Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q42559546)
Watch
English
Of mice and men: heritable skeletal disorders
scientific article published on February 1994
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
editorial
0 references
title
Of mice and men: heritable skeletal disorders
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
author name string
O Jacenko
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
B R Olsen
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
M L Warman
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
language of work or name
English
0 references
publication date
1 February 1994
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
volume
54
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
page(s)
163-168
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
cites work
The genetics of skeletal development.
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=1918165
retrieved
28 May 2018
Osteoarthritis associated with mild chondrodysplasia in transgenic mice expressing alpha 1(IX) collagen chains with a central deletion
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=1918165
retrieved
28 May 2018
Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1
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=1918165
retrieved
28 May 2018
Amino acid substitutions of conserved residues in the carboxyl-terminal domain of the alpha 1(X) chain of type X collagen occur in two unrelated families with metaphyseal chondrodysplasia type Schmid
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=1918165
retrieved
28 May 2018
A type X collagen mutation causes Schmid metaphyseal chondrodysplasia
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=1918165
retrieved
28 May 2018
Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis
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=1918165
retrieved
28 May 2018
Association of pancreatic insufficiency and chronic neutropenia in childhood
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=1918165
retrieved
28 May 2018
Pattern recognition in bone dysplasias.
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=1918165
retrieved
28 May 2018
Nonexpression of cartilage type II collagen in a case of Langer-Saldino achondrogenesis
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=1918165
retrieved
28 May 2018
Cartilage hair hypoplasia: immunological aspects and their clinical implications
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=1918165
retrieved
28 May 2018
Metaphyseal chondrodysplasia, Schmid type. Clinical and radiographic delineation with a review of the literature
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=1918165
retrieved
28 May 2018
Kniest dysplasia is characterized by an apparent abnormal processing of the C-propeptide of type II cartilage collagen resulting in imperfect fibril assembly
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=1918165
retrieved
28 May 2018
The Stickler syndrome: evidence for close linkage to the structural gene for type II collagen
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=1918165
retrieved
28 May 2018
Transgenic mouse model of the mild dominant 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=1918165
retrieved
28 May 2018
Mutations in collagen genes: causes of rare and some common diseases in humans
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=1918165
retrieved
28 May 2018
Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice
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=1918165
retrieved
28 May 2018
Reduced amounts of cartilage collagen fibrils and growth plate anomalies in transgenic mice harboring a glycine-to-cysteine mutation in the mouse type II procollagen alpha 1-chain 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=1918165
retrieved
28 May 2018
Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasia
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=1918165
retrieved
28 May 2018
Organization and regulation 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=1918165
retrieved
28 May 2018
A linkage map spanning the locus for diastrophic dysplasia (DTD).
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=1918165
retrieved
28 May 2018
Chondrodysplasia in transgenic mice harboring a 15-amino acid deletion in the triple helical domain of pro alpha 1(II) collagen chain
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=1918165
retrieved
28 May 2018
Targeted disruption of the mouse transforming growth factor-beta 1 gene results in multifocal inflammatory disease
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=1918165
retrieved
28 May 2018
The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGF beta 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=1918165
retrieved
28 May 2018
Patients with Ehlers-Danlos syndrome type IV lack type III collagen
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=1918165
retrieved
28 May 2018
Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect
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=1918165
retrieved
16 August 2018
Perinatal lethal osteogenesis imperfecta in transgenic mice bearing an engineered mutant pro-alpha 1(I) collagen 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=1918165
retrieved
16 August 2018
Bone and haematopoietic defects in mice lacking c-fos
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=1918165
retrieved
1 December 2018
Gli3 expression is affected in the morphogenetic mouse mutants add and Xt
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8304335
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID 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
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8304335
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1918165
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
PubMed publication ID
8304335
1 reference
stated in
Europe PubMed Central
PMC publication ID
1918165
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8304335%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit