Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q83443112)
Watch
English
Advances in molecular genetics of congenital heart disease
scientific article published on 01 March 2009
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19268067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19268067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
editorial
0 references
title
Advances in molecular genetics of congenital heart disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19268067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19268067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
main subject
molecular genetics
1 reference
based on heuristic
inferred from title
congenital heart disease
1 reference
based on heuristic
inferred from title
author name string
José Marín-García
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19268067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19268067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
publication date
1 March 2009
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19268067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19268067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
published in
Revista Española de Cardiología
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19268067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19268067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
volume
62
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19268067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19268067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19268067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19268067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
page(s)
242-245
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19268067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19268067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
cites work
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical and molecular genetics of Alagille syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in NOTCH1 cause aortic valve disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PTPN11 mutations in LEOPARD syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ventricular septal defect and cardiomyopathy in mice lacking the transcription factor CHF1/Hey2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RXR alpha mutant mice establish a genetic basis for vitamin A signaling in heart morphogenesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nf1 has an essential role in endothelial cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Double-outlet right ventricle and overriding tricuspid valve reflect disturbances of looping, myocardialization, endocardial cushion differentiation, and apoptosis in TGF-beta(2)-knockout mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The molecular basis of congenital cardiac disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital heart disease and genetic syndromes: specific correlation between cardiac phenotype and genotype.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
[Regulation of myocardial gene expression during heart development].
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1885-5857%2809%2971552-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1885-5857(09)71552-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19268067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19268067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
PubMed publication ID
19268067
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19268067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19268067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 January 2020
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit