The Dominant Negative LQT2 Mutation A561V Reduces Wild-type HERG Expression
Open Access
- 1 April 2000
- journal article
- Published by Elsevier
- Vol. 275 (15), 11241-11248
- https://doi.org/10.1074/jbc.275.15.11241
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- The Long QT Syndrome: Ion Channel Diseases of the HeartMayo Clinic Proceedings, 1998
- Cotranslational Biogenesis of NF-κB p50 by the 26S ProteasomeCell, 1998
- Pathophysiology of ion channel mutationsCurrent Opinion in Genetics & Development, 1996
- Glycerol Reverses the Misfolding Phenotype of the Most Common Cystic Fibrosis MutationJournal of Biological Chemistry, 1996
- A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndromeCell, 1995
- Ubiquitin, proteasomes, and the regulation of intracellular protein degradationCurrent Opinion in Cell Biology, 1995
- Efficient in vitro folding of the three‐disulfide derivatives of hen lysozyme in the presence of glycerolFEBS Letters, 1992
- Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus OocytesScience, 1991
- Determination of the subunit stoichiometry of a voltage-activated potassium channelNature, 1991
- Role of the environment in the refolding of reduced pancreatic trypsin inhibitorJournal of Molecular Biology, 1980