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English
Protein consequences of the Col2a1 C-propeptide mutation in the chondrodysplastic Dmm mouse
scientific article published on September 1, 2003
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scholarly article
1 reference
stated in
PubMed
PubMed ID
14614991
retrieved
25 January 2017
title
Protein consequences of the Col2a1 C-propeptide mutation in the chondrodysplastic Dmm mouse
(English)
1 reference
stated in
PubMed
PubMed ID
14614991
retrieved
25 January 2017
main subject
Collagen, type II, alpha 1
1 reference
stated in
GOA release 2020-03-11
author name string
Russell J. Fernandes
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
14614991
retrieved
25 January 2017
Robert E. Seegmiller
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
14614991
retrieved
25 January 2017
Whitney R. Nelson
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
14614991
retrieved
25 January 2017
David R. Eyre
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
14614991
retrieved
25 January 2017
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed ID
14614991
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14614991
retrieved
1 April 2024
publication date
1 September 2003
1 reference
stated in
PubMed
PubMed ID
14614991
retrieved
25 January 2017
full work available at URL
https://api.elsevier.com/content/article/PII:S0945053X03000775?httpAccept=text/xml
1 reference
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Crossref
DOI
10.1016/S0945-053X(03)00077-5
reference URL
https://api.crossref.org/works/10.1016/S0945-053X(03)00077-5
retrieved
1 April 2024
https://api.elsevier.com/content/article/PII:S0945053X03000775?httpAccept=text/plain
1 reference
stated in
Crossref
DOI
10.1016/S0945-053X(03)00077-5
reference URL
https://api.crossref.org/works/10.1016/S0945-053X(03)00077-5
retrieved
1 April 2024
published in
Matrix Biology
1 reference
stated in
PubMed
PubMed ID
14614991
retrieved
25 January 2017
volume
22
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PubMed
PubMed ID
14614991
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25 January 2017
issue
5
1 reference
stated in
PubMed
PubMed ID
14614991
retrieved
25 January 2017
page(s)
449–453
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PubMed
PubMed ID
14614991
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25 January 2017
cites work
Stickler syndrome. A mutation in the nonhelical 3' end of type II procollagen gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A COL2A1 mutation in achondrogenesis type II results in the replacement of type II collagen by type I and III collagens in cartilage
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Procollagen II amino propeptide processing by ADAMTS-3. Insights on dermatosparaxis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assembly of collagen types II, IX and XI into nascent hetero-fibrils by a rat chondrocyte cell line
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Building collagen molecules, fibrils, and suprafibrillar structures.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorder
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Histochemical, immunofluorescence, and ultrastructural differences in fetal cartilage among three genetically distinct chondrodystrophic mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Double heterozygosity for pseudoachondroplasia and spondyloepiphyseal dysplasia congenita.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A specific collagen type II gene (COL2A1) mutation presenting as spondyloperipheral dysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0945-053X%2803%2900077-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disproportionate micromelia (Dmm): an incomplete dominant mouse dwarfism with abnormal cartilage matrix
series ordinal
2
1 reference
stated in
Crossref
DOI
10.1016/S0945-053X(03)00077-5
reference URL
https://api.crossref.org/works/10.1016/S0945-053X(03)00077-5
retrieved
1 April 2024
Identifiers
DOI
10.1016/S0945-053X(03)00077-5
0 references
PubMed ID
14614991
1 reference
stated in
PubMed
PubMed ID
14614991
retrieved
25 January 2017
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