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Heart Rhythm|November 6, 2008
A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncopeGeorges Christé, Olivier Thériault, Mohamed Chahine, et al.
Nature Communications|December 14, 2017
Voltage-gated sodium channels assemble and gate as dimersJérôme Clatot, Malcolm Hoshi, Xiaoping Wan, et al.
The Journal of Clinical Investigation|February 13, 2018
Physiological genomics identifies genetic modifiers of long QT syndrome type 2 severitySam Chai, Xiaoping Wan, Angelina Ramirez-Navarro, et al.
Gene|December 17, 2013
The variant hERG/R148W associated with LQTS is a mutation that reduces current density on co-expression with the WTAsma Mechakra, Yohann Vincent, Philippe Chevalier, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|September 25, 2009
The human cardiac K2P3.1 (TASK-1) potassium leak channel is a molecular target for the class III antiarrhythmic drug amiodaroneJakob Gierten, Eckhard Ficker, Ramona Bloehs, et al.
Molecular Biology of the Cell|October 25, 2013
Ubiquitination-dependent quality control of hERG K+ channel with acquired and inherited conformational defect at the plasma membranePirjo M Apaja, Brian Foo, Tsukasa Okiyoneda, et al.
British Journal of Pharmacology|November 2, 2002
The antihistamine fexofenadine does not affect I(Kr) currents in a case report of drug-induced cardiac arrhythmiaConstanze R Scherer, Christian Lerche, Niels Decher, et al.
Molecular Pharmacology|June 24, 2004
Mechanisms of arsenic-induced prolongation of cardiac repolarizationEckhard Ficker, Yuri A Kuryshev, Adrienne T Dennis, et al.
Elife|March 7, 2017
KChIP2 is a core transcriptional regulator of cardiac excitabilityDrew M Nassal, Xiaoping Wan, Haiyan Liu, et al.
Heart Rhythm|October 14, 2008
In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: compound effects of hERG pore region mutation and SCN5A N-terminus variantMing-Tai Lin, Mei-Hwan Wu, Chien-Chih Chang, et al.
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