Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current
about
Sudden infant death syndrome-associated mutations in the sodium channel beta subunitsChannelopathies from mutations in the cardiac sodium channel protein complexMolecular and genetic basis of sudden cardiac deathSudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditionsSequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Dataα1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium CurrentRole of risk stratification and genetics in sudden cardiac death.Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.A perspective on SIDS pathogenesis. the hypotheses: plausibility and evidenceGenomic risk factors in sudden infant death syndromeDiseases caused by mutations in Nav1.5 interacting proteinsSCN5A rare variants in familial dilated cardiomyopathy decrease peak sodium current depending on the common polymorphism H558R and common splice variant Q1077del.The common African American polymorphism SCN5A-S1103Y interacts with mutation SCN5A-R680H to increase late Na currentCardiac ion channelopathies and the sudden infant death syndromeNew insights into the roles of Xin repeat-containing proteins in cardiac development, function, and disease.Caveolin-3 suppresses late sodium current by inhibiting nNOS-dependent S-nitrosylation of SCN5A.Pathophysiology of the cardiac late Na current and its potential as a drug target.LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype.Sudden infant death syndrome due to long QT syndrome: a brief review of the genetic substrate and prevalence.Gene variants predisposing to SIDS: current knowledge.Genetics of sudden death: focus on inherited channelopathies.Cardiac channelopathies and sudden infant death syndrome.Biology of cardiac sodium channel Nav1.5 expression.Sodium channel haploinsufficiency and structural change in ventricular arrhythmogenesis.Murine Electrophysiological Models of Cardiac Arrhythmogenesis.Rare variants in genes encoding the cardiac sodium channel and associated compounds and their impact on outcome of catheter ablation of atrial fibrillation.Sudden infant death syndrome and inherited cardiac conditions.The gene encoding the inwardly rectifying potassium channel Kir4.1 may be involved in sudden infant death syndrome.
P2860
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P2860
Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Alpha1-syntrophin mutations id ...... in late cardiac sodium current
@ast
Alpha1-syntrophin mutations id ...... in late cardiac sodium current
@en
type
label
Alpha1-syntrophin mutations id ...... in late cardiac sodium current
@ast
Alpha1-syntrophin mutations id ...... in late cardiac sodium current
@en
prefLabel
Alpha1-syntrophin mutations id ...... in late cardiac sodium current
@ast
Alpha1-syntrophin mutations id ...... in late cardiac sodium current
@en
P2093
P2860
P1476
Alpha1-syntrophin mutations id ...... in late cardiac sodium current
@en
P2093
Argelia Medeiros-Domingo
Bi-hua Tan
Carmen Valdivia
Craig T January
David J Tester
David W Van Norstrand
Jianding Cheng
Jonathan C Makielski
Matteo Vatta
P2860
P304
P356
10.1161/CIRCEP.109.891440
P577
2009-12-01T00:00:00Z