Monogenic atrial fibrillation as pathophysiological paradigms (Q34575292)

3 August 2017

1 reference

title

Monogenic atrial fibrillation as pathophysiological paradigms (English)

1 reference

3 August 2017

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1 reference

2

Steven A Lubitz

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3 August 2017

5

Patrick T Ellinor

1 reference

3 August 2017

3

Michiel Rienstra

1 reference

3 August 2017

1

Saagar Mahida

1 reference

3 August 2017

David J Milan

4

1 reference

3 August 2017

30 November 2010

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3 August 2017

Cardiovascular Research

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3 August 2017

89

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3 August 2017

4

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3 August 2017

692-700

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Left-to-right atrial inward rectifier potassium current gradients in patients with paroxysmal versus chronic atrial fibrillation

3 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Rare variants create synthetic genome-wide associations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Common genetic variation and human traits

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

IK1 heterogeneity affects genesis and stability of spiral waves in cardiac myocyte monolayers

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Prevalence of early-onset atrial fibrillation in congenital long QT syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Atrial-selective approaches for the treatment of atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Status of the epidemiology of atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Variants conferring risk of atrial fibrillation on chromosome 4q25.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

A common polymorphism in SCN5A is associated with lone atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Potassium channel gene mutations rarely cause atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Atrial distribution of connexin 40 and 43 in patients with intermittent, persistent, and postoperative atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Familial aggregation of atrial fibrillation in Iceland

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Expression and transcriptional control of human KCNE genes

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Atrial natriuretic peptide promotes cardiomyocyte survival by cGMP-dependent nuclear accumulation of zyxin and Akt.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Atrial fibrillation in KCNE1-null mice

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Ionic determinants of functional reentry in a 2-D model of human atrial cells during simulated chronic atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Expression of multiple KCNE genes in human heart may enable variable modulation of I(Ks).

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Incidence, clinical implications and prognosis of atrial arrhythmias in Brugada syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Renin-angiotensin system gene polymorphisms and atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Potassium channel subunits encoded by the KCNE gene family: physiology and pathophysiology of the MinK-related peptides (MiRPs).

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Remodeling of cardiomyocyte ion channels in human atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Familial atrial fibrillation is a genetically heterogeneous disorder.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Molecular dissection of the inward rectifier potassium current (IK1) in rabbit cardiomyocytes: evidence for heteromeric co-assembly of Kir2.1 and Kir2.2.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Atrial Electrophysiology and Mechanisms of Atrial Fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Regulating access to the genome: nucleocytoplasmic transport throughout the cell cycle

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

KCNQ1 gain-of-function mutation in familial atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Cellular electrophysiology of atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

New ideas about atrial fibrillation 50 years on.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

The role of myocardial gap junctions in electrical conduction and arrhythmogenesis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Inward rectifiers in the heart: an update on I(K1).

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

M-type KCNQ2-KCNQ3 potassium channels are modulated by the KCNE2 subunit

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Changes in the mRNA levels of delayed rectifier potassium channels in human atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Molecular basis of functional voltage-gated K+ channel diversity in the mammalian myocardium

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA)

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Cardiac conduction defects associate with mutations in SCN5A

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Differential distribution of inward rectifier potassium channel transcripts in human atrium versus ventricle

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Identification of a genetic locus for familial atrial fibrillation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Independent risk factors for atrial fibrillation in a population-based cohort. The Framingham Heart Study

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Polymorphism of the gene encoding a human minimal potassium ion channel (minK)

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Evidence for reentry as a mechanism of cardiac arrhythmias

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Atrial fibrillation and dementia in a population-based study. The Rotterdam Study.

7 July 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

A population-based study of the long-term risks associated with atrial fibrillation: 20-year follow-up of the Renfrew/Paisley study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Temporal Relations of Atrial Fibrillation and Congestive Heart Failure and Their Joint Influence on Mortality

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Incidence of and risk factors for atrial fibrillation in older adults.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

A mutation in the sodium channel is responsible for the association of long QT syndrome and familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Mechanisms by which atrial fibrillation-associated mutations in the S1 domain of KCNQ1 slow deactivation of IKs channels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

The contribution of ionic currents to changes in refractoriness of human atrial myocytes associated with chronic atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Rectification of the background potassium current: a determinant of rotor dynamics in ventricular fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Polymorphism screening in the cardiac K+ channel gene KCNA5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Cardiac sodium channel mutation in atrial fibrillation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

High risk for bradyarrhythmic complications in patients with Brugada syndrome caused by SCN5A gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Mechanisms of atrial fibrillation termination by pure sodium channel blockade in an ionically-realistic mathematical model.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

An increase of late sodium current induces delayed afterdepolarizations and sustained triggered activity in atrial myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Relationship between connexins and atrial activation during human atrial fibrillation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

A new role for extracellular Ca2+ in gap-junction remodeling: studies in humans and rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Atrial natriuretic peptide has dose-dependent, autonomically mediated effects on atrial refractoriness and repolarization in anesthetized dogs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Angiotensinogen and ACE gene polymorphisms and risk of atrial fibrillation in the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

The -174G/C interleukin-6 polymorphism influences postoperative interleukin-6 levels and postoperative atrial fibrillation. Is atrial fibrillation an inflammatory complication?

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039248

Analysis of minK and eNOS genes as candidate loci for predisposition to non-valvular atrial fibrillation

27 October 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Lone and secondary nonvalvular atrial fibrillation: Role of a genetic susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

The variation of the sarcolipin gene (SLN) in atrial fibrillation, long QT syndrome and sudden arrhythmic death syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FCVR%2FCVQ381

Locus for atrial fibrillation maps to chromosome 6q14-16

21 January 2018

1 reference

12 December 2020

Disorganization of gap junction distribution in dilated atria of patients with chronic atrial fibrillation

1 reference

12 December 2020

Genetic susceptibility to atrial fibrillation in patients with congestive heart failure

1 reference

12 December 2020

Stretch-sensitive KCNQ1 mutation A link between genetic and environmental factors in the pathogenesis of atrial fibrillation?

1 reference

12 December 2020

The association of human connexin 40 genetic polymorphisms with atrial fibrillation

1 reference

12 December 2020

Genetic factors for lone atrial fibrillation

1 reference

12 December 2020

Renin-angiotensin system gene polymorphisms and atrial fibrillation: a regression approach for the detection of gene-gene interactions in a large hospitalized population

1 reference

12 December 2020

Ion channel remodeling is related to intraoperative atrial effective refractory periods in patients with paroxysmal and persistent atrial fibrillation

1 reference

12 December 2020

The gap-junctional protein connexin40 is elevated in patients susceptible to postoperative atrial fibrillation

1 reference

12 December 2020

Effects of chronic atrial fibrillation on gap junction distribution in human and rat atria

1 reference

12 December 2020

Ionic mechanisms of electrical remodeling in human atrial fibrillation

1 reference

12 December 2020

Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation

1 reference

12 December 2020

Role of up-regulation of IK1 in action potential shortening associated with atrial fibrillation in humans

1 reference

12 December 2020

G-Protein beta(3)-subunit 825T allele is associated with enhanced human atrial inward rectifier potassium currents

1 reference

12 December 2020

Structural correlate of atrial fibrillation in human patients

1 reference

12 December 2020

Atrial fibrillation and atrial vulnerability in patients with Brugada syndrome

1 reference

12 December 2020

Comparison of expression of connexin in right atrial myocardium in patients with chronic atrial fibrillation versus those in sinus rhythm

1 reference

12 December 2020

Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation

1 reference

12 December 2020

C825T polymorphism of the G-protein beta3 subunit gene and atrial fibrillation: association of the TT genotype with a reduced risk for atrial fibrillation

1 reference

12 December 2020

Epidemiologic features of chronic atrial fibrillation: the Framingham study

1 reference

12 December 2020

Coronary heart disease and atrial fibrillation: the Framingham Study

1 reference

12 December 2020

Comparison of potassium currents in rabbit atrial and ventricular cells

1 reference

12 December 2020

Effects of atrionatriuretic factor on Ca2+ current and Cai-independent transient outward K+ current in human atrial cells

1 reference

12 December 2020

Electrophysiological effects of atrial natriuretic peptide on the cardiac conduction system in man

1 reference

12 December 2020

Delayed rectifier outward current and repolarization in human atrial myocytes

1 reference

12 December 2020

The natural history of atrial fibrillation: incidence, risk factors, and prognosis in the Manitoba Follow-Up Study

1 reference

12 December 2020

Outward K+ current densities and Kv1.5 expression are reduced in chronic human atrial fibrillation

1 reference

12 December 2020

1 reference

12 December 2020

Mechanisms of atrial fibrillation: mother rotors or multiple daughter wavelets, or both?

1 reference

12 December 2020

Familial aggregation in lone atrial fibrillation

1 reference

12 December 2020

Identifiers

DOI

10.1093/CVR/CVQ381

1 reference

3 August 2017

1 reference

3 August 2017

1 reference

PubMed ID

21123219