Cardiac IKr Channels Minimally Comprise hERG 1a and 1b Subunits
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference25 articles.
1. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
2. A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel
3. HERG, a Human Inward Rectifier in the Voltage-Gated Potassium Channel Family
4. Two Isoforms of the Mouse Ether-a-go-go –Related Gene Coassemble to Form Channels With Properties Similar to the Rapidly Activating Component of the Cardiac Delayed Rectifier K + Current
5. Electrophysiological Characterization of an Alternatively Processed ERG K + Channel in Mouse and Human Hearts
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5. The impact of uncertainty in hERG binding mechanism on in silico predictions of drug‐induced proarrhythmic risk;British Journal of Pharmacology;2023-11-08
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