The missing bone (Q41496768)

1 October 2017

title

The missing bone (English)

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1 October 2017

Rodan GA

1

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1 October 2017

Harada S

series ordinal

2

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1 October 2017

publication date

1 May 1997

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1 October 2017

language of work or name

0 references

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1 October 2017

volume

89

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1 October 2017

issue

5

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1 October 2017

page(s)

677-680

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publication type of scholarly work

1 October 2017

review article

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Two distinct osteoblast-specific cis-acting elements control expression of a mouse osteocalcin gene

cites work

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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

A PEBP2 alpha/AML-1-related factor increases osteocalcin promoter activity through its binding to an osteoblast-specific cis-acting element

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Embryonic patterning: to BMP or not to BMP, that is the question

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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Bone morphogenetic proteins: multifunctional regulators of vertebrate development

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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Somatic development in cleidocranial dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

PEBP2/PEA2 represents a family of transcription factors homologous to the products of the Drosophila runt gene and the human AML1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

1 reference

7 January 2021

Bone morphogenetic proteins: an unconventional approach to isolation of first mammalian morphogens.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Identification of a minimal sequence of the mouse pro-alpha 1(I) collagen promoter that confers high-level osteoblast expression in transgenic mice and that binds a protein selectively present in osteoblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Expression of the Runt domain-encoding PEBP2 alpha genes in T cells during thymic development

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Gamma-ray-induced dominant mutations that cause skeletal abnormalities in mice. II. Description of proved mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Animal model: skeletal anomalies in mice with cleidocranial dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Stimulation of adipogenesis in fibroblasts by PPAR gamma 2, a lipid-activated transcription factor

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980249-4

7 January 2021

10.1016/S0092-8674(00)80249-4

Identifiers

DOI

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1 October 2017

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