A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.
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- Type
- article
- Published
- 1995-03-10
- Cited by
- 2,354
- References
- 38
- Access
- Open access
- OpenAlex
- https://openalex.org/W2074705578
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:17466679
Keywords
hERG, Long QT syndrome, Biology, Missense mutation, Genetics
References
- The 1993–94 Généthon human genetic linkage map
- Functional expression of a rat homologue of the voltage gated either á go‐go potassium channel reveals differences in selectivity and activation kinetics between the Drosophila channel and its mammalian counterpart.
- Cardiac Electrophysiology: From Cell to Bedside
- Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.
- Clinical relevance of cardiac arrhythmias generated by afterdepolarizations. Role of M cells in the generation of U waves, triggered activity and torsade de pointes.
- Electrophysiologic substrate of torsade de pointes: dispersion of repolarization or early afterdepolarizations?
- CONGENITAL CARDIAC ARRHYTHMIA.
- Shaker, Shal, Shab, and Shaw express independent K+ current systems.
- Identification of a family of muscarinic acetylcholine receptor genes.
- Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene.
- The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome.
- The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis.
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.
- Locus heterogeneity of autosomal dominant long QT syndrome.
- Early Afterdepolarizations: Mechanism of Induction and Block A Role for L‐Type Ca2+ Current
- Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products.
- The long QT syndrome.
- Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
- Linkage Analysis and Long QT Syndrome: Using Genetics to Study Cardiovascular Disease
- Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.
Cited by
- Stereoselective interactions between local anesthetics and ion channels.
- On the trail of genetic culprits in Williams syndrome.
- Long QT and ventricular arrhythmias in transgenic mice expressing the N terminus and first transmembrane segment of a voltage-gated potassium channel.
- Stress (heat shock) proteins: molecular chaperones in cardiovascular biology and disease.
- Functional knockout of the transient outward current, long-QT syndrome, and cardiac remodeling in mice expressing a dominant-negative Kv4 alpha subunit.
- Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.
- Homozygous premature truncation of the HERG protein : the human HERG knockout.
- Diverse behavioural defects caused by mutations in Caenorhabditis elegans unc-43 CaM Kinase II
- A plethora of mechanisms in the HERG-related long QT syndrome. Genetics meets electrophysiology.
- Channelopathies can cause epilepsy in man
- A Simple Method for Evaluating Abnormal Lengthening of the QT Interval During the Face Immersion Test
- Defective Human Ether-à-go-go-related Gene Trafficking Linked to an Endoplasmic Reticulum Retention Signal in the C Terminus*
- Genotyping of Drug Targets
- Bertosamil blocks HERG potassium channels in their open and inactivated states
- Physiology of EAG K+ Channels
- Psychotropic Drugs, Cardiac Arrhythmia, and Sudden Death
- Expression and function of KCNH2 (HERG) in the human jejunum.
- ERG K+ currents regulate pacemaker activity in ICC.
- Molecular Genetics of Arrhythmias and Cardiovascular Conditions Associated with Arrhythmias
- Changes in cardiac repolarization during clinical episodes of nocturnal hypoglycaemia in adults with Type 1 diabetes
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