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Journal of Pharmacological Sciences|December 6, 2008
Hydroxyzine, a first generation H(1)-receptor antagonist, inhibits human ether-a-go-go-related gene (HERG) current and causes syncope in a patient with the HERG mutationTomoko Sakaguchi, Hideki Itoh, Wei-Guang Ding, et al.Circulation. Arrhythmia and Electrophysiology|April 16, 2011
KCNE5 (KCNE1L) variants are novel modulators of Brugada syndrome and idiopathic ventricular fibrillationSeiko Ohno, Dimitar P Zankov, Wei-Guang Ding, et al.International Journal of Cardiology|August 12, 2008
A novel KCNH2 mutation as a modifier for short QT intervalHideki Itoh, Tomoko Sakaguchi, Takashi Ashihara, et al.Journal of Cardiology|November 18, 2017
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndromeDaisuke Fukumoto, Wei-Guang Ding, Yuko Wada, et al.Scientific Reports|February 17, 2018
A hERG mutation E1039X produced a synergistic lesion on I<sub>Ks</sub> together with KCNQ1-R174C mutation in a LQTS family with three compound mutationsJie Wu, Yuka Mizusawa, Seiko Ohno, et al.Journal of Cardiovascular Electrophysiology|January 10, 2014
Gain-of-function KCNH2 mutations in patients with Brugada syndromeQ I Wang, Seiko Ohno, Wei-Guang Ding, et al.Journal of Cardiology|November 7, 2016
Contribution of a KCNH2 variant in genotyped long QT syndrome: Romano-Ward syndrome under double mutations and acquired long QT syndrome under heterozygoteYusuke Fujii, Yuichi Matsumoto, Kenshi Hayashi, et al.Journal of the American College of Cardiology|August 22, 2009
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndromeYukiko Nishio, Takeru Makiyama, Hideki Itoh, et al.Heart Rhythm|January 1, 2010
KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disordersJie Wu, Wataru Shimizu, Wei-Guang Ding, et al.Circulation. Cardiovascular Genetics|May 17, 2012
Phenotype variability in patients carrying KCNJ2 mutationsHiromi Kimura, Jun Zhou, Mihoko Kawamura, et al.Pageof 7