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English
Genetic control of cell differentiation in the skeleton
scientific article published on 01 October 1998
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Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
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6 December 2019
review article
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Europe PubMed Central
title
Genetic control of cell differentiation in the skeleton
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
main subject
cell differentiation
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author name string
P Ducy
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
G Karsenty
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
publication date
1 October 1998
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stated in
Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
published in
Current Opinion in Cell Biology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
volume
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
page(s)
614-619
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
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The membranous skeleton: the role of cell condensations in vertebrate skeletogenesis
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Alternatively spliced type II procollagen mRNAs define distinct populations of cells during vertebral development: differential expression of the amino-propeptide
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The matrix Gla protein gene is a marker of the chondrogenesis cell lineage during mouse development
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Analysis of chondroprogenitor frequency and cartilage differentiation in a novel family of clonal chondrogenic rat cell lines
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Modulation of osteoclast differentiation
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7 January 2021
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SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse
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7 January 2021
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Parallel expression of Sox9 and Col2a1 in cells undergoing chondrogenesis
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Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9
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7 January 2021
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SOX9 is a potent activator of the chondrocyte-specific enhancer of the pro alpha1(II) collagen gene
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7 January 2021
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SOX9 directly regulates the type-II collagen gene
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Crossref
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A parathyroid hormone-related protein implicated in malignant hypercalcemia: cloning and expression
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Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene
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PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth
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A constitutively active mutant PTH-PTHrP receptor in Jansen-type metaphyseal chondrodysplasia
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HedgehogandBmpGenes Are Coexpressed at Many Diverse Sites of Cell–Cell Interaction in the Mouse Embryo
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Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein
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Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
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Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia
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Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.
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MMP-9/gelatinase B is a key regulator of growth plate angiogenesis and apoptosis of hypertrophic chondrocytes
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Two distinct osteoblast-specific cis-acting elements control expression of a mouse osteocalcin gene
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A PEBP2 alpha/AML-1-related factor increases osteocalcin promoter activity through its binding to an osteoblast-specific cis-acting element
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The tissue-specific nuclear matrix protein, NMP-2, is a member of the AML/CBF/PEBP2/runt domain transcription factor family: interactions with the osteocalcin gene promoter
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The localized requirements for a gene affecting segmentation in Drosophila: analysis of larvae mosaic for runt
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7 January 2021
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inferred from DOI database lookup
The Runt domain identifies a new family of heteromeric transcriptional regulators.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of the Runt domain-encoding PEBP2 alpha genes in T cells during thymic development
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Osteopetrosis in mice lacking haematopoietic transcription factor PU.1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Osteoprotegerin: a novel secreted protein involved in the regulation of bone density
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Osteoprotegerin ligand is a cytokine that regulates osteoclast differentiation and activation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/RANKL
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Bone and haematopoietic defects in mice lacking c-fos
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
c-Fos: a key regulator of osteoclast-macrophage lineage determination and bone remodeling
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Pleiotropic effects of a null mutation in the c-fos proto-oncogene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Requirement for NF-kappaB in osteoclast and B-cell development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980037-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0955-0674(98)80037-9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
PubMed publication ID
9818172
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9818172
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9818172%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
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