about
Gene regulatory networks in cardiac conduction system developmentA reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsionsInteraction with GM130 during HERG ion channel trafficking. Disruption by type 2 congenital long QT syndrome mutations. Human Ether-à-go-go-Related Gene.Differential sialylation modulates voltage-gated Na+ channel gating throughout the developing myocardiumSingle-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome.Model organisms illuminate human genetics and disease.A second-generation computational modeling of cardiac electrophysiology: response of action potential to ionic concentration changes and metabolic inhibition.Heat shock protein 70 gene polymorphisms' influence on the electrophysiology of long QT syndrome.Re-trafficking of hERG reverses long QT syndrome 2 phenotype in human iPS-derived cardiomyocytes.Ile-177 and Ser-180 in the S1 segment are critically important in Kv1.1 channel function.The long QT syndrome with impaired atrioventricular conduction: a malignant variant in infants.
P2860
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P2860
description
1996 nî lūn-bûn
@nan
1996 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Pathophysiology of ion channel mutations.
@ast
Pathophysiology of ion channel mutations.
@en
Pathophysiology of ion channel mutations.
@nl
type
label
Pathophysiology of ion channel mutations.
@ast
Pathophysiology of ion channel mutations.
@en
Pathophysiology of ion channel mutations.
@nl
prefLabel
Pathophysiology of ion channel mutations.
@ast
Pathophysiology of ion channel mutations.
@en
Pathophysiology of ion channel mutations.
@nl
P1476
Pathophysiology of ion channel mutations.
@en
P2093
Keating MT
Sanguinetti MC
P304
P356
10.1016/S0959-437X(96)80010-4
P577
1996-06-01T00:00:00Z