Genetic variation in SCN10A influences cardiac conduction
about
Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndromeIdentification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome scienceImpact of New Genomic Technologies on Understanding Adverse Drug ReactionsIon Channels in the HeartGene regulatory networks in cardiac conduction system developmentLate Sodium Current in Human Atrial Cardiomyocytes from Patients in Sinus Rhythm and Atrial FibrillationThe cardiac conduction systemNav1.7 and other voltage-gated sodium channels as drug targets for pain reliefCommon variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathSequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.Genome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmiasGenome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility lociFine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations.Novel loci associated with PR interval in a genome-wide association study of 10 African American cohortsGenome-wide association studies of the PR interval in African AmericansSudden cardiac death prediction and prevention: report from a National Heart, Lung, and Blood Institute and Heart Rhythm Society Workshop.The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence Data.Novel SCN10A variants associated with Brugada syndrome.Deleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT.Genome-wide identification of expression quantitative trait loci (eQTLs) in human hearteMERGEing progress in genomics-the first seven years.OccuPeak: ChIP-Seq peak calling based on internal background modellingSingle-nucleotide variations in cardiac arrhythmias: prospects for genomics and proteomics based biomarker discovery and diagnostics.Improved understanding of the pathophysiology of atrial fibrillation through the lens of discrete pathological pathwaysGenetic determinants of P wave duration and PR segmentFine-scale estimation of location of birth from genome-wide single-nucleotide polymorphism dataThe trafficking of Na(V)1.8.Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model.Fine-mapping and initial characterization of QT interval loci in African Americans.Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease.Genetics of hypertension and cardiovascular disease and their interconnected pathways: lessons from large studies.SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillationCommon genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.Personalized medicine and the genotype-phenotype dilemma.Informatic and functional approaches to identifying a regulatory region for the cardiac sodium channel.Common and rare variants in SCN10A modulate the risk of atrial fibrillation.A novel selective and orally bioavailable Nav 1.8 channel blocker, PF-01247324, attenuates nociception and sensory neuron excitability.Hypermorphic mutation of the voltage-gated sodium channel encoding gene Scn10a causes a dramatic stimulus-dependent neurobehavioral phenotype.Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.
P2860
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P2860
Genetic variation in SCN10A influences cardiac conduction
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Genetic variation in SCN10A influences cardiac conduction
@ast
Genetic variation in SCN10A influences cardiac conduction
@en
Genetic variation in SCN10A influences cardiac conduction
@en-gb
Genetic variation in SCN10A influences cardiac conduction
@nl
type
label
Genetic variation in SCN10A influences cardiac conduction
@ast
Genetic variation in SCN10A influences cardiac conduction
@en
Genetic variation in SCN10A influences cardiac conduction
@en-gb
Genetic variation in SCN10A influences cardiac conduction
@nl
prefLabel
Genetic variation in SCN10A influences cardiac conduction
@ast
Genetic variation in SCN10A influences cardiac conduction
@en
Genetic variation in SCN10A influences cardiac conduction
@en-gb
Genetic variation in SCN10A influences cardiac conduction
@nl
P2093
P50
P921
P3181
P356
P1433
P1476
Genetic variation in SCN10A influences cardiac conduction
@en
P2093
Amol Lotlikar
Cesare M N Terracciano
Connie R Bezzina
Guohong Deng
Ismail El-Hamamsy
James Scott
Jaspal S Kooner
Joban S Sehmi
John C Chambers
John N Wood
P2888
P304
P3181
P356
10.1038/NG.516
P407
P577
2010-01-10T00:00:00Z
P6179
1052780791