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Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
10742104
retrieved
25 January 2017
title
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
(English)
1 reference
stated in
PubMed
PubMed ID
10742104
retrieved
25 January 2017
main subject
Msh homeobox 2
1 reference
stated in
GOA release 2020-03-11
Msh homeobox 1
1 reference
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GOA release 2020-03-11
pleiotropy
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based on heuristic
inferred from title
author name string
I. Satokata
series ordinal
1
1 reference
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PubMed
PubMed ID
10742104
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25 January 2017
L. Ma
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
10742104
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25 January 2017
H. Ohshima
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
10742104
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25 January 2017
M. Bei
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4
1 reference
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PubMed
PubMed ID
10742104
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25 January 2017
I. Woo
series ordinal
5
1 reference
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PubMed
PubMed ID
10742104
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25 January 2017
K. Nishizawa
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6
1 reference
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PubMed
PubMed ID
10742104
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T. Maeda
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7
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PubMed
PubMed ID
10742104
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25 January 2017
Y. Takano
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8
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PubMed
PubMed ID
10742104
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25 January 2017
M. Uchiyama
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PubMed
PubMed ID
10742104
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S. Heaney
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10
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PubMed
PubMed ID
10742104
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H. Peters
series ordinal
11
1 reference
stated in
PubMed
PubMed ID
10742104
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25 January 2017
Z. Tang
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12
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PubMed
PubMed ID
10742104
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R. Maxson
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13
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PubMed
PubMed ID
10742104
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25 January 2017
R. Maas
series ordinal
14
1 reference
stated in
PubMed
PubMed ID
10742104
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25 January 2017
language of work or name
English
0 references
publication date
1 April 2000
1 reference
stated in
PubMed
PubMed ID
10742104
retrieved
25 January 2017
published in
Nature Genetics
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stated in
PubMed
PubMed ID
10742104
retrieved
25 January 2017
volume
24
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PubMed
PubMed ID
10742104
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25 January 2017
page(s)
391–395
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PubMed
PubMed ID
10742104
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25 January 2017
issue
4
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PubMed
PubMed ID
10742104
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25 January 2017
cites work
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: a possible mechanism for MSX2-mediated craniosynostosis in humans.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ectopic Msx2 overexpression inhibits and Msx2 antisense stimulates calvarial osteoblast differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reciprocal regulation of osteocalcin transcription by the homeodomain proteins Msx2 and Dlx5.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Haploinsufficiency of parathyroid hormone-related peptide (PTHrP) results in abnormal postnatal bone development
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The cells and molecules that make a cerebellum.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FGF5 as a regulator of the hair growth cycle: evidence from targeted and spontaneous mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary cranium bifidum and symmetric parietal foramina are the same entity
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aplasia cutis congenita and enlarged parietal foramina (Catlin marks) in a family
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Syndromic foramina parietalia permagna
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epithelial cytodifferentiation and extracellular matrix formation in enamel-free areas of the occlusal cusp during development of mouse molars: light and electron microscopic studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A comprehensive guide for the recognition and classification of distinct stages of hair follicle morphogenesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Basal cell carcinomas in mice overexpressing sonic hedgehog
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F74231
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/74231
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1784916
Dimensions Publication ID
1037936629
0 references
OpenCitations bibliographic resource ID
1784916
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1784916
PubMed ID
10742104
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1784916
ResearchGate publication ID
12574420
0 references
Springer Nature article ID
10.1038/74231
0 references
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