A common polymorphism in SCN5A is associated with lone atrial fibrillation. - Wikidata - wikimedia - TriplyDB

A common polymorphism in SCN5A is associated with lone atrial fibrillation.

A common polymorphism in SCN5A is associated with lone atrial fibrillation.

http://www.wikidata.org/entity/Q35914701

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Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study Scn3b knockout mice exhibit abnormal sino-atrial and cardiac conduction properties Role of risk stratification and genetics in sudden cardiac death.Tox-database.net: a curated resource for data describing chemical triggered in vitro cardiac ion channels inhibition.Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgery Cardiac sodium channelopathies.Atrial fibrillation in congestive heart failure.Monogenic atrial fibrillation as pathophysiological paradigms.Lack of replication in polymorphisms reported to be associated with atrial fibrillation Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmias.Genetics of atrial fibrillation and possible implications for ischemic stroke.Recent advances in the molecular pathophysiology of atrial fibrillation.Atrial fibrillation: current knowledge and future directions in epidemiology and genomics.Transforming Growth Factor-β1 T869C Gene Polymorphism Is Associated with Acquired Sick Sinus Syndrome via Linking a Higher Serum Protein Level Interleukin-6 promoter polymorphisms and susceptibility to atrial fibrillation in elderly Han Chinese patients with essential hypertension Ion channel mutations in AF: signal or noise?Comparison of Atrial Fibrillation in the Young versus That in the Elderly: A Review.Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.X-linked nonsyndromic sinus node dysfunction and atrial fibrillation caused by emerin mutation.A genotype-dependent intermediate ECG phenotype in patients with persistent lone atrial fibrillation genotype ECG-phenotype correlation in atrial fibrillation.Common candidate gene variants are associated with QT interval duration in the general population.Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae.Molecular genetics of atrial fibrillation.Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect.Atrial fibrillation in cardiac channelopathies.Arrhythmia pharmacogenomics: methodological considerations.Atrial-selective sodium channel block for the treatment of atrial fibrillation.The rs6817105 polymorphism on chromosome 4q25 is associated with the risk of atrial fibrillation in the Chinese Han population.Cilostazol ameliorates atrial ionic remodeling in long-term rapid atrial pacing dogs.Different aspects of atrial fibrillation genetics.Atrial selectivity of antiarrhythmic drugs.Genetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice.Association of the angiotensinogen M235T polymorphism with recurrence after catheter ablation of acquired atrial fibrillation.Is endothelin gene polymorphism associated with postoperative atrial fibrillation in patients undergoing coronary artery bypass grafting?Atrial arrhythmogenicity in aged Scn5a+/DeltaKPQ mice modeling long QT type 3 syndrome and its relationship to Na+ channel expression and cardiac conduction.LKB1 deletion causes early changes in atrial channel expression and electrophysiology prior to atrial fibrillation.Genetic variants in post myocardial infarction patients presenting with electrical storm of unstable ventricular tachycardia.Long QT molecular autopsy in sudden unexplained death in the young (1-40 years old): Lessons learnt from an eight year experience in New Zealand.Polymorphism H558R in the human cardiac sodium channel SCN5A gene is associated with atrial fibrillation.Polymorphisms but not mutations of the KCNQ1 gene are associated with lone atrial fibrillation in the Chinese Han population.

P2860

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P2860

A common polymorphism in SCN5A is associated with lone atrial fibrillation.

http://www.wikidata.org/entity/Q35914701

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2007 nî lūn-bûn

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2007年の論文

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2007年論文

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name

A common polymorphism in SCN5A is associated with lone atrial fibrillation.

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A common polymorphism in SCN5A is associated with lone atrial fibrillation.

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A common polymorphism in SCN5A is associated with lone atrial fibrillation.

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A common polymorphism in SCN5A is associated with lone atrial fibrillation.

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A common polymorphism in SCN5A is associated with lone atrial fibrillation.

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A common polymorphism in SCN5A is associated with lone atrial fibrillation.

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Clinical Pharmacology & Therapeutics

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A common polymorphism in SCN5A is associated with lone atrial fibrillation.

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J D Ballew

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K J Herron

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L Y Chen

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R J Rodeheffer

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T M Olson

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P2860

Cardiac conduction defects associate with mutations in SCN5A

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

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

KCNQ1 gain-of-function mutation in familial atrial fibrillation

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

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

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

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts

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atrial fibrillation

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