(Q24307366)

T-box transcription factor 5

1 reference

positive regulation of transcription, DNA-templated

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NK2 homeobox 5

1 reference

GATA binding protein 4

1 reference

Vidu Garg

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Irfan S Kathiriya

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Robert Barnes

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Marie K Schluterman

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Isabelle N King

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Cheryl A Butler

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Caryn R Rothrock

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Reenu S Eapen

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Kayoko Hirayama-Yamada

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Kunitaka Joo

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Rumiko Matsuoka

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Jonathan C Cohen

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Deepak Srivastava

Incidence of congenital heart disease: I. Postnatal incidence.

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language of work or name

English

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publication date

24 July 2003

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published in

Nature

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volume

424

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issue

6947

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page(s)

443-7

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Congenital heart disease caused by mutations in the transcription factor NKX2-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

A genetic blueprint for cardiac development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

An mRNA surveillance mechanism that eliminates transcripts lacking termination codons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

The erythroid-specific transcription factor Eryf1: a new finger protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Cloning of cDNA for the major DNA-binding protein of the erythroid lineage through expression in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Mouse GATA-4: a retinoic acid-inducible GATA-binding transcription factor expressed in endodermally derived tissues and heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

GATA3 haplo-insufficiency causes human HDR syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

The zinc finger-containing transcription factors GATA-4, -5, and -6. Ubiquitously expressed regulators of tissue-specific gene expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Transcription factor GATA-4 regulates cardiac muscle-specific expression of the alpha-myosin heavy-chain gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Involvement of multiple cis elements in basal- and alpha-adrenergic agonist-inducible atrial natriuretic factor transcription. Roles for serum response elements and an SP-1-like element

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

GATA-4 activates transcription via two novel domains that are conserved within the GATA-4/5/6 subfamily

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

The mutation spectrum in Holt-Oram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Three novel TBX5 mutations in Chinese patients with Holt-Oram syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827

GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE01827