KCNQ1 gain-of-function mutation in familial atrial fibrillation - Wikidata - awgldk - TriplyDB

KCNQ1 gain-of-function mutation in familial atrial fibrillation

KCNQ1 gain-of-function mutation in familial atrial fibrillation

http://www.wikidata.org/entity/Q24338486

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Kcne2 deletion uncovers its crucial role in thyroid hormone biosynthesis Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy O-glycosylation of the cardiac I(Ks) complex Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation Regulation of the Kv2.1 potassium channel by MinK and MiRP1 Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.KCNE variants reveal a critical role of the beta subunit carboxyl terminus in PKA-dependent regulation of the IKs potassium channel Dynamic partnership between KCNQ1 and KCNE1 and influence on cardiac IKs current amplitude by KCNE2 Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans Neuronal and Cardiovascular Potassium Channels as Therapeutic Drug Targets: Promise and Pitfalls Mink S38G gene polymorphism and atrial fibrillation in the Chinese population: a meta-analysis of 1871 participants Ion Channels in the Heart Emerging directions in the genetics of atrial fibrillation CaMKII regulation of cardiac K channels Driving with no brakes: molecular pathophysiology of Kv7 potassium channels Structure of KCNE1 and Implications for How It Modulates the KCNQ1 Potassium Channel † ‡The Genetic Basis of Coronary Artery Disease and Atrial Fibrillation: A Search for Disease Mechanisms and Therapeutic Targets IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation Ablation of a Ca2+-activated K+ channel (SK2 channel) results in action potential prolongation in atrial myocytes and atrial fibrillation Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation KCNE2 and the K (+) channel: the tail wagging the dog Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death.KCNE1 alters the voltage sensor movements necessary to open the KCNQ1 channel gate Genetics of type 2 diabetes: pathophysiologic and clinical relevance Sodium channel mutations and susceptibility to heart failure and atrial fibrillation Inhibition of HERG potassium channels by celecoxib and its mechanism Life sciences and biotechnology in China.A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation Atrial Fibrillation: Epidemiology, Pathophysiology, and Clinical Outcomes.Conformational changes of an ion-channel during gating and emerging electrophysiologic properties: Application of a computational approach to cardiac Kv7.1.Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.Regulation of KCNQ/Kv7 family voltage-gated K+ channels by lipids.Characterization of KCNQ1 atrial fibrillation mutations reveals distinct dependence on KCNE1.European ancestry as a risk factor for atrial fibrillation in African Americans

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P2860

KCNQ1 gain-of-function mutation in familial atrial fibrillation

http://www.wikidata.org/entity/Q24338486

description

2003 nî lūn-bûn

@nan

2003 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2003 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2003年の論文

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2003年論文

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2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

name

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@ast

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@en

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@en-gb

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@nl

type

label

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@ast

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@en

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@en-gb

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@nl

prefLabel

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@ast

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@en

KCNQ1 gain-of-function mutation in familial atrial fibrillation

@en-gb

KCNQ1 gain-of-function mutation in familial atrial fibrillation

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SCIENCE.1077771

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KCNQ1 gain-of-function mutation in familial atrial fibrillation

@en

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Chun-Ping Mou

http://www.w3.org/2001/XMLSchema#string

Hao Sun

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Hong-Ju Xu

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Hong-Wei Jin

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Jacques Barhanin

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Ning Ma

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Qi-Nan Zhuang

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Said Bendahhou

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Shi-Jie Xu

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Wei Huang

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251-4

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1968962

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10.1126/SCIENCE.1077771

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299

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2003-01-10T00:00:00Z

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12522251

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P921

Potassium voltage-gated channel subfamily E regulatory subunit 1

membrane repolarization during atrial cardiac muscle cell action potential

Potassium voltage-gated channel subfamily Q member 1

atrial fibrillation