Monogenic atrial fibrillation as pathophysiological paradigms. - Wikidata - awgldk - TriplyDB

Monogenic atrial fibrillation as pathophysiological paradigms.

Monogenic atrial fibrillation as pathophysiological paradigms.

http://www.wikidata.org/entity/Q34575292

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Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation Ion Channels in the Heart IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation Expression and function of Kv1.1 potassium channels in human atria from patients with atrial fibrillation.Association between KCNE1 G38S gene polymorphism and risk of atrial fibrillation: A PRISMA-compliant meta-analysis.Single-nucleotide variations in cardiac arrhythmias: prospects for genomics and proteomics based biomarker discovery and diagnostics.Personalized medicine and atrial fibrillation: will it ever happen?Recent advances in the molecular pathophysiology of atrial fibrillation.Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation.Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation.New advances in the genetic basis of atrial fibrillation.Atrial fibrillation: the role of common and rare genetic variants.Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation Variant rs2200733 on chromosome 4q25 confers increased risk of atrial fibrillation: evidence from a meta-analysis.New directions in antiarrhythmic drug therapy for atrial fibrillation.Lone atrial fibrillation - an overview.Cardiac Delayed Rectifier Potassium Channels in Health and Disease.Destruction Of Medium Already Afected By Destructive Disorder: Fibrillating Atria Conceptually Need Therapeutic Help Rather Than Surgical Or Ablative Destruction.Ablatogenomics: can genotype guide catheter ablation for cardiac arrhythmias?A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation.A KCNQ1 mutation causes age-dependant bradycardia and persistent atrial fibrillation.Value of multilocus genetic risk score for atrial fibrillation in end-stage kidney disease patients in a Polish population.A Chromosome 4q25 Variant is Associated with Atrial Fibrillation Recurrence After Catheter Ablation: A Systematic Review and Meta-Analysis.Electroanatomic Mapping and Late Gadolinium Enhancement MRI in a Genetic Model of Arrhythmogenic Atrial Cardiomyopathy

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P2860

Monogenic atrial fibrillation as pathophysiological paradigms.

http://www.wikidata.org/entity/Q34575292

description

2010 nî lūn-bûn

@nan

2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

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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

Monogenic atrial fibrillation as pathophysiological paradigms.

@ast

Monogenic atrial fibrillation as pathophysiological paradigms.

@en

Monogenic atrial fibrillation as pathophysiological paradigms.

@nl

type

label

Monogenic atrial fibrillation as pathophysiological paradigms.

@ast

Monogenic atrial fibrillation as pathophysiological paradigms.

@en

Monogenic atrial fibrillation as pathophysiological paradigms.

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prefLabel

Monogenic atrial fibrillation as pathophysiological paradigms.

@ast

Monogenic atrial fibrillation as pathophysiological paradigms.

@en

Monogenic atrial fibrillation as pathophysiological paradigms.

@nl

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P1433

Cardiovascular Research

P1476

Monogenic atrial fibrillation as pathophysiological paradigms.

@en

P2093

David J Milan

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

Michiel Rienstra

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

Patrick T Ellinor

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Saagar Mahida

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Steven A Lubitz

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P2860

Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA

Cardiac conduction defects associate with mutations in SCN5A

Molecular cloning and characterization of two voltage-gated K+ channel cDNAs from human ventricle

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

Atrial natriuretic peptide modulates the hyperpolarization-activated current (If) in human atrial myocytes

Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans

Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation

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

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation

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692-700

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10.1093/CVR/CVQ381

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4

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89

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2010-11-30T00:00:00Z

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49650451

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21123219

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pathophysiology

atrial fibrillation

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3039248

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