(Q54454396)

30 May 2018

title

GATA4 mutations in Chinese patients with congenital cardiac septal defects. (English)

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30 May 2018

author name string

Ming-wu Chen

1

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30 May 2018

Yu-sheng Pang

2

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30 May 2018

Ying Guo

3

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30 May 2018

Jia-hua Pan

4

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30 May 2018

Bing-li Liu

5

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30 May 2018

Jie Shen

6

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30 May 2018

Tang-wei Liu

7

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30 May 2018

publication date

14 November 2009

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30 May 2018

published in

Pediatric Cardiology

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30 May 2018

volume

31

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30 May 2018

issue

1

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30 May 2018

page(s)

85-89

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30 May 2018

https://scigraph.springernature.com/pub.10.1007/s00246-009-9576-1

exact match

0 references

cites work

The cardiac tissue-restricted homeobox protein Csx/Nkx2.5 physically associates with the zinc finger protein GATA4 and cooperatively activates atrial natriuretic factor gene expression

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00246-009-9576-1

GATA4 is essential for formation of the proepicardium and regulates cardiogenesis

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00246-009-9576-1

GATA4 transcription factor is required for ventral morphogenesis and heart tube formation

21 January 2018

1 reference

12 December 2020

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

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12 December 2020

Transcription factors and congenital heart defects

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12 December 2020

A GATA-dependent right ventricular enhancer controls dHAND transcription in the developing heart

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12 December 2020

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

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12 December 2020

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

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12 December 2020

GATA4 sequence variants in patients with congenital heart disease

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12 December 2020

Mutation in myosin heavy chain 6 causes atrial septal defect

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12 December 2020

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

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12 December 2020

Insights into the genetic basis of congenital heart disease.

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12 December 2020

Towards a structural basis of human non-synonymous single nucleotide polymorphisms

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12 December 2020

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

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12 December 2020

Familial atrial septal defect and atrioventricular conduction disturbance associated with a point mutation in the cardiac homeobox gene CSX/NKX2-5 in a Japanese patient

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12 December 2020

Mutations in NOTCH1 cause aortic valve disease

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12 December 2020

Spectrum of heart disease associated with murine and human GATA4 mutation

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12 December 2020

Assignment of the human GATA4 gene to 8p23.1-->p22 using fluorescence in situ hybridization analysis

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12 December 2020

The genetics of congenital heart disease: a point in the revolution

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12 December 2020

Incidence of congenital heart disease: I. Postnatal incidence.

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A calcineurin-dependent transcriptional pathway for cardiac hypertrophy

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12 December 2020

Gata5 is required for the development of the heart and endoderm in zebrafish.

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12 December 2020

The cardiac transcription factors Nkx2-5 and GATA-4 are mutual cofactors

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12 December 2020

GATA-dependent recruitment of MEF2 proteins to target promoters

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12 December 2020

The incidence of congenital heart disease

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12 December 2020

Predicting deleterious amino acid substitutions

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12 December 2020

Requirement of the transcription factor GATA4 for heart tube formation and ventral morphogenesis

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12 December 2020

Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).

1 reference

12 December 2020

Prediction of deleterious human alleles

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12 December 2020

Screening and biochemical analysis of GATA4 sequence variations identified in patients with congenital heart disease

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12 December 2020

SIFT: Predicting amino acid changes that affect protein function

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12 December 2020

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

1 reference

12 December 2020

The zinc finger proteins Pannier and GATA4 function as cardiogenic factors in Drosophila.

1 reference

12 December 2020

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

1 reference

12 December 2020

10.1007/S00246-009-9576-1

Identifiers

DOI

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30 May 2018

1 reference

30 May 2018