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English
The developmental genetics of congenital heart disease.
scientific article published on February 2008
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
18288184
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288184%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
review article
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Europe PubMed Central
title
The developmental genetics of congenital heart disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18288184
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288184%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
main subject
congenital disorder
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author
Benoit G. Bruneau
series ordinal
1
1 reference
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Europe PubMed Central
PubMed ID
18288184
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288184%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
author name string
Benoit G Bruneau
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1
1 reference
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Europe PubMed Central
PubMed ID
18288184
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18 August 2017
language of work or name
English
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publication date
1 February 2008
1 reference
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Europe PubMed Central
PubMed ID
18288184
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288184%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
published in
Nature
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Europe PubMed Central
PubMed ID
18288184
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288184%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
volume
451
1 reference
stated in
Europe PubMed Central
PubMed ID
18288184
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288184%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
page(s)
943-948
1 reference
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Europe PubMed Central
PubMed ID
18288184
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288184%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
issue
7181
1 reference
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Europe PubMed Central
PubMed ID
18288184
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288184%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
exact match
https://scigraph.springernature.com/pub.10.1038/nature06801
0 references
cites work
The incidence of congenital heart disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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Incidence of congenital heart disease: I. Postnatal incidence.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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inferred from DOI database lookup
Abnormal brain development in newborns with congenital heart disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
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Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pedia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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Major congenital malformations after first-trimester exposure to ACE inhibitors
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
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Gene regulatory networks in the evolution and development of the heart
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
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inferred from DOI database lookup
Making or breaking the heart: from lineage determination to morphogenesis
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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Building the mammalian heart from two sources of myocardial cells
1 reference
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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Multipotent flk-1+ cardiovascular progenitor cells give rise to the cardiomyocyte, endothelial, and vascular smooth muscle lineages
1 reference
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https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
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inferred from DOI database lookup
Developmental origin of a bipotential myocardial and smooth muscle cell precursor in the mammalian heart.
1 reference
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
based on heuristic
inferred from DOI database lookup
Multipotent embryonic isl1+ progenitor cells lead to cardiac, smooth muscle, and endothelial cell diversification
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Wnt/beta-catenin signaling and cardiogenesis: timing does matter
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vessel and blood specification override cardiac potential in anterior mesoderm
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
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Retinoic acid signaling restricts the cardiac progenitor pool
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An Nkx2-5/Bmp2/Smad1 negative feedback loop controls heart progenitor specification and proliferation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Baf60c is essential for function of BAF chromatin remodelling complexes in heart development
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
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inferred from DOI database lookup
Histone deacetylases 1 and 2 redundantly regulate cardiac morphogenesis, growth, and contractility
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
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inferred from DOI database lookup
Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital heart disease caused by mutations in the transcription factor NKX2-5
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
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inferred from DOI database lookup
Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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inferred from DOI database lookup
Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5
1 reference
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
based on heuristic
inferred from DOI database lookup
TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
based on heuristic
inferred from DOI database lookup
Role of TBX1 in human del22q11.2 syndrome
1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors.
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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inferred from DOI database lookup
Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes.
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
based on heuristic
inferred from DOI database lookup
Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family
1 reference
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
based on heuristic
inferred from DOI database lookup
Okihiro syndrome is caused by SALL4 mutations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Missense mutations and gene interruption in PROSIT240, a novel TRAP240-like gene, in patients with congenital heart defect (transposition of the great arteries).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Intracardiac fluid forces are an essential epigenetic factor for embryonic cardiogenesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional modulation of cardiac form through regionally confined cell shape changes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Haemodynamics determined by a genetic programme govern asymmetric development of the aortic arch.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in myosin heavy chain 6 causes atrial septal defect
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Early events in valvulogenesis: a signaling perspective
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Notch promotes epithelial-mesenchymal transition during cardiac development and oncogenic transformation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in NOTCH1 cause aortic valve disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the human Jagged1 gene are responsible for Alagille syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
based on heuristic
inferred from DOI database lookup
Germline gain-of-function mutations in RAF1 cause Noonan syndrome
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
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inferred from DOI database lookup
Germline gain-of-function mutations in SOS1 cause Noonan syndrome
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
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7 January 2021
based on heuristic
inferred from DOI database lookup
The functions of animal microRNAs
1 reference
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Crossref
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https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MicroRNAs: powerful new regulators of heart disease and provocative therapeutic targets
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Serum response factor regulates a muscle-specific microRNA that targets Hand2 during cardiogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dysregulation of cardiogenesis, cardiac conduction, and cell cycle in mice lacking miRNA-1-2
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The adult with congenital heart disease: born to be bad?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gata4 is required for maintenance of postnatal cardiac function and protection from pressure overload-induced heart failure
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Modulation of morphogenesis by noncanonical Wnt signaling requires ATF/CREB family-mediated transcriptional activation of TGFbeta2
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Murine T-box transcription factor Tbx20 acts as a repressor during heart development, and is essential for adult heart integrity, function and adaptation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An essential role of Bmp4 in the atrioventricular septation of the mouse heart
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spectrum of heart disease associated with murine and human GATA4 mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNATURE06801
retrieved
7 January 2021
based on heuristic
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Identifiers
DOI
10.1038/NATURE06801
1 reference
stated in
Europe PubMed Central
PubMed ID
18288184
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288184%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
Dimensions Publication ID
1029098383
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Fatcat ID
release_inkoxotjendmbcu6ny65tdm5mq
1 reference
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Fatcat
reference URL
https://api.fatcat.wiki/v0/release/inkoxotjendmbcu6ny65tdm5mq
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
PubMed ID
18288184
1 reference
stated in
Europe PubMed Central
PubMed ID
18288184
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18288184%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 January 2020
ResearchGate publication ID
5564283
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