(Q43741626)

26 November 2017

title

GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect (English)

1 reference

26 November 2017

0 references

Dong Wei

1

1 reference

26 November 2017

Han Bao

2

1 reference

26 November 2017

Ning Zhou

3

1 reference

26 November 2017

Gui-Fen Zheng

4

1 reference

26 November 2017

Xing-Yuan Liu

5

1 reference

26 November 2017

Yi-Qing Yang

6

1 reference

26 November 2017

publication date

9 September 2012

1 reference

26 November 2017

1 reference

26 November 2017

volume

34

1 reference

26 November 2017

issue

3

1 reference

26 November 2017

page(s)

504-511

1 reference

https://scigraph.springernature.com/pub.10.1007/s00246-012-0482-6

26 November 2017

exact match

0 references

cites work

Examining the cardiac NK-2 genes in early heart development.

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

Genetic origins of pediatric heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

The developmental genetics of congenital heart disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

GATA4 mutations in 357 unrelated patients with congenital heart malformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

GATA4 mutations in Chinese patients with congenital cardiac septal defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

The contribution of chromosomal abnormalities to congenital heart defects: a population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

Using the zebrafish model to study GATA transcription factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

The development and structure of the ventricles in the human heart.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

GATA5 interacts with GATA4 and GATA6 in outflow tract development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

Congenital heart disease and brain development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

GATA transcription factors in the developing and adult heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

Spectrum of heart disease associated with murine and human GATA4 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

Pathophysiology of congenital heart disease in the adult: part I: Shunt lesions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

GATA4 sequence variants in patients with congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

GATA4 mutations in 486 Chinese patients with congenital heart disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

Submicroscopic Chromosomal Copy Number Variations Identified in Children With Hypoplastic Left Heart Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

BMP-4-responsive regulation of dorsal–ventral patterning by the homeobox protein Mix.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-012-0482-6

Involvement of a novel GATA4 mutation in atrial septal defects

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation

1 reference

12 December 2020

Ventricular septal defects

1 reference

12 December 2020

Congenital Cardiac Defects: A Possible Association of Aminopterin Syndrome and In Utero Methotrexate Exposure?

1 reference

12 December 2020

A novel GATA6 mutation associated with congenital ventricular septal defect.

1 reference

12 December 2020

A novel GATA4 mutation responsible for congenital ventricular septal defects.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A novel mutation of GATA4 in a familial atrial septal defect

1 reference

12 December 2020

Novel GATA4 mutations in patients with congenital ventricular septal defects.

1 reference

12 December 2020

10.1007/S00246-012-0482-6

Identifiers

DOI

1 reference

Dimensions Publication ID

26 November 2017

1031006213

0 references

1 reference