Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome
about
Differential association between HERG and KCNE1 or KCNE2Cloning of a new mouse two-P domain channel subunit and a human homologue with a unique pore structureKCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channelKCNE4 is an inhibitory subunit to the KCNQ1 channelElectrogram prolongation and nifedipine-suppressible ventricular arrhythmias in mice following targeted disruption of KCNE1Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.Congenital long QT syndromes: clinical features, molecular genetics and genetic testing.Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different?Genotype-phenotype analysis of three Chinese families with Jervell and Lange-Nielsen syndrome.Jervell and Lange-Nielsen syndrome in a father and daughter from a large highly inbred family: a 16-year follow-up of 59 living members.Deleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT.Functional interactions between KCNE1 C-terminus and the KCNQ1 channel.Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndromeDysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia.A new spontaneous mouse mutation in the Kcne1 geneThe genetics of cardiac arrhythmias.Unraveling monogenic channelopathies and their implications for complex polygenic diseasePrevention of ventricular arrhythmias in the congenital long QT syndrome.Pore- and state-dependent cadmium block of I(Ks) channels formed with MinK-55C and wild-type KCNQ1 subunitsMutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias.Peripheral channelopathies as targets for potassium channel openers.Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.Molecular genetics of arrhythmias and cardiovascular conditions associated with arrhythmias.LQT4 gene: the "missing" ankyrin.Modelling and imaging cardiac repolarization abnormalities.Computational biology in the study of cardiac ion channels and cell electrophysiology.Molecular mechanisms underlying KVS-1-MPS-1 complex assembly.Kcnq1 contributes to an adrenergic-sensitive steady-state K+ current in mouse heart.Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome.MinK subdomains that mediate modulation of and association with KvLQT1.Genetic testing in heritable cardiac arrhythmia syndromes: differentiating pathogenic mutations from background genetic noise.Mouse models of human arrhythmia syndromes.KCNE1 and KCNE3: The yin and yang of voltage-gated K(+) channel regulationVoltage-gated potassium channels as therapeutic targets.Genotype- and phenotype-guided management of congenital long QT syndrome.An Examination of KCNE1 Mutations and Common Variants in Chronic Tinnitus.Repolarization of the cardiac action potential. Does an increase in repolarization capacity constitute a new anti-arrhythmic principle?
P2860
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P2860
Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Mutation of the gene for IsK a ...... Ward forms of Long-QT syndrome
@ast
Mutation of the gene for IsK a ...... Ward forms of Long-QT syndrome
@en
Mutation of the gene for IsK a ...... Ward forms of Long-QT syndrome
@nl
type
label
Mutation of the gene for IsK a ...... Ward forms of Long-QT syndrome
@ast
Mutation of the gene for IsK a ...... Ward forms of Long-QT syndrome
@en
Mutation of the gene for IsK a ...... Ward forms of Long-QT syndrome
@nl
prefLabel
Mutation of the gene for IsK a ...... Ward forms of Long-QT syndrome
@ast
Mutation of the gene for IsK a ...... Ward forms of Long-QT syndrome
@en
Mutation of the gene for IsK a ...... Ward forms of Long-QT syndrome
@nl
P2093
P356
P1433
P1476
Mutation of the gene for IsK a ...... Ward forms of Long-QT syndrome
@en
P2093
D Wattanasirichaigoon
J Villafane
M R Vesely
P356
10.1161/01.CIR.97.2.142
P407
P577
1998-01-20T00:00:00Z