The Binding Site for Channel Blockers That Rescue Misprocessed Human Long QT Syndrome Type 2 ether-a-gogo-related Gene (HERG) Mutations
Open Access
- 1 February 2002
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 277 (7), 4989-4998
- https://doi.org/10.1074/jbc.m107345200
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Analysis of the Cyclic Nucleotide Binding Domain of the HERG Potassium Channel and Interactions with KCNE2Published by Elsevier ,2001
- The Dominant Negative LQT2 Mutation A561V Reduces Wild-type HERG ExpressionPublished by Elsevier ,2000
- The Structure of the Potassium Channel: Molecular Basis of K + Conduction and SelectivityScience, 1998
- The inward rectification mechanism of the HERG cardiac potassium channelNature, 1996
- Glycerol Reverses the Misfolding Phenotype of the Most Common Cystic Fibrosis MutationJournal of Biological Chemistry, 1996
- A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channelCell, 1995
- A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeCell, 1995
- The internal quaternary ammonium receptor site of Shaker potassium channelsNeuron, 1993
- Inactivation of potassium current in squid axon by a variety of quaternary ammonium ions.The Journal of general physiology, 1981
- Interaction of Tetraethylammonium Ion Derivatives with the Potassium Channels of Giant AxonsThe Journal of general physiology, 1971