(Q34415806)

2 August 2017

title

Ventricular septal defect and cardiomyopathy in mice lacking the transcription factor CHF1/Hey2. (English)

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ventricular septal defect

2 August 2017

main subject

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2 August 2017

Yasuhiko Sakata

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2 August 2017

Caramai N Kamei

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2 August 2017

Roderick Bronson

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2 August 2017

James K Liao

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2 August 2017

Michael T Chin

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2 August 2017

language of work or name

English

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publication date

26 November 2002

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Proceedings of the National Academy of Sciences of the United States of America

2 August 2017

published in

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2 August 2017

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2 August 2017

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2 August 2017

page(s)

16197-16202

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Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice

2 August 2017

cites work

1 reference

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

6 July 2018

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6 July 2018

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6 July 2018

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Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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The transcription factor NF-ATc is essential for cardiac valve formation

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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Cardiomyopathy in zebrafish due to mutation in an alternatively spliced exon of titin

6 July 2018

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Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy

27 October 2018

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Gridlock signalling pathway fashions the first embryonic artery

27 October 2018

1 reference

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Bmp6 and Bmp7 are required for cushion formation and septation in the developing mouse heart

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=138588

The basic helix-loop-helix transcription factor HESR1 regulates endothelial cell tube formation

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=138588

Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=138588

The mammalian Tolloid-like 1 gene, Tll1, is necessary for normal septation and positioning of the heart.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=138588

Formation of the atrioventricular septal structures in the normal mouse.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=138588

Familial fatal fetal cardiomyopathy with isolated myocardial calcifications: a new syndrome?

27 October 2018

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12 December 2020

Early postnatal cardiac changes and premature death in transgenic mice overexpressing a mutant form of serum response factor

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12 December 2020

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12 December 2020

Alcohol and congenital heart defects: an experimental study in mice

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12 December 2020

The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)

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12 December 2020

Identifiers

DOI

10.1073/PNAS.252648999

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2 August 2017

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2 August 2017

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