A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y - sprookjes - yvandenbroek - TriplyDB

A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y

A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y

http://www.wikidata.org/entity/Q34331339

about

Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3 Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome Sudden unexplained death in infants and children: the role of undiagnosed inherited cardiac conditions A novel and lethal de novo LQT-3 mutation in a newborn with distinct molecular pharmacology and therapeutic response Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans Sudden cardiac death prediction and prevention: report from a National Heart, Lung, and Blood Institute and Heart Rhythm Society Workshop.Sudden infant death syndrome.Alternative translation initiation in rat brain yields K2P2.1 potassium channels permeable to sodium Part 10: Pediatric basic and advanced life support: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science With Treatment Recommendations.Risk stratification in young patients with channelopathies.SCN5A allelic expression imbalance in African-Americans heterozygous for the common variant p.Ser1103Tyr Targeting device therapy: genomics of sudden death.Prevention of torsade de pointes in hospital settings: a scientific statement from the American Heart Association and the American College of Cardiology Foundation.A CACNA1C variant associated with reduced voltage-dependent inactivation, increased CaV1.2 channel window current, and arrhythmogenesis.Genomic risk factors in sudden infant death syndrome Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation.SCN5A variation is associated with electrocardiographic traits in the Jackson Heart Study.SUMO modification of cell surface Kv2.1 potassium channels regulates the activity of rat hippocampal neurons The S1103Y cardiac sodium channel variant is associated with implantable cardioverter-defibrillator events in blacks with heart failure and reduced ejection fraction The common African American polymorphism SCN5A-S1103Y interacts with mutation SCN5A-R680H to increase late Na current Arrhythmogenic Biophysical Phenotype for SCN5A Mutation S1787N Depends upon Splice Variant Background and Intracellular Acidosis.KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties.Sudden infant death syndrome and long QT syndrome: the zealots versus the naysayers.SIDS: genetic and environmental influences may cause arrhythmia in this silent killer The genetics of sudden cardiac death.Cardiac ion channelopathies and the sudden infant death syndrome Drug-induced arrhythmia: pharmacogenomic prescribing?Investigation of unexplained infant deaths in Jerusalem, Israel 1996-2003 Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome.Risk factors in sudden death in epilepsy (SUDEP): the quest for mechanisms.Identifying genetic risk factors for serious adverse drug reactions: current progress and challenges.The biophysical characterization of the first SCN5A mutation R1512W identified in Chinese sudden unexplained nocturnal death syndrome.Cardiac sodium channels and inherited electrophysiologic disorders: a pharmacogenetic overview.Pediatric basic and advanced life support: 2010 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular Care Science with Treatment Recommendations.Pathophysiology of the cardiac late Na current and its potential as a drug target.Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention Sudden infant death syndrome: do ion channels play a role?Protein kinase A-dependent biophysical phenotype for V227F-KCNJ2 mutation in catecholaminergic polymorphic ventricular tachycardia.

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A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y

http://www.wikidata.org/entity/Q34331339

description

2006 nî lūn-bûn

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2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

A common cardiac sodium channe ...... frican Americans, SCN5A S1103Y

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A common cardiac sodium channe ...... frican Americans, SCN5A S1103Y

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A common cardiac sodium channe ...... frican Americans, SCN5A S1103Y

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A common cardiac sodium channe ...... frican Americans, SCN5A S1103Y

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A common cardiac sodium channe ...... frican Americans, SCN5A S1103Y

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A common cardiac sodium channe ...... frican Americans, SCN5A S1103Y

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A common cardiac sodium channe ...... frican Americans, SCN5A S1103Y

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A common cardiac sodium channe ...... frican Americans, SCN5A S1103Y

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A common cardiac sodium channe ...... frican Americans, SCN5A S1103Y

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Journal of Clinical Investigation

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A common cardiac sodium channe ...... frican Americans, SCN5A S1103Y

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Leigh D Plant

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Matthew W State

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Peter N Bowers

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Qianyong Liu

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Rick A Kittles

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Thomas Morgan

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Tingting Zhang

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Weidong Chen

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P2860

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

Cardiac conduction defects associate with mutations in SCN5A

Basic Mechanisms of Cardiac Impulse Propagation and Associated Arrhythmias

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

The sodium channel beta-subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heart

A common polymorphism associated with antibiotic-induced cardiac arrhythmia

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

Infant mortality statistics from the 2001 period linked birth/infant death data set.

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430-435

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10.1172/JCI25618

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2

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116

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Steve Goldstein

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2006-02-01T00:00:00Z

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7321244

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16453024

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1359045

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