Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development
- 30 May 1997
- journal article
- research article
- Published by Elsevier
- Vol. 89 (5) , 765-771
- https://doi.org/10.1016/s0092-8674(00)80259-7
Abstract
No abstract availableKeywords
Funding Information
- National Institutes of Health (AR36819, 134/1–1)
- U.S. Department of Energy (AR36819, 134/1–1)
- Biotechnology and Biological Sciences Research Council (AR36819, 134/1–1)
- Deutsche Forschungsgemeinschaft (AR36819, 134/1–1)
This publication has 17 references indexed in Scilit:
- The CBFβ Subunit Is Essential for CBFα2 (AML1) Function In VivoCell, 1996
- Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity.Journal of Medical Genetics, 1996
- Structural alterations in the transcription factor PEBP2/CBF linked to four different types of leukemiaZeitschrift für Krebsforschung und Klinische Onkologie, 1996
- AML1, the Target of Multiple Chromosomal Translocations in Human Leukemia, Is Essential for Normal Fetal Liver HematopoiesisCell, 1996
- A PEBP2α/AML-1-related Factor Increases Osteocalcin Promoter Activity through Its Binding to an Osteoblast-specific cis-Acting ElementPublished by Elsevier ,1995
- Toward a molecular understanding of skeletal developmentCell, 1995
- A New Transcription Factor Family Associated with Human LeukemiasCritical Reviews™ in Eukaryotic Gene Expression, 1995
- AML1, AML2, and AML3, the Human Members of the runt domain Gene-Family: cDNA Structure, Expression, and Chromosomal LocalizationGenomics, 1994
- Animal model: Skeletal anomalies in mice with cleidocranial dysplasiaAmerican Journal of Medical Genetics, 1987
- Gamma-Ray-Induced Dominant Murtation That Cause Skeletal Abnormalities In MiceMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1978