NKX2.5mutations in patients with congenital heart disease (Q55671009)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14607454 AND SRC:MED&resulttype=core&format=json

20 December 2019

title

NKX2.5 mutations in patients with congenital heart disease (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14607454 AND SRC:MED&resulttype=core&format=json

20 December 2019

NKX2.5mutations in patients with congenital heart disease (English)

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https://api.crossref.org/works/10.1016/J.JACC.2003.05.004

Cardiology and cardiovascular medicine

30 March 2024

main subject

patient

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congenital heart disease

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based on heuristic

inferred from title

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https://api.crossref.org/works/10.1016/J.JACC.2003.05.004

30 March 2024

5

Elizabeth Goldmuntz

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20 December 2019

author name string

Elizabeth Geiger

2

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20 December 2019

Joshua Blinder

3

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20 December 2019

Doff B. McElhinney

1

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30 March 2024

D. Woodrow Benson

4

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30 March 2024

language of work or name

English

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publication date

1 November 2003

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20 December 2019

5 November 2003

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14607454

full work available at URL

30 March 2024

https://doi.org/10.1016/j.jacc.2003.05.004

online access status

open access

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https://api.elsevier.com/content/article/PII:S0735109703010829?httpAccept=text/xml

30 March 2024

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https://api.elsevier.com/content/article/PII:S0735109703010829?httpAccept=text/plain

30 March 2024

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Journal of the American College of Cardiology

30 March 2024

published in

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20 December 2019

volume

42

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20 December 2019

issue

9

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20 December 2019

page(s)

1650-1655

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

20 December 2019

cites work

1

1 reference

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

30 March 2024

2

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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

30 March 2024

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NKX2.5 mutations in patients with tetralogy of fallot

30 March 2024

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Frequency of 22q11 deletions in patients with conotruncal defects

30 March 2024

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Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes

30 March 2024

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Csx: a murine homeobox-containing gene specifically expressed in the developing heart

30 March 2024

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NK-2 homeobox genes and heart development

30 March 2024

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tinman and bagpipe: two homeo box genes that determine cell fates in the dorsal mesoderm of Drosophila

30 March 2024

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Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5

30 March 2024

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Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5

30 March 2024

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Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand

30 March 2024

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Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation

30 March 2024

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BMP signaling regulates Nkx2-5 activity during cardiomyogenesis

30 March 2024

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The combinatorial activities of Nkx2.5 and dHAND are essential for cardiac ventricle formation

30 March 2024

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Combinatorial expression of GATA4, Nkx2-5, and serum response factor directs early cardiac gene activity.

30 March 2024

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

30 March 2024

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1 reference

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Characterization of homo- and heterodimerization of cardiac Csx/Nkx2.5 homeoprotein

30 March 2024

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Identifiers

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20 December 2019

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