Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia. - Wikidata - awgldk - TriplyDB

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

http://www.wikidata.org/entity/Q33148058

about

Human population genetic structure and inference of group membership Associations between genetic variants in the NOS1AP (CAPON) gene and cardiac repolarization in the old order Amish Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome Facilitating arrhythmia simulation: the method of quantitative cellular automata modeling and parallel running The role of late I Na in development of cardiac arrhythmias Clinical and genetic determinants of torsade de pointes risk Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction The ARVD/C genetic variants database: 2014 update Sodium channel mutations and susceptibility to heart failure and atrial fibrillation Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes α1-Syntrophin Variant Identified in Drug-Induced Long QT Syndrome Increases Late Sodium Current CD36 overexpression predisposes to arrhythmias but reduces infarct size in spontaneously hypertensive rats: gene expression profile analysis Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.Impact of ancestry and common genetic variants on QT interval in African Americans.A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans Functional decorations: post-translational modifications and heart disease delineated by targeted proteomics.Genome-wide association studies of the PR interval in African Americans Tox-database.net: a curated resource for data describing chemical triggered in vitro cardiac ion channels inhibition.A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation.Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.Inherited and acquired vulnerability to ventricular arrhythmias: cardiac Na+ and K+ channels.The long QT syndrome family of cardiac ion channelopathies: a HuGE review.A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illness Long QT syndrome in African-Americans Torsades de pointes during complete atrioventricular block: Genetic factors and electrocardiogram correlates.Risk stratification in young patients with channelopathies.Congenital and drug-induced long-QT syndrome: an update.Patterns of population differentiation of candidate genes for cardiovascular disease.SCN5A allelic expression imbalance in African-Americans heterozygous for the common variant p.Ser1103Tyr Targeting device therapy: genomics of sudden death.Sodium channel carboxyl-terminal residue regulates fast inactivation.Genomics, heart failure and sudden cardiac death.Inherited disorders of voltage-gated sodium channels.Genetics of acquired long QT syndrome.Etiology of sudden death in the community: results of anatomical, metabolic, and genetic evaluation Genome-wide association studies in cardiac electrophysiology: recent discoveries and implications for clinical practice 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.

P2860

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P2860

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

http://www.wikidata.org/entity/Q33148058

description

2002 nî lūn-bûn

@nan

2002 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2002 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2002年の論文

@ja

2002年学术文章

@wuu

2002年学术文章

@zh-cn

2002年学术文章

@zh-hans

2002年学术文章

@zh-my

2002年学术文章

@zh-sg

2002年學術文章

@yue

name

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

@ast

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

@en

type

label

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

@ast

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

@en

prefLabel

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

@ast

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

@en

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P356

SCIENCE.1073569

P1433

P1476

Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.

@en

P2093

Alan H Beggs

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

Alka Malhotra

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

Colleen E Clancy

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

Francesco P Cappuccio

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

Giuseppe A Sagnella

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

Igor Splawski

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

Katherine W Timothy

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

Mark T Keating

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

Michihiro Tateyama

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

Robert S Kass

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

P304

1333-1336

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P31

scholarly article

P356

10.1126/SCIENCE.1073569

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P407

P433

5585

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P478

297

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P577

2002-08-01T00:00:00Z

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P5875

11194026

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P698

12193783

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P921

heart arrhythmia