E, Fukuhara, S, Mochizuki N, akiyama T, Itoh H, Christiansen M, McKeown P, Miyamoto K, Kamakura S, Tsutsui H, Schwartz PJ, George AL Jr, Roden DM
- Journal Title
  
  J Ctin Invest
  
  Volume: 118(6) Pages: 2219-2229
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-20117004
[Journal Article] SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmia.2008
- Author(s)
  Shan L, Makita N, et. al.
- Journal Title
  
  Mol Genet Metab 93
  
  Pages: 468-474
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Absence of a Trafficking Defect in R1232W/T1620M, a Double SCN5A Mutant Responsible For Brugada Syndrome2008
- Author(s)
  Makita N, Mochizuki N , et. al.
- Journal Title
  
  Circ J (印刷中)
- NAID
  110006783843
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmia2008
- Author(s)
  Shan L, Makita N , et. al.
- Journal Title
  
  Mol Genet Metab 93
  
  Pages: 468-474
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Absence of a Trafficking Defect in R1232W/T1620M, a Double SCN5A Mutant Responsible For Brugada Syndrome2008
- Author(s)
  Makita N, Mochizuki N, et. al.
- Journal Title
  
  Circ J (印刷中)
- NAID
  110006783843
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Brugada症候群の病因と発生機序2007
- Author(s)
  蒔田直昌, ら
- Journal Title
  
  心臓 39
  
  Pages: 4-9
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Genetic polymorphisms and arrhythmia susceptibility2007
- Author(s)
  Makita N, et. al.
- Journal Title
  
  Circ J 71
- NAID
  110006318434
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Genetic polymorphisms and arrhythmia susceptibility2007
- Author(s)
  Makita N , et. al.
- Journal Title
  
  Circ J 71
- NAID
  110006318434
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Novel SCN5A mutation (Q55X) associated with age-dependent expression of Brugada syndrome presenting as neurally mediated syncope2007
- Author(s)
  Makita N, et al.
- Journal Title
  
  Heart Rhythm (In press)
- NAID
  120000965174
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Brugada症候群の遺伝子変異と多型2007
- Author(s)
  佐々木孝治, 蒔田直昌, ら
- Journal Title
  
  Heart View 11
  
  Pages: 49-53
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Genetic polymorphisms and arrhythmia susceptibility2007
- Author(s)
  Makita N, Tsutsui H.
- Journal Title
  
  Circ J 71
- NAID
  110006318434
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Novel SCN5A mutation (Q55X) associated with age-dependent expression of Brugada syndrome presenting as neurally mediated syncope2007
- Author(s)
  Makita N, et. al.
- Journal Title
  
  Heart Rhythm 4
  
  Pages: 516-519
- NAID
  120000965174
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Novel SCN5A mutation (Q55X) associated with age-dependent expression of Brugada syndrome presenting as neurally mediated syncope.2007
- Author(s)
  Makita N , et. al.
- Journal Title
  
  Heart Rhythm 4
  
  Pages: 516-519
- NAID
  120000965174
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] 失神に関する遺伝子異常の最近の話題2006
- Author(s)
  蒔田直昌, ら
- Journal Title
  
  Heart View 10
  
  Pages: 72-76
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] 心臓突然死の分子遺伝学基盤2006
- Author(s)
  蒔田直昌, ら
- Journal Title
  
  心電図 26
  
  Pages: 118-124
- NAID
  10017545469
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Brugada症候群とその類縁疾患における遺伝子異常2006
- Author(s)
  蒔田直昌, ら
- Journal Title
  
  心電図 26・S4
  
  Pages: 5-9
- NAID
  130004245426
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] 心筋Naチャネル病2006
- Author(s)
  蒔田直昌, ら
- Journal Title
  
  医学の歩み 217
  
  Pages: 653-656
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] 不整脈の遺伝子診断2006
- Author(s)
  蒔田直昌, ら
- Journal Title
  
  Heart View 10
  
  Pages: 556-559
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] 臨床遺伝子学'06 循環器系疾患の遺伝子学2006
- Author(s)
  蒔田直昌, ら
- Journal Title
  
  最新医学 20
  
  Pages: 1883-1894
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] 薬物によるQT延長の遺伝的要因を含めた患者要因2006
- Author(s)
  蒔田直昌
- Journal Title
  
  臨床薬理 37
  
  Pages: 215-219
- NAID
  10018228106
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] 薬剤性QTL延長症候群と遺伝子変異2005
- Author(s)
  蒔田直昌
- Journal Title
  
  心電図 25
  
  Pages: 105-109
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] Double SCN5A mutation underlying asymptomatic Brugada syndrome.2005
- Author(s)
  Yokoi H, Makita N, Sasaki K, Takagi Y, Okumura Y, Nishino T, Makiyama T, Kitabatake A, Horie M, Watanabe I, Tsutsui H.
- Journal Title
  
  Heart Rhythm 2
  
  Pages: 285-292
- NAID
  120000961095
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] Intrinsic mechanism of the enhanced rate-dependent QT shortening in R1623Q mutant of the LQT3 syndrome.2005
- Author(s)
  Oginosawa Y, Nagatomo T, Abe H, Makita N, Makielski JC, Nakashima Y
- Journal Title
  
  Cardiovasc Res 65
  
  Pages: 138-147
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] 薬剤性QT延長症候群と遺伝子変異2005
- Author(s)
  蒔田直昌
- Journal Title
  
  心電図 25
  
  Pages: 105-109
- NAID
  10014429777
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] Unexpected mexiletine responses of a mutant cardiac Na^+ channel implicate the selectivity filter as a structural determinant of antiarrhythmic drug access.2004
- Author(s)
  Sasaki K, Makita N, Sunami A, Sakurada H, Shirai N, Yokoi H, Kimura A, Tohse N, Hiraoka M, Kitabatake A.
- Journal Title
  
  Mol Pharmacol 66
  
  Pages: 330-336
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] 致死性不整脈の最近の話題2004
- Author(s)
  蒔田直昌
- Journal Title
  
  札幌市内科医会会報 11
  
  Pages: 8-9
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] State-dependent blocking actions of azimilide dihydrochloride (NE-10064) on human cardiac Na^+ channels.2004
- Author(s)
  Miake J, Kurata Y, Iizuka K, Furuichi H, Manabe K, Sasaki N, Yamamoto Y, Hoshikawa Y, Taniguchi S, Yoshida A, Igawa O, Makita N, Shiota G, Nanba E, Ohgi S, Narahashi T, Hisatome I.
- Journal Title
  
  Circ J. 68
  
  Pages: 703-711
- NAID
  110002692181
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] Brugada症候群の基礎2004
- Author(s)
  佐々木孝治, 横井久卓, 蒔田直昌
- Journal Title
  
  循環器科 55
  
  Pages: 333-338
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] A cardiac sodium channel mutation identified in Brugada syndrome associated with at rial standstill.2004
- Author(s)
  Takehara N, Makita N, Kawabe J, Sato N, Kawamura Y, Kitabatake A, Kikuchi K
- Journal Title
  
  J Int Med 255
  
  Pages: 137-142
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] ここまでわかったBrugada症候群2004
- Author(s)
  佐々木孝治, 蒔田直昌
- Journal Title
  
  内科 94
  
  Pages: 735-738
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline2004
- Author(s)
  Kamiya K, Kaneda M, Sugawara T, Mazaki E, Okamura N, Mental M, Makita N, Tanaka M, Fukushima K, Fujiwara T, Inoue Y, Yamakawa K.
- Journal Title
  
  J Neurosci 24
  
  Pages: 2690-2698
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] 心室性不整脈の分子背景-Brugada症候群2004
- Author(s)
  蒔田直昌
- Journal Title
  
  Molecular Medicine 41
  
  Pages: 845-850
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] Cold induces shifts of voltage-dependence in a mutant SCN4A causing hypokalemic periodic paralysis.2003
- Author(s)
  Sugiura Y, Makita N, Li L, Noble P.J, Kimura J, Kumagai Y, Soeda T, Yamamoto T.
- Journal Title
  
  Neurology 61
  
  Pages: 914-918
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] 遺伝子異常による不整脈の現況2003
- Author(s)
  蒔田直昌
- Journal Title
  
  診断と治療 91
  
  Pages: 1917-1921
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] 心筋Na^+チャネル病の分子病態2003
- Author(s)
  蒔田直昌
- Journal Title
  
  臨床と研究 80
  
  Pages: 939-942
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article] Induction of Tissue Factor Expression in Endothelial Cells by Basic Fibroblast Growth Factor and its Modulation by Fenofibric acid.2003
- Author(s)
  Kaneko T, Fujii S, Matsumoto A, Goto D, Makita N, Hamada J, Moriuchi T, Kitabatake A.
- Journal Title
  
  Thromb J. 1
  
  Pages: 6-6
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590711
[Journal Article]
- Author(s)
  蒔田直昌
- Journal Title
  
  Brugada症候群(中山書店)
  
  Pages: 143-147
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] A nonsynonymous polymorphism in Semaphorin 3A as a risk factor forhuman unexplained cardiac arrest with documented ventricular fibrillation.
- Author(s)
  Nakano Y, Makita N, et al
- Journal Title
  
  PLOS Genet
  
  Volume: (In press)
- NAID
  120006985866
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390199
[Journal Article] Absence of a trafficking defect in R1232W/ T1620M, a double SCN5A mutant responsible for Brugada syndrome.
- Author(s)
  Makita N, Mochizuki N , et. al.
- Journal Title
  
  Circ J (In press)
- NAID
  110006783843
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Journal Article] Similarities and differences in genetic and clinical characteristics between early repolarization syndrome and Brugada syndrome
- Author(s)
  Watanabe H, Makita N, et al
- Journal Title
  
  Circ Arrhythm Electrophysiol
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590921
[Journal Article] Single common mutation in the cardiac sodium channel gene SCN5A with diverse clinical phenotypes
- Author(s)
  Makita N, Mochizuki N , et. al.
- Journal Title
  
  J Clin Invest (In press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] Pupulation-specific and cross-ancestry genome-wide association study indentifies shared gemetic architecture and 6 new risk loci including CAMK2D associated with Brugada syndrome2023
- Author(s)
  Naomasa Makita et al.
- Organizer
  European Society of Cardiology Congress 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02920
[Presentation] Non-coding Deletion Induces 3D Chromatin Remodelling And Pitx2 Expression Dysregulation Associated With A Syndromic Cardiac Disorder2022
- Author(s)
  Baudic, M. Makita, N et al
- Organizer
  Heart Rhythm Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02920
[Presentation] Development of an Oligonucleotide-Based Therapeutic Approach for Calmodulinopathy2021
- Author(s)
  Makiyama T, Yamamoto Y, Kondoh Y, Gao J, Kashiwa A, Aizawa T, Imamura T, Huang H, Kohjitani H, Ishikawa T, Yoshida Y, Ohno S, Makita N, Horie M, Kimura T.
- Organizer
  第85回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08416
[Presentation] 網羅的遺伝子解析と不整脈研究の進歩2021
- Author(s)
  蒔田直昌
- Organizer
  第57回日本小児循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-21H02920
[Presentation] Brugada Syndrome Risk Prediction2021
- Author(s)
  Makita N.
- Organizer
  Taiwan Heart Rhythm Society Autumn Forum
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21H02920
[Presentation] ブルガダ症候群の突然死リスクを遺伝的にどう評価するか2021
- Author(s)
  蒔田直昌
- Organizer
  第30回東京循環器小児科治療AGORA
- Invited
- Data Source
  KAKENHI-PROJECT-21H02920
[Presentation] Functionally Validated SCN5A Variants Allow Interpretation of Pathogenicity and Prediction of Lethal Events in Brugada Syndrome2021
- Author(s)
  Makita N.
- Organizer
  第67回日本不整脈心電学会学術大会
- Invited
- Data Source
  KAKENHI-PROJECT-21H02920
[Presentation] ブルガダ症候群の突然死リスクを遺伝的にどう評価するか2021
- Author(s)
  蒔田直昌
- Organizer
  第30回東京循環器小児科治療AGORA
- Invited
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Genetic Analysis of Young-onset Atrial Fibrillation with Family History2021
- Author(s)
  熊埜御堂淳, 大江征嗣, 服部悠一, 伊藤章吾, 堀賢介, 石川泰輔, 蒔田直昌, 福本義弘
- Organizer
  第85回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08416
[Presentation] Development of an Oligonucleotide-Based Therapeutic Approach for Calmodulinopathy2021
- Author(s)
  Makiyama T, Yamamoto Y, Ishikawa T, Makita N, Horie M, Kimura T et al.
- Organizer
  第85回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Modeling Inherited Arrhythmias Associated with Ryanodine Receptor Dysfunction using iPS Cells2021
- Author(s)
  Makiyama T, Gao J, Yamamoto Y, Ishikawa T, Makita N, Kimura T et al.
- Organizer
  第85回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Rare Variant of the Glycerol-3-Phosphate Dehydrogenase-1 Like (GPD1-L) Gene in Japanese Patients with Brugada Syndrome2021
- Author(s)
  Usuda K, Hayashi K, Ishikawa T, Aizawa Y, Kato T, Tsuda T, Kusayama T, Niwa S, Usui S, Sakata K, Kawashiri M, Mishima H, Yoshiura K, Makita N, Takamura M.
- Organizer
  第85回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08416
[Presentation] Functionally Validated SCN5A Variants Allow Interpretation of Pathogenicity and Prediction of Lethal Events in Brugada Syndrome2021
- Author(s)
  Makita N.
- Organizer
  第67回日本不整脈心電学会学術大会
- Invited
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Brugada症候群の突然死リスクを遺伝的にどう評価するか2021
- Author(s)
  蒔田直昌
- Organizer
  第67回日本不整脈心電学会学術大会
- Invited
- Data Source
  KAKENHI-PROJECT-21H02920
[Presentation] Modeling Inherited Arrhythmias Associated with Ryanodine Receptor Dysfunction using iPS Cells2021
- Author(s)
  Makiyama T, Gao J, Yamamoto Y, Ishikawa T, Makita N, Kimura T et al.
- Organizer
  第85回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08416
[Presentation] 網羅的遺伝子解析と不整脈研究の進歩2021
- Author(s)
  蒔田直昌
- Organizer
  第57回日本小児循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Brugada Syndrome Risk Prediction2021
- Author(s)
  Makita N.
- Organizer
  Taiwan Heart Rhythm Society Autumn Forum
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Brugada症候群の突然死リスクを遺伝的にどう評価するか2021
- Author(s)
  蒔田直昌
- Organizer
  第67回日本不整脈心電学会学術大会
- Invited
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Cardiac Emerinopathy, Novel Non-syndromic X-linked Left Ventricular Noncompaction Associated with Progressive Atrial Conduction Disturbance2020
- Author(s)
  Ishikawa T, Mishima H, Barc J, Hirono K, Terada S, Kowase S, Sato T, Yui Y, Mukai Y, Ohkubo K, Kimoto H, Watanabe H, Hata Y, Aiba T, Ohno S, Chishaki A, Shimizu W, Horie M, Ichida F, Nogami A, Yoshiura K, Makita N.
- Organizer
  第84回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08416
[Presentation] Genetic Risks of Sudden Death in Brugada Syndrome2020
- Author(s)
  Makita N.
- Organizer
  第84回日本循環器学会学術集会
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Cardiac Emerinopathy, Novel Non-syndromic X-linked Left Ventricular Noncompaction Associated with Progressive Atrial Conduction Disturbance2020
- Author(s)
  Ishikawa T, Aiba T, Ohno S, Yoshiura K, Makita N et al.
- Organizer
  第84回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] 患者由来iPS 細胞モデルを用いたCav 1.2イオン選択性を障害するCACNA1C-E1115K変異がQT 延長症候群、Brugada 症候群を発症するメカニズムの解析2020
- Author(s)
  柏麻美, 牧山武, 糀谷泰, マウリッセントーマス, ウリヤンハイイミン, 山本雄大, ガオジンシャン, ファンハイ, 今村知彦, 相澤卓範, 石川泰輔, 大野聖子, 豊田太, 佐藤誠一, 高橋一浩, ウォルツェンクヌート, 堀江稔, 蒔田直昌, 木村剛
- Organizer
  第97回日本生理学会大会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] 進行性心臓伝導障害患者の網羅的遺伝子解析とin vitro 機能解析系を用いて明らかになった心臓コネキシン病の分子病態2020
- Author(s)
  石川泰輔, 関明子, 蒔田直昌
- Organizer
  第97回日本生理学会大会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Cardiac Emerinopathy, Novel Non-syndromic X-linked Left Ventricular Noncompaction Associated with Progressive Atrial Conduction Disturbance2020
- Author(s)
  Ishikawa T, Aiba T, Ohno S, Yoshiura K, Makita N et al.
- Organizer
  第84回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Cardiac Emerinopathy, Novel Non-syndromic X-linked Left Ventricular Noncompaction Associated with Progressive Atrial Conduction Disturbance2020
- Author(s)
  Ishikawa T, Aiba T, Ohno S, Yoshiura K, Makita N et al.
- Organizer
  第84回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Genetic Risks of Sudden Death in Brugada Syndrome2020
- Author(s)
  Makita N.
- Organizer
  第84回日本循環器学会学術集会
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Genetic Risks of Sudden Death in Brugada Syndrome2020
- Author(s)
  Makita N.
- Organizer
  第84回日本循環器学会学術集会
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Cardiac Emerinopathy, Novel Non-syndromic X-linked Left Ventricular Noncompaction Associated with Progressive Atrial Conduction Disturbance2020
- Author(s)
  Ishikawa T, Aiba T, Ohno S, Yoshiura K, Makita N et al
- Organizer
  第84回日本循環器学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Inhibition of Late Sodium Current Attenuates Prolonged Action Potential Durations in CACNA1C-E1115K iPS Cell Model with Disrupted Cav1.2 ion Selectivity2020
- Author(s)
  Kashiwa A, Makiyama T, Ishikawa T, Makita N, Kimura T et al.
- Organizer
  The Heart Rhythm Society's Annual Scientific Sessions 2020
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Functional Reappraisal of SCN5A Mutations Reemphasize Their Predictive Value for Lethal Cardiac Events in Brugada Syndrome2019
- Author(s)
  Ishikawa T., Makita N.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Single Cell Electrophysiological Analysis of iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Potential Imaging System2019
- Author(s)
  Yamamoto Y., Makiyama T., Wuriyanghai Y., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Genetic of cardiac conduction disturbance2019
- Author(s)
  Makita N.
- Organizer
  12th Asia Pacific heart Rhythm Society Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Automatic Computational Action Potential Analyzing System Enables Accurate Drug Response Interpretation and Prediction in Human Induced Pluripotent Stem Cell-derived Cardiomyocytes2019
- Author(s)
  Ishikawa T, Makita N.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Modeling Overlapping Phenotypes of Long-QT and Brugada Syndrome with CACNA1C-E1115K that Alters Ion Selectivity of the Cardiac L-Type Calcium Channel Using Induced Pluripotent Stem Cells2019
- Author(s)
  Kashiwa A., Makiyama T., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Modeling Overlap Syndrome of Long QT and Brugada Syndrome Associated with Induced Pluripotent Stem Cells2019
- Author(s)
  Kashiwa A, Makiyama T, Kohjitani H, Wuriyanghai Y, Yamamoto Y, Jungshan G, Huang H, Ishikawa T, Ohno S, Toyoda F, Sato S, Horie M, Makita N, Kimura T.
- Organizer
  The 40th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Single Cell Electrophysiological Analysis of iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Potential Imaging System2019
- Author(s)
  Yamamoto Y., Makiyama T., Wuriyanghai Y., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] 次世代シーケンス解析による特発性心室細動の遺伝背景の解明2019
- Author(s)
  謝颯琴, 高橋篤, 大野聖子, 鎌倉令, 石川泰輔, 植田初江, 斯波真理子, 南野直人, 林研至, 八木原伸江, 中野由紀子, 伊藤英樹, 宮本恵宏, 田中敏博, 蒔田直昌, 堀江稔, 清水渉, 草野研吾, 安田聡, 相庭武司
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Genetic of cardiac conduction disturbance2019
- Author(s)
  Makita N.
- Organizer
  12th Asia Pacific heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Genetics and Clinical Aspects of Congenital Long-QT Syndrome: Results from the Japanese Multicenter Registry2019
- Author(s)
  清水渉, 山形研一郎, 野田崇, 草野研吾, 宮崎文, 牧山武, 伊藤英樹, 大野聖子, 渡部裕, 林研至, 森田宏, 吉永正夫, 福田恵一, 宮本恵宏, 鎌倉史郎, 田中敏博, 住友直方, 萩原誠久, 蒔田直昌, 堀江稔, 相庭武司
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] 発症前診断を行ったQT延長症候群の姉妹2019
- Author(s)
  松下悠紀, 永田弾尺, 小川昌宣, 鹿田佐和子, 石川泰輔, 蒔田直昌
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Genetic of cardiac conduction disturbance2019
- Author(s)
  Makita N.
- Organizer
  12th Asia Pacific heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] KCNQ1 Channel Dysfunction in human induced pluripotent stem cell-derived cardiomyocytes carrying a CALM2-N98S mutation associated with long QT syndrome2019
- Author(s)
  Yamamoto Y, Makiyama T, Ishiakawa T, Makita N, Kimura T et al.
- Organizer
  American Heart Association Scientific Sessions 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] 進行性心臓伝導障害患者の網羅的遺伝子解析とin vitro 機能解析系を用いて明らかになった心臓コネキシン病の分子病態2019
- Author(s)
  石川泰輔, 関明子, 蒔田直昌
- Organizer
  第97回日本生理学会大会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Brugada症候群の予後予測に対する分子生理学的アプローチ2019
- Author(s)
  石川泰輔, 蒔田直昌
- Organizer
  第67回日本心臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Comprehensive Analyses Using Functional Evaluation and Whole-exome Sequencings to Decipher the Genetic predispositions for Sudden Death in Brugada Syndrome2019
- Author(s)
  Makita N., Ishikawa T., Japanese Brugada Exome Consortium Investigators
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Modeling Overlapping Phenotypes of Long-QT and Brugada Syndrome with CACNA1C-E1115K that Alters Ion Selectivity of the Cardiac L-Type Calcium Channel Using Induced Pluripotent Stem Cells2019
- Author(s)
  Kashiwa A, Makiyama T, Kohjitani H, Hirose S, Gao J, Kashiwa A, Huang H, Ishikawa T, Ohno S, Chonabayashi K, Suda K, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Cardiac Emerinopathy, Novel Nonsyndromic Xlinked Left Ventricular Noncompaction Associated With Progressive Atrial Conduction Disturbance2019
- Author(s)
  Ishikawa T., Barc J., Mishima H., Hirono K., Terada S., Kowase S., Sato T., Mukai Y., Yui Y., Ohkubo K., Kimoto H., Hata Y., Aiba T., Ohno S., Chishaki A., Shimizu W., Horie M., Ichida F., Nogami A., Yoshiura K., Schott JJ., Makita N.
- Organizer
  The 40th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Comprehensive Analyses Using Functional Evaluation and Whole-exome Sequencings to Decipher the Genetic predispositions for Sudden Death in Brugada Syndrome2019
- Author(s)
  Makita N., Ishikawa T., Japanese Brugada Exome Consortium Investigators
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] A case report of juvenile onset familial atrial fibrillation due to genetic defect2019
- Author(s)
  Kumanomidou J, Makita N.
- Organizer
  12th Asia Pacific Heart Rhythm Society Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Cardiac Emerinopathy, Novel Nonsyndromic Xlinked Left Ventricular Noncompaction Associated With Progressive Atrial Conduction Disturbance2019
- Author(s)
  Ishikawa T., Barc J., Mishima H., Hirono K., Terada S., Kowase S., Sato T., Mukai Y., Yui Y., Ohkubo K., Kimoto H., Hata Y., Aiba T., Ohno S., Chishaki A., Shimizu W., Horie M., Ichida F., Nogami A., Yoshiura K., Schott JJ., Makita N.
- Organizer
  The 40th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] 発症前診断を行ったQT延長症候群の姉妹2019
- Author(s)
  松下悠紀, 永田弾尺, 小川昌宣, 鹿田佐和子, 石川泰輔, 蒔田直昌
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Single Cell Electrophysiological Analysis of iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Potential Imaging System2019
- Author(s)
  Yamamoto Y, Makiyama T, Wuriyanghai Y, Kohjitani H, Hirose S, Gao J, Kashiwa A, Huang H, Ishikawa T, Ohno S, Chonabayashi K, Suda K, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Functional reappraisal of SCN5A mutations reemphasize their predictive value for lethal cardiac events in Brugada syndrome2019
- Author(s)
  Ishikawa T., Kimoto H., Yamagata K., Asakura K., Aiba T., Kusano K., Shimizu W., Makita N.
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] 若年発症の家族性心房細動症例で遺伝子異常を認めた1例2019
- Author(s)
  岩橋英明, 熊埜御堂淳, 高橋淳彌, 大渕綾, 本多亮博, 平方佐季, 大塚昌紀, 大江征嗣, 蒔田直昌, 福本義弘
- Organizer
  日本内科学会第326回九州地方会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] 次世代シーケンス解析による特発性心室細動の遺伝背景の解明2019
- Author(s)
  謝颯琴, 高橋篤, 大野聖子, 鎌倉令, 石川泰輔, 植田初江, 斯波真理子, 南野直人, 林研至, 八木原伸江, 中野由紀子, 伊藤英樹, 宮本恵宏, 田中敏博, 蒔田直昌, 堀江稔, 清水渉, 草野研吾, 安田聡, 相庭武司
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Modeling Overlap Syndrome of Long QT and Brugada Syndrome Associated with Induced Pluripotent Stem Cells2019
- Author(s)
  Kashiwa A., Makiyama T., Kohjitani H., Wuriyanghai Y., Yamamoto Y., Jungshan G., Huang H., Ishikawa T., Ohno S., Toyoda F., Sato S., Horie M., Makita N., Kimura T.
- Organizer
  The 40th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Modeling Overlap Syndrome of Long QT and Brugada Syndrome Associated with Induced Pluripotent Stem Cells2019
- Author(s)
  Kashiwa A., Makiyama T., Kohjitani H., Wuriyanghai Y., Yamamoto Y., Jungshan G., Huang H., Ishikawa T., Ohno S., Toyoda F., Sato S., Horie M., Makita N., Kimura T.
- Organizer
  The 40th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Modeling Overlap Syndrome of Long QT and Brugada Syndrome Associated with Induced Pluripotent Stem Cells2019
- Author(s)
  Kashiwa A., Makiyama T., Kohjitani H., Wuriyanghai Y., Yamamoto Y., Jungshan G., Huang H., Ishikawa T., Ohno S., Toyoda F., Sato S., Horie M., Makita N., Kimura T.
- Organizer
  The 40th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] 若年発症の家族性心房細動症例で遺伝子異常を認めた1例2019
- Author(s)
  岩橋英明, 熊埜御堂淳, 高橋淳彌, 大渕綾, 本多亮博, 平方佐季, 大塚昌紀, 大江征嗣, 蒔田直昌, 福本義弘
- Organizer
  日本内科学会第326回九州地方会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] 患者由来iPS 細胞モデルを用いたCav 1.2イオン選択性を障害するCACNA1C-E1115K変異がQT 延長症候群、Brugada 症候群を発症するメカニズムの解析2019
- Author(s)
  柏麻美, 牧山武, 糀谷泰, マウリッセントーマス, ウリヤンハイイミン, 山本雄大, ガオジンシャン, ファンハイ, 今村知彦, 相澤卓範, 石川泰輔, 大野聖子, 豊田太, 佐藤誠一, 高橋一浩, ウォルツェンクヌート, 堀江稔, 蒔田直昌, 木村剛
- Organizer
  第97回日本生理学会大会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] 若年発症の家族性心房細動症例で遺伝子異常を認めた1例2019
- Author(s)
  岩橋英明, 熊埜御堂淳, 高橋淳彌, 大渕綾, 本多亮博, 平方佐季, 大塚昌紀, 大江征嗣, 蒔田直昌, 福本義弘
- Organizer
  日本内科学会第326回九州地方会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] 患者由来iPS 細胞モデルを用いたCav 1.2イオン選択性を障害するCACNA1C-E1115K変異がQT 延長症候群、Brugada 症候群を発症するメカニズムの解析2019
- Author(s)
  柏麻美, 牧山武, 糀谷泰, マウリッセントーマス, ウリヤンハイイミン, 山本雄大, ガオジンシャン, ファンハイ, 今村知彦, 相澤卓範, 石川泰輔, 大野聖子, 豊田太, 佐藤誠一, 高橋一浩, ウォルツェンクヌート, 堀江稔, 蒔田直昌, 木村剛
- Organizer
  第97回日本生理学会大会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] A case report of juvenile onset familial atrial fibrillation due to genetic defect2019
- Author(s)
  Kumanomidou J., Makita N.
- Organizer
  12th Asia Pacific Heart Rhythm Society Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] 進行性心臓伝導障害患者の網羅的遺伝子解析とin vitro 機能解析系を用いて明らかになった心臓コネキシン病の分子病態2019
- Author(s)
  石川泰輔, 関明子, 蒔田直昌
- Organizer
  第97回日本生理学会大会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Brugada症候群の予後予測に対する分子生理学的アプローチ2019
- Author(s)
  石川泰輔, 蒔田直昌
- Organizer
  第67回日本心臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Genetic Background in Patients with Idiopathic Ventricular Fibrillation: Known Gene Screening from Whole Exome Analysis Data2019
- Author(s)
  Aiba T., Cha, Pei-Chieng, Takahashi A., Ohno S., Kamakura T., Ishikawa T., Ishibashi-Ueda H., Harada-Shiba M., Minamino N., Hayashi K., Yagihara N., Nakano Y., Itoh H., Miyamoto Y., Tanaka T., Makita N., Horie M., Shimizu W., Kusano K., Yasuda S.
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Functional Reappraisal of SCN5A Mutations Reemphasize Their Predictive Value for Lethal Cardiac Events in Brugada Syndrome2019
- Author(s)
  Ishikawa T., Makita N.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Brugada症候群の予後予測に対する分子生理学的アプローチ2019
- Author(s)
  石川泰輔, 蒔田直昌
- Organizer
  第67回日本心臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Whole-Exome Sequencing to Discover Novel Responsible Genes for Brugada Syndrome: A Multicenter Japanese Registry2019
- Author(s)
  Ishikawa T., Makita N., Japanese Brugada Exome project
- Organizer
  第83回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] A case report of juvenile onset familial atrial fibrillation due to genetic defect2019
- Author(s)
  Kumanomidou J., Makita N.
- Organizer
  12th Asia Pacific Heart Rhythm Society Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Brugada症候群の予後予測に対する分子生理学的アプローチ2019
- Author(s)
  石川泰輔, 蒔田直昌
- Organizer
  第67回日本心臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Cardiac Emerinopathy, Novel Nonsyndromic Xlinked Left Ventricular Noncompaction Associated With Progressive Atrial Conduction Disturbance2019
- Author(s)
  Ishikawa T, Barc J, Mishima H, Hirono K, Terada S, Kowase S, Sato T, Mukai Y, Yui Y, Ohkubo K, Kimoto H, Hata Y, Aiba T, Ohno S, Chishaki A, Shimizu W, Horie M, Ichida F, Nogami A, Yoshiura K, Schott JJ, Makita N.
- Organizer
  The 40th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] 次世代シーケンス解析による特発性心室細動の遺伝背景の解明2019
- Author(s)
  謝颯琴, 高橋篤, 大野聖子, 鎌倉令, 石川泰輔, 植田初江, 斯波真理子, 南野直人, 林研至, 八木原伸江, 中野由紀子, 伊藤英樹, 宮本恵宏, 田中敏博, 蒔田直昌, 堀江稔, 清水渉, 草野研吾, 安田聡, 相庭武司
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Single Cell Electrophysiological Analysis of iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Potential Imaging System2019
- Author(s)
  Yamamoto Y., Makiyama T., Wuriyanghai Y., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Modeling Overlapping Phenotypes of Long-QT and Brugada Syndrome with CACNA1C-E1115K that Alters Ion Selectivity of the Cardiac L-Type Calcium Channel Using Induced Pluripotent Stem Cells2019
- Author(s)
  Kashiwa A., Makiyama T., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Modeling Overlapping Phenotypes of Long-QT and Brugada Syndrome with CACNA1C-E1115K that Alters Ion Selectivity of the Cardiac L-Type Calcium Channel Using Induced Pluripotent Stem Cells2019
- Author(s)
  Kashiwa A., Makiyama T., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] 若年発症の家族性心房細動症例で遺伝子異常を認めた1例2019
- Author(s)
  岩橋英明, 熊埜御堂淳, 高橋淳彌, 大渕綾, 本多亮博, 平方佐季, 大塚昌紀, 大江征嗣, 蒔田直昌, 福本義弘
- Organizer
  日本内科学会第326回九州地方会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] 発症前診断を行ったQT延長症候群の姉妹2019
- Author(s)
  松下悠紀, 永田弾尺, 小川昌宣, 鹿田佐和子, 石川泰輔, 蒔田直昌
- Organizer
  日本人類遺伝学会第64回大会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Cardiac Emerinopathy, Novel Nonsyndromic Xlinked Left Ventricular Noncompaction Associated With Progressive Atrial Conduction Disturbance2019
- Author(s)
  Ishikawa T., Barc J., Mishima H., Hirono K., Terada S., Kowase S., Sato T., Mukai Y., Yui Y., Ohkubo K., Kimoto H., Hata Y., Aiba T., Ohno S., Chishaki A., Shimizu W., Horie M., Ichida F., Nogami A., Yoshiura K., Schott JJ., Makita N.
- Organizer
  The 40th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Functional Reappraisal of SCN5A Mutations Reemphasize Their Predictive Value for Lethal Cardiac Events in Brugada Syndrome2019
- Author(s)
  Ishikawa T., Makita N.
- Organizer
  第66回日本不整脈心電学会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Lack Of Genotype-phenotype Correlation In Brugada Syndrome And Sudden Arrhythmic Death Syndrome Families With Reported Pathogenic SCN1B Variants2018
- Author(s)
  Gray B. , Hasdemir C. , Ingles J. , Aiba T., Makita N. , PROBST V. , Wilde A., Semsarian C. , Sy R., Behr E.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] CaMKII as a target for novel therapy to treat lethal ventricular tachyarrhythmias2018
- Author(s)
  辻幸臣, 蒔田直昌
- Organizer
  第57回日本生体医工学学会大会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Torsadogenic Action Of Late Na+ Current In Experimental Electrical Storm2018
- Author(s)
  Yamazaki M., Tsuji Y. , Niwa R., Tomii N., Arafune T., Honjo H., Dobrev D., Nattel S., Kodama I., Sakuma I., Makita N.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Rare Coding Variants in Genes Other Than SCN5A Are Minimal Genetic Burden on the Prognosis of Brugada Syndrome2018
- Author(s)
  Ishikawa T., Mishima H., Ohno S., T. Aiba, Nakano Y., Aizawa Y., Nakajima T., Hayashi K., Murakoshi N., Yagihara N., Kimoto H., Makiyama T., Watanabe H., Morita H., Yoshiura K., Nogami A., Shimizu W., Horie M., Tanaka T., Makita N.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] The inactivation of L-type Ca2+ Channel was impaired in Human iPS Cell Model of Long-QT Syndrome with CALM2-D134H Mutation.2018
- Author(s)
  Yamamoto Y., Makiyama T., Harita T., Hayano M., Nishiuchi S., Wuriyanghai Y., Kohjitani H., Hirose S., Yokoi F., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Duration Predicts Events In Caucasians With E1784K-SCN5A: The E1784K International Consortium2018
- Author(s)
  Wijeyeratne Y. , Makita N. et al
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] CaMKII as a target for novel therapy to treat lethal ventricular tachyarrhythmias.2018
- Author(s)
  辻幸臣, 蒔田直昌
- Organizer
  第57回日本生体医工学学会大会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] 不整脈症候群で心臓が構造的に正常な患者における心筋症の原因遺伝子変異の特定2018
- Author(s)
  八木原伸江, 渡部裕, 蒔田直昌, 堀江稔, 清水渉, 大野聖子, 長谷川奏恵, 相庭武司, 田中敏博, 角田達彦, 重水大智, 徹南野
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] CALM2関連性QT延長症候群iPSCモデルにおいて、l-cis-diltiazemは遅延したL型calciumチャネルの不活性化をさらに強める2018
- Author(s)
  横井文香, 牧山武, 山本雄大, 張田健志, Yimin Wuriyanghai, 早野護, 西内英, 糀谷泰彦, 廣瀬紗也子, 高景山, 大野聖子, 豊田太, 吉田善紀, 蒔田直昌, 堀江稔, 木村剛
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Pathophysiology of Inherited Arrhythmias Associated with Ca Handling Abnormality2018
- Author(s)
  Makita N.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Invited
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Novel Arrhythmia Syndrome Associated with Gap Junction Mutations2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] The inactivation of L-type Ca2+ Channel was impaired in Human iPS Cell Model of Long-QT Syndrome with CALM2-D134H Mutation.2018
- Author(s)
  Yamamoto Y., Makiyama T., Harita T., Hayano M., Nishiuchi S., Wuriyanghai Y., Kohjitani H., Hirose S., Yokoi F., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] CaMKII as a target for novel therapy to treat lethal ventricular tachyarrhythmias.2018
- Author(s)
  辻幸臣, 蒔田直昌
- Organizer
  第57回日本生体医工学学会大会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Clinical Manifestations and Long-term Mortality in Lamin A/C Mutation Carriers from the Japanese Multicenter Registry2018
- Author(s)
  Nakajima K., Aiba T., Makiyama T., Nishiuchi S., Ohno S., Doi T., Shizuta S., Onoue K., Yagihara N., Ishikawa T., Watanabe I., Oginosawa Y., Nogami A., Aonuma K., Saitoh Y., Kimura T., Makita N., Shimizu W., Horie M., Kusano K.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Cardiac Connexin Syndrome: A New Inherited Cardiac Conduction Disease Entity with Distinct Electrophysiological and Extracardiac Manifestations.2018
- Author(s)
  Ishikawa T., Seki A., Hagiwara N., Makita N.
- Organizer
  第82回日本循環器学会学術大会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Pathophysiology of Inherited Arrhythmias Associated with Ca Handling Abnormality2018
- Author(s)
  Makita N.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Mutation Hot-spot-based Risk Stratification In Long QT Syndrome Type 1: Data From A Nationwide Japanese LQT Registry2018
- Author(s)
  Kashiwa A., Aiba T., Makimoto H., Yamagata K. , Keiko S. , Yagihara N., Watanabe H. , Ohno S., Hayashi K. , Sumitomo N., Yoshinaga M. , Morita H., Miyamoto Y. , Makita N. , Horie M., Yasuda S., Kusano K., Shimizu W. , The_Japanese_LQTS_registry_investigators.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] CALM2関連性QT延長症候群iPSCモデルにおいて、l-cis-diltiazemは遅延したL型calciumチャネルの不活性化をさらに強める2018
- Author(s)
  横井文香, 牧山武, 山本雄大, 張田健志, Yimin Wuriyanghai, 早野護, 西内英, 糀谷泰彦, 廣瀬紗也子, 高景山, 大野聖子, 豊田太, 吉田善紀, 蒔田直昌, 堀江稔, 木村剛
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Mechanisms of Electrical Storm Associated With QT Prolongation: Successful Mapping of Torsades de Pointes in Rabbits2018
- Author(s)
  Tsuji Y., Yamazaki M., Niwa R., Tomii N., Arafune T., Honjo H., Dobrev D., Nattel S., Kodama I., Sakuma I., Makita N
- Organizer
  American Heart Association Annual Scientific Sessions 2018
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Duration Predicts Events In Caucasians With E1784K-SCN5A: The E1784K International Consortium2018
- Author(s)
  Wijeyeratne Y. ,Makita N. et al
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Clinical and Genetic Basis of Calmodulinopathy2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Rare Coding Variants in Genes Other Than SCN5A Are Minimal Genetic Burden on the Prognosis of Brugada Syndrome2018
- Author(s)
  Ishikawa T., Mishima H., Ohno S., T. Aiba, Nakano Y., Aizawa Y., Nakajima T., Hayashi K., Murakoshi N., Yagihara N., Kimoto H., Makiyama T., Watanabe H., Morita H., Yoshiura K., Nogami A., Shimizu W., Horie M., Tanaka T., Makita N.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Single Cell Electrophysiological Analysis of Human iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Voltage Imaging System2018
- Author(s)
  Yamamoto Y., Makiyama T, Wuriyanghai Y., Kohjitani H., Hirose S., Gao J, Kashiwa A., Kimura T., Ishikawa T., Motomura H., Makita N, Ohno S., Chonabayashi K., Yoshida Y., Suda K., Horie M
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Single Cell Electrophysiological Analysis of Human iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Voltage Imaging System2018
- Author(s)
  Yamamoto Y., Makiyama T, Wuriyanghai Y., Kohjitani H., Hirose S., Gao J, Kashiwa A., Kimura T., Ishikawa T., Motomura H., Makita N, Ohno S., Chonabayashi K., Yoshida Y., Suda K., Horie M
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Lack Of Genotype-phenotype Correlation In Brugada Syndrome And Sudden Arrhythmic Death Syndrome Families With Reported Pathogenic SCN1B Variants2018
- Author(s)
  Gray B. , Hasdemir C. , Ingles J. , Aiba T., Makita N., Probst V., Wilde A., Semsarian C., Sy R, Behr E.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Novel Arrhythmia Syndrome Associated with Gap Junction Mutations2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Torsadogenic Action Of Late Na+ Current In Experimental Electrical Storm2018
- Author(s)
  Yamamoto Y., Makiyama T, Wuriyanghai Y., Kohjitani H., Hirose S., Gao J, Kashiwa A., Kimura T., Ishikawa T., Motomura H., Makita N, Ohno S., Chonabayashi K., Yoshida Y., Suda K., Horie M
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Mutation Hot-spot-based Risk Stratification In Long QT Syndrome Type 1: Data From A Nationwide Japanese LQT Registry2018
- Author(s)
  Kashiwa A., Aiba T., Makimoto H., Yamagata K. , Keiko S. , Yagihara N., Watanabe H. , Ohno S., Hayashi K. , Sumitomo N., Yoshinaga M. , Morita H., Miyamoto Y. , Makita N. , Horie M., Yasuda S., Kusano K., Shimizu W. , The_Japanese_LQTS_registry_investigators.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Cardiac Connexin Syndrome: A New Inherited Cardiac Conduction Disease Entity with Distinct Electrophysiological and Extracardiac Manifestations.2018
- Author(s)
  Ishikawa T., Seki A., Hagiwara N., Makita N.
- Organizer
  第82回日本循環器学会学術大会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] 不整脈症候群で心臓が構造的に正常な患者における心筋症の原因遺伝子変異の特定2018
- Author(s)
  八木原伸江, 渡部裕, 蒔田直昌, 堀江稔, 清水渉, 大野聖子, 長谷川奏恵, 相庭武司, 田中敏博, 角田達彦, 重水大智, 南野徹
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Atrial Conduction Defects Caused by a Connexin45 Mutation2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Rare Coding Variants in Genes Other Than SCN5A Are Minimal Genetic Burden on the Prognosis of Brugada Syndrome2018
- Author(s)
  Ishikawa T., Mishima H., Ohno S., T. Aiba, Nakano Y., Aizawa Y., Nakajima T., Hayashi K., Murakoshi N., Yagihara N., Kimoto H., Makiyama T., Watanabe H., Morita H., Yoshiura K., Nogami A., Shimizu W., Horie M., Tanaka T., Makita N.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Clinical and Genetic Basis of Calmodulinopathy2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Genotype-Dependent Differences in Short QT Syndrome2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] The inactivation of L-type Ca2+ Channel was impaired in Human iPS Cell Model of Long-QT Syndrome with CALM2-D134H Mutation.2018
- Author(s)
  Yamamoto Y., Makiyama T., Harita T., Hayano M., Nishiuchi S., Wuriyanghai Y., Kohjitani H., Hirose S., Yokoi F., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Torsadogenic Action Of Late Na+ Current In Experimental Electrical Storm2018
- Author(s)
  Yamazaki M., Tsuji Y. , Niwa R., Tomii N., Arafune T., Honjo H., Dobrev D., Nattel S., Kodama I., Sakuma I., Makita N.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Atrial Conduction Defects Caused by a Connexin45 Mutation2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Clinical Manifestations and Long-term Mortality in Lamin A/C Mutation Carriers from the Japanese Multicenter Registry2018
- Author(s)
  Nakajima K., Aiba T., Makiyama T., Nishiuchi S., Ohno S., Doi T., Shizuta S., Onoue K., Yagihara N., Ishikawa T., Watanabe I., Oginosawa Y., Nogami A., Aonuma K., Saitoh Y., Kimura T., Makita N., Shimizu W., Horie M., Kusano K.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Lack Of Genotype-phenotype Correlation In Brugada Syndrome And Sudden Arrhythmic Death Syndrome Families With Reported Pathogenic SCN1B Variants2018
- Author(s)
  Gray B. , Hasdemir C. , Ingles J. , Aiba T., Makita N. , PROBST V. , Wilde A., Semsarian C. , Sy R., Behr E.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Mechanisms of Electrical Storm Associated With QT Prolongation: Successful Mapping of Torsades de Pointes in Rabbits2018
- Author(s)
  Tsuji Y., Yamazaki M., Niwa R., Tomii N., Arafune T., Honjo H., Dobrev D., Nattel S., Kodama I., Sakuma I., Makita N
- Organizer
  American Heart Association Annual Scientific Sessions 2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Mechanisms of Electrical Storm Associated With QT Prolongation: Successful Mapping of Torsades de Pointes in Rabbits2018
- Author(s)
  Tsuji Y., Yamazaki M., Niwa R., Tomii N., Arafune T., Honjo H., Dobrev D., Nattel S., Kodama I., Sakuma I., Makita N
- Organizer
  American Heart Association Annual Scientific Sessions 2018
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] HCN4 Polymorphisms and Tachycardia Induced Cardiomyopathy2018
- Author(s)
  Nakano Y., Ochi H., Onohara Y., Sairaku A., Tokuyama T., Motoda C., Matsumura H., Tomomori S., Amioka M., Hironobe N., Ohkubo Y., Okamura S., Makita N., Yoshida Y., Chayama K., Kihara Y.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Novel Arrhythmia Syndrome Associated with Gap Junction Mutations2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Novel Arrhythmia Syndrome Associated with Gap Junction Mutations2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] CALM2関連性QT延長症候群iPSCモデルにおいて、l-cis-diltiazemは遅延したL型calciumチャネルの不活性化をさらに強める2018
- Author(s)
  横井文香, 牧山武, 山本雄大, 張田健志, Yimin Wuriyanghai, 早野護, 西内英, 糀谷泰彦, 廣瀬紗也子, 高景山, 大野聖子, 豊田太, 吉田善紀, 蒔田直昌, 堀江稔, 木村剛
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Mutation Hot-spot-based Risk Stratification In Long QT Syndrome Type 1: Data From A Nationwide Japanese LQT Registry2018
- Author(s)
  Kashiwa A., Aiba T., Makimoto H., Yamagata K. , Keiko S. , Yagihara N., Watanabe H. , Ohno S., Hayashi K. , Sumitomo N., Yoshinaga M. , Morita H., Miyamoto Y. , Makita N. , Horie M., Yasuda S., Kusano K., Shimizu W. , The_Japanese_LQTS_registry_investigators.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Pathophysiology of Inherited Arrhythmias Associated with Ca Handling Abnormality2018
- Author(s)
  Makita N.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Mutation Hot-spot-based Risk Stratification In Long QT Syndrome Type 1: Data From A Nationwide Japanese LQT Registry2018
- Author(s)
  Kashiwa A., Aiba T., Makimoto H., Yamagata K. , Keiko S. , Yagihara N., Watanabe H. , Ohno S., Hayashi K. , Sumitomo N., Yoshinaga M. , Morita H., Miyamoto Y. , Makita N. , Horie M., Yasuda S., Kusano K., Shimizu W. , The_Japanese_LQTS_registry_investigators.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Atrial Conduction Defects Caused by a Connexin45 Mutation2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Clinical and Genetic Basis of Calmodulinopathy2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Duration Predicts Events In Caucasians With E1784K-SCN5A: The E1784K International Consortium2018
- Author(s)
  Wijeyeratne Y. ,Makita Naomasa et al.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Genotype-Dependent Differences in Short QT Syndrome2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] 不整脈症候群で心臓が構造的に正常な患者における心筋症の原因遺伝子変異の特定2018
- Author(s)
  八木原伸江, 渡部裕, 蒔田直昌, 堀江稔, 清水渉, 大野聖子, 長谷川奏恵, 相庭武司, 田中敏博, 角田達彦, 重水大智, 南野徹
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Lack Of Genotype-phenotype Correlation In Brugada Syndrome And Sudden Arrhythmic Death Syndrome Families With Reported Pathogenic SCN1B Variants2018
- Author(s)
  Gray B. , Hasdemir C. , Ingles J. , Aiba T., Makita N. , PROBST V. , Wilde A., Semsarian C. , Sy R., Behr E.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] 不整脈症候群で心臓が構造的に正常な患者における心筋症の原因遺伝子変異の特定2018
- Author(s)
  八木原伸江, 渡部裕, 蒔田直昌, 堀江稔, 清水渉, 大野聖子, 長谷川奏恵, 相庭武司, 田中敏博, 角田達彦, 重水大智, 徹南野
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Clinical Manifestations and Long-term Mortality in Lamin A/C Mutation Carriers from the Japanese Multicenter Registry2018
- Author(s)
  Nakajima K., Aiba T., Makiyama T., Nishiuchi S., Ohno S., Doi T., Shizuta S., Onoue K., Yagihara N., Ishikawa T., Watanabe I., Oginosawa Y., Nogami A., Aonuma K., Saitoh Y., Kimura T., Makita N., Shimizu W., Horie M., Kusano K.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] HCN4 Polymorphisms and Tachycardia Induced Cardiomyopathy2018
- Author(s)
  Nakano Y., Ochi H., Onohara Y., Sairaku A., Tokuyama T., Motoda C., Matsumura H., Tomomori S., Amioka M., Hironobe N., Ohkubo Y., Okamura S., Makita N., Yoshida Y., Chayama K., Kihara Y.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] CaMKII as a target for novel therapy to treat lethal ventricular tachyarrhythmias.2018
- Author(s)
  辻幸臣, 蒔田直昌
- Organizer
  第57回日本生体医工学学会大会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Torsadogenic Action Of Late Na+ Current In Experimental Electrical Storm2018
- Author(s)
  Yamazaki M., Tsuji Y. , Niwa R., Tomii N., Arafune T., Honjo H., Dobrev D., Nattel S., Kodama I., Sakuma I., Makita N.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Atrial Conduction Defects Caused by a Connexin45 Mutation2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] The inactivation of L-type Ca2+ Channel was impaired in Human iPS Cell Model of Long-QT Syndrome with CALM2-D134H Mutation.2018
- Author(s)
  Yamamoto Y., Makiyama T., Harita T., Hayano M., Nishiuchi S., Wuriyanghai Y., Kohjitani H., Hirose S., Yokoi F., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] HCN4 Polymorphisms and Tachycardia Induced Cardiomyopathy2018
- Author(s)
  Nakano Y., Ochi H., Onohara Y., Sairaku A., Tokuyama T., Motoda C., Matsumura H., Tomomori S., Amioka M., Hironobe N., Ohkubo Y., Okamura S., Makita N., Yoshida Y., Chayama K., Kihara Y.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Torsadogenic Action Of Late Na+ Current In Experimental Electrical Storm2018
- Author(s)
  Yamazaki M., Tsuji Y. , Niwa R., Tomii N., Arafune T., Honjo H., Dobrev D., Nattel S., Kodama I., Sakuma I., Makita N.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Mechanisms of Electrical Storm Associated With QT Prolongation: Successful Mapping of Torsades de Pointes in Rabbits2018
- Author(s)
  Tsuji Y., Yamazaki M., Niwa R., Tomii N., Arafune T., Honjo H., Dobrev D., Nattel S., Kodama I., Sakuma I., Makita N
- Organizer
  American Heart Association Annual Scientific Sessions 2018
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Cardiac Connexin Syndrome: A New Inherited Cardiac Conduction Disease Entity with Distinct Electrophysiological and Extracardiac Manifestations.2018
- Author(s)
  Ishikawa T., Seki A., Hagiwara N., Makita N.
- Organizer
  第82回日本循環器学会学術大会
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Genotype-Dependent Differences in Short QT Syndrome2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Cardiac Connexin Syndrome: A New Inherited Cardiac Conduction Disease Entity with Distinct Electrophysiological and Extracardiac Manifestations.2018
- Author(s)
  Ishikawa T., Seki A., Hagiwara N., Makita N.
- Organizer
  第82回日本循環器学会学術大会
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Clinical Manifestations and Long-term Mortality in Lamin A/C Mutation Carriers from the Japanese Multicenter Registry2018
- Author(s)
  Nakajima K., Aiba T., Makiyama T., Nishiuchi S., Ohno S., Doi T., Shizuta S., Onoue K., Yagihara N., Ishikawa T., Watanabe I., Oginosawa Y., Nogami A., Aonuma K., Saitoh Y., Kimura T., Makita N., Shimizu W., Horie M., Kusano K.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Rare Coding Variants in Genes Other Than SCN5A Are Minimal Genetic Burden on the Prognosis of Brugada Syndrome2018
- Author(s)
  Ishikawa T., Mishima H., Ohno S., T. Aiba, Nakano Y., Aizawa Y., Nakajima T., Hayashi K., Murakoshi N., Yagihara N., Kimoto H., Makiyama T., Watanabe H., Morita H., Yoshiura K., Nogami A., Shimizu W., Horie M., Tanaka T., Makita N.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Duration Predicts Events In Caucasians With E1784K-SCN5A: The E1784K International Consortium2018
- Author(s)
  Wijeyeratne Y., Makita N., Roden D., Probst V., Ackerman M., Aiba T., Behr E. et al.
- Organizer
  The 39th Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] CALM2関連性QT延長症候群iPSCモデルにおいて、l-cis-diltiazemは遅延したL型calciumチャネルの不活性化をさらに強める2018
- Author(s)
  横井文香, 牧山武, 山本雄大, 張田健志, Yimin Wuriyanghai, 早野護, 西内英, 糀谷泰彦, 廣瀬紗也子, 高景山, 大野聖子, 豊田太, 吉田善紀, 蒔田直昌, 堀江稔, 木村剛
- Organizer
  第82回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] Clinical and Genetic Basis of Calmodulinopathy2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H02808
[Presentation] Single Cell Electrophysiological Analysis of Human iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Voltage Imaging System2018
- Author(s)
  Yamamoto Y., Makiyama T, Wuriyanghai Y., Kohjitani H., Hirose S., Gao J, Kashiwa A., Kimura T., Ishikawa T., Motomura H., Makita N, Ohno S., Chonabayashi K., Yoshida Y., Suda K., Horie M
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Genotype-Dependent Differences in Short QT Syndrome2018
- Author(s)
  Makita N.
- Organizer
  The 11th Asia Pacific Heart Rhythm Society Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K19550
[Presentation] HCN4 Polymorphisms and Tachycardia Induced Cardiomyopathy2018
- Author(s)
  Nakano Y., Ochi H., Onohara Y., Sairaku A., Tokuyama T., Motoda C., Matsumura H., Tomomori S., Amioka M., Hironobe N., Ohkubo Y., Okamura S., Makita N., Yoshida Y., Chayama K., Kihara Y.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Pathophysiology of Inherited Arrhythmias Associated with Ca Handling Abnormality2018
- Author(s)
  Makita N.
- Organizer
  The 65th Annual Meeting of the Japan Heart Rhythm Society
- Data Source
  KAKENHI-PROJECT-18KK0245
[Presentation] Mutation in L-type Calcium Channel Cav1.3 (CACNA1D) Underlying a Consanguineous Family Associated with Congenital AV Block and Deaf-Blindness2017
- Author(s)
  Kimoto H, Ishikawa T, Mishima H, Hasdemir C, Yoshiura K, Makita N.
- Organizer
  The 10th Asia Pacific Heart Rhythm Society Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] CALM2-D134H Mutation Associated With Long-QT Syndrome Delayed Inactivation of L-type Ca2+ Currents in Human iPS Cells Derived Cardiomyocytes.2017
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Hayano M, Nishiuchi S, Wuriyanghai Y, Kohjitani H, Hirose S, Yokoi F, Ishikawa T, Ohno S, Chonabayashi K, Suda K, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  American Heart Association Annual Scientific Session 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers2017
- Author(s)
  Nishiuchi S, Makiyama T, Aiba T, Nakajima K, Ishikawa T, Murakoshi N, Watanabe H, Ohno S, Doi T, Shizuta S, Minamino T, Saito Y, Oginosawa Y, Nogami A, Aonuma K, Kusano K, Makita N, Shimizu W, Horie M, Kimura T.
- Organizer
  The 10th Asia Pacific Heart Rhythm Sosiety Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Mutation Spot-sensitive Clinical Features and Risk of Life-threatening Arrhythmia in Long QT Syndrome Type 1 in Japan2017
- Author(s)
  Aiba T, Makimoto H, Yagihara N, Watanabe H, Ohno S, Hayashi K, Sumitomo N, Yoshinaga M, Morita H, Miyamoto Y, Makita N, Horie M, Yasuda S, Kusano K, Shimizu W.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] De novo and Familial Connexin45 Mutant R75H Causes Progressive Atrioventricular Block Associated with Craniofacial and Dentodigital Dysmorphisms2017
- Author(s)
  Makita N, Seki A, Ishikawa T, Dawmy X, Mishima H, Barc J, Sasaki R, Nishii K, Saito K, Urano M, Ohno S, Otsuki S, Kimoto H, Baruteau A, Aurelie T, Swanny F, Stephanie B, Parent P, Shibata Y, Perrin JJ, Le Marec H, Hagiwara N, Mercier S, Horie M, Probst V, Yoshiura K, Redon R, Schott J, J.
- Organizer
  Printemps de la Cardiologie Recherche Fondamentale et Clinique
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers in Japan2017
- Author(s)
  Nishiuchi S, Aiba T, Makiyama T, Nakajima K, Yagihara N, Ishikawa T, Onoue K, Murakoshi N, Watanabe I, Ohkubo K, Watanabe H, Ohno S, Doi T, Shizuta S, Minamino T, Saito Y, Oginosawa Y, Nogami A, Aonuma K, Kusano K, Makita N, Shimizu W, Horie M, Kimura T.
- Organizer
  American Heart Association Annual Scientific Session 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] lL-cis-Diltiazem Ameliorates Impaired Calcium Channel Inactivation in a Patient-Specific Stem Cell Model of Long-QT Syndrome with a Calmodulin Mutation2017
- Author(s)
  Yokoi F, Makiyama T, Harita T, Yamamoto Y, Hayano M, Nishiuchi S, Kohjitani H, Wuriyanghai Y, Hirose S, Toyoda F, Yoshida Y, Makita N, Horie M, Kimura T.
- Organizer
  The 10th Asia Pacific Heart Rhythm Society Scientific Session
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Calmodulin Mutations Responsible for Long QT Syndrome and Functional Rescue using a CRISPR/Cas9 System2017
- Author(s)
  蒔田直昌.
- Organizer
  第94回日本生理学会大会
- Invited
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Genetic Mutation of Brugada Syndrome2017
- Author(s)
  Makita N.
- Organizer
  Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Genetics of Familial Atrial Fibrillation2017
- Author(s)
  Ishikawa T, Makita N.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Mutation Spot-sensitive Clinical Features and Risk of Life-threatening Arrhythmia in Long QT Syndrome Type 1 in Japan2017
- Author(s)
  Aiba T, Makimoto H, Yagihara N, Watanabe H, Ohno S, Hayashi K, Sumitomo N, Yoshinaga M, Morita H, Miyamoto Y, Makita N, Horie M, Yasuda S, Kusano K, Shimizu W.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] lL-cis-Diltiazem Ameliorates Impaired Calcium Channel Inactivation in a Patient-Specific Stem Cell Model of Long-QT Syndrome with a Calmodulin Mutation2017
- Author(s)
  Yokoi F, Makiyama T, Harita T, Yamamoto Y, Hayano M, Nishiuchi S, Kohjitani H, Wuriyanghai Y, Hirose S, Toyoda F, Yoshida Y, Makita N, Horie M, Kimura T.
- Organizer
  The 10th Asia Pacific Heart Rhythm Society Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Genetic-based risk stratification for cardiac disorders in LMNA mutation carriers2017
- Author(s)
  Nishiuchi S, Aiba T, Nakajima K, Hirose S, Kohjitani H, Yamamoto Y, Harita T, Hayano M, Sasaki K, Ishikawa T, Onoue K, Saito Y, Kusano K, Makita N, Shimizu W, Horie M, Kimura T.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Multinational genome-wide association study in long QT syndrome identifies a role for common genetic variation in disease susceptibility and points to a polygenic architecture in mutation-negative cases2017
- Author(s)
  Lahrouchi N, Makita N, et al.
- Organizer
  Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Multinational genome-wide association study in long QT syndrome identifies a role for common genetic variation in disease susceptibility and points to a polygenic architecture in mutation-negative cases2017
- Author(s)
  Lahrouchi N, Makita N et al.
- Organizer
  Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] De novo and Familial Connexin45 Mutant R75H Causes Progressive Atrioventricular Block Associated with Craniofacial and Dentodigital Dysmorphisms2017
- Author(s)
  Makita N, Seki A, Ishikawa T, Dawmy X, Mishima H, Barc J, Sasaki R, Nishii K, Saito K, Urano M, Ohno S, Otsuki S, Kimoto H, Baruteau A, Aurelie T, Swanny F, St?phanie B, Parent P, Shibata Y, Perrin JJ, Le Marec H, Hagiwara N, Mercier S, Horie M, Probst V, Yoshiura K, Redon R, Schott J, J.
- Organizer
  Printemps de la Cardiologie Recherche Fondamentale et Clinique
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Sick sinus syndrome caused by HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular non-compaction2017
- Author(s)
  Ishikawa T, Ohno S, Murakami T, Yoshida K, Fukuoka T, Mishima H, Kimoto H, Aiba T, Nogami A, Sumitomo N, Shimizu W, Horigome H, Yoshiura KI, Horie M, Makita N.
- Organizer
  Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Mutations in Desmin Gene Uncover Phenotypic Overlap between Progressive Cardiac Conduction Defect with Muscular Dystrophy and Cardiomyopathy2017
- Author(s)
  木本浩樹, 町田紘子, 森田宏, 住友直方, 中村一文, 伊藤浩, バーク・ジュリアン, ショット・ジョンジャック, 蒔田直昌.
- Organizer
  第81回日本循環器学会学術集会
- Place of Presentation
  石川県立音楽堂音楽堂（石川県金沢市）
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Sick sinus syndrome caused by HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular non-compaction2017
- Author(s)
  Ishikawa T, Ohno S, Murakami T, Yoshida K, Fukuoka T, Mishima H, Kimoto H, Aiba T, Nogami A, Sumitomo N, Shimizu W, Horigome H, Yoshiura KI, Horie M, Makita N.
- Organizer
  Heart Rhythm Society Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Calmodulin Mutations Responsible for Long QT Syndrome and Functional Rescue using a CRISPR/Cas9 System2017
- Author(s)
  蒔田直昌.
- Organizer
  第94回日本生理学会大会
- Invited
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Calmodulin Mutations Responsible for Long QT Syndrome and Functional Rescue using a CRISPR/Cas9 System2017
- Author(s)
  Makita N.
- Organizer
  第94回日本生理学会大会
- Place of Presentation
  アクトシティ浜松（静岡県浜松市）
- Invited
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Mutation in L-type Calcium Channel Cav1.3 (CACNA1D) Underlying a Consanguineous Family Associated with Congenital AV Block and Deaf-Blindness2017
- Author(s)
  Kimoto H, Ishikawa T, Mishima H, Hasdemir C, Yoshiura K, Makita N.
- Organizer
  The 10th Asia Pacific Heart Rhythm Society Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers2017
- Author(s)
  Nishiuchi S, Makiyama T, Aiba T, Nakajima K, Ishikawa T, Murakoshi N, Watanabe H, Ohno S, Doi T, Shizuta S, Minamino T, Saito Y, Oginosawa Y, Nogami A, Aonuma K, Kusano K, Makita N, Shimizu W, Horie M, Kimura T.
- Organizer
  The 10th Asia Pacific Heart Rhythm Sosiety Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation2017
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Sasaki K, Wuriyanghai Y, Nishiuchi S, Kohjitani H, Hirose S, Ishikawa T, Motomura H, Ohno S, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers in Japan2017
- Author(s)
  Nishiuchi S, Aiba T, Makiyama T, Nakajima K, Yagihara N, Ishikawa T, Onoue K, Murakoshi N, Watanabe I, Ohkubo K, Watanabe H, Ohno S, Doi T, Shizuta S, Minamino T, Saito Y, Oginosawa Y, Nogami A, Aonuma K, Kusano K, Makita N, Shimizu W, Horie M, Kimura T.
- Organizer
  American Heart Association Annual Scientific Session 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Genetics of Familial Atrial Fibrillation2017
- Author(s)
  Ishikawa T, Makita N.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Genotype-Phenotype Correlation of SCN5A Mutations for the Clinical and Electrocardiographic Characteristics of Probands with Brugada Syndrome: A Japanese Multicenter Registry2017
- Author(s)
  Yamagata K, Horie M, Aiba T, Ogawa S, Aizawa Y, Ohe T, Yamagishi M, Makita N, Sakurada H, Tanaka T, Shimizu A, Hagiwara N, Kishi R, Nakano Y, Takagi M, Makiyama T, Ohno S, Fukuda K, Watanabe H, Morita H, Hayashi K, Fukushima-Kusano K, Kamakura S, Yasuda S, Ogawa H, Y. M, Kapplinger J, Ackerman M, Shimizu W.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Brugada Syndrome: Basic and Clinical Updates, Advancement of Basic Research2017
- Author(s)
  Makita N.
- Organizer
  13th Annual Congress European Cardiac Arrhythmia Society
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Genetic-based risk stratification for cardiac disorders in LMNA mutation carriers2017
- Author(s)
  Nishiuchi S, Aiba T, Nakajima K, Hirose S, Kohjitani H, Yamamoto Y, Harita T, Hayano M, Sasaki K, Ishikawa T, Onoue K, Saito Y, Kusano K, Makita N, Shimizu W, Horie M, Kimura T.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] CALM2-D134H Mutation Associated with Long-QT Syndrome Prevents Inactivation of L-type Ca2+ Currents in Human iPS Cell Derived Cardiomyocytes.2017
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Hayano M, Nishiuchi S, Wuriyanghai Y, Kohjitani H, Hirose S, Yokoi F, Ishikawa T, Ohno S, Chinabayashi K, Suda K, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  The 10th Asia Pacific Heart Rhythm Society Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation2017
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Sasaki K, Wuriyanghai Y, Nishiuchi S, Kohjitani H, Hirose S, Ishikawa T, Motomura H, Ohno S, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Brugada Syndrome: Basic and Clinical Updates, Advancement of Basic Research2017
- Author(s)
  Makita N.
- Organizer
  13th Annual Congress European Cardiac Arrhythmia Society
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Sick sinus syndrome caused by HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular non-compaction2017
- Author(s)
  Ishikawa T, Ohno S, Murakami T, Yoshida K, Fukuoka T, Mishima H, Kimoto H, Aiba T, Nogami A, Sumitomo N, Shimizu W, Horigome H, Yoshiura K. I, Horie M, Makita N.
- Organizer
  Heart Rhythm Society Scientific Sessions
- Place of Presentation
  Chicago, USA
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] CALM2-D134H Mutation Associated with Long-QT Syndrome Prevents Inactivation of L-type Ca2+ Currents in Human iPS Cell Derived Cardiomyocytes.2017
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Hayano M, Nishiuchi S, Wuriyanghai Y, Kohjitani H, Hirose S, Yokoi F, Ishikawa T, Ohno S, Chinabayashi K, Suda K, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  The 10th Asia Pacific Heart Rhythm Society Scientific Session
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Genotype-Phenotype Correlation of SCN5A Mutations for the Clinical and Electrocardiographic Characteristics of Probands with Brugada Syndrome: A Japanese Multicenter Registry2017
- Author(s)
  Yamagata K, Horie M, Aiba T, Ogawa S, Aizawa Y, Ohe T, Yamagishi M, Makita N, Sakurada H, Tanaka T, Shimizu A, Hagiwara N, Kishi R, Nakano Y, Takagi M, Makiyama T, Ohno S, Fukuda K, Watanabe H, Morita H, Hayashi K, Fukushima-Kusano K, Kamakura S, Yasuda S, Ogawa H, Y. M, Kapplinger J, Ackerman M, Shimizu W.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Genetic and Biophysical Basis of Calmodulinopathy, and Functional Rescue by Genome-Editing in Patient-Derived iPS Cardiomyocytes2017
- Author(s)
  Makita N.
- Organizer
  20th International Symposium on Calcium Binding Proteins and Calcium Function in Health and Disease
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] ブルガダ症候群の予後予測を目指す変異心筋Naチャネルの機能解析2017
- Author(s)
  下河舞子, 木本浩貴, 石川泰輔, 蒔田直昌.
- Organizer
  第68回西日本生理学会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Mutations in Desmin Gene Uncover Phenotypic Overlap between Progressive Cardiac Conduction Defect with Muscular Dystrophy and Cardiomyopathy2017
- Author(s)
  木本浩貴, 石川泰輔, 町田紘子, 森田宏, 住友直方, 中村一文, 伊藤浩, バーク・ジュリアン, ショット・ジョンジャック, 蒔田直昌.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] ブルガダ症候群の予後予測を目指す変異心筋Naチャネルの機能解析2017
- Author(s)
  下河舞子, 木本浩貴, 石川泰輔, 蒔田直昌.
- Organizer
  第68回西日本生理学会
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] De novo and Familial Connexin45 Mutant R75H Causes Progressive Atrioventricular Block Associated with Craniofacial and Dentodigital Dysmorphisms2017
- Author(s)
  Makita N, Seki A, Ishikawa T, Schott JJ. et al.
- Organizer
  Printemps de la Cardiologie Recherche Fondamentale et Clinique
- Place of Presentation
  La Cite des Congres, Nantes, France
- Invited
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Genetic and Biophysical Basis of Calmodulinopathy, and Functional Rescue by Genome-Editing in Patient-Derived iPS Cardiomyocytes2017
- Author(s)
  Makita N.
- Organizer
  20th International Symposium on Calcium Binding Proteins and Calcium Function in Health and Disease
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] CALM2-D134H Mutation Associated With Long-QT Syndrome Delayed Inactivation of L-type Ca2+ Currents in Human iPS Cells Derived Cardiomyocytes.2017
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Hayano M, Nishiuchi S, Wuriyanghai Y, Kohjitani H, Hirose S, Yokoi F, Ishikawa T, Ohno S, Chonabayashi K, Suda K, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  American Heart Association Annual Scientific Session 2017
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Multinational genome-wide association study in long QT syndrome identifies a role for common genetic variation in disease susceptibility and points to a polygenic architecture in mutation-negative cases2017
- Author(s)
  Lahrouchi N, Tadros R, Makita N. et al
- Organizer
  Heart Rhythm Society Scientific Sessions
- Place of Presentation
  Chicago, USA
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Genetic Mutation of Brugada Syndrome2017
- Author(s)
  Makita N.
- Organizer
  Heart Rhythm Society Scientific Sessions
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Mutations in Desmin Gene Uncover Phenotypic Overlap between Progressive Cardiac Conduction Defect with Muscular Dystrophy and Cardiomyopathy2017
- Author(s)
  木本浩貴, 石川泰輔, 町田紘子, 森田宏, 住友直方, 中村一文, 伊藤浩, バーク・ジュリアン, ショット・ジョンジャック, 蒔田直昌.
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Utility of QT dynamics for identyfying genetic testing candidates in children with borderline QT interval prolongation2016
- Author(s)
  Takahashi K, Makita N, Shimizu W
- Organizer
  第80回日本循環器学会学術集会
- Place of Presentation
  仙台市、せんだい青葉山交流広場
- Year and Date
  2016-03-20
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Catheter Ablation of Brugada Syndrome：Further Evidence of Conduction Delay in the Right Ventricular Subepicardium as Mechanism of Brugada ECG and Ventricular Fibrillation2016
- Author(s)
  Nakagawa H, Sakamoto Y, Yamashiro K, Takagi M, Kusano K, Noda T, Yamazaki M, Honjo H, Makita N, Tsuchiya T, Hoogeudiik MG, Nademanee K.
- Organizer
  第63回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Dose-Sensitive Relationship of an SCN10A Pore Mutation and Enhancer SNPs Identified in a Brugada Syndrome Family with Different Expressivity2016
- Author(s)
  Ishikawa T, Ohkubo K, Yamaguchi R, Harrell DT, Tsuji Y, Watanabe I, Makita N.
- Organizer
  第80回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Selective therapeutic targeting of ion channel rare variants predisposing to lone atrial fibrillation2016
- Author(s)
  Hayashi K, Fujino N, Tsuda T, Tanaka Y, Ino H, Makita N, Yamagishi M.
- Organizer
  第63回日本不整脈心電学会学術大会
- Place of Presentation
  札幌コンベンションセンター（北海道札幌市）
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Broader Genetic Spectrum of Familial Atrial Arrhythmias Involving Rare Variations in the Common Arrhythmia-Susceptible Genes2016
- Author(s)
  Ishikawa T, Mishima H, Ohno S, Harrell DT, Tsuji Y, Yoshiura K, Horie M, Makita N.
- Organizer
  第63回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Modeling of long-QT syndrome associated with a calmodulin mutation using human induced pluripotent stem cells2016
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Sasaki K, Hayano M, Nishiuchi S, Wuriyanghai Y, Kohjitani H, Hirose S, Cheng J, Ishikawa T, Ohno S, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  第63回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] 歯牙骨格形成異常を合併する洞不全症候群に固定されたコネキシン45遺伝子変異と機能異常.2016
- Author(s)
  木本浩樹, 石川泰輔, 西井明子, 斎藤加代子, 三嶋博之, 大槻早紀, 辻幸臣, 吉浦孝一郎, 萩原誠久, 蒔田直昌.
- Organizer
  第67回西日本生理学会
- Place of Presentation
  レインボー桜島（鹿児島県鹿児島市）
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] ECG Screening of 1-month-old Infants May Prevent Out-of-hospital Cardiac Arrest in Infancy2016
- Author(s)
  Yoshinaga M, Ohno S, Ushinohama H, Sato S, Miyamoto T, Tauchi N, Horigome H, Sumitomo N, Shiraishi H, Ichida F, Hata T, Nomura Y, Horie M, Makita N, Nagashima M.
- Organizer
  American Heat Association Scientific Meeting 2016
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Common genetic variants at SCN5A, SCN10A, and HEY2 are associated with cardiac conduction disturbance in patients with Brugada syndrome2016
- Author(s)
  Murakoshi N, Xu D, Nogami A, Makita N, Sekiguchi Y, Kurosaki K, Kowase S, Naruse Y, Aonuma K.
- Organizer
  第63回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Overview of Genes Related to Cardiac Conduction2016
- Author(s)
  Makita N.
- Organizer
  Korean Heart Rhythm Society 8th Annual Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] International Calmodulinopathy Registry (ICaMR)2016
- Author(s)
  Crotti L, Makita N.
- Organizer
  American Heart Association's Scientific Sessions
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] 心臓刺激伝導系と心室の電気的興奮現象のマルチスケールシミュレーション研究2016
- Author(s)
  稲田慎, ハーレルダニエル, 原口亮, 芦原貴司, 相庭武司, 山下富義, 柴田仁太郎, 池田隆徳, 三井和幸, 蒔田直昌, 本荘晴朗, ボエットマーク, 中沢一雄
- Organizer
  第93回日本生理学会大会
- Place of Presentation
  札幌市、札幌コンベンションセンター
- Year and Date
  2016-03-23
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Catheter Ablation of Brugada Syndrome：Further Evidence of Conduction Delay in the Right Ventricular Subepicardium as Mechanism of Brugada ECG and Ventricular Fibrillation2016
- Author(s)
  Nakagawa H, Sakamoto Y, Yamashiro K, Takagi M, Kusano K, Noda T, Yamazaki M, Honjo H, Makita N, Tsuchiya T, Hoogeudiik MG, Nademanee K.
- Organizer
  第63回日本不整脈心電学会学術大会
- Place of Presentation
  札幌コンベンションセンター（北海道札幌市）
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] 心臓刺激伝導系と心室の電気的興奮現象のマルチスケールシミュレーション研究2016
- Author(s)
  稲田慎, ハーレルダニエル, 原口亮, 芦原貴司, 相庭武司, 山下富義, 柴田仁太郎, 池田隆徳, 三井和幸, 蒔田直昌, 本荘晴朗, ボエットマーク, 中沢一雄.
- Organizer
  第93回日本生理学会大会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] ECG Screening of 1-month-old Infants May Prevent Out-of-hospital Cardiac Arrest in Infancy2016
- Author(s)
  Yoshinaga M, Ohno S, Ushinohama H, Sato S, Miyamoto T, Tauchi N, Horigome H, Sumitomo N, Shiraishi H, Ichida F, Hata T, Nomura Y, Horie M, Makita N, Nagashima M.
- Organizer
  American Heat Association Scientific Meeting 2016
- Place of Presentation
  New Orleans Convention Center, USA
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Novel de novo Calmodulin Mutation in a Pre-school boy Experiencing Aborted Cardiac Arrest2016
- Author(s)
  Takahashi K, Makita N.
- Organizer
  第63回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Conditional knockout mice recapitulated two families with congenital AV block and sick sinus syndrome with a novel connexin 45 mutation.2016
- Author(s)
  Nishii A, Ishikawa T, Daumy X, Urano M, Saito K, Baruteau A, Nishii K, Shibata Y, Kobayashi Y, Redon R, Schott JJ, Probst V, Hagiwara N, Makita N
- Organizer
  第80回日本循環器学会学術集会
- Place of Presentation
  仙台市、仙台市民会館
- Year and Date
  2016-03-18
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Naチャネル遺伝子のバリエーションと致死性不整脈の罹患性との関連2016
- Author(s)
  蒔田直昌, 石川泰輔.
- Organizer
  第93回日本生理学会大会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Genetic Background of Inherited Bradyarrhythmia2016
- Author(s)
  Makita N.
- Organizer
  Korean Heart Rhythm Society 8th Annual Scientific Session
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Overview of Genes Related to Cardiac Conduction2016
- Author(s)
  Makita N.
- Organizer
  Korean Heart Rhythm Society 8th Annual Scientific Session
- Place of Presentation
  KINTEX,Korea
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] International Calmodulinopathy Registry (ICaMR)2016
- Author(s)
  Crotti L, Makita N.
- Organizer
  American Heart Association's Scientific Sessions
- Place of Presentation
  New Orleands, USA
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Dose-Sensitive Relationship of an SCN10A Pore Mutation and Enhancer SNPs Identified in a Brugada Syndrome Family with Different Expressivity2016
- Author(s)
  Ishikawa T, Ohkubo K, Yamaguchi R, Harrell DT, Tsuji Y, Watanabe I, Makita N
- Organizer
  第80回日本循環器学会学術集会
- Place of Presentation
  仙台市、仙台市民会館
- Year and Date
  2016-03-18
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Novel de novo Calmodulin Mutation in a Pre-school boy Experiencing Aborted Cardiac Arrest2016
- Author(s)
  Takahashi K, Makita N.
- Organizer
  第63回日本不整脈心電学会学術大会
- Place of Presentation
  札幌コンベンションセンター（北海道札幌市）
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Genetic Background of Inherited Bradyarrhythmia2016
- Author(s)
  Makita N.
- Organizer
  Korean Heart Rhythm Society 8th Annual Scientific Session
- Place of Presentation
  KINTEX,Korea
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Naチャネル遺伝子のバリエーションと致死性不整脈の罹患性との関連2016
- Author(s)
  蒔田直昌, 石川泰輔
- Organizer
  第93回日本生理学会大会
- Place of Presentation
  札幌市、札幌コンベンションセンター
- Year and Date
  2016-03-23
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Conditional knockout mice recapitulated two families with congenital AV block and sick sinus syndrome with a novel connexin 45 mutation.2016
- Author(s)
  Nishii A, Ishikawa T, Daumy X, Urano M, Saito K, Baruteau A, Nishii K, Shibata Y, Kobayashi Y, Redon R, Schott JJ, Probst V, Hagiwara N, Makita N.
- Organizer
  第80回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Utility of QT dynamics for identyfying genetic testing candidates in children with borderline QT interval prolongation2016
- Author(s)
  Takahashi K, Makita N, Shimizu W.
- Organizer
  第80回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Common genetic variants at SCN5A, SCN10A, and HEY2 are associated with cardiac conduction disturbance in patients with Brugada syndrome2016
- Author(s)
  Murakoshi N, Xu D, Nogami A, Makita N, Sekiguchi Y, Kurosaki K, Kowase S, Naruse Y, Aonuma K.
- Organizer
  第63回日本不整脈心電学会学術大会
- Place of Presentation
  札幌コンベンションセンター（北海道札幌市）
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Selective therapeutic targeting of ion channel rare variants predisposing to lone atrial fibrillation2016
- Author(s)
  Hayashi K, Fujino N, Tsuda T, Tanaka Y, Ino H, Makita N, Yamagishi M.
- Organizer
  第63回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Broader Genetic Spectrum of Familial Atrial Arrhythmias Involving Rare Variations in the Common Arrhythmia-Susceptible Genes2016
- Author(s)
  Ishikawa T, Mishima H, Ohno S, Harrell DT, Tsuji Y, Yoshiura K, Horie M, Makita N.
- Organizer
  第63回日本不整脈心電学会学術大会
- Place of Presentation
  札幌コンベンションセンター（北海道札幌市）
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] Modeling of long-QT syndrome associated with a calmodulin mutation using human induced pluripotent stem cells2016
- Author(s)
  Yamamoto Y, Makiyama T, Harita T, Sasaki K, Hayano M, Nishiuchi S, Wuriyanghai Y, Kohjitani H, Hirose S, Cheng J, Ishikawa T, Ohno S, Yoshida Y, Horie M, Makita N, Kimura T.
- Organizer
  第63回日本不整脈心電学会学術大会
- Place of Presentation
  札幌コンベンションセンター（北海道札幌市）
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] 歯牙骨格形成異常を合併する洞不全症候群に固定されたコネキシン45遺伝子変異と機能異常2016
- Author(s)
  木本浩貴, 石川泰輔, 西井明子, 斎藤加代子, 三嶋博之, 大槻早紀, 辻幸臣, 吉浦孝一郎, 萩原誠久, 蒔田直昌.
- Organizer
  第67回西日本生理学会
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] New genes for Progressive Cardiac Conduction Disease.2015
- Author(s)
  Makita,N.
- Organizer
  Heart Rhythm Society
- Place of Presentation
  Boston,USA
- Year and Date
  2015-05-14
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] SCN5A and ventricular arrhythmias2015
- Author(s)
  Makita N
- Organizer
  Asian Pacific Heart Rhythm Society
- Place of Presentation
  Melbourne, Australia
- Year and Date
  2015-11-22
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Ventricular arrhythmias generated from purkinje fiber network with gap junction mutation －A simulation study－2015
- Author(s)
  Inada S, Harrell DT, Haraguchi R, Ashihara T, Makita N, Nakazawa K
- Organizer
  多階層生体機能学「終了記念シンポジウム」
- Place of Presentation
  大阪市、大阪大学中之島センター
- Year and Date
  2015-03-06
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Emerging link between genetic variations of sodium channels and susceptibility to lethal arrhythmias.2015
- Author(s)
  Makita N, Ishikawa T, Schott JJ, Bezzina CR
- Organizer
  第88回日本薬理学会
- Place of Presentation
  名古屋市、名古屋国際会議場
- Year and Date
  2015-03-19
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] SCN5A and ventricular arrhythmias.2015
- Author(s)
  Makita N
- Organizer
  Asian Pacific Heart Rhythm Society
- Place of Presentation
  Melbourne, Australia.
- Year and Date
  2015-11-22
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] 重症不整脈を伴うQT延長症候群の新規原因遺伝子CALM2の同定2015
- Author(s)
  石川泰輔, 須田憲治, 本村秀樹, 山本雄大, 牧山武, ダニエルハーレル, 辻幸臣, 蒔田直昌
- Organizer
  第66回西日本生理学会
- Place of Presentation
  久留米市、久留米大学
- Year and Date
  2015-10-10
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Study of long QT syndrome type 3 using human iPS cell-derived cardiomyocytes.2015
- Author(s)
  Furukawa T, Okata S, Yuasa S, Suzuki T, Makita N, Kurokawa J, Egashira T, Yamakawa H, Seki T, Aizawa Y, Hashimoto H, Kuroda Y, Tanaka A, Yae K, Murata M, Aiba T, Shimizu W, Horie M, Kamiya K, Fukuda K
- Organizer
  第30回日本不整脈学会学術大会・第32回日本心電学会学術集会
- Place of Presentation
  京都市、国立京都国際会館
- Year and Date
  2015-07-31
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Meta-analysis of Short QT Syndrome discloses genotype-dependent clinical characteristics in age of manifestation and arrhythmia complications.2015
- Author(s)
  Harrell DT, Ashihara T, Ishikawa T, Mazzanti A, Takahashi K, Oginosawa Y, Abe H, Maemura K, Sumitomo N, Uno K, Takano M, Priori SG, Makita N
- Organizer
  第30回日本不整脈学会学術大会・第32回日本心電学会学術集会
- Place of Presentation
  京都市、国立京都国際会館
- Year and Date
  2015-07-30
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Dose-Sensitive Relationship of an SCN10A Pore Mutation and Enhancer SNPs Identified in a Brugada Syndrome Family with Different Expressivity2015
- Author(s)
  Ishikawa T, Ohkubo K, Yamaguchi R, Harrell DT, Tsuji Y, Watanabe I, Makita N
- Organizer
  第30回日本不整脈学会学術大会・第32回日本心電学会学術集会
- Place of Presentation
  京都市、国立京都国際会館
- Year and Date
  2015-07-30
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] New genes for Progressive Cardiac Conduction Disease.2015
- Author(s)
  Makita, N.
- Organizer
  Academic Medical Center Research Seminar
- Place of Presentation
  AMC,Amsterdam,The Netherlands
- Year and Date
  2015-05-21
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Translational Perspective on Pathophysiology of Frequent ICD-shocked Ventricular Tachyarrhythmias.2015
- Author(s)
  Tsuji Y, Harrell DT, Ishikawa T, Makita N
- Organizer
  第30回日本不整脈学会学術大会・第32回日本心電学会学術集会
- Place of Presentation
  京都市、国立京都国際会館
- Year and Date
  2015-07-31
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] New genes for Progressive Cardiac Conduction Disease2015
- Author(s)
  Makita N
- Organizer
  Heart Rhythm Society
- Place of Presentation
  Boston,USA.
- Year and Date
  2015-05-14
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K15311
[Presentation] SCN5A and ventricular arrhythmias2015
- Author(s)
  Makita N
- Organizer
  Asian Pacific Heart Rhythm Society,
- Place of Presentation
  Melbourne, Australia.
- Year and Date
  2015-11-22
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] Can computer simulation technique contribute regenerative medicine?2015
- Author(s)
  Inada S, Harrell DT, Haraguchi R, Ashihara T, Aiba T, Ikeda T, Mitsui K, Honjo H, Shibata N, Makita N, Kamiya K, Kodama I, Nakazawa K
- Organizer
  第30回日本不整脈学会学術大会・第32回日本心電学会学術集会
- Place of Presentation
  京都市、国立京都国際会館
- Year and Date
  2015-07-31
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 乳幼児突然死症例に対する次世代シークエンサーを用いた脂肪酸代謝異常の遺伝子解析2015
- Author(s)
  大崎琢弥, 山本琢磨, 石川泰輔, 三嶋博之, 深堀友希, 梅原敬弘, 村瀬壮彦, 吉浦孝一郎, 蒔田直昌, 池松和哉
- Organizer
  日本法医学会学術九州地方集会
- Place of Presentation
  宮崎市、宮崎県医師会館
- Year and Date
  2015-10-16
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Ventricular arrhythmias generated from purkinje fiber network with gap junction mutation －A simulation study－2015
- Author(s)
  Inada S, Harrell DT, Haraguchi R, Ashihara T, Makita N, Nakazawa K
- Organizer
  多階層生体機能学「終了記念シンポジウム」
- Place of Presentation
  大阪市、大阪大学中之島センター
- Year and Date
  2015-03-06
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] New genes for Progressive Cardiac Conduction Disease.2015
- Author(s)
  Makita N
- Organizer
  Heart Rhythm Society
- Place of Presentation
  Boston, USA
- Year and Date
  2015-05-14
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04823
[Presentation] 心臓イオンチャネルの遺伝子異常と機能破綻の分子基盤2015
- Author(s)
  蒔田直昌
- Organizer
  多階層生体機能学「最終成果報告会」
- Place of Presentation
  大阪市、大阪大学中之島センター
- Year and Date
  2015-03-05
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Dose-Sensitive Relationship of an SCN10A Pore Mutation and Enhancer SNPS Identified in a Brugada Syndrome Family with Different Expressivity2015
- Author(s)
  Ishikawa T, Ohkubo K, Yamaguchi R, Harrell DT, Tsuji Y, Watanabe I, Makita N
- Organizer
  Heart Rhythm Society
- Place of Presentation
  Boston, USA
- Year and Date
  2015-05-15
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Emerging link between genetic variations of sodium channels and susceptibility to lethal arrhythmias.2015
- Author(s)
  Makita N, Ishikawa T, Schott JJ, Bezzina CR
- Organizer
  第88回日本薬理学会
- Place of Presentation
  名古屋市、名古屋国際会議場
- Year and Date
  2015-03-19
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 心臓イオンチャネルの遺伝子異常と機能破綻の分子基盤2015
- Author(s)
  蒔田直昌
- Organizer
  多階層生体機能学「最終成果報告会」
- Place of Presentation
  大阪市、大阪大学中之島センター
- Year and Date
  2015-03-05
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 家族性心臓伝導障害に同定されたコネキシン遺伝子変異とその機能異常2015
- Author(s)
  石川泰輔, 西井明子, 斎藤加代子, 三嶋博之, 大槻早紀, 稲田慎, ダニエルハーレル, 辻幸臣, 中沢一雄, 吉浦孝一郎, 萩原誠久, 蒔田直昌
- Organizer
  心血管膜輸送研究会2015
- Place of Presentation
  岡崎市、生理学研究所
- Year and Date
  2015-10-30
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] A Novel Splicing Mutation in a Sarcomeric Gene MYPN Responsible for Familial Sick Sinus Syndrome Identified by Whole Exome Sequencing2015
- Author(s)
  Ishikawa T, Nogami A, Kowase S, Harrell DT, Tsuji Y, Arimura T, Kimura A, Makita N
- Organizer
  第79回日本循環器学会学術集会
- Place of Presentation
  大阪市、大阪国際会議場
- Year and Date
  2015-04-26
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Distinct Clinical Characteristics in Short QT Syndrome Associated with Mutations in KCNH2 and KCNQ12015
- Author(s)
  Harrell DT, Ishikawa T, Komiya N, Takahashi K, Oginosawa Y, Abe H, Maemura K, Sumitomo N, Uno K, Makita N
- Organizer
  第79回日本循環器学会学術集会
- Place of Presentation
  大阪市、大阪国際会議場
- Year and Date
  2015-04-25
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] A Novel Mutation in Atrial Myosin Heavy Chain Coding Gene MYH6 Causes Sick Sinus Syndrome2014
- Author(s)
  Ishikawa T, Nogami A, Kowase S, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N
- Organizer
  第29回日本不整脈学会・第31回日本心電学会合同学術大会
- Place of Presentation
  東京都港区、ザ・プリンスパークタワー東京
- Year and Date
  2014-07-24
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Paradigm Shifts in the Genetics of Inherited Arrhythmias Brought on by High-throughput Sequencing and Genome-wide Association Studies2014
- Author(s)
  Makita N
- Organizer
  第29回日本不整脈学会・第31回日本心電学会合同学術大会
- Place of Presentation
  東京都港区、ザ・プリンスパークタワー東京
- Year and Date
  2014-07-24
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Electrical Storm in Inherited Arrhythmia Syndromes2014
- Author(s)
  Tsuji Y, Ishikawa T, Makita N
- Organizer
  第29回日本不整脈学会・第31回日本心電学会合同学術大会
- Place of Presentation
  東京都港区、ザ・プリンスパークタワー東京
- Year and Date
  2014-07-23
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 遺伝性不整脈の病態における最近の知見2014
- Author(s)
  蒔田直昌
- Organizer
  第23回東葛地区不整脈研究会
- Place of Presentation
  松戸市、松戸市立病院
- Year and Date
  2014-05-31
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Genetic modifiers in carriers of the SCN5A E1784K mutation with variable phenotypic expression - Long QT3 / Brugada syndrome overlap disease2014
- Author(s)
  Wileyeratne YD, Muggenthaler M, Tanck M, Schott JJ, Kyndt F, Probst V, Borggrefe M, McKeown P, Veltmann C, L C, Schwarts P, Sharma S, Makita N, Roden D, Behr ER
- Organizer
  British Cardiovascular Society annual meeting
- Place of Presentation
  Manchester,UK
- Year and Date
  2014-05-01
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Ventricular arrhythmia induced by the Purkinje network with reduced gap junction conductance - A simulation study -2014
- Author(s)
  Inada S, Harrell DT, Haraguchi R, Ashihara T, Makita N, Nakazawa K
- Organizer
  第53回日本生体医工学会
- Place of Presentation
  仙台市、仙台国際センター
- Year and Date
  2014-06-24
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Electrical Storm in Inherited Arrhythmia Syndromes2014
- Author(s)
  Tsuji Y, Ishikawa T, Makita N
- Organizer
  第29回日本不整脈学会・第31回日本心電学会合同学術大会
- Place of Presentation
  東京都港区、ザ・プリンスパークタワー東京
- Year and Date
  2014-07-23
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Ethnicity and phenotype in the SCN5A E1784K mutation.2014
- Author(s)
  Wijeyeratne Y, Probst V, Veltmann C, Shimizu W, Crotti L, Horie M, McKeown P, Makita N, Roden D, Behr ER
- Organizer
  European Society of Cardiology
- Place of Presentation
  Barcelona,Spain
- Year and Date
  2014-08-31
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 不整脈の新規病因解明を目指す全エクソン解析とiPS技術のハイブリッドアプローチ2014
- Author(s)
  石川泰輔, 牧山武, 蒔田直昌
- Organizer
  新学術研究領域「統合的多階層生体機能学領域の確立とその応用」
- Place of Presentation
  秋田市、秋田大学
- Year and Date
  2014-08-05
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Genotype-Phenotype Associations in Early Repolarization Syndrome2014
- Author(s)
  Sonoda K, Watanabe H, Nogami A, Ohkubo K, Makiyama T, Takehara N, Kawamura Y, Hosaka Y, Sato M, Fukae S, Chinushi M, Oda H, Okabe M, Shimizu W, Kimura A, Maemura K, Watanabe I, Kamakura S, Burashnikov E, Antzelevitch C, Horie M, Aizawa Y, Minamino T, Makita N
- Organizer
  35th Annual Scientific Sessions,Heart Rhythm
- Place of Presentation
  San Francisco, USA
- Year and Date
  2014-05-08
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Role of Ca2+/calmodulin -dependent Protein Kinase ll in Atrial and Ventricular Remodeling and Arrhythmias2014
- Author(s)
  Tsuji Y, Ishikawa T, Makita N
- Organizer
  第29回日本不整脈学会・第31回日本心電学会合同学術大会
- Place of Presentation
  東京都港区、ザ・プリンスパークタワー東京
- Year and Date
  2014-07-24
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Genetic modifiers in the long QT3/Brugada overlap-syndrome caused by E1784K.2014
- Author(s)
  Muggenthaler M, Tanck MW, Schott JJ, Kyndt F, Borggrefe M, McKeown P, Makita N, Schwartz P, Roden D, Behr ER
- Organizer
  European Society of Cardiology
- Place of Presentation
  Barcelona,Spain
- Year and Date
  2014-09-02
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Diverse Gender Difference of Arrhythmic Risk in Patients With Congenital Long QT Syndrome:From Japanese Congenital LQTS Multicenter Registry2014
- Author(s)
  Aiba T, Makimoto H, Makiyama T, Watanabe H, Hayashi K, Nakano Y, Miyauchi Y, Morita H, Aonuma K, Hagiwara N, Fukuda K, Yoshinaga M, Horigome H, Sumitomo N, Tanaka T, Sekine A, Shiraishi I, Kusano K, Miyamoto Y, Kamakura S, Yasuda S, Ogawa H, Makita N, Horie M, Shimizu W
- Organizer
  American Heart Association Scientific Sessions
- Place of Presentation
  Chicago,USA
- Year and Date
  2014-11-16
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] A novel cardiac alpha-myosin heavy chain (MYH6) mutation impairing sarcomere structure responsible for familial sick sinus syndrome2014
- Author(s)
  Ishikawa T, Nogami A, Kowase S, Harrell D, Tsuji Y, Arimura T, Kimura A, Makita N
- Organizer
  European Society of Cardiology
- Place of Presentation
  Barcelona,Spain
- Year and Date
  2014-09-02
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Role of Ca2+/calmodulin -dependent Protein Kinase ll in Atrial and Ventricular Remodeling and Arrhythmias2014
- Author(s)
  Tsuji Y, Ishikawa T, Makita N
- Organizer
  第29回日本不整脈学会・第31回日本心電学会合同学術大会
- Place of Presentation
  東京都港区、ザ・プリンスパークタワー東京
- Year and Date
  2014-07-24
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Genotype-Phenotype Associations in Early Repolarization Syndrome2014
- Author(s)
  Sonoda K, Watanabe H, Nogami A, Ohkubo K, Makiyama T, Takehara N, Kawamura Y, Hosaka Y, Sato M, Fukae S, Chinushi M, Oda H, Okabe M, Shimizu W, Kimura A, Maemura K, Watanabe I, Kamakura S, Burashnikov E, Antzelevitch C, Horie M, Aizawa Y, Minamino T, Makita N
- Organizer
  35th Annual Scientific Sessions,Heart Rhythm
- Place of Presentation
  San Francisco,USA
- Year and Date
  2014-05-08
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] A Novel Cardiac a-Myosin Heavy Chain (MYH6) Mutation Associated with Familial Sick Sinus Syndrome Altering Sarcomeric Organization2014
- Author(s)
  Ishikawa T, Nogami A, Kowase S, Arimura T, Kimura A, Makita N
- Organizer
  35th Annual Scientific Sessions,Heart Rhythm
- Place of Presentation
  San Francisco, USA
- Year and Date
  2014-05-08
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] The Spectrum of Most Frequent Mutation in Short QT Syndrome2014
- Author(s)
  Hu D, Zhang J, Li Y, Gollob M, Healey J, Harrell DT, Makita N, Abe H, Sun Y, Zhang L, Yan G, Mah D, Walsh E, Leopold H, Giustetto C, Gaita F, Martinez HB, Antzelevitch C
- Organizer
  35th Annual Scientific Sessions, Heart Rhythm
- Place of Presentation
  San Francisco,USA
- Year and Date
  2014-05-08
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Ventricular arrhythmia induced by the Purkinje network with reduced gap junction conductance - A simulation study -2014
- Author(s)
  Inada S, Harrell DT, Haraguchi R, Ashihara T, Makita N, Nakazawa K
- Organizer
  第53回日本生体医工学会
- Place of Presentation
  仙台市、仙台国際センター
- Year and Date
  2014-06-24
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Ethnicity and phenotype in the SCN5A E1784K mutation.2014
- Author(s)
  Wijeyeratne Y, Probst V, Veltmann C, Shimizu W, Crotti L, Horie M, McKeown P, Makita N, Roden D, Behr ER
- Organizer
  European Society of Cardiology
- Place of Presentation
  Barcelona,Spain
- Year and Date
  2014-08-31
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Genetic modifiers in the long QT3/Brugada overlap-syndrome caused by E1784K.2014
- Author(s)
  Muggenthaler M, Tanck MW, Schott JJ, Kyndt F, Borggrefe M, McKeown P, Makita N, Schwartz P, Roden D, Behr ER
- Organizer
  European Society of Cardiology
- Place of Presentation
  Barcelona,Spain
- Year and Date
  2014-09-02
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] A novel cardiac alpha-myosin heavy chain (MYH6) mutation impairing sarcomere structure responsible for familial sick sinus syndrome2014
- Author(s)
  Ishikawa T, Nogami A, Kowase S, Harrell D, Tsuji Y, Arimura T, Kimura A, Makita N
- Organizer
  European Society of Cardiology
- Place of Presentation
  Barcelona,Spain
- Year and Date
  2014-09-02
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] A Novel Cardiac a-Myosin Heavy Chain (MYH6) Mutation Associated with Familial Sick Sinus Syndrome Altering Sarcomeric Organization2014
- Author(s)
  Ishikawa T, Nogami A, Kowase S, Arimura T, Kimura A, Makita N
- Organizer
  35th Annual Scientific Sessions,Heart Rhythm
- Place of Presentation
  San Francisco,USA
- Year and Date
  2014-05-08
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] The Spectrum of Most Frequent Mutation in Short QT Syndrome2014
- Author(s)
  Hu D, Zhang J, Li Y, Gollob M, Healey J, Harrell DT, Makita N, Abe H, Sun Y, Zhang L, Yan G, Mah D, Walsh E, Leopold H, Giustetto C, Gaita F, Martinez HB, Antzelevitch C
- Organizer
  35th Annual Scientific Sessions, Heart Rhythm
- Place of Presentation
  San Francisco, USA
- Year and Date
  2014-05-08
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Paradigm Shifts in the Genetics of Inherited Arrhythmias Brought on by High-throughput Sequencing and Genome-wide Association Studies2014
- Author(s)
  Makita N
- Organizer
  第29回日本不整脈学会・第31回日本心電学会合同学術大会
- Place of Presentation
  東京都港区、ザ・プリンスパークタワー東京
- Year and Date
  2014-07-24
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Diverse Gender Difference of Arrhythmic Risk in Patients With Congenital Long QT Syndrome:From Japanese Congenital LQTS Multicenter Registry2014
- Author(s)
  Aiba T, Makimoto H, Makiyama T, Watanabe H, Hayashi K, Nakano Y, Miyauchi Y, Morita H, Aonuma K, Hagiwara N, Fukuda K, Yoshinaga M, Horigome H, Sumitomo N, Tanaka T, Sekine A, Shiraishi I, Kusano K, Miyamoto Y, Kamakura S, Yasuda S, Ogawa H, Makita N, Horie M, Shimizu W
- Organizer
  American Heart Association Scientific Sessions
- Place of Presentation
  Chicago,USA
- Year and Date
  2014-11-16
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 遺伝性不整脈の病態における最近の知見2014
- Author(s)
  蒔田直昌
- Organizer
  第23回東葛地区不整脈研究会
- Place of Presentation
  松戸市、松戸市立病院
- Year and Date
  2014-05-31
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] A Novel Mutation in Atrial Myosin Heavy Chain Coding Gene MYH6 Causes Sick Sinus Syndrome2014
- Author(s)
  Ishikawa T, Nogami A, Kowase S, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N
- Organizer
  第29回日本不整脈学会・第31回日本心電学会合同学術大会
- Place of Presentation
  東京都港区、ザ・プリンスパークタワー東京
- Year and Date
  2014-07-24
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Genetic modifiers in carriers of the SCN5A E1784K mutation with variable phenotypic expression - Long QT3 / Brugada syndrome overlap disease2014
- Author(s)
  Wileyeratne YD, Muggenthaler M, Tanck M, Schott JJ, Kyndt F, Probst V, Borggrefe M, McKeown P, Veltmann C, L C, Schwarts P, Sharma S, Makita N, Roden D, Behr ER
- Organizer
  British Cardiovascular Society annual meeting
- Place of Presentation
  Manchester,UK
- Year and Date
  2014-05-01
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 不整脈の新規病因解明を目指す全エクソン解析とiPS技術のハイブリッドアプローチ2014
- Author(s)
  石川泰輔, 牧山武, 蒔田直昌
- Organizer
  新学術研究領域「統合的多階層生体機能学領域の確立とその応用」
- Place of Presentation
  秋田市、秋田大学
- Year and Date
  2014-08-05
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Clinical and Genetic Characteristics of Short QT Symdrome in Japan.2013
- Author(s)
  Harrell D, Makita N, et al
- Organizer
  The 77th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Yokohama Japan
- Year and Date
  2013-03-16
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Clinical Manifestations and Electrophysiological Characteristics of K Channel Mutations Responsible for Short QT Syndrome.2013
- Author(s)
  Harrell D, Makita N, et al
- Organizer
  第90回日本生理学会大会
- Place of Presentation
  横浜
- Year and Date
  2013-03-29
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] グレリン、CCK-8およびLPS誘発の摂食行動に及ぼす求心性迷走神経内臓枝の役割2013
- Author(s)
  松本逸郎、蒔田直昌、他
- Organizer
  第90回日本生理学会大会
- Place of Presentation
  横浜
- Year and Date
  2013-03-27
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Clinical Manifestations and Electrophysiological Characteristics of K Channel Mutations Responsible for Short QT Syndrome.2013
- Author(s)
  Harrell D, Makita N, et al
- Organizer
  第90回日本生理学会大会
- Place of Presentation
  横浜
- Year and Date
  2013-03-29
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] グレリン、CCK-8およびLPS誘発の摂食行動に及ぼす求心性迷走神経内臓枝の役割2013
- Author(s)
  松本逸郎、蒔田直昌、他
- Organizer
  第90回日本生理学会大会
- Place of Presentation
  横浜
- Year and Date
  2013-03-27
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 致死性不整脈の遺伝子基盤:特発性心室細動と伝導障害2013
- Author(s)
  蒔田直昌
- Organizer
  第13回近畿心不全・不整脈カンファレンス
- Place of Presentation
  大阪(招待講演)
- Year and Date
  2013-02-16
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 致死性不整脈の遺伝子基盤：特発性心室細動と伝導障害2013
- Author(s)
  蒔田直昌
- Organizer
  第13回近畿心不全・不整脈カンファレンス
- Place of Presentation
  大阪
- Year and Date
  2013-02-16
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Clinical and Genetic Characteristics of Short QT Symdrome in Japan.2013
- Author(s)
  Harrell D, Makita N, et al
- Organizer
  The 77th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Yokohama Japan
- Year and Date
  2013-03-16
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] グレリン誘発の摂食促進には迷走神経胃枝および肝・門脈枝の求心性神経終末部の2型ヒスタミンレセプターを介する神経入力が関与する2012
- Author(s)
  松本逸郎、蒔田直昌, 他
- Organizer
  第89回日本生理学会大会
- Place of Presentation
  松本
- Year and Date
  2012-03-29
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Arrhythmia-associated Variants in the SCN5A Promoter and Regulatory Regions.2012
- Author(s)
  Yagihara N, Makita N, et al
- Organizer
  American Heart Association Scientific Sessions 2012
- Place of Presentation
  Los Angeles USA
- Year and Date
  2012-11-04
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 進行性心臓伝導障害2012
- Author(s)
  蒔田直昌
- Organizer
  第41回日本心脈管作動物質学会
- Place of Presentation
  秋田
- Year and Date
  2012-02-11
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] EP臨床医に必要な遺伝子診断の知識2012
- Author(s)
  蒔田直昌
- Organizer
  第27回日本不整脈学会学術大会
- Place of Presentation
  横浜
- Year and Date
  2012-07-07
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] A Novel Mechanism of Brugada Syndrome : Mutation of Sarcolemmal Membrane-associated Protein (SLMAP) Gene Impaired hNav1.5 Function2012
- Author(s)
  Ishikawa T, Makita N, et al
- Organizer
  The 76th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Fukuoka
- Year and Date
  2012-03-16
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Arrhythmia-associated Variants in the SCN5A Promoter and RegulatoryRegions.2012
- Author(s)
  Yagihara N, Makita N, et al
- Organizer
  American Heart Association Scientific Sessions 2012
- Place of Presentation
  Los Angeles USA
- Year and Date
  2012-11-04
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 家族性進行性心臓伝導障害の重症家系に同定されたコネキシン40遺伝子変異2012
- Author(s)
  蒔田直昌
- Organizer
  第89回日本生理学会大会
- Place of Presentation
  松本
- Year and Date
  2012-03-30
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 進行性心臓伝導障害の全国レジストリー2012
- Author(s)
  蒔田直昌、堀江稔、他
- Organizer
  第27回日本不整脈学会学術大会
- Place of Presentation
  横浜
- Year and Date
  2012-07-06
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 致死性不整脈の原因はどこまでわかったか2012
- Author(s)
  蒔田直昌
- Organizer
  佐世保市不整脈学術講演会
- Place of Presentation
  佐世保
- Year and Date
  2012-02-24
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Biophysical Properties of Na Channel in the S5-S6 High Risk LQT3 Mutations of the Long QT Syndrome.2012
- Author(s)
  Aiba T, Makita N, et al
- Organizer
  American Heart Association Scientific Sessions 2012
- Place of Presentation
  Los Angeles USA
- Year and Date
  2012-11-07
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Genetic Diagnosis of Hereditary Lethal Arrhythmias2012
- Author(s)
  Makita N
- Organizer
  The 76th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Fukuoka
- Year and Date
  2012-03-17
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 遺伝性致死性不整脈の基礎と臨床2012
- Author(s)
  蒔田直昌
- Organizer
  第34回高知不整脈研究会
- Place of Presentation
  高知
- Year and Date
  2012-01-13
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 家族性進行性心臓伝導障害の重症家系に同定されたコネキシン40遺伝子変異2012
- Author(s)
  蒔田直昌
- Organizer
  第89回日本生理学会大会
- Place of Presentation
  松本
- Year and Date
  2012-03-30
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 致死性不整脈の遺伝子異常に関する最近の知見2012
- Author(s)
  蒔田直昌
- Organizer
  お茶の水ハートリズム研究会
- Place of Presentation
  東京
- Year and Date
  2012-06-02
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Is it the Prime Time to Treat the Patients with Early Repolarization?2012
- Author(s)
  Makita N
- Organizer
  The 5th Asia Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Taipei Taiwan
- Year and Date
  2012-10-05
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈の分子病態2012
- Author(s)
  蒔田直昌
- Organizer
  第4回鴨川循環器フォーラム
- Place of Presentation
  京都
- Year and Date
  2012-09-11
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 進行性心臓伝導障害の基礎と臨床2012
- Author(s)
  蒔田直昌
- Organizer
  第27回犬山不整脈カンファランス
- Place of Presentation
  東京(招待講演)
- Year and Date
  2012-08-18
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Clinical Features and Genetic Basis of 63 Patients with Progressive Cardiac Conduction Defect.2012
- Author(s)
  Makita N, Delmar M, et al
- Organizer
  Heart Rhythm Society 33rd Annual Scientific Sessions 2012
- Place of Presentation
  Boston USA
- Year and Date
  2012-05-09
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 薬剤誘発性QT延長症候群の遺伝子基盤2012
- Author(s)
  蒔田直昌
- Organizer
  医療薬学フォーラム2012
- Place of Presentation
  福岡
- Year and Date
  2012-07-15
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Biophysical Properties of Na Channel in the S5-S6 High Risk LQT3 Mutations of the Long QT Syndrome.2012
- Author(s)
  Aiba T, Makita N, et al
- Organizer
  American Heart Association Scientific Sessions 2012
- Place of Presentation
  Los Angeles USA
- Year and Date
  2012-11-07
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 器質的心疾患を伴わない心室細動の診断と治療2012
- Author(s)
  蒔田直昌
- Organizer
  第39回日本集中治療医学会学術集会
- Place of Presentation
  千葉
- Year and Date
  2012-02-29
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 致死性不整脈の原因はどこまでわかったか2012
- Author(s)
  蒔田直昌
- Organizer
  佐世保市不整脈学術講演会
- Place of Presentation
  佐世保
- Year and Date
  2012-02-24
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 致死性不整脈の遺伝子異常2012
- Author(s)
  蒔田直昌
- Organizer
  第29回岐阜不整脈研究会
- Place of Presentation
  岐阜
- Year and Date
  2012-11-15
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 進行性心臓伝導障害2012
- Author(s)
  蒔田直昌
- Organizer
  第41回日本心脈管作動物質学会
- Place of Presentation
  秋田
- Year and Date
  2012-02-11
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 薬剤誘発性QT延長症候群の遺伝子基盤2012
- Author(s)
  蒔田直昌
- Organizer
  医療薬学フォーラム2012
- Place of Presentation
  福岡
- Year and Date
  2012-07-15
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈の臨床と遺伝子診断2012
- Author(s)
  蒔田直昌
- Organizer
  第23回九州不整脈研究会
- Place of Presentation
  福岡
- Year and Date
  2012-07-21
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈のトピックス2012
- Author(s)
  蒔田直昌
- Organizer
  不整脈アカデミー
- Place of Presentation
  岡山
- Year and Date
  2012-05-22
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] A Novel Mechanism of Brugada Syndrome : Mutation of Sarcolemmal Membrane-associated Protein (SLMAP) Gene Impaired hNav1.5 Function2012
- Author(s)
  Ishikawa T, Makita N, et al
- Organizer
  The 76th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Fukuoka
- Year and Date
  2012-03-16
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Genetic Diagnosis of Hereditary Lethal Arrhythmias2012
- Author(s)
  Makita N
- Organizer
  The 76th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Fukuoka
- Year and Date
  2012-03-17
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical Features and Genetic Basis of 63 Patients with Progressive Cardiac Conduction Defect.2012
- Author(s)
  Makita N, Delmar M, et al
- Organizer
  Heart Rhythm Society 33rd Annual Scientific SesSions 2012
- Place of Presentation
  Boston USA
- Year and Date
  2012-05-09
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 進行性心臓伝導障害の全国レジストリー2012
- Author(s)
  蒔田直昌、堀江　稔、他
- Organizer
  第27回日本不整脈学会学術大会
- Place of Presentation
  横浜
- Year and Date
  2012-07-06
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈のトピックス2012
- Author(s)
  蒔田直昌
- Organizer
  不整脈アカデミー
- Place of Presentation
  岡山(招待講演)
- Year and Date
  2012-05-22
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 致死性不整脈の臨床と遺伝子診断2012
- Author(s)
  蒔田直昌
- Organizer
  第23回九州不整脈研究会
- Place of Presentation
  福岡(招待講演)
- Year and Date
  2012-07-21
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 致死性不整脈の遺伝子異常に関する最近の知見2012
- Author(s)
  蒔田直昌
- Organizer
  お茶の水ハートリズム研究会
- Place of Presentation
  東京(招待講演)
- Year and Date
  2012-06-02
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Mutation Site-specific Differences in Arrhythmic Risk in the LQT3 Form of Congenital Long QT Syndrome2012
- Author(s)
  Aiba T, Makita N, et al
- Organizer
  The 76th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Fukuoka
- Year and Date
  2012-03-16
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 致死性不整脈の分子病態2012
- Author(s)
  蒔田直昌
- Organizer
  第4回鴨川循環器フォーラム
- Place of Presentation
  京都(招待講演)
- Year and Date
  2012-09-11
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Molecular and Physiological Basis of Familial Progressive Heart Block Type-I2012
- Author(s)
  Makita N
- Organizer
  The 1st HD Physiology International Symposium
- Place of Presentation
  Tokyo
- Year and Date
  2012-01-21
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈の遺伝子異常2012
- Author(s)
  蒔田直昌
- Organizer
  第29回岐阜不整脈研究会
- Place of Presentation
  岐阜(招待講演)
- Year and Date
  2012-11-15
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] グレリン誘発の摂食促進には迷走神経胃枝および肝・門脈枝の求心性神経終末部の2型ヒスタミンレセプターを介する神経入力が関与する2012
- Author(s)
  松本逸郎、蒔田直昌, 他
- Organizer
  第89回日本生理学会大会
- Place of Presentation
  松本
- Year and Date
  2012-03-29
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 進行性心臓伝導障害の基礎と臨床2012
- Author(s)
  蒔田直昌
- Organizer
  第27回犬山不整脈カンファランス
- Place of Presentation
  東京
- Year and Date
  2012-08-18
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Is it the Prime Time to Treat the Patients with Early Repolarization?2012
- Author(s)
  Makita N
- Organizer
  The 5th Asia Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Taipei Taiwan(招待講演)
- Year and Date
  2012-10-05
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 遺伝性致死性不整脈の基礎と臨床2012
- Author(s)
  蒔田直昌
- Organizer
  第34回高知不整脈研究会
- Place of Presentation
  高知
- Year and Date
  2012-01-13
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] EP臨床医に必要な遺伝子診断の知識2012
- Author(s)
  蒔田直昌
- Organizer
  第27回日本不整脈学会学術大会
- Place of Presentation
  横浜
- Year and Date
  2012-07-07
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Molecular and Physiological Basis of Familial Progressive Heart Block Type-I2012
- Author(s)
  Makita N
- Organizer
  The 1st HD Physiology International Symposium
- Place of Presentation
  Tokyo
- Year and Date
  2012-01-21
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Mutation Site-specific Differences in Arrhythmic Risk in the LQT3 Form of Congenital Long QT Syndrome2012
- Author(s)
  Aiba T, Makita N, et al
- Organizer
  The 76th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Fukuoka
- Year and Date
  2012-03-16
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 器質的心疾患を伴わない心室細動の診断と治療2012
- Author(s)
  蒔田直昌
- Organizer
  第39回日本集中治療医学会学術集会
- Place of Presentation
  千葉
- Year and Date
  2012-02-29
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Clinical and Genetic Features of Japanese Patient with Congenital Long QT Syndrome2011
- Author(s)
  Makimoto H, Makita N, et al
- Organizer
  4th Asia Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Fukuoka
- Year and Date
  2011-09-20
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 早期再分極を伴った特発性心室細動の遺伝子解析と機能解析2011
- Author(s)
  蒔田直昌
- Organizer
  平成23年度生理学研究所研究会
- Place of Presentation
  岡崎
- Year and Date
  2011-11-30
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 先天性洞不全症候群2家系に同定された心筋Naチャネル異変の機能解析2011
- Author(s)
  阿部圭祐、蒔田直昌, 他
- Organizer
  第62回西日本生理学会
- Place of Presentation
  佐賀
- Year and Date
  2011-10-15
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Clinical features and Genetic Basis of Progressive Cardiac Conduction Defect : Japanese PCCD Registry2011
- Author(s)
  Makita N, et al
- Organizer
  26th Annual Scientific Session of the Japanese Society of Electrocardiology
- Place of Presentation
  Fukuoka
- Year and Date
  2011-09-20
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] J Wave Syndrome・Brugada Syndromeの遺伝子異常-Overview-2011
- Author(s)
  蒔田直昌
- Organizer
  第26回犬山不整脈カンファランス
- Place of Presentation
  名古屋
- Year and Date
  2011-08-20
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] ブルガタ症候群患者に見出されたSCN3B遺伝子V110I変異とその機能解析2011
- Author(s)
  石川泰輔、蒔田直昌, 他
- Organizer
  第56回日本人類遺伝学会・第11回東アジア人類遺伝学会共同大会
- Place of Presentation
  千葉
- Year and Date
  2011-11-10
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical Features and Genetic Basis of Progressive Cardiac Conduction Defect : Japanese PCCD Registry2011
- Author(s)
  Makita N, et al
- Organizer
  4th Asia Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Fukuoka
- Year and Date
  2011-09-20
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical and Genetic Features of Japanese Patient with Congenital Long QT Syndrome2011
- Author(s)
  Makimoto H, Makita N, et al
- Organizer
  4th Asia Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Fukuoka
- Year and Date
  2011-09-20
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 早期再分極を伴った特発性心室細動の遺伝子解析と機能解析2011
- Author(s)
  蒔田直昌
- Organizer
  平成23年度生理学研究所研究会
- Place of Presentation
  岡崎
- Year and Date
  2011-11-30
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] J Wave Syndrome・Brugada Syndromeの遺伝子異常-Overview-2011
- Author(s)
  蒔田直昌
- Organizer
  第26回犬山不整脈カンファランス
- Place of Presentation
  名古屋
- Year and Date
  2011-08-20
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈研究の進歩2011
- Author(s)
  蒔田直昌
- Organizer
  第14回大分心電図研究会
- Place of Presentation
  大分
- Year and Date
  2011-01-07
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Clinical Features and Genetic Basis of Progressive Cardiac Conduction Defect : Japanese PCCD Registry2011
- Author(s)
  Makita N, et al
- Organizer
  4th Asia Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Fukuoka
- Year and Date
  2011-09-20
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Symposium 7-6, A New Approach to the Pathophysiology of Hereditary Sudden Cardiac Death Syndrome, Clinical and Genetic Features of Japanese Patient with Congenital Long QT Syndrome2011
- Author(s)
 Makimoto H, Makita N, Sumitomo N, et al
- Organizer
 The 74^<th> Japanese Circulation Society
- Place of Presentation
 Yokohama
- Data Source
 KAKENHI-PROJECT-21590921
[Presentation] 遺伝性不整脈の基礎と臨床2011
- Author(s)
  蒔田直昌
- Organizer
  第24回九州小児不整脈研究会学術集会・症例検討会
- Place of Presentation
  熊本
- Year and Date
  2011-11-05
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical and Genetic Features of Japanese Patient with Congenital Long QT Syndrome2011
- Author(s)
  Makimoto H, Makita N, et al
- Organizer
  26th Annual Scientific Session of the Japanese Society of Electrocardiology
- Place of Presentation
  Fukuoka
- Year and Date
  2011-09-20
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] ブルガタ症候群患者に見出されたSCN3B遺伝子V110I変異とその機能解析2011
- Author(s)
  石川泰輔、蒔田直昌, 他
- Organizer
  第56回日本人類遺伝学会・第11回東アジア人類遺伝学会共同大会
- Place of Presentation
  千葉
- Year and Date
  2011-11-10
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Overview of cardiac ion channelopathies2011
- Author(s)
  Makita N
- Organizer
  36 th Annual ISCE Conference
- Place of Presentation
  San Jose USA
- Year and Date
  2011-04-14
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical and Genetic Features of Japanese Patient with Congenital Long QT Syndrome2011
- Author(s)
  Makimoto H, Makita N, et al
- Organizer
  26th Annual Scientific Session of the Japanese Society of Electrocardiology
- Place of Presentation
  Fukuoka
- Year and Date
  2011-09-20
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Functional Basis of Type 3 Long QT Syndrome2011
- Author(s)
  Makita N
- Organizer
  The 75th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Yokohama
- Year and Date
  2011-08-04
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Symposium 7-6, A New Approach to the Pathophysiology of Hereditary Sudden Cardiac Death Syndrome, Clinical and Genetic Features of Japanese Patient with Congenital Long QT Syndrome2011
- Author(s)
 Makimoto H, Makita N, et al
- Organizer
 The 74^<th> Japanese Circulation Society
- Place of Presentation
 Yokohama
- Data Source
 KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈の基礎と臨床2011
- Author(s)
  蒔田直昌
- Organizer
  第64回福岡不整脈同好会
- Place of Presentation
  福岡
- Year and Date
  2011-01-22
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] What Influences ss-blocker Resistance for Secondary Prevention of Cardiac Events in Patients with Congenital Long QT Syndrome2011
- Author(s)
 Makimoto H, Makita N, Sumitomo N, et al
- Organizer
 The 74^<th> Japanese Circulation Society
- Place of Presentation
 Yokohama
- Data Source
 KAKENHI-PROJECT-21590921
[Presentation] Functional Basis of Type 3 Long QT Syndrome2011
- Author(s)
  Makita N
- Organizer
  The 75th Annual Scientific Meeting of the Japanese Circulation Society
- Place of Presentation
  Yokohama
- Year and Date
  2011-08-04
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] QT延長症候群の診断と治療2011
- Author(s)
  蒔田直昌
- Organizer
  Daiichi-Sankyo循環器ファーラム2011
- Place of Presentation
  東京
- Year and Date
  2011-12-10
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈の基礎と臨床2011
- Author(s)
  蒔田直昌
- Organizer
  第64回福岡不整脈同好会
- Place of Presentation
  福岡
- Year and Date
  2011-01-22
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical features and Genetic Basis of Progressive Cardiac Conduction Defect : Japanese PCCD Registry2011
- Author(s)
  Makita N, et al
- Organizer
  26th Annual Scientific Session of the Japanese Society of Electrocardiology
- Place of Presentation
  Fukuoka
- Year and Date
  2011-09-20
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Overview of cardiac ion channelopathies2011
- Author(s)
  Makita N
- Organizer
  36 th Annual ISCE Conference
- Place of Presentation
  San Jose USA
- Year and Date
  2011-04-14
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Jwave Syndrome2011
- Author(s)
  蒔田直昌
- Organizer
  第13回札幌ハートリズムカンファレンス
- Place of Presentation
  札幌
- Year and Date
  2011-01-29
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Jwave Syndrome2011
- Author(s)
  蒔田直昌
- Organizer
  第13回札幌ハートリズムカンファレンス
- Place of Presentation
  札幌
- Year and Date
  2011-01-29
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] A New Approach to the Pathophysiology of Hereditary Sudden Cardiac Death Syndrome, Clinical and Genetic Features of Japanese Patient with Congenital Long QT Syndrome2011
- Author(s)
 Makimoto H, Makita N, Sumitomo N, et al
- Organizer
 The 74^<th> Japanese Circulation Society
- Place of Presentation
 Yokohama
- Data Source
 KAKENHI-PROJECT-21590921
[Presentation] 致死性不整脈研究の進歩2011
- Author(s)
  蒔田直昌
- Organizer
  第14回大分心電図研究会
- Place of Presentation
  大分
- Year and Date
  2011-01-07
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 先天性洞不全症候群2家系に同定された心筋Naチャネル異変の機能解析2011
- Author(s)
  阿部圭祐、蒔田直昌, 他
- Organizer
  第62回西日本生理学会
- Place of Presentation
  佐賀
- Year and Date
  2011-10-15
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 遺伝性不整脈の基礎と臨床2011
- Author(s)
  蒔田直昌
- Organizer
  第24回九州小児不整脈研究会学術集会・症例検討会
- Place of Presentation
  熊本
- Year and Date
  2011-11-05
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] QT延長症候群の診断と治療2011
- Author(s)
  蒔田直昌
- Organizer
  Daiichi-Sankyo循環器ファーラム2011
- Place of Presentation
  東京
- Year and Date
  2011-12-10
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical Features of Congenital Long QT Syndrome in Pre-elementary-age Children2010
- Author(s)
  Makimoto H, Makita N, et al
- Organizer
  American Heart Association Scientific Sessions 2010
- Place of Presentation
  Chicago USA
- Year and Date
  2010-11-15
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] QT延長症候群に対するエプレレノンの有効性について2010
- Author(s)
  蒔田直昌
- Organizer
  Meet the specialist滋賀循環器講演
- Place of Presentation
  滋賀
- Year and Date
  2010-05-14
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Molecular basis of cardiac conduction defect2010
- Author(s)
  Makita N, Schot, J-J
- Organizer
  Annual European-SAKURA meeting
- Place of Presentation
  Nantes France
- Year and Date
  2010-12-06
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Electrocardiographic risk factors for complete atrioventricular block : The Niigata Preventive Medicine Study2010
- Author(s)
  Watanabe H, Makita N, et al
- Organizer
  American Heart Association Scientific Sessions 2010
- Place of Presentation
  Chicago USA.
- Year and Date
  2010-11-16
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Electrocardiographic risk factors for complete atrioventricular block : The Niigata Preventive Medicine Study2010
- Author(s)
  Watanabe H, Makita N, et al
- Organizer
  American Heart Association Scientific Sessions 2010
- Place of Presentation
  Chicago USA
- Year and Date
  2010-11-16
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Brugada症候群とその類縁疾患の病態2010
- Author(s)
  蒔田直昌
- Organizer
  第27回日本心電学会学術集会ランチョンセミナー
- Place of Presentation
  大分
- Year and Date
  2010-10-08
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Molecular basis of cardiac conduction defect.2010
- Author(s)
  Makita N, Schot, J-J
- Organizer
  Annual European-SAKURA meeting-
- Place of Presentation
  Nantes France
- Year and Date
  2010-12-06
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Molecular genetics of Brugada syndrome.2010
- Author(s)
  Makita N
- Organizer
  XXth World Congress of the International Society for Heart Research 2010 Kyoto
- Place of Presentation
  Kyoto
- Year and Date
  2010-05-13
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Novel Mechanisms of Trafficking Defect Caused by KCNQ1 Mutations Found in Long QT Syndrome2010
- Author(s)
  Arimura T, Makita N, et al
- Organizer
  The 3nd Asia-Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Jeju Korea
- Year and Date
  2010-10-29
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical Phenotype and Prognosis of Probands with Brugada Syndrome in Relation to SCN5A Mutaiton.2010
- Author(s)
  Yamagata K, Makita N, et al
- Organizer
  第74回日本循環器学会総会・学術集会
- Place of Presentation
  京都
- Year and Date
  2010-03-06
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Electrocardiographic risk factors for complete atrioventricular block : The Niigata Preventive Medicine Study2010
- Author(s)
  Watanabe H, Makita N, et al
- Organizer
  American Heart Association Scientific Sessions 2010
- Place of Presentation
  Chicago USA.
- Year and Date
  2010-11-16
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈の基礎と臨床2010
- Author(s)
  蒔田直昌
- Organizer
  第96回日本循環器学会中国・四国合同地方会
- Place of Presentation
  鳥取
- Year and Date
  2010-06-11
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Molecular genetics of Brugada syndrome.2010
- Author(s)
  Makita N
- Organizer
  XXth World Congress of the International Society for Heart Research 2010 Kyoto
- Place of Presentation
  Kyoto
- Year and Date
  2010-05-13
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Cardiac Conduction Disturbance and Connexins2010
- Author(s)
  Makita N
- Organizer
  The 3nd Asia-Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Jeju Korea
- Year and Date
  2010-10-30
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Special Session Molecular Basis of Congenital Long QT and Related Arrhythmia Syndromes2010
- Author(s)
  Makita N
- Organizer
  第74回日本循環器学会総会・学術集会
- Place of Presentation
  京都
- Year and Date
  2010-03-06
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 心電図QT時間の遺伝的素因2010
- Author(s)
  蒔田直昌
- Organizer
  第27回日本心電学会学術集会モーニングセミナー
- Place of Presentation
  大分
- Year and Date
  2010-10-09
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Brugada症候群とその類縁疾患の病態2010
- Author(s)
  蒔田直昌
- Organizer
  第27回日本心電学会学術集会ランチョンセミナー
- Place of Presentation
  大分
- Year and Date
  2010-10-08
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Genetic basis of age-dependent manifestation of cardiac conduction defect2010
- Author(s)
  Makita N
- Organizer
  The 3rd Nagasaki-Hallym International Joint Meeting on Aging and Neurodegenerative Diseases
- Place of Presentation
  長崎
- Year and Date
  2010-11-29
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Cardiac Conduction Disturbance and Connexins.2010
- Author(s)
  Makita N
- Organizer
  The 3nd Asia-Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Jeju Korea
- Year and Date
  2010-10-30
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 心電図QT時間の遺伝的素因2010
- Author(s)
  蒔田直昌
- Organizer
  第27回日本心電学会学術集会モーニングセミナー
- Place of Presentation
  大分
- Year and Date
  2010-10-09
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical Features of Long QT Syndrome in Pre-Elementary Age.2010
- Author(s)
  Makimoto H, Makita N, et al
- Organizer
  第74回日本循環器学会総会・学術集会
- Place of Presentation
  京都
- Year and Date
  2010-03-05
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Novel Mechanisms of Trafficking Defect Caused by KCNQ1 Mutations Found in Long QT Syndrome.2010
- Author(s)
  Arimura T, Makita N, et al
- Organizer
  The 3nd Asia-Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Jeju Korea
- Year and Date
  2010-10-29
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Cardiac Conduction Disturbance and Connexins.2010
- Author(s)
  Makita N
- Organizer
  The 3nd Asia-Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Jeju Korea
- Year and Date
  2010-10-30
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Novel Mechanisms of Trafficking Defect Caused by KCNQ1 Mutations Found in Long QT Syndrome.2010
- Author(s)
  Arimura T, Makita N, et al
- Organizer
  The 3nd Asia-Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Jeju Korea
- Year and Date
  2010-10-29
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] QT延長症候群に対するエプレレノンの有効性について2010
- Author(s)
  蒔田直昌
- Organizer
  Meet the specialist滋賀循環器講演
- Place of Presentation
  滋賀
- Year and Date
  2010-05-14
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 致死性不整脈の基礎と臨床2010
- Author(s)
  蒔田直昌
- Organizer
  第96回日本循環器学会中国・四国合同地方会
- Place of Presentation
  鳥取
- Year and Date
  2010-06-11
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Molecular basis of cardiac conduction defect.2010
- Author(s)
  Makita N, Schot, J-J
- Organizer
  Annual European-SAKURA meeting-
- Place of Presentation
  Nantes France
- Year and Date
  2010-12-06
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Genetic basis of age-dependent manifestation of cardiac conduction defect2010
- Author(s)
  Makita N
- Organizer
  The 3rd Nagasaki-Hallym International Joint Meeting on Aging and Neurodegenerative Diseases
- Place of Presentation
  長崎
- Year and Date
  2010-11-29
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical Features of Congenital Long QT Syndrome in Pre-elementary-age Children2010
- Author(s)
  Makimoto H, Makita N, et al
- Organizer
  American Heart Association Scientific Sessions 2010
- Place of Presentation
  Chicago USA
- Year and Date
  2010-11-15
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Novel Mechanisms of Trafficking Defect Caused by KCNQ1 Mutations Found in Long QT Syndrome2010
- Author(s)
  Sato A, Makita N, et al
- Organizer
  The 3nd Asia-Pacific Heart Rhythm Society Scientific Session
- Place of Presentation
  Jeju Korea
- Year and Date
  2010-10-30
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Clinical Phenotype and Prognosis of Probands With Brugada Syndrome in Relation to SCN5A Mutation.-Japanese Brugada Syndrome Multicenter Registry2009
- Author(s)
  Yamagata K, Makita N, et al
- Organizer
  American Heart Association Scientific Sessions 2009
- Place of Presentation
  Orlando, USA
- Year and Date
  2009-11-18
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Brugada症候群におけるSCN5A遺伝子変異と臨床像-多施設登録による検討-2009
- Author(s)
  山形研一郎、蒔田直昌, 他
- Organizer
  第24回日本不整脈学会学術大会・第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都
- Year and Date
  2009-07-02
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] ClinicaI Phenotype of Japanese LQT3 Form of CongenitaI Long QT Syndrome by Location and Coding Type from Japanese Multicenter Registry2009
- Author(s)
  Yamagata K, Makita N, et al
- Organizer
  13th Congress of International Society for Holter and Noninvasive Electrocardiology
- Place of Presentation
  横浜
- Year and Date
  2009-06-05
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 家族性進行性心臓伝導障害に同定されたconnexin40遺伝子GJA5異変の機能異常2009
- Author(s)
  蒔田直昌、住友直方、関明子
- Organizer
  心電学フロンティア2009(第44回理論心電図研究会)
- Place of Presentation
  京都
- Year and Date
  2009-07-03
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Overlap Between LQT3 and Brugada Syndrome : Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms2009
- Author(s)
  Makita N, et al
- Organizer
  第24回日本不整脈学会学術大会・第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都
- Year and Date
  2009-07-03
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Overlap between LQT3 and Brugada Syndrome : Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms2009
- Author(s)
  Makita N
- Organizer
  13th Congress of International Society for Holter and Noninvasive Electrocardiology
- Place of Presentation
  横浜
- Year and Date
  2009-06-05
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Clinical Phenotype of Japanese LQT3 Form of Congenital Long QT Syndrome by Location and Coding Type from Japanese Multicenter Registr2009
- Author(s)
  Yamagata K, Makita N, et al
- Organizer
  13th Congress of International Society for Holter and Noninvasive Electrocardiology
- Place of Presentation
  横浜
- Year and Date
  2009-06-05
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Familial isolated cardiac conduction defect associated with a mutation in the connexin40 gene GJA52009
- Author(s)
  Makita N, Sumitomo N, Seki A, et al
- Organizer
  The 36th Congress of the International Union of Physiological Sciences
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 家族性進行性心臓伝導障害に同定されたconnexin40遺伝子変異の機能異常2009
- Author(s)
  蒔田直昌、住友直方、関明子
- Organizer
  第8回コネキシン研究会
- Place of Presentation
  福岡
- Year and Date
  2009-11-27
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 家族性進行性心臓伝導障害のコネキシン40遺伝子異変と機能解析2009
- Author(s)
  蒔田直昌、住友直方、関明子
- Organizer
  平成21年度生理学研究所研究会
- Place of Presentation
  岡崎
- Year and Date
  2009-11-25
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Overlap Between LQT3 and Brugada Syndrome : Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms.2009
- Author(s)
  Makita N, et al
- Organizer
  第24回日本不整脈学会学術大会・第26回日本心電学会学術集会合同学術集会
- Place of Presentation
  京都
- Year and Date
  2009-07-03
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] Overlap between LQT3 and Brugada Syndrome : Clinical Features in a Common Mutation and Underlying Bionhvsical Mechanisms2009
- Author(s)
  Makita N
- Organizer
  13th Congress of International Society for Holter and Noninvasive Electrocardiology
- Place of Presentation
  横浜
- Year and Date
  2009-06-05
- Data Source
  KAKENHI-PROJECT-21590921
[Presentation] 心筋Naチャネル遺伝子異常と薬物誘発性不整脈2007
- Author(s)
  蒔田直昌
- Organizer
  第24回日本心電学会
- Place of Presentation
  名古屋
- Year and Date
  2007-10-05
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] SCN5Aキャリアにおける先天性洞不全症候群発生の遺伝的要因2007
- Author(s)
  蒔田直昌
- Organizer
  第24回日本心電学会
- Place of Presentation
  名古屋
- Year and Date
  2007-10-05
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] Overlap Between LQT3 and Brugada Syndrome: Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms.2007
- Author(s)
 Makita N. , et. al.
- Organizer
 80^<th> American Heart Association
- Place of Presentation
 Orlando
- Year and Date
 2007-11-05
- Description
 「研究成果報告書概要(欧文)」より
- Data Source
 KAKENHI-PROJECT-18590757
[Presentation] Overlap Between LQT3 and Brugada Syndrome: Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms.2007
- Author(s)
  Makita N. , et. al.
- Organizer
  XIII World Congress on Cardiac Pacing and Electrophysiology.
- Place of Presentation
  Rome
- Year and Date
  2007-12-04
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] Brugada症候群とLQT3のオーバーラップ:SCN5A変異の臨床的特徴と分子メカニズム2007
- Author(s)
  蒔田直昌
- Organizer
  第55回日本心臓病学会学術集会
- Place of Presentation
  浦安
- Year and Date
  2007-09-11
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] Overlap Between LQT3 and Brugada Syndrome: Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms2007
- Author(s)
  Makita N
- Organizer
  80th American Heart Association
- Place of Presentation
  オーランド
- Year and Date
  2007-11-05
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] Overlap Between LQT3 and Brugada Syndrome: Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms2007
- Author(s)
  Makita N
- Organizer
  XIII World Congress on Cardiac Pacing and Electrophysiology
- Place of Presentation
  ローマ
- Year and Date
  2007-12-04
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] Left Ventricular Noncompaction Associated With Mutations in Cardiac Na Channel Gene SCN5A2006
- Author(s)
 Makita N , et. al.
- Organizer
 79^<th> American Heart Association
- Place of Presentation
 Chicago
- Year and Date
 2006-11-17
- Description
 「研究成果報告書概要(欧文)」より
- Data Source
 KAKENHI-PROJECT-18590757
[Presentation] Genetic factors conferring congenital sick sinus syndrome in SCN5A mutation carriers2006
- Author(s)
  Makita N
- Organizer
  The 9th Cardiovascular Genomics and Atheros clerosis Symposium
- Place of Presentation
  ソウル
- Year and Date
  2006-11-21
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] Genetic Factors Conferring Congenital Sick Sinus Syndrome in SCN5A Mutation Carriers2006
- Author(s)
 Makita N , et. al.
- Organizer
 79^<th> American Heart Association
- Place of Presentation
 Chicago
- Year and Date
 2006-11-17
- Description
 「研究成果報告書概要(欧文)」より
- Data Source
 KAKENHI-PROJECT-18590757
[Presentation] Genetic factors conferring congenital sick sinus syndrome in SCN5A mutation carriers2006
- Author(s)
  Makita N.
- Organizer
  The 9th Cardiovascular Genomics and Atherosclerosis Symposium.
- Place of Presentation
  Seoul
- Year and Date
  2006-11-21
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] Left Ventricular Noncompaction Associated With Mutations in Cardiac Na Channel Gene SCN5A2006
- Author(s)
  Makita N
- Organizer
  79th American Heart Association
- Place of Presentation
  シカゴ
- Year and Date
  2006-11-17
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] Genetic Factors Conferring Congenital Sick Sinus Syndrome in SCN5A Mutation Carriers2006
- Author(s)
  Makita N
- Organizer
  79th American Heart Association
- Place of Presentation
  シカゴ
- Year and Date
  2006-11-17
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590757
[Presentation] ギャップ結合変異を有するプルキンエ線維から発生する心室性不整脈に関するシミュレーション研究
- Author(s)
  稲田慎, ダニエル・トシオ・ハーレル, 原口亮, 芦原貴司, 蒔田直昌, 中沢一雄
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島　鹿児島大学
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Electrical storm in inherited arrhythmia syndromes
- Author(s)
  Yukiomi Tsuji, Taisuke Ishikawa, Naomasa Makita
- Organizer
  第29回日本不整脈学会・第31回日本心電学会合同学術集会
- Place of Presentation
  ザ・プリンスパークタワー東京
- Year and Date
  2014-07-22 – 2014-07-25
- Invited
- Data Source
  KAKENHI-PROJECT-26461074
[Presentation] Is It the Prime Time to Treat the Patients with Early Repolarization?
- Author(s)
  N. Makita
- Organizer
  6th APHRS CARDIO RHYTHM 2013
- Place of Presentation
  Hong Kong, China
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] ラミン遺伝子関連心筋症の家族内発生が疑われた家系の発端者に対して施行した右室心筋生検
- Author(s)
  石松卓, 河野浩章, 荒川修司, 土居寿志, 深江学芸, 武野正義, 小出優史, 前村浩二, 蒔田直昌
- Organizer
  第35回心筋生検研究会
- Place of Presentation
  東京, 東京女子医科大学弥生記念講堂
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] A loss-of-function mutation in SCN5A associated with monomorphic ventricular tachycardia in brugada syndrome
- Author(s)
  K. Sonoda, H. Watanabe, T. Ashihara, A. Sato, N. Yagihara, S. Otuki, K. Hasegawa, G. Katsuumi, K. Iijima, D. Izumi, H. Furushima, M. Horie, N. Makita , T. Minamino
- Organizer
  6th APHRS CARDIO RHYTHM 2013
- Place of Presentation
  Hong Kong, China
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Genome-Wide Association Analysis Identifies 3 Common Variants Predisposing to Brugada Syndrome, a Rare Disease With High Risk of Sudden Cardiac Death
- Author(s)
  J. Barc, C. Bezzina, Y. Mizusawa, C. Remme, J. Gourraud, A. Verkerk, P. Schwartz, P. Guicheney, C. Antzelevitch, E. Schulze-Bahr, E. Behr, J. Tfelt-Hanson, S. Kaab, H. Watanabe, M. Horie, N. Makita, W. Shimizu, P. Froguel, D. Roden, V. Christoffels, M. Gessler, A. Wilde, V. Probst, J. J. Schott, C. Dina and R. Redon
- Organizer
  American Heart Association Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Disease Modeling Using iPS Cells
- Author(s)
  Furukawa T, Okata S, Yuasa S, Suzuki T, Makita N, Kurokawa J, Egashira T, Yamakawa H, Seki T, Aizawa T, Hashimoto H, Kuroda Y, Tanaka A, Yae K, Murata M, Aiba T, Shimizu W, Horie M, Kodama I, Ogawa S, Fukuda K
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Ventricular fibrillation storm and Ca2+/calmodulin-dependent kinase II
- Author(s)
  辻幸臣, 蒔田直昌
- Organizer
  The 2nd HD Physiology International Symposium: Multi-Level Systems Biology
- Place of Presentation
  東京丸の内My Plaza Hall
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] A Novel Mutation in Atrial Myosin Heavy Chain Coding Gene MYH6 Causes Sick Sinus Syndrome
- Author(s)
  Ishikawa T, Nogami A, Kowase S, Arimura T, Kimura A, Makita N
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] A loss-of-function mutation in SCN5A associated with monomorphic ventricular tachycardia in brugada syndrome
- Author(s)
  K. Sonoda, H. Watanabe, T. Ashihara, A. Sato, N. Yagihara, S. Otuki, K. Hasegawa, G. Katsuumi, K. Iijima, D. Izumi, H. Furushima, M. Horie, N. Makita and T. Minamino
- Organizer
  6th APHRS CARDIO RHYTHM 2013
- Place of Presentation
  Hong Kong, China
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Efficacy of Bepridil to Prevent Ventricular Fibrillation in Early Repolarization Syndrome
- Author(s)
  G. Katsuumi, W. Shimizu, H. Watanabe, T. Noda, A. Nogami, K. Ohkubo, N. Takehara, Y. Kawamura, Y. Hosaka, T. Makiyama, M. Sato, S. Fukae, M. Chinushi, H. Oda, M. Okabe, A. Kimura, K. Maemura, I. Watanabe, S. Kamakura, M. Horie, Y. Aizawa, N. Makita and T. Minamino
- Organizer
  American Heart Association Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] A Cardiac α-Myosin Heavy Chain (MYH6) Mutation Impairing Sarcomere Structure Responsible for Familial Sick Sinus Syndrome
- Author(s)
  T. Ishikawa, A. Nogami, S. Kowase, A. Kimura and N. Makita
- Organizer
  American Heart Association Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈の分子病態に関する新展開
- Author(s)
  蒔田直昌
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島　鹿児島大学
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] QT短縮症候群に同定されたKチャネル変異の電気生理学的特性と臨床像
- Author(s)
  ダニエル・トシオ・ハーレル, 芦原貴司, 冨永伊知子, 阿部圭祐, 石川泰輔, 住友直方, 鵜野起久也, 鷹野誠 , 蒔田直昌
- Organizer
  第64回西日本生理学会
- Place of Presentation
  北九州市、産業医科大学　ラマッツィーニホール
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Nonsynonymous Polymorphism in Semaphorin 3A as a Risk Factor for Human Unexplained Cardiac Arrest With Documented Ventricular Fibrillation
- Author(s)
  Y. Nakano, N. Makita（30人中29番目）et al
- Organizer
  American Heart Association Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Electrical stormに伴う心機能障害のメカニズム：頻発するVFエピソードを有する実験モデル動物での検討
- Author(s)
  辻幸臣, 蒔田直昌
- Organizer
  第23回日本循環薬理学会
- Place of Presentation
  福岡　福岡大学メディカルホール
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Nonsynonymous Polymorphism in Semaphorin 3A is a New Genetic Risk Factor for Human Idiopathic Ventricular Fibrillation
- Author(s)
  Nakano Y, Toshisige M, Ochi H, Tokuyama T, Sairaku A, Oda N, Kajiahara K, Uchimura Y, Fujiwara M, Watanabe Y, Kawazoe H, Motoda C, Matumura M, Oda N, Aiba T, Watanabe H, Shimizu W, Horie M, Makita N, Chayama K, Kihara Y
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Na+ Channel beta-subunit affects the phenotype in long QT syndrome type 3 and Brugada syndrome induced pluripotent stem cell-derived cardiomyocytes
- Author(s)
  Okata S, Yuasa S, Suzuki T, Egashira T, Kuroda Y, Tanaka A, Makita N, Kurokawa J, Furukawa T, Fukuda K
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Role of Ca2+/calmodulin-dependent protein kinase II in atrial and ventricular remodeling and arrhythmias
- Author(s)
  Yukiomi Tsuji, Taisuke Ishikawa, Naomasa Makita
- Organizer
  第29回日本不整脈学会・第31回日本心電学会合同学術集会
- Place of Presentation
  ザ・プリンスパークタワー東京
- Year and Date
  2014-07-22 – 2014-07-25
- Invited
- Data Source
  KAKENHI-PROJECT-26461074
[Presentation] 心室細動成立に果たすカルモジュリンキナーゼの役割とは？
- Author(s)
  辻幸臣, 蒔田直昌
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島　鹿児島大学
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] A Cardiac α-Myosin Heavy Chain (MYH6) Mutation Impairing Sarcomere Structure Responsible for Familial Sick Sinus Syndrome
- Author(s)
  T. Ishikawa, A. Nogami, S. Kowase, A. Kimura and N. Makita
- Organizer
  American Heart Association Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Nonsynonymous Polymorphism in Semaphorin 3A is a New Genetic Risk Factor for Human Idiopathic Ventricular Fibrillation
- Author(s)
  Nakano Y, Toshisige M, Ochi H, Tokuyama T, Sairaku A, Oda N, Kajiahara K, Uchimura Y, Fujiwara M, Watanabe Y, Kawazoe H, Motoda C, Matumura M, Oda N, Aiba T, Watanabe H, Shimizu W, Horie M, Makita N, Chayama K, Kihara Y
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 右室自由壁心外膜側の遅延電位記録部位への冷凍凝固により胸部誘導ST上昇消失と心室細動の抑制が認められたBrugada症候群の1例：病理学・遺伝子学的検討
- Author(s)
  小和瀬晋弥, 篠田康俊, 成瀬代士久, 川越純志, 黒崎健司, 井川修, 蒔田直昌 , 野上明彦
- Organizer
  第25回カテーテルアブレーション委員会公開研究会
- Place of Presentation
  横浜、パシフィコ横浜
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Clinical Manifestations and Electrophysiological Characteristics of K Channel Mutations Responsible for Short QT Syndrome
- Author(s)
  D. T. Harrell, I. Tominaga, K. Abe, T. Watabe, Y. Oginosawa, H. Abe, N. Sumitomo, K. Uno, M. Takano and N. Makita
- Organizer
  Heart Rhythm Society 34th Annual Scientific Sessions
- Place of Presentation
  Denver USA
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Genetic mutations in early repolrization syndrome
- Author(s)
  N. Makita
- Organizer
  Venice Arrhythmias 2013
- Place of Presentation
  Venice, Italy
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Brugada症候群とQT延長症候群のオーバーラップを認めた一症例
- Author(s)
  白石亜季, 深江学芸, 森内拓治, 坂口能理子, 古島早苗, 森永芳智, 蒔田直昌, 前村浩二, 栁原克紀
- Organizer
  日本臨床検査医学会　九州支部（第59回）
- Place of Presentation
  熊本,熊本市医師会館
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 家族性洞不全症候群患者に同定された心房型ミオシン重鎖遺伝子(MYH6)変異と機能解析
- Author(s)
  石川泰輔, 小和瀬晋弥, 有村卓朗, 野上昭彦, 辻幸臣, 木村彰方 , 蒔田直昌
- Organizer
  第64回西日本生理学会
- Place of Presentation
  北九州市、産業医科大学　ラマッツィーニホール
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Nonsynonymous Polymorphism in Semaphorin 3A as a Risk Factor for Human Unexplained Cardiac Arrest With Documented Ventricular Fibrillation
- Author(s)
  Y. Nakano, N. Makita（30人中29番目）et al
- Organizer
  American Heart Association Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Variable Expressivity of Phenotype in The V1764fsx 1786 Mutation of Cardiac Sodium Channel Scn5a
- Author(s)
  H. Kawakami, T. Aiba, H. Okayama, Y. Kazatani, I. Nakajima, K. Miyamoto, Y. Yamada, H. Okamura, T. Noda, K. Satomi, S. Kamakura, N. Makita and W. Shimizu
- Organizer
  Heart Rhythm Society 34th Annual Scientific Sessions
- Place of Presentation
  Denver USA
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 家族性洞不全症候群患者に同定された心房型ミオシン重鎖遺伝子(MYH6)変異と機能解析
- Author(s)
  石川泰輔, 小和瀬晋弥, 有村卓朗, 野上昭彦, 辻幸臣, 木村彰方, 蒔田直昌
- Organizer
  第64回西日本生理学会
- Place of Presentation
  北九州市、産業医科大学　ラマッツィーニホール
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] QT短縮症候群患者に同定された新規K+チャネル変異の電気生理学的特性と臨床像
- Author(s)
  ダニエル・トシオ・ハーレル, 冨永伊知子, 阿部圭祐, 渡部太一, 荻ノ原泰司, 安部治彦, 住友直方, 鵜野起久也, 鷹野誠 ,蒔田直昌
- Organizer
  第30回日本心電学会学術集会
- Place of Presentation
  青森、リンステーションホール青森
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Na+ Channel beta-subunit affects the phenotype in long QT syndrome type 3 and Brugada syndrome induced pluripotent stem cell-derived cardiomyocytes
- Author(s)
  Okata S, Yuasa S, Suzuki T, Egashira T, Kuroda Y, Tanaka A, Makita N, Kurokawa J, Furukawa T, Fukuda K
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] A Novel Mutation in Atrial Myosin Heavy Chain Coding Gene MYH6 Causes Sick Sinus Syndrome
- Author(s)
  Ishikawa T, Nogami A, Kowase S, Arimura T, Kimura A, Makita N
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] A Gap Junction Mutation Expressed in the Purkinje Network and Lethal Ventricular Arrhythmias -A Simulation Study-
- Author(s)
  Inada S, Harrell DT, Haraguchi R, Ashihara T, Makita N, Nakazawa K
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 家族性心臓伝導障害家系に同定されたcoonexin40の遺伝子変異と機能異常
- Author(s)
  蒔田直昌, 関明子
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島　鹿児島大学
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] ラミン遺伝子関連心筋症の家族内発生が疑われた家系の発端者に対して施行した右室心筋生検
- Author(s)
  石松卓, 河野浩章, 荒川修司, 土居寿志, 深江学芸, 武野正義, 小出優史, 前村浩二 ,蒔田直昌
- Organizer
  第35回心筋生検研究会
- Place of Presentation
  東京東京女子医科大学弥生記念講堂
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 致死性不整脈の遺伝子基盤に関する新展開
- Author(s)
  蒔田直昌
- Organizer
  第18回日本小児心電学会
- Place of Presentation
  宮崎市、宮崎県医師会館
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Reentrant beat in the Purkinje network associated with gap junction mutation
- Author(s)
  Inada S, Harrell DT, Haraguchi R, Ashihara T, Makita N, Nakazawa K
- Organizer
  2nd HD Physiology International Symposium:Multilevel system biology
- Place of Presentation
  東京丸の内My Plaza Hall
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 家族性心臓伝導障害家系に同定されたcoonexin40の遺伝子変異と機能異常
- Author(s)
  蒔田直昌, 関明子
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島　鹿児島大学
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Common Variants at SCN5A, SCN10A, and HEY2 are Associated with Cardiac Conduction Disturbance in Patients with Brugada Syndrome
- Author(s)
  Xu D, Murakoshi N, Nogami A, Makita N, Sekiguchi Y, Igarashi M, Isaka Y, Kurosaki K, Kowase S, Naruse Y, Aonuma K
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] CALM2 Mutations Associated With Atypical Juvenile Long QT Syndrome
- Author(s)
  N. Makita, T. Ishikawa（28人中8番目）, Y. Tsuji（28人中13番目）et al
- Organizer
  American Heart Association Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Common Variants at SCN5A, SCN10A, and HEY2 are Associated with Cardiac Conduction Disturbance in Patients with Brugada Syndrome
- Author(s)
  Xu D, Murakoshi N, Nogami A, Makita N, Sekiguchi Y, Igarashi M, Isaka Y, Kurosaki K, Kowase S, Naruse Y, Aonuma K
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Electrophysiological Characteristics and Clinical Manifestation of K Channel Mutations Responsible for Short QT Syndrome
- Author(s)
  Harrell DT, Tominaga I, Abe K, Watanabe T, Oginosawa Y, Abe H, Sumitomo N, Uno K, Takano M, Makita N
- Organizer
  2nd HD Physiology International Symposium: Multilevel system biology
- Place of Presentation
  東京丸の内My Plaza Hall
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Electrical stormに伴う心機能障害のメカニズム：頻発するVFエピソードを有する実験モデル動物での検討
- Author(s)
  辻幸臣, 蒔田直昌
- Organizer
  第23回日本循環薬理学会
- Place of Presentation
  福岡　アクロス福岡
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Efficacy of Bepridil to Prevent Ventricular Fibrillation in Early Repolarization Syndrome
- Author(s)
  Katsuumi G, Watanabe H, Chinushi M, Fukae S, Noda T, Ohkubo K, Nogami A, Hosaka Y, Oda H, Sato H, Okabe M, Aizawa Y, Kimura A, Makiyama T, Horie M, Maemura K, Makita N, Minamino T
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Efficacy of Bepridil to Prevent Ventricular Fibrillation in Early Repolarization Syndrome
- Author(s)
  G. Katsuumi, W. Shimizu, H. Watanabe, T. Noda, A. Nogami, K. Ohkubo, N. Takehara, Y. Kawamura, Y. Hosaka, T. Makiyama, M. Sato, S. Fukae, M. Chinushi, H. Oda, M. Okabe, A. Kimura, K. Maemura, I. Watanabe, S. Kamakura, M. Horie, Y. Aizawa, N. Makita and T. Minamino
- Organizer
  American Heart Association Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Clinical Manifestations and Electrophysiological Characteristics of K Channel Mutations Responsible for Short QT Syndrome
- Author(s)
  D. T. Harrell, I. Tominaga, K. Abe, T. Watabe, Y. Oginosawa, H. Abe, N. Sumitomo, K. Uno, M. Takano and N. Makita
- Organizer
  Heart Rhythm Society 34th Annual Scientific Sessions
- Place of Presentation
  Denver USA
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Genetic Basis in familial Sick Sinus Syndrome
- Author(s)
  石川泰輔, 蒔田直昌
- Organizer
  International symposium of inherited arrhythmia 2014
- Place of Presentation
  東京、東京ステーションカンファレンス
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Electrophysiological Characteristics and Clinical Manifestation of K Channel Mutations Responsible for Short QT Syndrome
- Author(s)
  Harrell DT, Tominaga I, Abe K, Watanabe T, Oginosawa Y, Abe H, Sumitomo N, Uno K, Takano M, Makita N
- Organizer
  2nd HD Physiology International Symposium: Multilevel system biology
- Place of Presentation
  東京　丸の内My Plaza Hall
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Ventricular fibrillation storm and Ca2+/calmodulin-dependent kinase II
- Author(s)
  辻幸臣, 蒔田直昌
- Organizer
  The 2nd HD Physiology International Symposium: Multi-Level Systems Biology
- Place of Presentation
  東京　丸の内My Plaza Hall
- Invited
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Mutations in SCN5A Associated with Monomorphic Ventricular Tachycardia, Conduction Disease, and J-Wave Syndrome
- Author(s)
  Sonoda K, Watanabe H, Sato A, Yagihara N, Hasegawa K, Iijima K, Izumi D, Furushima H, Ashihara T, Horie M, Makita N, Minamino T
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] ギャップ結合変異を有するプルキンエ線維から発生する心室性不整脈に関するシミュレーション研究
- Author(s)
  稲田慎, ダニエル・トシオ・ハーレル, 原口亮, 芦原貴司, 蒔田直昌, 中沢一雄
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島　鹿児島大学
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Disease Modeling Using iPS Cells
- Author(s)
  Furukawa T, Okata S, Yuasa S, Suzuki T, Makita N, Kurokawa J, Egashira T, Yamakawa H, Seki T, Aizawa T, Hashimoto H, Kuroda Y, Tanaka A, Yae K, Murata M, Aiba T, Shimizu W, Horie M, Kodama I, Ogawa S, Fukuda K
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Reentrant beat in the Purkinje network associated with gap junction mutation
- Author(s)
  Inada S, Harrell DT, Haraguchi R, Ashihara T, Makita N, Nakazawa K
- Organizer
  2nd HD Physiology International Symposium:Multilevel system biology
- Place of Presentation
  東京　丸の内My Plaza Hall
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Genetic mutationｓin early repolarization syndrome
- Author(s)
  N. Makita
- Organizer
  Venice Arrhythmias 2013
- Place of Presentation
  Venice, Italy
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Brugada症候群とQT延長症候群のオーバーラップを認めた一症例
- Author(s)
  白石亜季, 深江学芸, 森内拓治, 坂口能理子, 古島早苗, 森永芳智, 蒔田直昌, 前村浩二, 栁原克紀
- Organizer
  日本臨床検査医学会　九州支部（第59回）
- Place of Presentation
  熊本,熊本市医師会館
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 運動負荷試験にて伝導障害が顕在化し、SCN5Aの遺伝子変異が判明した完全左脚ブロックの1例
- Author(s)
  白井加奈子, 泉田直己, 石井卓, 土井庄三郎 , 蒔田直昌
- Organizer
  第18回日本小児心電学会
- Place of Presentation
  宮崎市、宮崎県医師会館
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] CALM2 Mutations Associated With Atypical Juvenile Long QT Syndrome
- Author(s)
  N. Makita, Y. Tsuji（28人中13番目）et al
- Organizer
  American Heart Association Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] QT短縮症候群患者に同定された新規K+チャネル変異の電気生理学的特性と臨床像
- Author(s)
  ダニエル・トシオ・ハーレル, 冨永伊知子, 阿部圭祐, 渡部太一, 荻ノ原泰司, 安部治彦, 住友直方, 鵜野起久也, 鷹野誠 , 蒔田直昌
- Organizer
  第30回日本心電学会学術集会
- Place of Presentation
  青森、リンステーションホール青森
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 運動負荷試験にて伝導障害が顕在化し、SCN5Aの遺伝子変異が判明した完全左脚ブロックの1例
- Author(s)
  白井加奈子, 泉田直己, 石井卓, 土井庄三郎, 蒔田直昌
- Organizer
  第18回日本小児心電学会
- Place of Presentation
  宮崎市、宮崎県医師会館
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Variable Expressivity of Phenotype in The V1764fsx 1786 Mutation of Cardiac Sodium Channel Scn5a
- Author(s)
  H. Kawakami, T. Aiba, H. Okayama, Y. Kazatani, I. Nakajima, K. Miyamoto, Y. Yamada, H. Okamura, T. Noda, K. Satomi, S. Kamakura, N. Makita and W. Shimizu
- Organizer
  Heart Rhythm Society 34th Annual Scientific Sessions
- Place of Presentation
  Denver, USA
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] QT短縮症候群に同定されたKチャネル変異の電気生理学的特性と臨床像
- Author(s)
  ダニエル・トシオ・ハーレル, 芦原貴司, 冨永伊知子, 阿部圭祐, 石川泰輔, 住友直方, 鵜野起久也, 鷹野誠 ,蒔田直昌
- Organizer
  第64回西日本生理学会
- Place of Presentation
  北九州市、産業医科大学　ラマッツィーニホール
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 心室細動成立に果たすカルモジュリンキナーゼの役割とは？
- Author(s)
  辻幸臣, 蒔田直昌
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島　鹿児島大学
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 致死性不整脈の遺伝子基盤に関する新展開
- Author(s)
  蒔田直昌
- Organizer
  第18回日本小児心電学会
- Place of Presentation
  宮崎市、宮崎県医師会館
- Invited
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Efficacy of Bepridil to Prevent Ventricular Fibrillation in Early Repolarization Syndrome
- Author(s)
  Katsuumi G, Watanabe H, Chinushi M, Fukae S, Noda T, Ohkubo K, Nogami A, Hosaka Y, Oda H, Sato H, Okabe M, Aizawa Y, Kimura A, Makiyama T, Horie M, Maemura K, Makita N, Minamino T
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] 右室自由壁心外膜側の遅延電位記録部位への冷凍凝固により胸部誘導ST上昇消失と心室細動の抑制が認められたBrugada症候群の1例：病理学・遺伝子学的検討
- Author(s)
  小和瀬晋弥, 篠田康俊, 成瀬代士久, 川越純志, 黒崎健司, 井川修, 蒔田直昌 , 野上明彦
- Organizer
  第25回カテーテルアブレーション委員会公開研究会
- Place of Presentation
  横浜、パシフィコ横浜
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Familial neurally mediated syncope
- Author(s)
  M. Nakao, S. Kobayashi and N. Makita
- Organizer
  Venice Arrhythmias 2013
- Place of Presentation
  Venice, Italy
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Is It the Prime Time to Treat the Patients with Early Repolarization?
- Author(s)
  N. Makita
- Organizer
  6th APHRS CARDIO RHYTHM 2013
- Place of Presentation
  Hong Kong, China
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] Mutations in SCN5A Associated with Monomorphic Ventricular Tachycardia, Conduction Disease, and J-Wave Syndrome
- Author(s)
  Sonoda K, Watanabe H, Sato A, Yagihara N, Hasegawa K, Iijima K, Izumi D, Furushima H, Ashihara T, Horie M, Makita N, Minamino T
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PLANNED-22136007
[Presentation] A Gap Junction Mutation Expressed in the Purkinje Network and Lethal Ventricular Arrhythmias -A Simulation Study-
- Author(s)
  Inada S, Harrell DT, Haraguchi R, Ashihara T, Makita N, Nakazawa K
- Organizer
  第78回日本循環器学会
- Place of Presentation
  東京、東京フォーラム
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Genome-Wide Association Analysis Identifies 3 Common Variants Predisposing to Brugada Syndrome, a Rare Disease With High Risk of Sudden Cardiac Death
- Author(s)
  J. Barc, C. Bezzina, Y. Mizusawa, C. Remme, J. Gourraud, A. Verkerk, P. Schwartz, P. Guicheney, C. Antzelevitch, E. Schulze-Bahr, E. Behr, J. Tfelt-Hanson, S. Kaab, H. Watanabe, M. Horie, N. Makita, W. Shimizu, P. Froguel, D. Roden, V. Christoffels, M. Gessler, A. Wilde, V. Probst, J. J. Schott, C. Dina and R. Redon
- Organizer
  American Heart Association Scientific Sessions 2013
- Place of Presentation
  Dallas, USA
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] 致死性不整脈の分子病態に関する新展開
- Author(s)
  蒔田直昌
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島　鹿児島大学
- Data Source
  KAKENHI-PROJECT-24390199
[Presentation] Familial neurally mediated syncope
- Author(s)
  M. Nakao, S. Kobayashi and N. Makita
- Organizer
  Venice Arrhythmias 2013
- Place of Presentation
  Venice, Italy
- Data Source
  KAKENHI-PROJECT-24390199

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78. 国広なごみ

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MAKITA Naomasa 蒔田 直昌

Research Projects

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A multi-omics study to elucidate the novel molecular basis of the complex traits and ethnicity in Brugada syndromePrincipal Investigator

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Novel pathophysiology underlying cardiac conduction defect due to mutations of gap junction genesPrincipal Investigator

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Ethnicity-oriented genomic analysis of pathogenesis underlysing sudden cardiac death of unknown causePrincipal Investigator

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Novel molecular basis underlying lethal arrhythmic syndrome due to mutations in cardiac Na/Ca exchanger genePrincipal Investigator

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Novel molecular basis of cardriac conduction disturbance associated with a collagene gene mutationPrincipal Investigator

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Elucidation of novel pathophysiology underlysing lethal arrhythmia due to mutations in cardiac ion transportersPrincipal Investigator

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Identification of Novel Genes and Pathogenesis Responsible for Brugada Syndrome Using Whole Exome SequencingPrincipal Investigator

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Genetic and functional basis of cardiac ion channelopathyPrincipal Investigator

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Mutations in cardiac gap junction genes and the pathophysiology underlying progressive cardiac conduction defect.Principal Investigator

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MAKITA Naomasa 蒔田直昌

[Book] 週刊　医学の歩み2022

[Book] ゼロから学ぶ　Burugada症候群2020