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English
Key role for a minor collagen
scientific article published on 01 January 1995
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7704026
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7704026%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
title
Key role for a minor collagen
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7704026
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7704026%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
author name string
Francomano CA
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7704026
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7704026%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
publication date
1 January 1995
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7704026
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7704026%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7704026
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7704026%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
volume
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7704026
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7704026%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7704026
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7704026%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
page(s)
6-8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7704026
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7704026%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0195-6
0 references
cites work
Targeted mutation in the col5a2 gene reveals a regulatory role for type V collagen during matrix assembly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Collagens and their abnormalities in a wide spectrum of diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Post-translational processing of procollagens
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Brittle bones--fragile molecules: disorders of collagen gene structure and expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
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inferred from DOI database lookup
Mutation in a gene for type I procollagen (COL1A2) in a woman with postmenopausal osteoporosis: evidence for phenotypic and genotypic overlap with mild osteogenesis imperfecta
1 reference
stated in
Crossref
reference URL
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retrieved
7 January 2021
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Characterization of a type II collagen gene (COL2A1) mutation identified in cultured chondrocytes from human hypochondrogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
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Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia
1 reference
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Crossref
reference URL
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retrieved
7 January 2021
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Identification of the molecular defect in a family with spondyloepiphyseal dysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
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Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
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inferred from DOI database lookup
A mutation in the gene for type III procollagen (COL3A1) in a family with aortic aneurysms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
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inferred from DOI database lookup
Mice lacking alpha 1 (IX) collagen develop noninflammatory degenerative joint disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Normal long bone growth and development in type X collagen-null mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Type V collagen: molecular structure and fibrillar organization of the chicken alpha 1(V) NH2-terminal domain, a putative regulator of corneal fibrillogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
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inferred from DOI database lookup
Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
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inferred from DOI database lookup
Molecular genetics of Alport syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
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Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
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A missense mutation in type VII collagen in two affected siblings with recessive dystrophic epidermolysis bullosa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dominant dystrophic epidermolysis bullosa: identification of a Gly-->Ser substitution in the triple-helical domain of type VII collagen
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A type X collagen mutation causes Schmid metaphyseal chondrodysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0195-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0195-6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7704026
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7704026%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
PubMed publication ID
7704026
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7704026
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7704026%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
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