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MAKITA Naomasa  蒔田 直昌

ORCIDConnect your ORCID iD *help
Researcher Number 00312356
Other IDs
Affiliation (Current) 2019: 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
Affiliation (based on the past Project Information) *help 2019: 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
2012: 北海道大学, 大学院・医学研究科, 准教授 … More
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 / Cardiovascular medicine / Medium-sized Section 53:Organ-based internal medicine and related fields / Basic Section 53020:Cardiology-related / Circulatory organs internal medicine / Complex systems
Except Principal Investigator
Cardiovascular medicine / General physiology / Complex systems / Obstetrics and gynecology / Biological Sciences / Circulatory organs internal medicine
Keywords
Principal Investigator
致死性不整脈 / 遺伝子変異 / SCN5A / ゲノム編集 / イオンチャネル / 心臓伝導障害 / GWAS / Brugada syndrome / Brugada症候群 / QT短縮症候群 … More / エクソーム解析 / Na channel / Na/Ca交換体 / 遺伝子多型 / Akt / エクソーム / ブルガダ症候群 / Naチャネル / Na-Ca交換体 / 心室細動 / コンピュータシミュレーション / 進行性心臓伝導障害 / mutation / ゲノムワイド関連解析 / ギャップ結合 / 内科 / トランスポータ / lathal arrhythmia / SCN10A / CRISPR/cas9 / カルモジュリン / iPS / 網羅的遺伝子解析 / コラーゲン / CRISPR/CAS / 全エクソン解析 / 次世代シークエンサー / 心房停止 / パッチクランプ / 国際情報交換（フランス） / J波症候群 / サルコメア / MYH6 / 洞不全症候群 / プロモータ / 伝導障害 / 心臓突然死 / ノックインマウス / Transgenic mice / 光シグナルマッピング / ゼブラフィッシュ / リン酸化シグナル / トランスジェニックマウス / コネキシン / ion channel / Ventricular fibrillation / Long QT syndrome / 心拍数 / シミュレーション / polymorphism / 遺伝子 / 分子心臓学 / 光学マッピング / Lethal arrhythmias / ミオシン重鎖 / Kaplan-Meier解析 / atrial standstill / リン酸化 / トランスジェニック動物 / 歯骨格異常 / 遺伝子改変動物 / 突然死 / ギャップジャンクション / Mutations / phosphorylation / CRISPR/Cas9 / 不整脈 / 単一塩基多型 / QT延長症候群 / 遺伝性不整脈 … More
Except Principal Investigator
心筋症 / QT延長症候群 / 循環器 / アデノウイルス / estrogen / 拡張型心筋症 / 全身循環 / 病理所見 / ミトコンドリア / CaMKII / 心臓電気生理学 / rat / 薬物動態学 / 遅延ナトリウム電流 / Brugada症候群 / パッチクランプ / カルモジュリンキナーゼ / 遺伝子導入 / 静止膜電位 / プラコグロビン / カリウムチャネル / ストレス応答 / イオンチャネル / resting membrane potential / 植込み型除細動器 / mesenteric artery / endothelium-derived hyperpolarizing factor / 酸化ストレス / ovariectomy / 腸間脈動脈 / 心筋細胞 / 薬物動態 / コネキシン / 腸間膜動脈 / Na チャネル / 電子顕微鏡 / 電気的ストーム / トルサード・ド・ポアンツ / 内皮由来過分極因子 / 心室細動ストーム / 心室細動 / 活性酸素 / HERG / カリウムチャンネル / 心筋生検 / カテコラミン感受性多形心室頻拍 / 生物学 / 心臓 / システム生物学 / 生物物理 / connexin / Naチャネル / チャネル遺伝子 / ラット / ST上昇 / 心不全 / KvLQT1 / potassium channel / 心血管病 / 生物物理学 / 不整脈 / 免疫染色 / 生理学 / 代謝 / エストロゲン / 卵巣摘出 / SCN5A / 遺伝子解析 Less

  • Research Projects

    (19 results)

  • Research Products

    (531 results)

  • Co-Researchers

    (97 People)

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

    • Principal Investigator
      蒔田 直昌
    • 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
      Nagasaki University

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

    • Principal Investigator
      蒔田 直昌
    • Project Period (FY)
      2018 – 2020
    • Research Category
      Challenging Research (Exploratory)
    • Review Section
      Medium-sized Section 53:Organ-based internal medicine and related fields
    • Research Institution
      Nagasaki University

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

    • Principal Investigator
      蒔田 直昌
    • Project Period (FY)
      2018 – 2020
    • 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
      Nagasaki University

  •  各種心筋症の診断および臨床像における心筋病理組織評価の有用性の検討Ongoing

    • Principal Investigator
      河野 浩章
    • 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 InvestigatorOngoing

    • Principal Investigator
      蒔田 直昌
    • 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

All 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 2004 2003 Other

All Journal Article Presentation Book

  • [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] 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

      J Physiol

      Volume: 596 Pages: 809-825

    • DOI
      10.1113/jp275303
    • Open Access / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16H05124, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15K18967

  • [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

    • Int'l Joint Research / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K15311

  • [Journal Article] Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death2017
    • 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

      Journal of Human Genetics

      Volume: 62 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 Pages: 69-72

    • DOI
      10.1016/j.hrcr.2016.09.004
    • Open Access / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15H04823, 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, Makiyama T*, Harita T, Sasaki K, Wuriyanghai Y, Hayano M, Nishiuchi S, Kohjitani H, Hirose S, Chen J, Yokoi F, Ishikawa T, Ohno S, Chonabayashi K, Motomura H, Yoshida Y, Horie M, Makita N, Kimura T
    • Journal Title

      Human Molecular Genetics

      Volume: - Pages: 1670-1677

    • DOI
      10.1093/hmg/ddx073
    • Acknowledgement Compliant / Int'l Joint Research / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-16H05297, 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

    • Int'l Joint Research / Peer Reviewed
    • 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 Pages: 967-968

    • DOI
      10.1111/jvim.14781
    • Open Access / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15K15311

  • [Journal Article] Genotype-Phenotype Correlation of <i>SCN5A</i> Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter Registry.2017
    • Author(s)
      Yamagata K, Horie M, et al.
    • Journal Title

      Send to Circulation.

      Volume: 印刷中 Pages: 0-0

    • DOI
      10.1161/circulationaha.117.027983
    • Open Access / Int'l Joint Research / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-26461130, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15KK0302, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15K09082, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-15K15311

  • [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: 3 Pages: 727-743

    • DOI
      10.1016/j.jacep.2016.11.013
    • Int'l Joint Research / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15K15311

  • [Journal Article] Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction2017
    • Author(s)
      Ishikawa T, Horie M, et al.
    • Journal Title

      Heart rhythm

      Volume: 印刷中 Pages: 717-724

    • DOI
      10.1016/j.hrthm.2017.01.020
    • Open Access / Peer Reviewed
    • 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 cardiomyocytes2017
    • 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
    • Open Access / Peer Reviewed
    • 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 <i>LMNA</i> 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

      Circulation Cardiovascular Genetics

      Volume: 6

    • DOI
      10.1161/circgenetics.116.001603
    • Open Access / Int'l Joint Research / Peer Reviewed
    • 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 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 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 Pages: 358-370

    • DOI
      10.1016/j.jacc.2017.05.039
    • Int'l Joint Research / Peer Reviewed
    • 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] 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 Pages: 1658-1659

    • DOI
      10.1016/j.jacc.2016.01.032
    • Open Access / Int'l Joint Research / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823

  • [Journal Article] Electrical Storm Associated with Inherited Arrhythmia Syndromes : Cardiac Purkinje Fiber Arrhythmogenesis2016
    • Author(s)
      辻幸臣，Harrell DT，石川泰輔，蒔田直昌
    • Journal Title

      JPN.J

      Volume: 35 Issue: 2 Pages: 104-115

    • DOI
      10.5105/jse.35.104
    • ISSN
      0285-1660, 1884-2437
    • Year and Date
      2016-03-25
    • Language
      Japanese
    • Data Source
      KAKENHI-PROJECT-26461074

  • [Journal Article] Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I2016
    • Author(s)
      Daumy X, Amarouch MY, Lindenbaum P, 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
    • Acknowledgement Compliant / Int'l Joint Research / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823

  • [Journal Article] Novel mutation in the alpha-myosin heavy chain gene is associated with sick sinus syndrome2016
    • 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

      Circulation Arrhythmia and Electrophysiology

      Volume: 8 Pages: 400-108

    • DOI
      10.1161/circep.114.002534
    • Acknowledgement Compliant / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25670172, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25293181

  • [Journal Article] Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes2016
    • Author(s)
      Yagihara N,Minamino T,33名中28番
    • Journal Title

      Journal of American Heart Association

      Volume: 19 Pages: 644-650

    • DOI
      10.1161/jaha.116.003644
    • Open Access / Acknowledgement Compliant / Int'l Joint Research / Peer Reviewed
    • 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] Embryonic type Na+ channel beta-subunit, SCN3B masks the disease phenotype of Brugada syndrome2016
    • Author(s)
      Kushiyama Y, Honjo H, Niwa R, Takanari H, Yamazaki M, Takemoto Y, Sakuma I, Kodama I, Kamiya K
    • Journal Title

      Scientific Reports

      Volume: 311 Pages: 34198-34198

    • DOI
      10.1038/srep34198
    • Open Access / Acknowledgement Compliant / Int'l Joint Research / Peer Reviewed
    • 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 background2016
    • Author(s)
      Ishikawa T, Tsuji Y, Makita N
    • Journal Title

      J Arrhythm

      Volume: 印刷中 Pages: 352-358

    • DOI
      10.1016/j.joa.2015.09.009
    • Open Access / Acknowledgement Compliant / Int'l Joint Research / Peer Reviewed
    • 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

      Circulation Journal

      Volume: 79 Issue: 12 Pages: 2659-2668

    • DOI
      10.1253/circj.CJ-15-0416
    • ISSN
      1346-9843, 1347-4820
    • Language
      English
    • Peer Reviewed / Int'l Joint Research / Open Access
    • 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 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

    • Acknowledgement Compliant / Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390199

  • [Journal Article] Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation2015
    • 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 Pages: 1095-104

    • DOI
      10.1161/circep.114.002519
    • Open Access / Peer Reviewed
    • 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] Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome2015
    • Author(s)
      Harrell DT, Ashihara T, Ishikawa T, et al.
    • Journal Title

      Int J Cardio

      Volume: 190 Pages: 1095-1104

    • DOI
      10.1016/j.ijcard.2015.04.090
    • Open Access / Acknowledgement Compliant / Int'l Joint Research / Peer Reviewed
    • 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

    • Acknowledgement Compliant / Peer Reviewed
    • 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) Pages: 1976-1986

    • DOI
      10.1016/j.jacc.2015.08.862
    • Int'l Joint Research / Peer Reviewed
    • 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 syndrome.2014
    • Author(s)
      Hasegawa K, Ohno S, Itoh H, Makiyama T, Aiba T, Nakano Y, Shimizu W, Matsuura H, Makita N, Horie M
    • Journal Title

      Journal of Arrhythmia

      Volume: in press 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 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-compaction.2014
    • 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 Pages: 16461654-16461654

    • DOI
      10.1093/europace/eut382
    • Peer Reviewed / Acknowledgement Compliant
    • 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 tachyarrhythmias2014
    • Author(s)
      Tsuji Y, Ishikawa T, Makita N.
    • Journal Title

      Journal of Arrhythmia

      Volume: 30 Pages: 235-241

    • DOI
      10.1016/j.joa.2014.04.003
    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-26461074, KAKENHI-PROJECT-26860572

  • [Journal Article] Successful control of life-threatening polymorphic ventricular tachycardia by radiofrequency catheter ablation in an infant.2014
    • 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 Pages: 422-426

    • DOI
      10.1007/s00380-013-0390-6
    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199

  • [Journal Article] Efficacy of bepridil to prevent ventricular fibrillation in severe form of early repolarization syndrome. International journal of cardiology.2014
    • 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 Pages: 519-522

    • DOI
      10.1016/j.ijcard.2014.01.036
    • Open Access / Peer Reviewed
    • 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 (CALM2) 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 Pages: 466-474

    • DOI
      10.1161/circgenetics.113.000459
    • Open Access / Acknowledgement Compliant / Peer Reviewed
    • 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 Pages: 511-517

    • DOI
      10.1161/circep.113.001340
    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25461054, KAKENHI-PROJECT-25461113, KAKENHI-PROJECT-26860572

  • [Journal Article] Paradigm shifts in the genetics of inherited arrhythmias: Using next-generation sequencing technologies to uncover hidden etiologies.2013
    • Author(s)
      Makita N
    • Journal Title

      J Arrhythmia

      Volume: 29 Pages: 305-307

    • DOI
      10.1016/j.joa.2013.09.001
    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199

  • [Journal Article] Novel <i>SCN3B</i> Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.52013
    • Author(s)
      Ishikawa T
    • Journal Title

      Circulation Journal

      Volume: 77 Issue: 4 Pages: 959-67

    • DOI
      10.1253/circj.CJ-12-0995
    • 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] 【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 abnormalities.2013
    • 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

    • 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 the SCN5A/SCN10A and HEY2 loci predispose to 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

      Nature genetics

      Volume: 45 Pages: 1044-1049

    • DOI
      10.1038/ng.2712
    • Open Access / Peer Reviewed
    • 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

    • DOI
      10.1371/journal.pgen.1003364
    • Open Access / Peer Reviewed
    • 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] 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: -

    • 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

      International Journal of Cardiology

      Volume: 155 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 repolarization2012
    • Author(s)
      Watanabe H
    • Journal Title

      International J Cardiol

      Volume: 159 Pages: 238-240

    • 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 Pages: 236-241

    • DOI
      10.1097/hco.0b013e328352220e
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390199, KAKENHI-PLANNED-22136007

  • [Journal Article] A connexin40 mutation associated with a malignant variant of progressive familial heart block type I.2012
    • Author(s)
      Delmar M, Makita N
    • Journal Title

      Circ Arrhythm Electrophysiol.

      Volume: (in press) 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

    • Data Source
      KAKENHI-PLANNED-22136007

  • [Journal Article] Disease characterization using LQTS-specific induced pluripotent stem cElls2012
    • Author(s)
      Egashira T, Yuasa S, Suzuki T, Tohyama S, et al.
    • Journal Title

      Cardiovasc Res.

      Volume: 95 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

    • 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

    • 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 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

      Circulation Arrhythmia and Electrophysiology

      Volume: 5 Pages: 1098-107

    • 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

      Circulation : Arrhythmia and Electrophysiology

      Volume: 4 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

    • 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

    • 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

    • 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

    • 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)

    • 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)

    • 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

    • 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

    • 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)

    • 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

    • 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

    • 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

    • 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

    • 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

    • 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

    • 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

    • 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

    • 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

    • 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] Variable expressivity of phenotype in a frameshift mutation of cardiac sodium channel SCN5A.
    • Author(s)
      Kawakami H Makita N, et al
    • Journal Title

      J. Arrhythmia

      Volume: (In press)

    • DOI
      10.1016/j.joa.2013.04.005
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390199

  • [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)

    • 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)

    • 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] 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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] 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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
    • Int'l Joint Research / Invited
    • 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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.
    • 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] 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] 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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  • 4.  ISHIKAWA Taisuke (60708692)
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  • 12.  TSUTSUI Hiroyuki (70264017)
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  • 13.  KINUGAWA Shintaro (60399871)
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  • 43.  ARAI Yuji (30202724)
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