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DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
scientific article (publication date: March 2001)
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
title
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
main subject
T-box 1
1 reference
stated in
GOA release 2020-03-11
DiGeorge syndrome
1 reference
based on heuristic
inferred from title
phenotype
1 reference
based on heuristic
inferred from title
author
Virginia E Papaioannou
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
author name string
Jerome LA
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
language of work or name
English
0 references
publication date
1 March 2001
1 reference
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
volume
27
1 reference
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
page(s)
286-291
1 reference
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
cites work
The 22q11 deletion syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Velo-cardio-facial syndrome: a review of 120 patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Velo-cardio-facial syndrome. Intrafamilial variability of the phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Monozygotic twins with chromosome 22q11 deletion and discordant phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
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7 January 2021
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inferred from DOI database lookup
Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Goosecoid-like (Gscl), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pax genes and organogenesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of PAX9 is associated with oligodontia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
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7 January 2021
based on heuristic
inferred from DOI database lookup
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Derivation of completely cell culture-derived mice from early-passage embryonic stem cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Segmental identity can change independently in the hindbrain and rhombencephalic neural crest.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F85845
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/85845
2 references
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1085716
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
OpenCitations bibliographic resource ID
1085716
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1085716
PubMed ID
11242110
2 references
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1085716
stated in
Europe PubMed Central
PubMed ID
11242110
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11242110%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
ResearchGate publication ID
12090309
0 references
Springer Nature article ID
10.1038/85845
0 references
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