ISHIKAWA Taisuke 石川泰輔

… Alternative Names

石川泰輔イシカワタイスケ

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Researcher Number	50708716
Affiliation (based on the past Project Information) *help	2015: 長崎大学, 医歯薬学総合研究科(医学系), 助教 2013: 長崎大学, 医歯(薬)学総合研究科, 研究員
Review Section/Research Field	Except Principal Investigator Circulatory organs internal medicine
Keywords	Except Principal Investigator イオンチャネル / 次世代シークエンサー / 遺伝子多型 / 突然死 / SCN5A / 遺伝子変異 / エクソーム / SCN10A / GWAS / エクソーム解析 / 全エクソン解析 / ブルガダ症候群

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

All 2016 2015 2014 2013 2012 Other

All Journal Article Presentation Book

[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
[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] 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] 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] 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] 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] 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] 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 Nav1.5.2013
- 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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 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] 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 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] 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-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-PROJECT-24390199
[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] 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

1. MAKITA Naomasa (00312356)

# of Collaborated Projects: 1 results

# of Collaborated Products: 32 results
2. MAEMURA Koji (90282649)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
3. YOSHIURA Koichiro (00304931)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
4. TSUJI Yukiomi (60432217)

# of Collaborated Projects: 1 results

# of Collaborated Products: 17 results
5. 石川泰輔 (60708692)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. AIBA Takeshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
7. 木村彰方

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

ISHIKAWA Taisuke 石川 泰輔

石川 泰輔 イシカワ タイスケ

Research Projects

Research Products

Co-Researchers

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

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[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

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[Journal Article] Inherited bradyarrhythmia: A diverse genetic background.2016

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[Journal Article] Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias.2016

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DOI

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[Journal Article] A novel mutation in the α-myosin heavy chain gene is associated with sick sinus syndrome.2015

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[Journal Article] A novel mutation in alpha-myosin heavy chain gene is associated with sick sinus syndrome2015

Author(s)

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DOI

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[Journal Article] Molecular mechanisms of heart failure progression associated with implantable cardioverter-defibrillator shocks for ventricular tachyarrhythmias.2014

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[Journal Article] Novel calmodulin mutations associated with congenital arrhythmia susceptibility.2014

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[Journal Article] Sodium channelopathy underlying familial sick sinus syndrome with early onset and predominantly male characteristics.2014

Author(s)

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DOI

NAID

Data Source

[Journal Article] Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.2013

Author(s)

Journal Title

Data Source

[Journal Article] Novel <i>SCN3B</i> Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.52013

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[Journal Article] Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations2013

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[Journal Article] A novel disease gene for Brugada syndrome: sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.52012

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[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

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[Presentation] Dose-Sensitive Relationship of an SCN10A Pore Mutation and Enhancer SNPs Identified in a Brugada Syndrome Family with Different Expressivity2016

ISHIKAWA Taisuke 石川泰輔

石川泰輔イシカワタイスケ