(Q36501505)

14 August 2017

GATA5 loss-of-function mutations underlie tetralogy of fallot (English)

1 reference

14 August 2017

1 reference

Dong Wei

1

1 reference

14 August 2017

Han Bao

2

1 reference

14 August 2017

Xing-Yuan Liu

3

1 reference

14 August 2017

Ning Zhou

4

1 reference

14 August 2017

Qian Wang

5

1 reference

14 August 2017

Ruo-Gu Li

6

1 reference

14 August 2017

Ying-Jia Xu

7

1 reference

14 August 2017

Yi-Qing Yang

8

1 reference

14 August 2017

language of work or name

English

0 references

publication date

10 December 2012

1 reference

International Journal of Medical Sciences

14 August 2017

1 reference

14 August 2017

10

1 reference

14 August 2017

1

1 reference

14 August 2017

34-42

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GATA6 loss-of-function mutation in atrial fibrillation

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Sudden cardiac death and malignant arrhythmias: the scope of the problem in adult congenital heart patients

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

A contemporary assessment of the risk for sudden cardiac death in patients with congenital heart disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Heart disease and stroke statistics--2012 update: a report from the American Heart Association

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Infective endocarditis in congenital heart disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Quality of life experienced by adolescents and young adults with congenital heart disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Identification of GATA6 sequence variants in patients with congenital heart defects.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

From molecular mechanisms of cardiac development to genetic substrate of congenital heart diseases.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Tetralogy of fallot: yesterday and today

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

GATA4 sequence variants in patients with congenital heart disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Spectrum of heart disease associated with murine and human GATA4 mutation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Molecular pathway for the localized formation of the sinoatrial node

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

GATA and Nkx factors synergistically regulate tissue-specific gene expression and development in vivo

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Using the zebrafish model to study GATA transcription factors

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

The roles of GATA-4, -5 and -6 in vertebrate heart development

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

GATA transcription factors in the developing and adult heart

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Functional analysis and chromosomal mapping of Gata5, a gene encoding a zinc finger DNA-binding protein.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

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

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

A novel GATA6 mutation associated with congenital ventricular septal defect.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Prevalence and spectrum of GATA6 mutations associated with familial atrial fibrillation.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Novel GATA4 mutations in lone atrial fibrillation

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

GATA5 interacts with GATA4 and GATA6 in outflow tract development

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

A novel GATA4 mutation responsible for congenital ventricular septal defects.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Factors associated with surgery for active endocarditis in congenital heart disease

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Minor symptoms of depression in patients with congenital heart disease have a larger impact on quality of life than limited exercise capacity.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

GATA4 mutations in 357 unrelated patients with congenital heart malformation

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Exercise performance and quality of life is more impaired in Eisenmenger syndrome than in complex cyanotic congenital heart disease with pulmonary stenosis.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

GATA4 mutations in Chinese patients with congenital cardiac septal defects.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

GATA4 mutations in 486 Chinese patients with congenital heart disease.

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

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

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

GATA4 zinc finger mutations as a molecular rationale for septation defects of the human heart

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3534875

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect

21 September 2018

1 reference

12 December 2020

A novel mutation of GATA4 in a familial atrial septal defect

1 reference

12 December 2020

Brain maturity and brain injury in newborns with cyanotic congenital heart disease

1 reference

12 December 2020

Involvement of a novel GATA4 mutation in atrial septal defects

1 reference

12 December 2020

GATA4 loss-of-function mutations in familial atrial fibrillation

1 reference

12 December 2020

Outcomes and Risk Factors for Mortality in Premature Neonates With Critical Congenital Heart Disease

1 reference

12 December 2020

Measures of exercise capacity in adults with congenital heart disease

1 reference

12 December 2020

Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation

1 reference

12 December 2020

Identifiers

DOI

10.7150/IJMS.5270

1 reference

14 August 2017

1 reference

14 August 2017

PubMed publication ID

23289003

1 reference