Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias
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Sudden infant death syndrome-associated mutations in the sodium channel beta subunitsSodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humansCardiac Na+ current regulation by pyridine nucleotidesMexiletine differentially restores the trafficking defects caused by two brugada syndrome mutationsGPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5AMolecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndromeAn integrated approach for experimental target identification of hypoxia-induced miR-210Functional effects of KCNE3 mutation and its role in the development of Brugada syndromeThe Brugada Syndrome: A Rare Arrhythmia Disorder with Complex InheritanceGenetics of channelopathies associated with sudden cardiac deathChannelopathies from mutations in the cardiac sodium channel protein complexMolecular and genetic basis of sudden cardiac deathRegulation of ion channels by pyridine nucleotidesIon Channels in the HeartProtein assemblies of sodium and inward rectifier potassium channels control cardiac excitability and arrhythmogenesisElectrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical StudiesGenetics of Brugada syndromeIon channel macromolecular complexes in cardiomyocytes: roles in sudden cardiac deathPost-translational modifications of the cardiac Na channel: contribution of CaMKII-dependent phosphorylation to acquired arrhythmiasmiR-210: More than a silent player in hypoxiaGenetics of sudden cardiac death syndromesNovel loci associated with PR interval in a genome-wide association study of 10 African American cohortsPharmacogenomic and clinical data link non-pharmacokinetic metabolic dysregulation to drug side effect pathogenesisDistinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutationsAccelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndromeDrug-induced Brugada syndrome.Risk stratification in electrical cardiomyopathies.Recent developments in the management of patients at risk for sudden cardiac death.Genetic testing of inherited arrhythmias.A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome.The role of ion channelopathies in sudden cardiac death: implications for clinical practice.Risk stratification and treatment of brugada syndrome.Risk Stratification and Therapeutic Approach in Brugada Syndrome.A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotypeAbnormal repolarization as the basis for late potentials and fractionated electrograms recorded from epicardium in experimental models of Brugada syndrome.An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.J wave syndromes.Mitochondria and arrhythmias.Cardiac sodium channelopathies.A mutation causing Brugada syndrome identifies a mechanism for altered autonomic and oxidant regulation of cardiac sodium currents
P2860
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P2860
Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias
description
2007 nî lūn-bûn
@nan
2007 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@ast
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@en
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@en-gb
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@nl
type
label
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@ast
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@en
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@en-gb
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@nl
prefLabel
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@ast
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@en
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@en-gb
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@nl
P2093
P2860
P921
P3181
P1433
P1476
Mutation in glycerol-3-phospha ...... d causes inherited arrhythmias
@en
P2093
Arnold E Pfahnl
Barry London
Catherine J Baty
Dennis M McNamara
Haider Mehdi
Laurie Kerchner
Lijuan L Shang
Michael J Ackerman
Michael Michalec
Mohan Madhusudanan
P2860
P304
P3181
P356
10.1161/CIRCULATIONAHA.107.703330
P407
P577
2007-11-13T00:00:00Z