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The human type I collagen mutation database
scientific article published on January 1997
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
title
The human type I collagen mutation database
(English)
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
main subject
database
0 references
author name string
Dalgleish R
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
language of work or name
English
0 references
publication date
1 January 1997
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
published in
Nucleic Acids Research
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
volume
25
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
page(s)
181-187
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
cites work
Osteogenesis imperfecta type III: mutations in the type I collagen structural genes, COL1A1 and COL1A2, are not necessarily responsible
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=146420
retrieved
14 September 2017
Perinatal lethal osteogenesis imperfecta.
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=146420
retrieved
14 September 2017
Collagens: molecular biology, diseases, and potentials for therapy
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=146420
retrieved
14 September 2017
Intron-mediated recombination may cause a deletion in an alpha 1 type I collagen chain in a lethal form of osteogenesis imperfecta
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=146420
retrieved
14 September 2017
Brittle bones--fragile molecules: disorders of collagen gene structure and expression
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=146420
retrieved
14 September 2017
The family of collagen genes
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=146420
retrieved
14 September 2017
A substitution at a non-glycine position in the triple-helical domain of pro alpha 2(I) collagen chains present in an individual with a variant of the Marfan 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=146420
retrieved
14 September 2017
PvuII polymorphism at the COL1A2 locus
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=146420
retrieved
14 September 2017
A 9-base pair deletion in COL1A1 in a lethal variant of osteogenesis imperfecta
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=146420
retrieved
14 September 2017
G to A polymorphism in exon 45 of the COL1A1 gene
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=146420
retrieved
14 September 2017
The zipper-like folding of collagen triple helices and the effects of mutations that disrupt the zipper
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=146420
retrieved
14 September 2017
Genetic heterogeneity in osteogenesis imperfecta
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=146420
retrieved
14 September 2017
The collagen superfamily.
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=146420
retrieved
14 September 2017
A sequence polymorphism in the 3'-nontranslated region of the pro alpha 1 chain of type I procollagen
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=146420
retrieved
14 September 2017
Osteogenesis imperfecta: cloning of a pro-alpha 2(I) collagen gene with a frameshift mutation
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=146420
retrieved
17 June 2018
Multiexon deletion in an osteogenesis imperfecta variant with increased type III collagen mRNA.
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=146420
retrieved
17 June 2018
Complete nucleotide sequence of the region encompassing the first twenty-five exons of the human pro alpha 1(I) collagen gene (COL1A1)
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=146420
retrieved
17 June 2018
Internal deletion in a collagen gene in a perinatal lethal form of osteogenesis imperfecta.
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=146420
retrieved
20 August 2018
Three new polymorphisms at the COL1A2 locus
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=146420
retrieved
4 November 2018
Completion of the last half of the structure of the human gene for the Pro alpha 1 (I) chain of type I procollagen (COL1A1)
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9016532
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1093/NAR/25.1.181
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
DBLP publication ID
journals/nar/Dalgleish97
1 reference
stated in
DBLP Dataset 2021-01-02
retrieved
28 January 2021
PMCID
146420
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
PubMed ID
9016532
1 reference
stated in
Europe PubMed Central
PMCID
146420
retrieved
14 September 2017
ResearchGate publication ID
14191684
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