Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation (Q39354706)

11 September 2017

title

Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation (English)

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11 September 2017

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Jun Wang

1

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11 September 2017

Yu-Min Sun

series ordinal

2

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11 September 2017

Yi-Qing Yang

series ordinal

3

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11 September 2017

publication date

3 May 2012

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Molecular Biology Reports

11 September 2017

published in

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11 September 2017

volume

39

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11 September 2017

issue

8

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11 September 2017

page(s)

8127-8135

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Trends in the incidence and prevalence of atrial fibrillation in Iceland and future projections

11 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Lifetime risk for development of atrial fibrillation: the Framingham Heart Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Atrial fibrillation as an independent risk factor for stroke: the Framingham Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Impact of atrial fibrillation on the risk of death: the Framingham Heart Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Atrial fibrillation and congestive heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Atrial fibrillation in stroke-free patients is associated with memory impairment and hippocampal atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Impact of the control of symptomatic paroxysmal atrial fibrillation on health-related quality of life.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

2011 ACCF/AHA/HRS Focused Updates Incorporated Into the ACC/AHA/ESC 2006 Guidelines for the Management of Patients With Atrial Fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Familial aggregation of atrial fibrillation in Iceland

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Familial clustering of lone atrial fibrillation in patients with saddleback-type ST-segment elevation in right precordial leads

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Familial aggregation of atrial fibrillation: a study in Danish twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Familial Aggregation of Lone atrial Fibrillation in the Chinese Population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Association between familial atrial fibrillation and risk of new-onset atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Familial atrial fibrillation is a genetically heterogeneous disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Genetic insights into normal and abnormal heart development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

The developmental genetics of congenital heart disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Assignment of the transcription factor GATA4 gene to human chromosome 8 and mouse chromosome 14: Gata4 is a candidate gene for Ds (disorganization).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

GATA4 is a dosage-sensitive regulator of cardiac morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

GATA4 is essential for formation of the proepicardium and regulates cardiogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Spectrum of heart disease associated with murine and human GATA4 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Mutations in the cardiac transcription factor GATA4 in patients with lone atrial fibrillation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

GATA factors in vertebrate heart development and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Molecular genetics of congenital atrial septal defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Context-dependent transcriptional cooperation mediated by cardiac transcription factors Csx/Nkx-2.5 and GATA-4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Pitx2c and Nkx2-5 are required for the formation and identity of the pulmonary myocardium

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Basic electrophysiology of the pulmonary veins and their role in atrial fibrillation: precipitators, perpetuators, and perplexers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Molecular pathway for the localized formation of the sinoatrial node

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

A novel stop mutation truncating critical regions of the cardiac transcription factor NKX2-5 in a large family with autosomal-dominant inherited congenital heart disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

Novel connexin40 missense mutations in patients with familial atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

A common connexin-40 gene promoter variant affects connexin-40 expression in human atria and is associated with atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-012-1660-6

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

21 January 2018

1 reference

12 December 2020

The association of human connexin 40 genetic polymorphisms with atrial fibrillation

1 reference

12 December 2020

Genetics of atrial fibrillation

1 reference

12 December 2020

Novel GATA4 mutations in lone atrial fibrillation

1 reference

12 December 2020

Connexin40 nonsense mutation in familial atrial fibrillation

1 reference

12 December 2020

GATA4 loss-of-function mutations in familial atrial fibrillation

1 reference

12 December 2020

Familial aggregation in lone atrial fibrillation

1 reference

12 December 2020

Guidelines for the management of atrial fibrillation: the Task Force for the Management of Atrial Fibrillation of the European Society of Cardiology (ESC).

1 reference

12 December 2020

10.1007/S11033-012-1660-6

Identifiers

DOI

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release_4rqjsvajojcknicmwkci6cbhuy

11 September 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/4rqjsvajojcknicmwkci6cbhuy

24 November 2022

mapped directly with Wikidata item

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