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ISHIKAWA Taisuke  石川 泰輔

Researcher Number 60708692
Other IDs
  • ORCIDhttps://orcid.org/0000-0001-8195-4700
External Links
Affiliation (Current) 2025: 鹿児島大学, 共同獣医学部, 特任助教
Affiliation (based on the past Project Information) *help 2025: 鹿児島大学, 共同獣医学部, 特任助教
2021 – 2023: 国立研究開発法人国立循環器病研究センター, オープンイノベーションセンター, 客員研究員
2019 – 2020: 国立研究開発法人国立循環器病研究センター, オープンイノベーションセンター, 室長
2017 – 2019: 長崎大学, 医歯薬学総合研究科(医学系), 講師
2014 – 2015: 長崎大学, 医歯薬学総合研究科(医学系), 助教
Review Section/Research Field
Principal Investigator
Basic Section 53020:Cardiology-related / Cardiovascular medicine
Except Principal Investigator
Basic Section 53020:Cardiology-related / Basic Section 52050:Embryonic medicine and pediatrics-related / Medium-sized Section 53:Organ-based internal medicine and related fields / Cardiovascular medicine / Circulatory organs internal medicine / Complex systems
Keywords
Principal Investigator
突然死 / 心臓突然死 / 遺伝子変異 / 変異 / 遺伝性不整脈 / ノックインマウス / 膜タンパク / 特発性心室細動 / トランスポータ / リスク階層化 … More / 一次予防 / ゲノムワイド関連解析 / 致死性不整脈 / リスク予測 / プレシジョンメディスン / SNP / ゲノム / ブルガダ症候群患者 / 次世代シーケンス / リスク層別化 / ブルガダ症候群 / 心房性不整脈 / 洞不全症候群 / サルコメア / チャネル / ターゲットシークエンス / 遺伝子異常 / 次世代シークエンサー / 興奮伝導 / 心房 / 遺伝子解析 / 遺伝子 / 不整脈 / 徐脈 … More
Except Principal Investigator
ブルガダ症候群 / GWAS / ゲノムワイド関連解析 / 突然死 / SCN5A / 遺伝子変異 / エクソーム / 心臓伝導障害 / 致死性不整脈 / エクソーム解析 / イオンチャネル / リスク予測 / 複雑形質 / 人種特異性 / マルチオミックス解析 / リスク層別化 / ポリジニックリスクスコア / 選択的スプライシング / 人種横断的解析 / TGF-β / SMAD4 / endoglin / SMAD / BMPシグナル / Smad / BMP9 / ALK1 / ACVRL1 / 遺伝性出血性末梢血管拡張症 / Kaplan-Meier解析 / ゲノム編集 / 多遺伝子リスクスコア / 多因子疾患 / 生存曲線 / 心臓突然死 / 一塩基多型 / ポリジェニックリスクスコア / COX比例ハザード解析 / 個別化予防医療 / COX回帰解析 / 単一塩基多型 / CRISPR/CAS / CRISPR/cas9 / CRISPR/Cas9 / ノックインマウス / 進行性心臓伝導障害 / コラーゲン / 次世代シークエンサー / 遺伝子多型 / SCN10A / 全エクソン解析 / 遺伝子改変動物 / プロモータ / 伝導障害 / 国際情報交換(フランス) / ギャップ結合 / iPS / コンピュータシミュレーション / シミュレーション / 心拍数 / ゼブラフィッシュ / 網羅的遺伝子解析 / サルコメア / 遺伝性不整脈 / ミオシン重鎖 / MYH6 / 洞不全症候群 Less
  • Research Projects

    (10 results)
  • Research Products

    (169 results)
  • Co-Researchers

    (31 People)
  •  ブルガダ症候群の突然死リスク遺伝子を解明する人種横断メタ解析の国際共同研究Principal Investigator

    • Principal Investigator
      石川 泰輔
    • Project Period (FY)
      2025 – 2028
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 53020:Cardiology-related
    • Research Institution
      Kagoshima University
  •  A multi-omics study to elucidate the novel molecular basis of the complex traits and ethnicity in Brugada syndrome

    • Principal Investigator
      Makita Naomasa
    • Project Period (FY)
      2021 – 2023
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 53020:Cardiology-related
    • Research Institution
      National Cardiovascular Center Research Institute
  •  Integrated analysis of pathgenesis of hereditary hemorrhagic telangiectasia

    • Principal Investigator
      Iwasa Toru
    • Project Period (FY)
      2020 – 2022
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      National Cardiovascular Center Research Institute
  •  Elucidation of molecular pathogenesis for inherited lethal arrhythmia associated with transporter abnormalitiesPrincipal Investigator

    • Principal Investigator
      石川 泰輔
    • Project Period (FY)
      2020 – 2021
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 53020:Cardiology-related
    • Research Institution
      National Cardiovascular Center Research Institute
  •  Ethnicity-oriented genomic analysis of pathogenesis underlysing sudden cardiac death of unknown cause

    • Principal Investigator
      Makita Naomasa
    • Project Period (FY)
      2018 – 2021
    • Research Category
      Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
    • Review Section
      Medium-sized Section 53:Organ-based internal medicine and related fields
    • Research Institution
      National Cardiovascular Center Research Institute
      Nagasaki University
  •  Elucidation of genetic predispositions to cardiac sudden death in Brugada syndromePrincipal Investigator

    • Principal Investigator
      ISHIKAWA TAISUKE
    • Project Period (FY)
      2018 – 2019
    • Research Category
      Grant-in-Aid for Early-Career Scientists
    • Review Section
      Basic Section 53020:Cardiology-related
    • Research Institution
      National Cardiovascular Center Research Institute
      Nagasaki University
  •  Novel molecular basis of cardriac conduction disturbance associated with a collagene gene mutation

    • 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
  •  Elucadation of genetic disorders and molecular pathogenesis in inherited bradyarrhythmia due to the abnormalities in genes encoding sarcomere componentsPrincipal Investigator

    • Principal Investigator
      ISHIKAWA Taisuke
    • Project Period (FY)
      2014 – 2015
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Cardiovascular medicine
    • Research Institution
      Nagasaki University
  •  Identification of Novel Genes and Pathogenesis Responsible for Brugada Syndrome Using Whole Exome Sequencing

    • 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
  •  Genetic and functional basis of cardiac ion channelopathy

    • 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

All 2024 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 Other

All Journal Article Presentation Book

  • [Book] 週刊 医学の歩み2022

    • Author(s)
      蒔田直昌 石川泰輔
    • Total Pages
      6
    • Publisher
      医歯薬出版株式会社
    • Data Source
      KAKENHI-PROJECT-21H02920
  • [Book] ゼロから学ぶブルガダ症候群2020

    • Author(s)
      石川泰輔, 蒔田直昌
    • Total Pages
      133
    • Publisher
      大道学館出版部
    • ISBN
      9784924391840
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Book] ゼロから学ぶブルガダ症候群2020

    • Author(s)
      石川泰輔, 蒔田直昌
    • Total Pages
      133
    • Publisher
      大道学館出版部
    • ISBN
      9784924391840
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Book] 循環器科の心電図: ECG for Cardiologists2018

    • Author(s)
      石川泰輔、蒔田直昌 (村川裕二 編)
    • Total Pages
      215
    • Publisher
      南江堂
    • ISBN
      9784524237913
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Book] 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] 不整脈症候群-遺伝子変異から不整脈治療を捉える2015

    • Author(s)
      石川泰輔、蒔田直昌
    • Total Pages
      196
    • Publisher
      南江堂
    • Data Source
      KAKENHI-PROJECT-26860572
  • [Journal Article] Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci2024

    • Author(s)
      Ishikawa T, Makita N et al.
    • Journal Title

      European Heart Journal

      Volume: in press Issue: 26 Pages: 2320-2332

    • DOI

      10.1093/eurheartj/ehae251

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-21H02920
  • [Journal Article] Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian population2022

    • Author(s)
      Murakami Haruka、Tanimoto Yoko、Tanimoto Kojiro、Inoue Satomi、Ishikawa Taisuke、Makita Naomasa、Yamazawa Kazuki
    • Journal Title

      Human Genome Variation

      Volume: 9 Issue: 1 Pages: 28-28

    • DOI

      10.1038/s41439-022-00206-9

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-21K19751, KAKENHI-PROJECT-20K19082, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-23K24309
  • [Journal Article] Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome.2021

    • Author(s)
      Ishikawa T, Kimoto H, Mishima H, Yamagata K, Ogata S, Aizawa Y, Hayashi K, Morita H, Nakajima T, Nakano Y, Nagase S, Murakoshi N, Kowase S, Ohkubo K, Aiba T, Morimoto S, Ohno S, Kamakura S, Nogami A, Takagi M, Karakachoff M, Dina C, Schott JJ, Yoshiura KI, Horie M, Shimizu W, Nishimura K, Kusano K, Makita N.
    • Journal Title

      Eur Heart J.

      Volume: 42(29) Issue: 29 Pages: 2854-2863

    • DOI

      10.1093/eurheartj/ehab254

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17K09524, KAKENHI-PROJECT-18K15407, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-20H03591, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-20K08487, KAKENHI-PROJECT-21K07800, KAKENHI-PROJECT-21K08028, KAKENHI-PROJECT-21K08075, KAKENHI-PROJECT-20K08416
  • [Journal Article] Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> Variants2021

    • Author(s)
      Kozek K, Wada Y, Makita N, Ishikawa T, Crotti L, Kroncke BM, et al.
    • Journal Title

      Circulation: Genomic and Precision Medicine

      Volume: 14 Issue: 4

    • DOI

      10.1161/circgen.120.003289

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-20K08416
  • [Journal Article] Novel electrocardiographic criteria for short QT syndrome in children and adolescents2021

    • Author(s)
      Suzuki H, Horie M, Ishikawa T, Makita N, Nagashima M, et al.
    • Journal Title

      EP Europace

      Volume: 23 Issue: 12 Pages: 2029-2038

    • DOI

      10.1093/europace/euab097

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-20K08416
  • [Journal Article] Pathological Features of Lamin Cardiomyopathy2020

    • Author(s)
      Kawano, H., Ishimatsu, T., Ishijima, I., Hayashi, T., Ishikawa, T., Makita, N., Maemura,K.
    • Journal Title

      Circulation Journal

      Volume: -

    • NAID

      130007864268

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Journal Article] 遺伝性不整脈のPrecision medicine2020

    • Author(s)
      石川泰輔, 蒔田直昌
    • Journal Title

      週間 医学のあゆみ

      Volume: 272 Pages: 1279-1283

    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Journal Article] Pathological Features of Lamin Cardiomyopathy2020

    • Author(s)
      Kawano H., Ishimatsu T., Ishijima I., Hayashi T., Ishikawa T., Makita N., Maemura K.
    • Journal Title

      Circulation Journal

      Volume: -

    • NAID

      130007864268

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Journal Article] Desmin‐related myopathy characterized by non‐compaction cardiomyopathy, cardiac conduction defect, and coronary artery dissection2020

    • Author(s)
      Tamiya R., Saito Y., Fukamachi D., Nagashima K., Aizawa Y., Ohkubo K., Hatta T., Sezai A., Tanaka M, Ishikawa T., Makita N., Sumitomo N., Okumura Y.
    • Journal Title

      ESC Heart Failure

      Volume: - Issue: 3 Pages: 1338-1343

    • DOI

      10.1002/ehf2.12667

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894
  • [Journal Article] Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome2020

    • Author(s)
      Lahrouchi N, Tadros R, Crotti L, Makiyama T et al.
    • Journal Title

      Circulation

      Volume: 142 Issue: 4 Pages: 324-338

    • DOI

      10.1161/circulationaha.120.045956

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-20K08416
  • [Journal Article] TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway2020

    • Author(s)
      Miyao N., Hata Y., Izumi H., Nagaoka R., Oku Y., Takasaki I., Ishikawa T., Takarada S., Okabe M., Nakaoka H., Ibuki K., Ozawa S., Yoshida T., Hasegawa H., Makita N., Nishida N., Mori H., Ichida F., Hirono K.
    • Journal Title

      PLOS ONE

      Volume: 15 Issue: 4 Pages: 0227393-0227393

    • DOI

      10.1371/journal.pone.0227393

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PUBLICLY-19H04744, KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894, KAKENHI-PROJECT-18K07365, KAKENHI-PROJECT-20H03350
  • [Journal Article] Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome2020

    • Author(s)
      Lahrouchi N., Ishikawa T., Makita N., Bezzina C. R., et al.
    • Journal Title

      Circulation

      Volume: -

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Journal Article] 遺伝性不整脈のPrecision medicine2020

    • Author(s)
      石川泰輔, 蒔田直昌
    • Journal Title

      週間 医学のあゆみ

      Volume: 272 Pages: 1279-1283

    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Journal Article] Cardiac Emerinopathy2020

    • Author(s)
      Ishikawa Taisuke、Ichida Fukiko、Makita Naomasa et al
    • Journal Title

      Circulation: Arrhythmia and Electrophysiology

      Volume: 13 Issue: 10 Pages: 1165-1174

    • DOI

      10.1161/circep.120.008712

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-19K21724, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-20H03591, KAKENHI-PROJECT-18K07850, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-20K08416, KAKENHI-PROJECT-18H03083
  • [Journal Article] Pathological Features of Lamin Cardiomyopathy2020

    • Author(s)
      Kawano H, Ishimatsu T, Kawamura K, Ishijima M, Hayashi T, Ishikawa T, Makita N, Maemura K.
    • Journal Title

      Circ J

      Volume: 84 Issue: 7 Pages: 1193

    • DOI

      10.1253/circj.CJ-20-0187

    • NAID

      130007864268

    • ISSN
      1346-9843, 1347-4820
    • Year and Date
      2020-06-25
    • Language
      English
    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K08416
  • [Journal Article] SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families2020

    • Author(s)
      3.Wijeyeratne YD, Tanck MW, Mizusawa Y, Batchvarov V, Barc J, Crotti L, et al.
    • Journal Title

      Circulation: Genomic and Precision Medicine

      Volume: 13 Issue: 6

    • DOI

      10.1161/circgen.120.002911

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-20K08416
  • [Journal Article] Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls2020

    • Author(s)
      2.Walsh R, Lahrouchi N, Tadros R, Kyndt F, Glinge C, Postema PG, et al.
    • Journal Title

      Genetics in Medicine

      Volume: 23 Issue: 1 Pages: 47-58

    • DOI

      10.1038/s41436-020-00946-5

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-19K08505, KAKENHI-PROJECT-19K08538, KAKENHI-PROJECT-20K08473, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08100, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18K15407, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02888, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-20K08416
  • [Journal Article] Identification of transmembrane protein 168 mutation in familial Brugada syndrome.2020

    • Author(s)
      Shimizu A, Zankov DP, Sato A, Komeno M, Toyoda F, Yamazaki S, Makita T, Noda T, Ikawa M, Asano Y, Miyashita Y, Takashima S, Morita H, Ishikawa T, Makita N, Hitosugi M, Matsuura H, Ohno S, Horie M, Ogita H.
    • Journal Title

      FASEB Journal

      Volume: 34 Issue: 5 Pages: 6399-6417

    • DOI

      10.1096/fj.201902991r

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K08075, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-ORGANIZER-19H05749, KAKENHI-PROJECT-17F17418, KAKENHI-PROJECT-17K08536, KAKENHI-PROJECT-17K08627, KAKENHI-PROJECT-17K08657, KAKENHI-PROJECT-16H06276, KAKENHI-PROJECT-19K09408, KAKENHI-PROJECT-20K08489, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K08033, KAKENHI-PROJECT-19H03652, KAKENHI-PROJECT-18K19547, KAKENHI-PROJECT-21K08119
  • [Journal Article] Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome2020

    • Author(s)
      Lahrouchi N., Ishikawa T., Makita N., Connie R. B., et al.
    • Journal Title

      Circulation

      Volume: -

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Journal Article] 遺伝性不整脈の遺伝子診断:有効性と限界2019

    • Author(s)
      石川泰輔, 蒔田 直昌
    • Journal Title

      循環器病研究の進歩

      Volume: 40 Pages: 58-66

    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Journal Article] 遺伝性不整脈の遺伝子診断:有効性と限界2019

    • Author(s)
      石川泰輔, 蒔田 直昌
    • Journal Title

      循環器病研究の進歩

      Volume: 40 Pages: 58-66

    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Journal Article] Identification of a novel CCDC22 mutation in a patient with severe Epstein?Barr virus-associated hemophagocytic lymphohistiocytosis and aggressive natural killer cell leukemia2019

    • Author(s)
      Yamashita Y, Nishikawa A, Iwahashi Y, Fujimoto M, Sasaki I, Mishima H, Kinoshita A, Hemmi H, Kanazawa N, Ohshima K, Imadome KI, Murata SI、Yoshiura KI, Kaisho T, Sonoki T, Tamura S
    • Journal Title

      International Journal of Hematology

      Volume: 印刷中 Issue: 6 Pages: 744-750

    • DOI

      10.1007/s12185-019-02595-0

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K07071, KAKENHI-PROJECT-18K07850, KAKENHI-PUBLICLY-17H05799, KAKENHI-PROJECT-17H04088, KAKENHI-PROJECT-17K19568, KAKENHI-PROJECT-19K07628, KAKENHI-PROJECT-19K08821, KAKENHI-PROJECT-19K22913, KAKENHI-PROJECT-18KK0245, KAKENHI-PUBLICLY-19H04813, KAKENHI-PROJECT-16KT0112
  • [Journal Article] Overexpression of heart-specific small subunit of myosin light chain phosphatase results in heart failure and conduction disturbance2018

    • Author(s)
      Arimura Takuro、Muchir Antoine、Kuwahara Masayoshi、Morimoto Sachio、Ishikawa Taisuke、Du Cheng-Kun、Zhan Dong-Yun、Nakao Shu、Machida Noboru、Tanaka Ryo、Yamane Yoshihisa、Hayashi Takeharu、Kimura Akinori
    • Journal Title

      American Journal of Physiology-Heart and Circulatory Physiology

      Volume: epub Issue: 6 Pages: H1192-H1202

    • DOI

      10.1152/ajpheart.00696.2017

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-17H07258, KAKENHI-PROJECT-17K08540, KAKENHI-PROJECT-16H05296, KAKENHI-PROJECT-15K08210, KAKENHI-PROJECT-16K08514, KAKENHI-PROJECT-18K15894
  • [Journal Article] Clinical Manifestations and Long-Term Mortality in <i>Lamin A/C</i> Mutation Carriers From a Japanese Multicenter Registry2018

    • Author(s)
      14.Nakajima K, Aiba T, Makiyama T, Nishiuchi S, Ohno S, Kato K, Yamamoto Y, Doi T, Shizuta S, Onoue K, Yagihara N, Ishikawa T, Watanabe I, Kawakami H, Oginosawa Y, Murakoshi N, Nogami A, Aonuma K, Saito Y, Kimura T, Yasuda S, Makita N, Shimizu W, Horie M, Kusano K.
    • Journal Title

      Circ J

      Volume: 82 Issue: 11 Pages: 2707-2714

    • DOI

      10.1253/circj.CJ-18-0339

    • NAID

      40021697176

    • ISSN
      1346-9843, 1347-4820
    • Year and Date
      2018-10-25
    • Language
      English
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-18K07875, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18K15847, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894
  • [Journal Article] HCN4 pacemaker channels attenuate the parasympathetic response and stabilize the spontaneous firing of the sinoatrial node2018

    • Author(s)
      Kozasa Yuko、Nakashima Noriyuki、Ito Masayuki、Ishikawa Taisuke、Kimoto Hiroki、Ushijima Kazuo、Makita Naomasa、Takano Makoto
    • Journal Title

      The Journal of Physiology

      Volume: 596 Issue: 5 Pages: 809-825

    • DOI

      10.1113/jp275303

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16H05124, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15K18967, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894
  • [Journal Article] 進行性心臓伝導障害の病態と遺伝的背景2018

    • Author(s)
      石川泰輔, 蒔田直昌
    • Journal Title

      循環器内科

      Volume: 84 Pages: 721-728

    • NAID

      40021757390

    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Journal Article] Progressive atrial conduction system defects associated with bone malformation caused by a connexin45 mutation2017

    • Author(s)
      Seki A, Ishikawa T, Daumy X, Mishima H, Barc J, Sasaki R, Nishii K, Saito K, Urano M, Ohno S, Otsuki S, Kimoto H, Baruteau A, Thollet A, Fouchard S, Bonnaud S, Parent P, Shibata Y, Perrin JP, Le Marec H, Hagiwara N, Mercier S, Horie M, Probst V, Yoshiura KI, Redon R, Schott JJ, Makita N.
    • Journal Title

      J Am Coll Cardiol

      Volume: 印刷中

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15311
  • [Journal Article] Letter to the Editor2017

    • Author(s)
      Ishikawa T, Makita N, Aoki H, Saida Y
    • Journal Title

      J Vet Intern Med

      Volume: 31 Issue: 4 Pages: 967-968

    • DOI

      10.1111/jvim.14781

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15K15311
  • [Journal Article] Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.2017

    • Author(s)
      Seki A, Ishikawa T, Daumy X, Mishima H, Barc J, Sasaki R, Nishii K, Saito K, Urano M, Ohno S, Otsuki S, Kimoto H, Baruteau AE, Thollet A, Fouchard S, Bonnaud S, Parent P, Shibata Y, Perrin JP, Le Marec H, Hagiwara N, Mercier S, Horie M, Probst V, Yoshiura KI, Redon R, Schott JJ, Makita N.
    • Journal Title

      J Am Coll Cardiol.

      Volume: 70 Issue: 3 Pages: 358-370

    • DOI

      10.1016/j.jacc.2017.05.039

    • Peer Reviewed / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16KT0112, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-16H05159, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-15K15311
  • [Journal Article] Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death.2017

    • Author(s)
      Oshima Y, Yamamoto T, Ishikawa T, Mishima H, Matsusue A, Umehara T, Murase T, Abe Y, Kubo SI, Yoshiura KI, Makita N, Ikematsu K.
    • Journal Title

      J Hum Genet.

      Volume: 62 Issue: 11 Pages: 989-995

    • DOI

      10.1038/jhg.2017.79

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16KT0112, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-16H05159, KAKENHI-PROJECT-15K08892, KAKENHI-PROJECT-15K15311
  • [Journal Article] A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest2017

    • Author(s)
      Takahashi K, Ishikawa T, Makita N, Takefuta K, Nabeshima T, Nakayashiro M
    • Journal Title

      HeartRhythm Case Reports

      Volume: 3 Issue: 1 Pages: 69-72

    • DOI

      10.1016/j.hrcr.2016.09.004

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-15K15311
  • [Journal Article] Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction.2017

    • Author(s)
      Ishikawa T, Horie M, et al.
    • Journal Title

      Heart Rhythm

      Volume: 印刷中 Issue: 5 Pages: 717-724

    • DOI

      10.1016/j.hrthm.2017.01.020

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K09680, KAKENHI-PROJECT-16KT0112, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-16H05159, KAKENHI-PROJECT-15K15311
  • [Journal Article] Allele-specific Ablation Rescues Electrophysiological Abnormalities in a Human iPS Cell Model of Long-QT Syndrome with a CALM2 Mutation.2017

    • Author(s)
      Yamamoto Y, Horie M, et al.
    • Journal Title

      Human Molecular Genetics

      Volume: 印刷中 Issue: 9 Pages: 1670-1677

    • DOI

      10.1093/hmg/ddx073

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-16H05297
  • [Journal Article] Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers.2017

    • Author(s)
      Nishiuchi S, Makiyama T, Aiba T, Nakajima K, Hirose S, Kohjitani H, Yamamoto Y, Harita T, Hayano M, Wuriyanghai Y, Chen J, Sasaki K, Yagihara N, Ishikawa T, Onoue K, Murakoshi N, Watanabe I, Ohkubo K, Watanabe H, Ohno S, Doi T, Shizuta S, Minamino T, et.al
    • Journal Title

      Circ Cardiovasc Genet.

      Volume: 6 Issue: 6

    • DOI

      10.1161/circgenetics.116.001603

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K09421, KAKENHI-PROJECT-16K09499, KAKENHI-PROJECT-17K09495, KAKENHI-PROJECT-15H04823, KAKENHI-PLANNED-26115008, KAKENHI-PROJECT-15H04818, KAKENHI-PROJECT-17H06806, KAKENHI-PROJECT-15K09150, KAKENHI-PROJECT-15K09689, KAKENHI-PROJECT-15K15311
  • [Journal Article] Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias.2016

    • Author(s)
      Koizumi A, Sasano T, Kimura W, Miyamoto Y, Aiba T, Ishikawa T, Nogami A, Fukamizu S, Sakurada H, Takahashi Y, Nakamura H, Ishikura T, Koseki H, Arimura T, Kimura A, Hirao K, Isobe M, Shimizu W, Miura N, Furukawa T.
    • Journal Title

      European Heart Journal.

      Volume: 37 (18) Issue: 18 Pages: 1469-1475

    • DOI

      10.1093/eurheartj/ehv449

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K09150, KAKENHI-PUBLICLY-25136727, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-25461045, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25293181, KAKENHI-PROJECT-15H04817, KAKENHI-PROJECT-15K15049, KAKENHI-PROJECT-16K09494, KAKENHI-PROJECT-26293052
  • [Journal Article] Inherited bradyarrhythmia: A diverse genetic background.2016

    • Author(s)
      Ishikawa T, Tsuji Y, Makita N
    • Journal Title

      Journal of Arrhythmia

      Volume: 印刷中 Issue: 5 Pages: 352-358

    • DOI

      10.1016/j.joa.2015.09.009

    • Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-24390199
  • [Journal Article] A novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.2015

    • Author(s)
      Ishikawa T, Jou CJ, Nogami A, Kowase S, Arrington CB, Barnett SM, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N.
    • Journal Title

      Circ Arrhythm Electrophysiol.

      Volume: in press

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-24390199
  • [Journal Article] Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome.2015

    • Author(s)
      Harrell DT, Ashihara T, Ishikawa T, et al.
    • Journal Title

      International Journal of Cardiology.

      Volume: 190 Pages: 393-402

    • DOI

      10.1016/j.ijcard.2015.04.090

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-25461053, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-25461106, KAKENHI-PROJECT-25461113, KAKENHI-PROJECT-26670292, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-24300145, KAKENHI-PROJECT-24390199
  • [Journal Article] 徐脈性疾患と分子遺伝学2015

    • Author(s)
      石川泰輔 蒔田直昌
    • Journal Title

      循環器内科

      Volume: 4 Pages: 360-365

    • Data Source
      KAKENHI-PROJECT-26860572
  • [Journal Article] A novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.2015

    • Author(s)
      Ishikawa T, Jou CJ, Nogami A, Kowase S, Arrington CB, Barnett SM, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N.
    • Journal Title

      Circ Arrhythm Electrophysiol.

      Volume: in press

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PLANNED-22136007
  • [Journal Article] A novel mutation in alpha-myosin heavy chain gene is associated with sick sinus syndrome2015

    • Author(s)
      Ishikawa T, Jou CJ, Nogami A, Kowase S, Arrington CB, Barnett SM, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N
    • Journal Title

      Circ Arrhythm Electrophysiol

      Volume: 8 Issue: 2 Pages: 400-108

    • DOI

      10.1161/circep.114.002534

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-25670172, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-15K15311, KAKENHI-PROJECT-15H04823, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25293181
  • [Journal Article] Novel calmodulin mutations associated with congenital arrhythmia susceptibility.2014

    • Author(s)
      Makita N, Tsuji Y(39人中21番目)et al
    • Journal Title

      Circ Cardiovasc Genet.

      Volume: 7 Issue: 4 Pages: 466-474

    • DOI

      10.1161/circgenetics.113.000459

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591038, KAKENHI-PROJECT-24591086, KAKENHI-PUBLICLY-25110720, KAKENHI-PROJECT-25293181, KAKENHI-PROJECT-25670172, KAKENHI-PROJECT-25670420, KAKENHI-PROJECT-25713015, KAKENHI-PROJECT-26860572, KAKENHI-PROJECT-221S0002
  • [Journal Article] Molecular mechanisms of heart failure progression associated with implantable cardioverter-defibrillator shocks for ventricular tachyarrhythmias.2014

    • Author(s)
      Tsuji Y, Ishikawa T, Makita N.
    • Journal Title

      J Arrhythmia.

      Volume: 30 Issue: 4 Pages: 235-241

    • DOI

      10.1016/j.joa.2014.04.003

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-26461074, KAKENHI-PROJECT-26860572
  • [Journal Article] Sodium channelopathy underlying familial sick sinus syndrome with early onset and predominantly male characteristics.2014

    • Author(s)
      Abe K, Machida T, Sumitomo N, Yamamoto H, Ohkubo K, Watanabe I, Makiyama T, Fukae S, Kohno M, Harrell DT, Ishikawa T, Tsuji Y, Nogami A, Watabe T, Oginosawa Y, Abe H, Maemura K, Motomura H, Makita N.
    • Journal Title

      Circ Arrhythm Electrophysiol

      Volume: in press Issue: 3 Pages: 511-517

    • DOI

      10.1161/circep.113.001340

    • NAID

      120006986434

    • Peer Reviewed
    • Data Source
      KAKENHI-PLANNED-22136007, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25461054, KAKENHI-PROJECT-25461113, KAKENHI-PROJECT-26860572
  • [Journal Article] 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] Novel <i>SCN3B</i> Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.52013

    • Author(s)
      Ishikawa T
    • Journal Title

      Circ J

      Volume: 77 Issue: 4 Pages: 959-967

    • DOI

      10.1253/circj.CJ-12-0995

    • NAID

      10031138998

    • ISSN
      1346-9843, 1347-4820
    • Language
      English
    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390157, KAKENHI-PROJECT-23390209, KAKENHI-PROJECT-23659414, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-24591575
  • [Journal Article] Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations2013

    • Author(s)
      Arimura T, Onoue K, Takahashi-Tanaka Y, Ishikawa T, Kuwahara M, Setou M, Shigenbu S, Yamaguchi K, Bertrand AT, Machida N, Takayama K, Fukusato M, Tanaka R, Somekawa T, Nakano T, Yamane Y, Kuba K, Imai Y, Saito N, Bonne G, Kimura A
    • Journal Title

      Cardiovasc Res

      Volume: (in press) Issue: 3 Pages: 382-394

    • DOI

      10.1093/cvr/cvt106

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390157, KAKENHI-PROJECT-24390199, KAKENHI-PROJECT-25293181, KAKENHI-PROJECT-25670393, KAKENHI-PUBLICLY-23132507
  • [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] A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.52012

    • Author(s)
      Ishikawa T
    • Journal Title

      Circ Arrhythm Electrophysiol

      Volume: 5 Issue: 6 Pages: 1098-1107

    • DOI

      10.1161/circep.111.969972

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22390157, KAKENHI-PROJECT-23591031, KAKENHI-PROJECT-23659414, KAKENHI-PROJECT-24390199, KAKENHI-PLANNED-22136007
  • [Presentation] Development of an Oligonucleotide-Based Therapeutic Approach for Calmodulinopathy2021

    • Author(s)
      Makiyama T, Yamamoto Y, Kondoh Y, Gao J, Kashiwa A, Aizawa T, Imamura T, Huang H, Kohjitani H, Ishikawa T, Yoshida Y, Ohno S, Makita N, Horie M, Kimura T.
    • Organizer
      第85回日本循環器学会学術集会
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K08416
  • [Presentation] Modeling Inherited Arrhythmias Associated with Ryanodine Receptor Dysfunction using iPS Cells2021

    • Author(s)
      Makiyama T, Gao J, Yamamoto Y, Ishikawa T, Makita N, Kimura T et al.
    • Organizer
      第85回日本循環器学会学術集会
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K08416
  • [Presentation] Genetic Analysis of Young-onset Atrial Fibrillation with Family History2021

    • Author(s)
      熊埜御堂淳, 大江征嗣, 服部悠一, 伊藤章吾, 堀賢介, 石川泰輔, 蒔田直昌, 福本義弘
    • Organizer
      第85回日本循環器学会学術集会
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K08416
  • [Presentation] ブルガダ症候群における致死性不整脈発症に関連するゲノム領域の特定と個別化リスク予測法の樹立2021

    • Author(s)
      石川泰輔
    • Organizer
      バイエル循環器病研究助成第27回・第28回研究発表会
    • Invited
    • Data Source
      KAKENHI-PROJECT-20K08416
  • [Presentation] Rare Variant of the Glycerol-3-Phosphate Dehydrogenase-1 Like (GPD1-L) Gene in Japanese Patients with Brugada Syndrome2021

    • Author(s)
      Usuda K, Hayashi K, Ishikawa T, Aizawa Y, Kato T, Tsuda T, Kusayama T, Niwa S, Usui S, Sakata K, Kawashiri M, Mishima H, Yoshiura K, Makita N, Takamura M.
    • Organizer
      第85回日本循環器学会学術集会
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K08416
  • [Presentation] Cardiac Emerinopathy, Novel Non-syndromic X-linked Left Ventricular Noncompaction Associated with Progressive Atrial Conduction Disturbance2020

    • Author(s)
      Ishikawa T, Mishima H, Barc J, Hirono K, Terada S, Kowase S, Sato T, Yui Y, Mukai Y, Ohkubo K, Kimoto H, Watanabe H, Hata Y, Aiba T, Ohno S, Chishaki A, Shimizu W, Horie M, Ichida F, Nogami A, Yoshiura K, Makita N.
    • Organizer
      第84回日本循環器学会学術集会
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K08416
  • [Presentation] 患者由来iPS 細胞モデルを用いたCav 1.2イオン選択性を障害するCACNA1C-E1115K変異がQT 延長症候群、Brugada 症候群を発症するメカニズムの解析2020

    • Author(s)
      柏麻美, 牧山武, 糀谷泰, マウリッセン トーマス, ウリヤンハイ イミン, 山本雄大, ガオ ジンシャン, ファン ハイ, 今村知彦, 相澤卓範, 石川泰輔, 大野聖子, 豊田太, 佐藤誠一, 高橋一浩, ウォルツェン クヌート, 堀江稔, 蒔田直昌, 木村剛
    • Organizer
      第97回日本生理学会大会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] 進行性心臓伝導障害患者の網羅的遺伝子解析とin vitro 機能解析系を用いて明らかになった心臓コネキシン病の分子病態2020

    • Author(s)
      石川泰輔, 関明子, 蒔田直昌
    • Organizer
      第97回日本生理学会大会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Cardiac Emerinopathy, Novel Non-syndromic X-linked Left Ventricular Noncompaction Associated with Progressive Atrial Conduction Disturbance2020

    • Author(s)
      Ishikawa T, Aiba T, Ohno S, Yoshiura K, Makita N et al.
    • Organizer
      第84回日本循環器学会学術集会
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Inhibition of Late Sodium Current Attenuates Prolonged Action Potential Durations in CACNA1C-E1115K iPS Cell Model with Disrupted Cav1.2 ion Selectivity2020

    • Author(s)
      Yamamoto Y, Makiyama T, Kondo Y, Iriyama Y, Ishikawa R, Kimura T et al.
    • Organizer
      The Heart Rhythm Society's Annual Scientific Sessions 2020
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K08416
  • [Presentation] Preclinical Proof-of-Concept Study: Antisense-mediated Knockdown of CALM as a Therapeutic Strategy for Calmodulinopathy2020

    • Author(s)
      Yamamoto Y, Makiyama T, Kondo Y, Iriyama Y, Ishikawa R, Kimura T et al.
    • Organizer
      European Society of Cardiology Congress 2020
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-20K08416
  • [Presentation] 進行性心臓伝導障害患者の網羅的遺伝子解析とin vitro 機能解析系を用いて明らかになった心臓コネキシン病の分子病態2019

    • Author(s)
      石川泰輔, 関明子, 蒔田直昌
    • Organizer
      第97回日本生理学会大会
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Brugada症候群の予後予測に対する分子生理学的アプローチ2019

    • Author(s)
      石川泰輔, 蒔田直昌
    • Organizer
      第67回日本心臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Functional Reappraisal of SCN5A Mutations Reemphasize Their Predictive Value for Lethal Cardiac Events in Brugada Syndrome2019

    • Author(s)
      Ishikawa T., Makita N.
    • Organizer
      第66回日本不整脈心電学会
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] 患者由来iPS 細胞モデルを用いたCav 1.2イオン選択性を障害するCACNA1C-E1115K変異がQT 延長症候群、Brugada 症候群を発症するメカニズムの解析2019

    • Author(s)
      柏麻美, 牧山武, 糀谷泰, マウリッセン トーマス, ウリヤンハイ イミン, 山本雄大, ガオ ジンシャン, ファン ハイ, 今村知彦, 相澤卓範, 石川泰輔, 大野聖子, 豊田太, 佐藤誠一, 高橋一浩, ウォルツェン クヌート, 堀江稔, 蒔田直昌, 木村剛
    • Organizer
      第97回日本生理学会大会
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Brugada症候群の予後予測に対する分子生理学的アプローチ2019

    • Author(s)
      石川泰輔, 蒔田直昌
    • Organizer
      第67回日本心臓病学会学術集会
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Modeling Overlapping Phenotypes of Long-QT and Brugada Syndrome with CACNA1C-E1115K that Alters Ion Selectivity of the Cardiac L-Type Calcium Channel Using Induced Pluripotent Stem Cells2019

    • Author(s)
      Kashiwa A., Makiyama T., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
    • Organizer
      第66回日本不整脈心電学会
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] 次世代シーケンス解析による特発性心室細動の遺伝背景の解明2019

    • Author(s)
      謝颯琴, 高橋篤, 大野聖子, 鎌倉令, 石川泰輔, 植田初江, 斯波真理子, 南野直人, 林研至, 八木原伸江, 中野由紀子, 伊藤英樹, 宮本恵宏, 田中敏博, 蒔田直昌, 堀江稔, 清水渉, 草野研吾, 安田聡, 相庭武司
    • Organizer
      日本人類遺伝学会第64回大会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Comprehensive Analyses Using Functional Evaluation and Whole-exome Sequencings to Decipher the Genetic predispositions for Sudden Death in Brugada Syndrome2019

    • Author(s)
      Makita N., Ishikawa T., Japanese Brugada Exome Consortium Investigators
    • Organizer
      第83回日本循環器学会学術集会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Modeling Overlap Syndrome of Long QT and Brugada Syndrome Associated with Induced Pluripotent Stem Cells2019

    • Author(s)
      Kashiwa A., Makiyama T., Kohjitani H., Wuriyanghai Y., Yamamoto Y., Jungshan G., Huang H., Ishikawa T., Ohno S., Toyoda F., Sato S., Horie M., Makita N., Kimura T.
    • Organizer
      The 40th Heart Rhythm Society Scientific Sessions
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Single Cell Electrophysiological Analysis of iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Potential Imaging System2019

    • Author(s)
      Yamamoto Y., Makiyama T., Wuriyanghai Y., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
    • Organizer
      第66回日本不整脈心電学会
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Single Cell Electrophysiological Analysis of iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Potential Imaging System2019

    • Author(s)
      Yamamoto Y., Makiyama T., Wuriyanghai Y., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
    • Organizer
      第66回日本不整脈心電学会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Cardiac Emerinopathy, Novel Nonsyndromic Xlinked Left Ventricular Noncompaction Associated With Progressive Atrial Conduction Disturbance2019

    • Author(s)
      Ishikawa T., Barc J., Mishima H., Hirono K., Terada S., Kowase S., Sato T., Mukai Y., Yui Y., Ohkubo K., Kimoto H., Hata Y., Aiba T., Ohno S., Chishaki A., Shimizu W., Horie M., Ichida F., Nogami A., Yoshiura K., Schott JJ., Makita N.
    • Organizer
      The 40th Heart Rhythm Society Scientific Sessions
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Cardiac Emerinopathy, Novel Nonsyndromic Xlinked Left Ventricular Noncompaction Associated With Progressive Atrial Conduction Disturbance2019

    • Author(s)
      Ishikawa T., Barc J., Mishima H., Hirono K., Terada S., Kowase S., Sato T., Mukai Y., Yui Y., Ohkubo K., Kimoto H., Hata Y., Aiba T., Ohno S., Chishaki A., Shimizu W., Horie M., Ichida F., Nogami A., Yoshiura K., Schott JJ., Makita N.
    • Organizer
      The 40th Heart Rhythm Society Scientific Sessions
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] 発症前診断を行ったQT延長症候群の姉妹2019

    • Author(s)
      松下悠紀, 永田弾尺, 小川昌宣, 鹿田佐和子, 石川泰輔, 蒔田直昌
    • Organizer
      日本人類遺伝学会第64回大会
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Modeling Overlapping Phenotypes of Long-QT and Brugada Syndrome with CACNA1C-E1115K that Alters Ion Selectivity of the Cardiac L-Type Calcium Channel Using Induced Pluripotent Stem Cells2019

    • Author(s)
      Kashiwa A., Makiyama T., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
    • Organizer
      第66回日本不整脈心電学会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Novel common genetic predispositions to sudden death in Brugada syndrome distinct from those to diagnostic Brugada-ECG pattern2019

    • Author(s)
      Ishikawa T.
    • Organizer
      第3回日本循環器病学会基礎研究フォーラム
    • Invited
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] 次世代シーケンス解析による特発性心室細動の遺伝背景の解明2019

    • Author(s)
      謝颯琴, 高橋篤, 大野聖子, 鎌倉令, 石川泰輔, 植田初江, 斯波真理子, 南野直人, 林研至, 八木原伸江, 中野由紀子, 伊藤英樹, 宮本恵宏, 田中敏博, 蒔田直昌, 堀江稔, 清水渉, 草野研吾, 安田聡, 相庭武司
    • Organizer
      日本人類遺伝学会第64回大会
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Novel common genetic predispositions to sudden death in Brugada syndrome distinct from those to diagnostic Brugada-ECG pattern2019

    • Author(s)
      Ishikawa T.
    • Organizer
      第3回日本循環器病学会基礎研究フォーラム
    • Invited
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] 発症前診断を行ったQT延長症候群の姉妹2019

    • Author(s)
      松下悠紀, 永田弾尺, 小川昌宣, 鹿田佐和子, 石川泰輔, 蒔田直昌
    • Organizer
      日本人類遺伝学会第64回大会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Modeling Overlap Syndrome of Long QT and Brugada Syndrome Associated with Induced Pluripotent Stem Cells2019

    • Author(s)
      Kashiwa A., Makiyama T., Kohjitani H., Wuriyanghai Y., Yamamoto Y., Jungshan G., Huang H., Ishikawa T., Ohno S., Toyoda F., Sato S., Horie M., Makita N., Kimura T.
    • Organizer
      The 40th Heart Rhythm Society Scientific Sessions
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Functional Reappraisal of SCN5A Mutations Reemphasize Their Predictive Value for Lethal Cardiac Events in Brugada Syndrome2019

    • Author(s)
      Ishikawa T., Makita N.
    • Organizer
      第66回日本不整脈心電学会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Single Cell Electrophysiological Analysis of Human iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Voltage Imaging System2018

    • Author(s)
      Yamamoto Y., Makiyama T, Wuriyanghai Y., Kohjitani H., Hirose S., Gao J, Kashiwa A., Kimura T., Ishikawa T., Motomura H., Makita N, Ohno S., Chonabayashi K., Yoshida Y., Suda K., Horie M
    • Organizer
      The 11th Asia Pacific Heart Rhythm Society Scientific Session
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Cardiac Connexin Syndrome: A New Inherited Cardiac Conduction Disease Entity with Distinct Electrophysiological and Extracardiac Manifestations.2018

    • Author(s)
      Ishikawa T, Seki A, Hagiwara N and Makita N.
    • Organizer
      第82回日本循環器学会学術大会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Naチャネルβ1サブユニット SCN1Bは致死性不整脈の原因遺伝子か?2018

    • Author(s)
      石川泰輔, 佐藤誠一, 髙橋一浩 and 蒔田直昌
    • Organizer
      第16回特発性心室細動研究会
    • Invited
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Single Cell Electrophysiological Analysis of Human iPS Cell-Derived Cardiomyocytes Generated from Long-QT Syndrome Patients Carrying a CALM2 Mutation Using a Membrane Voltage Imaging System2018

    • Author(s)
      Yamamoto Y, Makiyama T, Wuriyanghai Y, Kohjitani H, Hirose S, Gao J, Kashiwa A, Kimura T, Ishikawa T, Motomura H, Makita N, Ohno S, Chonabayashi K, Yoshida Y, Suda K and Horie M.
    • Organizer
      The 11th Asia Pacific Heart Rhythm Society Scientific Session
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] The inactivation of L-type Ca2+ Channel was impaired in Human iPS Cell Model of Long-QT Syndrome with CALM2-D134H Mutation.2018

    • Author(s)
      Yamamoto Y., Makiyama T., Harita T., Hayano M., Nishiuchi S., Wuriyanghai Y., Kohjitani H., Hirose S., Yokoi F., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.
    • Organizer
      第82回日本循環器学会学術集会
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Attempts to identify the genetic risk loci for the lethal arrhythmia in Japanese Brugada syndrome population.2018

    • Author(s)
      Ishikawa T
    • Organizer
      第一回日本循環器学会基礎研究フォーラム
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Cardiac Connexin Syndrome: A New Inherited Cardiac Conduction Disease Entity with Distinct Electrophysiological and Extracardiac Manifestations.2018

    • Author(s)
      Ishikawa T., Seki A., Hagiwara N., Makita N.
    • Organizer
      第82回日本循環器学会学術大会
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Rare Coding Variants in Genes Other Than SCN5A Are Minimal Genetic Burden on the Prognosis of Brugada Syndrome2018

    • Author(s)
      Ishikawa T., Mishima H., Ohno S., T. Aiba, Nakano Y., Aizawa Y., Nakajima T., Hayashi K., Murakoshi N., Yagihara N., Kimoto H., Makiyama T., Watanabe H., Morita H., Yoshiura K., Nogami A., Shimizu W., Horie M., Tanaka T., Makita N.
    • Organizer
      The 65th Annual Meeting of the Japan Heart Rhythm Society
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] Clinical Manifestations and Long-term Mortality in Lamin A/C Mutation Carriers from the Japanese Multicenter Registry2018

    • Author(s)
      Nakajima K, Aiba T, Makiyama T, Nishiuchi S, Ohno S, Doi T, Shizuta S, Onoue K, Yagihara N, Ishikawa T, Watanabe I, Oginosawa Y, Nogami A, Aonuma K, Saitoh Y, Kimura T, Makita N, Shimizu W, Horie M and Kusano K.
    • Organizer
      The 65th Annual Meeting of the Japan Heart Rhythm Society
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Rare Coding Variants in Genes Other Than SCN5A Are Minimal Genetic Burden on the Prognosis of Brugada Syndrome2018

    • Author(s)
      Ishikawa T, Mishima H, Ohno S, T. A, Nakano Y, Aizawa Y, Nakajima T, Hayashi K, Murakoshi N, Yagihara N, Kimoto H, Makiyama T, Watanabe H, Morita H, Yoshiura K, Nogami A, Shimizu W, Horie M, Tanaka T and Makita N.
    • Organizer
      The 65th Annual Meeting of the Japan Heart Rhythm Society
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [Presentation] Clinical Manifestations and Long-term Mortality in Lamin A/C Mutation Carriers from the Japanese Multicenter Registry2018

    • Author(s)
      Nakajima K., Aiba T., Makiyama T., Nishiuchi S., Ohno S., Doi T., Shizuta S., Onoue K., Yagihara N., Ishikawa T., Watanabe I., Oginosawa Y., Nogami A., Aonuma K., Saitoh Y., Kimura T., Makita N., Shimizu W., Horie M., Kusano K.
    • Organizer
      The 65th Annual Meeting of the Japan Heart Rhythm Society
    • Data Source
      KAKENHI-PROJECT-18KK0245
  • [Presentation] The inactivation of L-type Ca2+ Channel was impaired in Human iPS Cell Model of Long-QT Syndrome with CALM2-D134H Mutation.2018

    • Author(s)
      Yamamoto Y, Makiyama T, Harita T, Hayano M, Nishiuchi S, Wuriyanghai Y, Kohjitani H, Hirose S, Yokoi F, Ishikawa T, Ohno S, Chonabayashi K, Suda K, Yoshida Y, Horie M, Makita N and Kimura T.
    • Organizer
      第82回日本循環器学会学術集会
    • Data Source
      KAKENHI-PROJECT-18K15894
  • [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] 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] 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] 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] De novo and Familial Connexin45 Mutant R75H Causes Progressive Atrioventricular Block Associated with Craniofacial and Dentodigital Dysmorphisms2017

    • Author(s)
      Makita N, Seki A, Ishikawa T, Dawmy X, Mishima H, Barc J, Sasaki R, Nishii K, Saito K, Urano M, Ohno S, Otsuki S, Kimoto H, Baruteau A, Aurelie T, Swanny F, Stephanie B, Parent P, Shibata Y, Perrin JJ, Le Marec H, Hagiwara N, Mercier S, Horie M, Probst V, Yoshiura K, Redon R, Schott J, J.
    • Organizer
      Printemps de la Cardiologie Recherche Fondamentale et Clinique
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K15311
  • [Presentation] Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation 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] 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] 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] 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] 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] 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
    • Place of Presentation
      札幌コンベンションセンター(北海道・札幌市)
    • Year and Date
      2016-03-23
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26860572
  • [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] 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] 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, D. T. Tsuji, Y. Watanabe, I. Makita, N.
    • Organizer
      第80回日本循環器学会学術集会
    • Place of Presentation
      仙台国際会議場(宮城県・仙台市)
    • Year and Date
      2016-03-18
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26860572
  • [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] 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] 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] 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] 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, D. T. Tsuji, Y. Watanabe, I. Makita, N.
    • Organizer
      Heart Rhythm Society
    • Place of Presentation
      ボストン(米国)
    • Year and Date
      2015-05-15
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26860572
  • [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] 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
      宮崎大学(宮崎県・宮崎市)
    • Year and Date
      2015-10-16
    • Data Source
      KAKENHI-PROJECT-26860572
  • [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] 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] 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
      久留米大学(福岡県・久留米市)
    • Year and Date
      2015-10-10
    • Data Source
      KAKENHI-PROJECT-26860572
  • [Presentation] Meta-analysis of Short QT Syndrome discloses genotype-dependent clinical characteristics in age of manifestation and arrhythmia complications.2015

    • Author(s)
      Harrell, D. T. Ashihara, T. Ishikawa, T. Mazzanti, A. Takahashi, K. Oginosawa, Y. Abe, H. Maemura, K. Sumitomo, N. Uno, K. Takano, M. Priori, S. G. 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
      京都国際会議場(京都府・京都市)
    • Year and Date
      2015-07-28
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-26860572
  • [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] 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-26860572
  • [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
      生理学研究所(愛知県・岡崎市)
    • Year and Date
      2015-10-30
    • Data Source
      KAKENHI-PROJECT-26860572
  • [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] 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] 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] 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] 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] 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] 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] A Novel Cardiac a-Myosin Heavy Chain (MYH6) Mutation Associated with Familial Sick Sinus Syndrome Altering Sarcomeric Organization.2014

    • Author(s)
      Ishikawa T, Nogami A, Kowase S, Arimura T, 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
      2014-07-23
    • Data Source
      KAKENHI-PROJECT-26860572
  • [Presentation] Electrical Storm in Inherited Arrhythmia Syndromes.2014

    • 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
    • Data Source
      KAKENHI-PROJECT-26860572
  • [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] 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] Role of Ca2+/calmodulin -dependent Protein Kinase ll in Atrial and Ventricular Remodeling and Arrhythmias2014

    • Author(s)
      Tsuji Y, Ishikawa T, Makita N
    • Organizer
      第29回日本不整脈学会・第31回日本心電学会合同学術大会
    • Place of Presentation
      東京都港区、ザ・プリンスパークタワー東京
    • Year and Date
      2014-07-24
    • Invited
    • Data Source
      KAKENHI-PLANNED-22136007
  • [Presentation] 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] A Novel Cardiac a-Myosin Heavy Chain (MYH6) Mutation Associated with Familial Sick Sinus Syndrome Altering Sarcomeric Organization.2014

    • 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
      2014-05-10
    • Data Source
      KAKENHI-PROJECT-26860572
  • [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] A novel cardiac alpha-myosin heavy chain (MYH6) mutation impairing sarcomere structure responsible for familial sick sinus syndrome2014

    • Author(s)
      Ishikawa T, Nogami A, Kowase S, Harrell D, Tsuji Y, Arimura T, Kimura A, Makita N
    • Organizer
      European Society of Cardiology
    • Place of Presentation
      Barcelona,Spain
    • Year and Date
      2014-09-02
    • Data Source
      KAKENHI-PLANNED-22136007
  • [Presentation] Role of Ca2+/calmodulin -dependent Protein Kinase ll in Atrial and Ventricular Remodeling and Arrhythmias2014

    • Author(s)
      Tsuji Y, Ishikawa T, Makita N
    • Organizer
      第29回日本不整脈学会・第31回日本心電学会合同学術大会
    • Place of Presentation
      東京都港区、ザ・プリンスパークタワー東京
    • Year and Date
      2014-07-24
    • Invited
    • Data Source
      KAKENHI-PROJECT-24390199
  • [Presentation] 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-26860572
  • [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-26860572
  • [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] 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] 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] 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] 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 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] 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] 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] 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] 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] 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] A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated

    • Author(s)
      石川泰輔
    • Organizer
      第30回日本心電学会
    • Place of Presentation
      青森市 リンステーションホール青森
    • 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] 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] 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
  • 1.  MAKITA Naomasa (00312356)
    # of Collaborated Projects: 6 results
    # of Collaborated Products: 102 results
  • 2.  MAEMURA Koji (90282649)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 3 results
  • 3.  TSUJI Yukiomi (60432217)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 23 results
  • 4.  YOSHIURA Koichiro (00304931)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 7 results
  • 5.  牧山 武 (30528302)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 11 results
  • 6.  ISHIKAWA Taisuke (50708716)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 7.  ARAI Yuji (30202724)
    # of Collaborated Projects: 1 results
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  • 8.  Iwasa Toru (80712843)
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  • 9.  高塚 賢二 (70378701)
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  • 10.  島本 恵子 (00792699)
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  • 11.  渡邉 裕介 (20562333)
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    # of Collaborated Products: 0 results
  • 12.  中川 修 (40283593)
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    # of Collaborated Products: 0 results
  • 13.  浦崎 明宏 (40550083)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 14.  黒嵜 健一 (40561460)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  白石 公 (80295659)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  岡田 随象 (70727411)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 17.  白井 学 (70294121)
    # of Collaborated Projects: 1 results
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  • 18.  沖田 孝一 (80382539)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 19.  塩谷 孝夫 (20253594)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 20.  YAMAZAWA Kazuki
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 21.  AIZAWA Yoshiyasu
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 22.  NAKAO Shu
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 23.  AIBA Takeshi
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 24.  芦原 貴司
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 25.  木村 彰方
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 26.  鷹野 誠
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 27.  堀江 稔
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 28.  市田 蕗子
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 29.  邊見 弘明
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 30.  南野 徹
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 31.  森田 宏
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