Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation. - Wikidata - wikimedia - TriplyDB

Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

http://www.wikidata.org/entity/Q36628071

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Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation Solution NMR structure of Apo-calmodulin in complex with the IQ motif of human cardiac sodium channel NaV1.5 Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison The role of late I Na in development of cardiac arrhythmias Cardiac sodium channel Nav1.5 mutations and cardiac arrhythmia Ion Channels in the Heart Emerging directions in the genetics of atrial fibrillation Aberrant sodium influx causes cardiomyopathy and atrial fibrillation in mice Prediction of gene-phenotype associations in humans, mice, and plants using phenologs Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation The implications of familial incidental findings from exome sequencing: the NIH Undiagnosed Diseases Program experience Clinical Toxicities of Histone Deacetylase Inhibitors.Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgery A contemporary review on the genetic basis of atrial fibrillation.Improved understanding of the pathophysiology of atrial fibrillation through the lens of discrete pathological pathways Atrial fibrillation in congestive heart failure.Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder.Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation Brugada syndrome risk loci seem protective against atrial fibrillation.Monogenic atrial fibrillation as pathophysiological paradigms.Atrial Fibrillation and SCN5A Variants.Genetics of atrial fibrillation: implications for future research directions and personalized medicine.SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A.Examining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note.Differential impact of race and risk factors on incidence of atrial fibrillation.Genetics of atrial fibrillation and possible implications for ischemic stroke.Common and rare variants in SCN10A modulate the risk of atrial fibrillation.Atrial fibrillation: current knowledge and future directions in epidemiology and genomics.Your Father and Grandfather's Atrial Fibrillation: A Review of the Genetics of the Most Common Pathologic Cardiac Dysrhythmia Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro Repolarization recipes for atrial fibrillation: beyond single channel variants Symptomatic response to antiarrhythmic drug therapy is modulated by a common single nucleotide polymorphism in atrial fibrillation.Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation The Role of Pharmacogenetics in Atrial Fibrillation Therapeutics: Is Personalized Therapy in Sight?A KCNJ8 mutation associated with early repolarization and atrial fibrillation.Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation.

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P2860

Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

http://www.wikidata.org/entity/Q36628071

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2008 nî lūn-bûn

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name

Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

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Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

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Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

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Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

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Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

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Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

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Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.

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P2093

Alfred L George

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Brian S Donahue

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Dan M Roden

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Gayle Kucera

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Prince J Kannankeril

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Tanya Stubblefield

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P2860

Cardiac conduction defects associate with mutations in SCN5A

ACC/AHA/ESC 2006 Guidelines for the Management of Patients With Atrial Fibrillation

Nav1.5 E1053K mutation causing Brugada syndrome blocks binding to ankyrin-G and expression of Nav1.5 on the surface of cardiomyocytes

KCNQ1 gain-of-function mutation in familial atrial fibrillation

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.

Haploview: analysis and visualization of LD and haplotype maps

A single Na(+) channel mutation causing both long-QT and Brugada syndromes

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

Prevalence of long-QT syndrome gene variants in sudden infant death syndrome

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15

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117

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Jonathan L Haines

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2008-03-31T00:00:00Z

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18378609

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atrial fibrillation

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2365761

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