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English
Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
title
Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization
(English)
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
main subject
haploinsufficiency
0 references
SRY (sex determining region Y)-box 9
1 reference
stated in
GOA release 2020-03-11
cartilage
1 reference
based on heuristic
inferred from title
author
Benoit de Crombrugghe
series ordinal
7
object named as
B. de Crombrugghe
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
author name string
W. Bi
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
W. Huang
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
D. J. Whitworth
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
J. M. Deng
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
Z. Zhang
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
R. R. Behringer
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
language of work or name
English
0 references
publication date
5 June 2001
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
volume
98
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
page(s)
6698–6703
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
issue
12
1 reference
stated in
PubMed
PubMed ID
11371614
retrieved
31 January 2017
cites work
The chondrogenic transcription factor Sox9 is a target of signaling by the parathyroid hormone-related peptide in the growth plate of endochondral bones
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=34415
retrieved
17 March 2017
Sox9 is required for cartilage formation
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=34415
retrieved
17 March 2017
A new long form of Sox5 (L-Sox5), Sox6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II 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=34415
retrieved
17 March 2017
SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse
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=34415
retrieved
17 March 2017
Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9
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=34415
retrieved
17 March 2017
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related 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=34415
retrieved
17 March 2017
A clinical and genetic study of campomelic dysplasia
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=34415
retrieved
17 March 2017
The DNA-binding specificity of SOX9 and other SOX proteins.
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=34415
retrieved
29 September 2017
Modeling stochastic gene expression: implications for haploinsufficiency
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=34415
retrieved
29 September 2017
SOX9 is a potent activator of the chondrocyte-specific enhancer of the pro alpha1(II) 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=34415
retrieved
29 September 2017
Chondrocyte differentiation
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=34415
retrieved
29 September 2017
The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971.
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=34415
retrieved
29 September 2017
Tissue-specific expression of the mouse alpha 2(I) collagen promoter. Studies in transgenic mice and in tissue culture cells
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=34415
retrieved
29 September 2017
Studies on transcription activation by the multimeric CCAAT-binding factor CBF.
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=34415
retrieved
3 June 2018
The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos.
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=34415
retrieved
3 June 2018
Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.
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=34415
retrieved
3 June 2018
Selective skeletal staining in whole chicken embryos; a rapid Alcian blue technique.
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=34415
retrieved
3 June 2018
Specific hybridization probes for mouse type I, II, III and IX collagen mRNAs.
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=34415
retrieved
3 June 2018
Parallel expression of Sox9 and Col2a1 in cells undergoing chondrogenesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1073%2FPNAS.111092198
retrieved
21 January 2018
Cell condensation in chondrogenic differentiation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11371614
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.111092198
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3554546
ADS bibcode
2001PNAS...98.6698B
0 references
OpenCitations bibliographic resource ID
3554546
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3554546
PMCID
34415
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3554546
PubMed ID
11371614
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3554546
ResearchGate publication ID
11965905
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