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A heart-hand syndrome gene: Tfap2b plays a critical role in the development and remodeling of mouse ductus arteriosus and limb patterning
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
title
A heart-hand syndrome gene: Tfap2b plays a critical role in the development and remodeling of mouse ductus arteriosus and limb patterning
(English)
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
main subject
Transcription factor AP-2 beta
1 reference
stated in
GOA release 2020-03-11
Transcription factor AP-2, alpha
1 reference
stated in
GOA release 2020-03-11
author name string
Feng Zhao
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
Anja-Katrin Bosserhoff
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
Reinhard Buettner
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
Markus Moser
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
language of work or name
English
0 references
publication date
1 January 2011
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
published in
PLOS One
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
volume
6
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
issue
7
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
page(s)
e22908
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
copyright license
Creative Commons Attribution 4.0 International
start time
29 July 2011
1 reference
stated in
April 2022 Public Data File from Crossref
copyright status
copyrighted
0 references
cites work
Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Identification and embryonic expression of a new AP-2 transcription factor, AP-2 epsilon
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Cardiac outflow tract defects in mice lacking ALK2 in neural crest cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Terminal renal failure in mice lacking transcription factor AP-2 beta
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Requirement for AP-2alpha in cardiac outflow tract morphogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Cloning and characterization of a novel mouse AP-2 transcription factor, AP-2delta, with unique DNA binding and transactivation properties
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Fate of the mammalian cardiac neural crest
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2beta
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Chromosomal mapping of the human and mouse homologues of two new members of the AP-2 family of transcription factors
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Transcription factor AP-2 essential for cranial closure and craniofacial development
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
Cloning and characterization of a second AP-2 transcription factor: AP-2 beta
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
19 March 2017
The incidence of congenital heart disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
7 April 2017
Disorganized olfactory bulb lamination in mice deficient for transcription factor AP-2epsilon
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
29 September 2017
Novel TFAP2B mutation in nonsyndromic patent ductus arteriosus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
29 September 2017
Transcriptional regulation during development of the ductus arteriosus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
29 September 2017
Bone morphogenetic protein signaling in limb outgrowth and patterning
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
29 September 2017
Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
29 September 2017
Molecular cloning and characterization of AP-2 epsilon, a fifth member of the AP-2 family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
29 September 2017
Molecular control of neural crest formation, migration and differentiation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
29 September 2017
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
29 September 2017
Ductus arteriosus blood flow during first 48 hours of life
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
29 September 2017
Cloning and expression of AP-2, a cell-type-specific transcription factor that activates inducible enhancer elements
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
29 September 2017
The pharmacology of the ductus arteriosus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
2 June 2018
Correlated heart/limb anomalies in Mendelian syndromes provide evidence for a cardiomelic developmental field
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
2 June 2018
Comparative analysis of AP-2 alpha and AP-2 beta gene expression during murine embryogenesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0022908
retrieved
21 January 2018
Transcription factor AP-2gamma is essential in the extra-embryonic lineages for early postimplantation development.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
27 November 2018
Drosophila transcription factor AP-2 in proboscis, leg and brain central complex development
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3146506
retrieved
27 November 2018
Char syndrome, an inherited disorder with patent ductus arteriosus, maps to chromosome 6p12-p21
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21829553
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Bmp4 in limb bud mesoderm regulates digit pattern by controlling AER development
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21829553
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1371/JOURNAL.PONE.0022908
0 references
ADS bibcode
2011PLoSO...622908Z
0 references
Fatcat ID
release_txe6qdtgwnghpagemv5evko3de
1 reference
stated in
Fatcat
reference URL
https://api.fatcat.wiki/v0/release/txe6qdtgwnghpagemv5evko3de
retrieved
24 November 2022
based on heuristic
mapped directly with Wikidata item
PMCID
3146506
0 references
PubMed ID
21829553
1 reference
stated in
PubMed
PubMed ID
21829553
retrieved
24 January 2017
ResearchGate publication ID
51559866
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