Suivre
Taisuke Ishikawa
Taisuke Ishikawa
国立循環器病研究センター 創薬オミックス解析センター
Adresse e-mail validée de ncvc.go.jp
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Année
Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1.
Y Kurihara, H Kurihara, H Oda, K Maemura, R Nagai, T Ishikawa, ...
The Journal of clinical investigation 96 (1), 293-300, 1995
4801995
Electrocardiographic Characteristics and SCN5A Mutations in Idiopathic Ventricular Fibrillation Associated With Early Repolarization
H Watanabe, A Nogami, K Ohkubo, H Kawata, Y Hayashi, T Ishikawa, ...
Circulation: Arrhythmia and Electrophysiology 4 (6), 874-881, 2011
2112011
Novel calmodulin mutations associated with congenital arrhythmia susceptibility
N Makita, N Yagihara, L Crotti, CN Johnson, BM Beckmann, MS Roh, ...
Circulation: Cardiovascular Genetics 7 (4), 466-474, 2014
2102014
Dilated cardiomyopathy‐associated BAG3 mutations impair Z‐disc assembly and enhance sensitivity to apoptosis in cardiomyocytes
T Arimura, T Ishikawa, S Nunoda, S Kawai, A Kimura
Human mutation 32 (12), 1481-1491, 2011
1622011
A novel disease gene for brugada syndrome: sarcolemmal membrane–associated protein gene mutations impair intracellular trafficking of hnav1. 5
T Ishikawa, A Sato, CA Marcou, DJ Tester, MJ Ackerman, L Crotti, ...
Circulation: Arrhythmia and Electrophysiology 5 (6), 1098-1107, 2012
1222012
Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome
N Lahrouchi, R Tadros, L Crotti, Y Mizusawa, PG Postema, L Beekman, ...
Circulation 142 (4), 324-338, 2020
1072020
Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation
Y Yamamoto, T Makiyama, T Harita, K Sasaki, Y Wuriyanghai, M Hayano, ...
Human Molecular Genetics 26 (9), 1670-1677, 2017
1032017
Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1. 5
T Ishikawa, N Takahashi, S Ohno, H Sakurada, K Nakamura, YK On, ...
Circulation Journal 77 (4), 959-967, 2013
862013
The effect of pimobendan on left atrial pressure in dogs with mitral valve regurgitation
S Suzuki, R Fukushima, T Ishikawa, L Hamabe, D Aytemiz, H Huai‐Che, ...
Journal of veterinary internal medicine 25 (6), 1328-1333, 2011
682011
Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias
A Koizumi, T Sasano, W Kimura, Y Miyamoto, T Aiba, T Ishikawa, ...
European Heart Journal 37 (18), 1469-1475, 2016
672016
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
R Walsh, N Lahrouchi, R Tadros, F Kyndt, C Glinge, PG Postema, ...
Genetics in medicine 23 (1), 47-58, 2021
652021
Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome
DT Harrell, T Ashihara, T Ishikawa, I Tominaga, A Mazzanti, K Takahashi, ...
International journal of cardiology 190, 393-402, 2015
652015
Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers
S Nishiuchi, T Makiyama, T Aiba, K Nakajima, S Hirose, H Kohjitani, ...
Circulation: cardiovascular genetics 10 (6), e001603, 2017
602017
Sodium channelopathy underlying familial sick sinus syndrome with early onset and predominantly male characteristics
K Abe, T Machida, N Sumitomo, H Yamamoto, K Ohkubo, I Watanabe, ...
Circulation: Arrhythmia and Electrophysiology 7 (3), 511-517, 2014
582014
Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction
T Ishikawa, S Ohno, T Murakami, K Yoshida, H Mishima, T Fukuoka, ...
Heart Rhythm 14 (5), 717-724, 2017
552017
Dilated cardiomyopathy-associated FHOD3 variant impairs the ability to induce activation of transcription factor serum response factor
T Arimura, R Takeya, T Ishikawa, T Yamano, A Matsuo, T Tatsumi, ...
Circulation Journal 77 (12), 2990-2996, 2013
542013
Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations
T Arimura, K Onoue, Y Takahashi-Tanaka, T Ishikawa, M Kuwahara, ...
Cardiovascular research 99 (3), 382-394, 2013
532013
HCN4 pacemaker channels attenuate the parasympathetic response and stabilize the spontaneous firing of the sinoatrial node
Y Kozasa, N Nakashima, M Ito, T Ishikawa, H Kimoto, K Ushijima, ...
The Journal of physiology 596 (5), 809-825, 2018
502018
SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families
YD Wijeyeratne, MW Tanck, Y Mizusawa, V Batchvarov, J Barc, L Crotti, ...
Circulation: Genomic and Precision Medicine 13 (6), e002911, 2020
482020
Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome
T Ishikawa, H Kimoto, H Mishima, K Yamagata, S Ogata, Y Aizawa, ...
European heart journal 42 (29), 2854-2863, 2021
472021
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