A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction.
about
Inherited and acquired vulnerability to ventricular arrhythmias: cardiac Na+ and K+ channels.Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.Congenital and drug-induced long-QT syndrome: an update.Alternans resonance and propagation block during supernormal conduction in cardiac tissue with decreased [K(+)](o)Genetic analysis of Brugada syndrome and congenital long-QT syndrome type 3 in the Chinese.Ion channel associated diseases: overview of molecular mechanismsMutational analysis of SCN5A gene in long QT syndromePharmacogenetics and anti-arrhythmic drug therapy: a theoretical investigation.The Na+ channel inactivation gate is a molecular complex: a novel role of the COOH-terminal domain.Sodium channel inactivation in heart: a novel role of the carboxy-terminal domain.Role of sodium channels in propagation in heart muscle: how subtle genetic alterations result in major arrhythmic disorders.Computational approaches to understand cardiac electrophysiology and arrhythmias.Molecular Pathophysiology of Congenital Long QT Syndrome.Long-QT syndrome-related sodium channel mutations probed by the dynamic action potential clamp technique.Functional Interactions between Distinct Sodium Channel Cytoplasmic Domains through the Action of Calmodulin.Computer simulation of wild-type and mutant human cardiac Na+ current.Structural effects of an LQT-3 mutation on heart Na+ channel gating.Contributions of sustained INa and IKv43 to transmural heterogeneity of early repolarization and arrhythmogenesis in canine left ventricular myocytes.Cardiac channelopathy causing sudden death as revealed by molecular autopsy.Sinus Bradycardia in Carriers of the SCN5A-1795insD Mutation: Unraveling the Mechanism through Computer Simulations.A Heart for Diversity: Simulating Variability in Cardiac Arrhythmia ResearchVariants: Association With Cardiac Disorders
P2860
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P2860
A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction.
description
2002 nî lūn-bûn
@nan
2002 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
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2002年学术文章
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2002年学术文章
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2002年学术文章
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2002年学术文章
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2002年学术文章
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2002年學術文章
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name
A novel SCN5A mutation associa ...... etics and channel dysfunction.
@ast
A novel SCN5A mutation associa ...... etics and channel dysfunction.
@en
type
label
A novel SCN5A mutation associa ...... etics and channel dysfunction.
@ast
A novel SCN5A mutation associa ...... etics and channel dysfunction.
@en
prefLabel
A novel SCN5A mutation associa ...... etics and channel dysfunction.
@ast
A novel SCN5A mutation associa ...... etics and channel dysfunction.
@en
P2093
P2860
P1476
A novel SCN5A mutation associa ...... netics and channel dysfunction
@en
P2093
Colleen E Clancy
Huajun Liu
Ilaria Rivolta
Robert S Kass
Silvia G Priori
P2860
P304
P356
10.1152/PHYSIOLGENOMICS.00039.2002
P50
P577
2002-09-03T00:00:00Z