Suppression of slow delayed rectifier current by a truncated isoform of KvLQT1 cloned from normal human heart
about
Amino-terminal determinants of U-type inactivation of voltage-gated K+ channelsPrimary structure and expression of a naturally truncated human P2X ATP receptor subunit from brain and immune systemExpression and coassociation of ERG1, KCNQ1, and KCNE1 potassium channel proteins in horse heartThe KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis.Molecular basis of functional voltage-gated K+ channel diversity in the mammalian myocardium.Novel truncated isoform of SK3 potassium channel is a potent dominant-negative regulator of SK currents: implications in schizophrenia.SK3-1C, a dominant-negative suppressor of SKCa and IKCa channels.Pore mutants of HERG and KvLQT1 downregulate the reciprocal currents in stable cell lines.Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias.KCNQ5/K(v)7.5 potassium channel expression and subcellular localization in primate retinal pigment epithelium and neural retinaModulation of KCNQ1 alternative splicing regulates cardiac IKs and action potential repolarization.Contribution of KCNQ1 to the regulatory volume decrease in the human mammary epithelial cell line MCF-7.Expression of potassium channel isoforms mRNA in normal human adrenals and aldosterone-secreting adenomas.Altered state dependence of c-type inactivation in the long and short forms of human Kv1.5.Electrical remodeling in a canine model of ischemic cardiomyopathy.Differential expression of KvLQT1 isoforms across the human ventricular wall.Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.Functional effects of mutations in KvLQT1 that cause long QT syndrome.Whole blood RNA offers a rapid, comprehensive approach to genetic diagnosis of cardiovascular diseases.
P2860
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P2860
Suppression of slow delayed rectifier current by a truncated isoform of KvLQT1 cloned from normal human heart
description
1997 nî lūn-bûn
@nan
1997 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Suppression of slow delayed re ...... cloned from normal human heart
@ast
Suppression of slow delayed re ...... cloned from normal human heart
@en
Suppression of slow delayed re ...... cloned from normal human heart
@en-gb
Suppression of slow delayed re ...... cloned from normal human heart
@nl
type
label
Suppression of slow delayed re ...... cloned from normal human heart
@ast
Suppression of slow delayed re ...... cloned from normal human heart
@en
Suppression of slow delayed re ...... cloned from normal human heart
@en-gb
Suppression of slow delayed re ...... cloned from normal human heart
@nl
prefLabel
Suppression of slow delayed re ...... cloned from normal human heart
@ast
Suppression of slow delayed re ...... cloned from normal human heart
@en
Suppression of slow delayed re ...... cloned from normal human heart
@en-gb
Suppression of slow delayed re ...... cloned from normal human heart
@nl
P2093
P2860
P356
P1476
Suppression of slow delayed re ...... cloned from normal human heart
@en
P2093
P2860
P304
P356
10.1074/JBC.272.39.24109
P407
P577
1997-09-26T00:00:00Z