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Microform holoprosencephaly in mice that lack the Ig superfamily member Cdon.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
title
Microform holoprosencephaly in mice that lack the Ig superfamily member Cdon
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
main subject
holoprosencephaly
1 reference
based on heuristic
inferred from title
Microform holoprosencephaly
1 reference
based on heuristic
inferred from title
author
Francesca Cole
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
author name string
Robert S Krauss
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
language of work or name
English
0 references
publication date
1 March 2003
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
published in
Current Biology
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
volume
13
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
page(s)
411-415
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
cites work
Genetics of ventral forebrain development and holoprosencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Holoprosencephaly: from Homer to Hedgehog.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple hits during early embryonic development: digenic diseases and holoprosencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in holoprosencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
BOC, an Ig superfamily member, associates with CDO to positively regulate myogenic differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CDO, a robo-related cell surface protein that mediates myogenic differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CDO: an oncogene-, serum-, and anchorage-regulated member of the Ig/fibronectin type III repeat family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sonic hedgehog participates in craniofacial morphogenesis and is down-regulated by teratogenic doses of retinoic acid
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The contribution of both forebrain and midbrain crest cells to the mesenchyme in the frontonasal mass of mouse embryos
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital nasal pyriform aperture stenosis. Isolated abnormality vs developmental field defect
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The midline craniofacial skeleton in holoprosencephalic fetuses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Agenesis of the nasal septal cartilage: Another sign in autosomal dominant holoprosencephaly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetics of craniofacial development and malformation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Signalling interactions during facial development.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0960-9822%2803%2900088-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0960-9822(03)00088-5
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
PubMed ID
12620190
1 reference
stated in
Europe PubMed Central
PubMed ID
12620190
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12620190%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
ResearchGate publication ID
10871219
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