Cbfa1 in bone development (Q77210704)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9729728%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

review article

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title

Cbfa1 in bone development (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9729728%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

T Komori

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3 December 2019

T Kishimoto

series ordinal

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3 December 2019

publication date

1 August 1998

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Current Opinion in Genetics & Development

3 December 2019

published in

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3 December 2019

volume

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3 December 2019

issue

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3 December 2019

page(s)

494-499

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The MyoD family and myogenesis: redundancy, networks, and thresholds

3 December 2019

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

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

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The CBFbeta subunit is essential for CBFalpha2 (AML1) function in vivo

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

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Proviral insertions induce the expression of bone-specific isoforms of PEBP2alphaA (CBFA1): evidence for a new myc collaborating oncogene

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7 January 2021

Genomic organization, expression of the human CBFA1 gene, and evidence for an alternative splicing event affecting protein function

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7 January 2021

Comparison of the human genomic structure of the Runt domain-encoding PEBP2/CBFalpha gene family

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7 January 2021

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

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7 January 2021

Runt homology domain proteins in osteoblast differentiation: AML3/CBFA1 is a major component of a bone-specific complex

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7 January 2021

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

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7 January 2021

Cleidocranial dysplasia in mice

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7 January 2021

AML1, AML2, and AML3, the human members of the runt domain gene-family: cDNA structure, expression, and chromosomal localization

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7 January 2021

Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.

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7 January 2021

The cDNA cloning of the transcripts of human PEBP2αA/CBFA1 mapped to 6p12.3-p21.1, the locus for cleidocranial dysplasia

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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

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7 January 2021

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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7 January 2021

An AML-1 consensus sequence binds an osteoblast-specific complex and transcriptionally activates the osteocalcin gene

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7 January 2021

Separate cis-acting DNA elements of the mouse pro-alpha 1(I) collagen promoter direct expression of reporter genes to different type I collagen-producing cells in transgenic mice

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7 January 2021

Regulation of COL1A1 expression in type I collagen producing tissues: identification of a 49 base pair region which is required for transgene expression in bone of transgenic mice

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7 January 2021

Expression of the PEBP2αA/AML3/CBFA1 Gene is Regulated by BMP4/7 Heterodimer and Its Overexpression Suppresses Type I Collagen and Osteocalcin Gene Expression in Osteoblastic and Nonosteoblastic Mesenchymal Cells

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7 January 2021

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Identifiers

DOI

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3 December 2019

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