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Minoru Horie

Showing results (251-260 of 428) with videos related to

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Circulation Journal : Official Journal of the Japanese Circulation Society|October 27, 2010
Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndromeYuko Oka, Hideki Itoh, Wei-Guang Ding, et al.
Heart Rhythm|November 26, 2013
A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylationDaniel C Bartos, John R Giudicessi, David J Tester, et al.
Heart Rhythm|August 23, 2011
Clinical and electrocardiographic characteristics of patients with short QT interval in a large hospital-based populationAkashi Miyamoto, Hideki Hayashi, Tomohide Yoshino, et al.
Journal of Atherosclerosis and Thrombosis|December 8, 2017
Association of Coronary Artery Calcification with Estimated Coronary Heart Disease Risk from Prediction Models in a Community-Based Sample of Japanese Men: The Shiga Epidemiological Study of Subclinical Atherosclerosis (SESSA), Akira Fujiyoshi, Hisatomi Arima, 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|April 15, 2014
Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypesMegumi Fukuyama, Qi Wang, Koichi Kato, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 25, 2008
In vivo and in vitro inhibition of monocyte adhesion to endothelial cells and endothelial adhesion molecules by eicosapentaenoic acidHideto Yamada, Masayuki Yoshida, Yasutaka Nakano, et al.
Journal of the American College of Cardiology|October 22, 2008
A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillationTakeru Makiyama, Masaharu Akao, Satoshi Shizuta, et al.
Journal of Cardiology Cases|July 23, 2025
Atypical Holt-Oram syndrome: Early-onset sick sinus syndrome in a Japanese family with a novel <i>TBX5</i> mutation, Q469Yoshihiro Nomura, Taisuke Ishikawa, Seiko Ohno, et al.
Cardiovascular Research|December 14, 2011
A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currentsTetsuhisa Hattori, Takeru Makiyama, Masaharu Akao, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 22, 2012
Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5Taisuke Ishikawa, Naohiko Takahashi, Seiko Ohno, et al.
Pageof 43

Showing results (251-260 of 428) with videos related to

Sort By:
Pageof 43
Circulation Journal : Official Journal of the Japanese Circulation Society|October 27, 2010
Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndromeYuko Oka, Hideki Itoh, Wei-Guang Ding, et al.
Heart Rhythm|November 26, 2013
A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylationDaniel C Bartos, John R Giudicessi, David J Tester, et al.
Heart Rhythm|August 23, 2011
Clinical and electrocardiographic characteristics of patients with short QT interval in a large hospital-based populationAkashi Miyamoto, Hideki Hayashi, Tomohide Yoshino, et al.
Journal of Atherosclerosis and Thrombosis|December 8, 2017
Association of Coronary Artery Calcification with Estimated Coronary Heart Disease Risk from Prediction Models in a Community-Based Sample of Japanese Men: The Shiga Epidemiological Study of Subclinical Atherosclerosis (SESSA), Akira Fujiyoshi, Hisatomi Arima, 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|April 15, 2014
Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypesMegumi Fukuyama, Qi Wang, Koichi Kato, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 25, 2008
In vivo and in vitro inhibition of monocyte adhesion to endothelial cells and endothelial adhesion molecules by eicosapentaenoic acidHideto Yamada, Masayuki Yoshida, Yasutaka Nakano, et al.
Journal of the American College of Cardiology|October 22, 2008
A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillationTakeru Makiyama, Masaharu Akao, Satoshi Shizuta, et al.
Journal of Cardiology Cases|July 23, 2025
Atypical Holt-Oram syndrome: Early-onset sick sinus syndrome in a Japanese family with a novel <i>TBX5</i> mutation, Q469Yoshihiro Nomura, Taisuke Ishikawa, Seiko Ohno, et al.
Cardiovascular Research|December 14, 2011
A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currentsTetsuhisa Hattori, Takeru Makiyama, Masaharu Akao, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 22, 2012
Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5Taisuke Ishikawa, Naohiko Takahashi, Seiko Ohno, et al.
Pageof 43