(Q54382691)

English

GATA transcription factors in congenital heart defects: a commentary on a novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect.

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

GATA transcription factors in congenital heart defects: a commentary on a novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect. (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

tetralogy of Fallot

1 reference

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inferred from title

author name string

Kazuki Kodo

1

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

Hiroyuki Yamagishi

2

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

publication date

26 August 2010

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

55

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

10

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

637-638

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

https://scigraph.springernature.com/pub.10.1038/jhg.2010.105

0 references

Development gone awry: congenital heart disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.105

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.105

21 January 2018

GATA-6 regulates semaphorin 3C and is required in cardiac neural crest for cardiovascular morphogenesis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.105

21 January 2018

Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.105

21 January 2018

Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.105

21 January 2018

Molecular embryology for an understanding of congenital heart diseases

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.105

21 January 2018

The del22q11.2 candidate gene Tbx1 controls regional outflow tract identity and coronary artery patterning

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.105

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.105

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2010.105

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/JHG.2010.105

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

Dimensions Publication ID

0 references

release_m7ldhepfofebtf2uuwvllv54cy

1 reference

https://api.fatcat.wiki/v0/release/m7ldhepfofebtf2uuwvllv54cy

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 May 2018

http://europepmc.org/abstract/MED/20739941

ResearchGate publication ID

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