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Journal of Arrhythmia|October 21, 2016
Inherited bradyarrhythmia: A diverse genetic backgroundTaisuke Ishikawa, Yukiomi Tsuji, Naomasa Makita
Beilstein Journal of Organic Chemistry|October 21, 2020
Catalytic trifluoromethylation of iodoarenes by use of 2-trifluoromethylated benzimidazoline as trifluoromethylating reagentTatsuhiro Uchikura, Nanami Kamiyama, Taisuke Ishikawa, et al.
The Journal of Biological Chemistry|August 31, 2010
Heart-specific small subunit of myosin light chain phosphatase activates rho-associated kinase and regulates phosphorylation of myosin phosphatase target subunit 1Daisuke Shichi, Takuro Arimura, Taisuke Ishikawa, et al.
Human Mutation|September 8, 2011
Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytesTakuro Arimura, Taisuke Ishikawa, Shinichi Nunoda, et al.
Journal of Pediatric Genetics|October 21, 2022
A Case Report: Two Young Children with Long QT Syndrome Type-2 Diagnosed by Presymptomatic Genetic TestingYuki Matsushita, Hazumu Nagata, Masanobu Ogawa, et al.
Human Genome Variation|August 8, 2022
Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian populationHaruka Murakami, Yoko Tanimoto, Kojiro Tanimoto, et al.
The Journal of Physiology|January 10, 2018
HCN4 pacemaker channels attenuate the parasympathetic response and stabilize the spontaneous firing of the sinoatrial nodeYuko Kozasa, Noriyuki Nakashima, Masayuki Ito, et al.
The Journal of Veterinary Medical Science|April 13, 2011
Echocardiographic estimation of left atrial pressure in beagle dogs with experimentally-induced mitral valve regurgitationTaisuke Ishikawa, Ryuji Fukushima, Shuji Suzuki, et al.
The Journal of Biological Chemistry|October 15, 2009
Novel mechanisms of trafficking defect caused by KCNQ1 mutations found in long QT syndromeAkinori Sato, Takuro Arimura, Naomasa Makita, et al.
Medical Molecular Morphology|March 2, 2021
Pathological findings of myocardium in a patient with cardiac conduction defect associated with an SCN5A mutationHiroaki Kawano, Koichi Kawamura, Masaki Kohno, et al.
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