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Seiko Ohno

Showing results (161-170 of 196) with videos related to

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Biochemistry and Biophysics Reports|September 29, 2017
Flecainide ameliorates arrhythmogenicity through NCX flux in Andersen-Tawil syndrome-iPS cell-derived cardiomyocytesYusuke Kuroda, Shinsuke Yuasa, Yasuhide Watanabe, et al.
Circulation. Cardiovascular Genetics|July 17, 2013
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndromeSabine Duchatelet, Lia Crotti, Rachel A Peat, et al.
Circulation. Arrhythmia and Electrophysiology|March 3, 2023
Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived CardiomyocytesJingshan Gao, Takeru Makiyama, Yuta Yamamoto, et al.
Circulation. Arrhythmia and Electrophysiology|October 22, 2009
Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndromeHideki Itoh, Tomoko Sakaguchi, Wei-Guang Ding, et al.
European Heart Journal|July 5, 2021
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndromeTaisuke Ishikawa, Hiroki Kimoto, Hiroyuki Mishima, et al.
Circulation|March 26, 2017
Genotype-Phenotype Correlation of <i>SCN5A</i> Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter RegistryKenichiro Yamagata, Minoru Horie, Takeshi Aiba, et al.
Journal of the American College of Cardiology|July 15, 2017
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 MutationAkiko Seki, Taisuke Ishikawa, Xavier Daumy, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|February 11, 2025
SCN5A variant type-dependent risk prediction in Brugada syndromeTakanori Aizawa, Takeru Makiyama, Hai Huang, et al.
Plos One|December 3, 2024
Correction: Targeted deep sequencing analyses of long QT syndrome in a Japanese populationYuki Nagata, Ryo Watanabe, Christian Eichhorn, et al.
Plos Genetics|April 18, 2013
A nonsynonymous polymorphism in semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillationYukiko Nakano, Kazuaki Chayama, Hidenori Ochi, et al.
Pageof 20

Showing results (161-170 of 196) with videos related to

Sort By:
Pageof 20
Biochemistry and Biophysics Reports|September 29, 2017
Flecainide ameliorates arrhythmogenicity through NCX flux in Andersen-Tawil syndrome-iPS cell-derived cardiomyocytesYusuke Kuroda, Shinsuke Yuasa, Yasuhide Watanabe, et al.
Circulation. Cardiovascular Genetics|July 17, 2013
Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndromeSabine Duchatelet, Lia Crotti, Rachel A Peat, et al.
Circulation. Arrhythmia and Electrophysiology|March 3, 2023
Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived CardiomyocytesJingshan Gao, Takeru Makiyama, Yuta Yamamoto, et al.
Circulation. Arrhythmia and Electrophysiology|October 22, 2009
Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndromeHideki Itoh, Tomoko Sakaguchi, Wei-Guang Ding, et al.
European Heart Journal|July 5, 2021
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndromeTaisuke Ishikawa, Hiroki Kimoto, Hiroyuki Mishima, et al.
Circulation|March 26, 2017
Genotype-Phenotype Correlation of <i>SCN5A</i> Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome: A Japanese Multicenter RegistryKenichiro Yamagata, Minoru Horie, Takeshi Aiba, et al.
Journal of the American College of Cardiology|July 15, 2017
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 MutationAkiko Seki, Taisuke Ishikawa, Xavier Daumy, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|February 11, 2025
SCN5A variant type-dependent risk prediction in Brugada syndromeTakanori Aizawa, Takeru Makiyama, Hai Huang, et al.
Plos One|December 3, 2024
Correction: Targeted deep sequencing analyses of long QT syndrome in a Japanese populationYuki Nagata, Ryo Watanabe, Christian Eichhorn, et al.
Plos Genetics|April 18, 2013
A nonsynonymous polymorphism in semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillationYukiko Nakano, Kazuaki Chayama, Hidenori Ochi, et al.
Pageof 20