DOI: 10.1016/s0092-8674(00)80259-7. Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development

Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development

10.1016/s0092-8674(00)80259-7

Crossref journal-article

Elsevier BV

Cell (78)

Bibliography

Otto, F., Thornell, A. P., Crompton, T., Denzel, A., Gilmour, K. C., Rosewell, I. R., Stamp, G. W. H., Beddington, R. S. P., Mundlos, S., Olsen, B. R., Selby, P. B., & Owen, M. J. (1997). Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development. Cell, 89(5), 765â771.

Authors 12

Florian Otto (first)
Anders P Thornell (additional)
Tessa Crompton (additional)
Angela Denzel (additional)
Kimberly C Gilmour (additional)
Ian R Rosewell (additional)
Gordon W.H Stamp (additional)
Rosa S.P Beddington (additional)
Stefan Mundlos (additional)
Bjorn R Olsen (additional)
Paul B Selby (additional)
Michael J Owen (additional)

References 19 Referenced 2,342

10.1073/pnas.93.10.4968 / Proc. Natl. Acad. Sci. USA / An AML-1 consensus sequence binds an osteoblast-specific complex and transcriptionally activates the osteocalcin gene by Banerjee (1996)
10.1242/dev.106.1.37 / Development / An in situ transgenic enzyme marker for the midgestation mouse embryo and the visualization of inner cell mass clones during early organogenesis by Beddington (1989)
10.1128/MCB.15.4.1858 / Mol. Cell. Biol. / Two distinct osteoblast-specific cis-acting elements control expression of a mouse osteocalcin gene by Ducy (1995)
10.1016/0092-8674(95)90487-5 / Cell / Toward a molecular understanding of skeletal development by Erlebacher (1995)
10.1074/jbc.270.52.30973 / J. Biol. Chem. / A PEBP2 alpha/AML-1 related factor increases osteocalcin promoter activity through its binding to an osteoblast-specific cis-acting element by Geoffroy (1995)
{'issue': '6', 'key': '10.1016/S0092-8674(00)80259-7_BIB5', 'first-page': 'S281', 'article-title': 'Encyclopedia of the mouse genome V', 'volume': '17. Mammalian Genome', 'author': 'Hamvas', 'year': '1996', 'journal-title': 'Mouse chromosome'} / Mouse chromosome / Encyclopedia of the mouse genome V by Hamvas (1996)
10.1007/BF01261402 / J. Cancer Res. Clin. Oncol. / Structural alterations in the transcription factors PEBP2/CBF linked to four different types of leukemia by Ito (1996)
{'year': '1992', 'series-title': 'The Atlas of Mouse Development', 'key': '10.1016/S0092-8674(00)80259-7_BIB7'} / The Atlas of Mouse Development (1992)
10.1006/geno.1994.1519 / Genomics / AML1, AML2 and AML3, the human members of the runt domain gene-family by Levanon (1994)
10.1136/jcp.35.10.1092 / J. Clin. Pathol. / Development of alkaline phosphatase to give a less soluble red end-product by Malik (1982)
10.1093/hmg/4.1.71 / Hum. Mol. Genet. / Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family by Mundlos (1995)
10.1016/S0092-8674(00)80986-1 / Cell / AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis by Okuda (1996)
10.1136/jmg.33.6.511 / J. Med. Genet. / Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity by Ramesar (1996)
10.1073/pnas.93.22.12359 / Proc. Natl. Acad. Sci. USA / Absence of fetal liver hematopoiesis in mice deficient in transcriptional coactivator core binding factor β by Sasaki (1996)
10.1016/S0027-5107(78)80019-0 / Mut. Res. / Gamma-ray-induced dominant mutations that cause skeletal abnormalities in mice by Selby (1978)
10.1002/ajmg.1320270109 / Am. J. Med. Genet. / Animal model by Sillence (1987)
10.1615/CritRevEukarGeneExpr.v5.i3-4.60 / Crit. Rev. Eukaryot. Gene Expr. / A new transcription factor family associated with human leukemias by Speck (1995)
10.1073/pnas.93.8.3444 / Proc. Natl. Acad. Sci. USA / Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis by Wang (1996)
10.1016/S0092-8674(00)81389-6 / Cell / The CBFβ subunit is essential for CBFα2 (AML1) function in vivo by Wang (1996)

Dates

Type	When
Created	21 years, 3 months ago (May 4, 2004, 6:14 a.m.)
Deposited	4 years, 2 months ago (June 17, 2021, 4:06 a.m.)
Indexed	3 hours, 19 minutes ago (Aug. 31, 2025, 7:16 p.m.)
Issued	28 years, 3 months ago (May 1, 1997)
Published	28 years, 3 months ago (May 1, 1997)
Published Print	28 years, 3 months ago (May 1, 1997)

Funders 4

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gov (National government)
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U.S. Department of Energy 10.13039/100000015
Region: Americas
gov (National government)
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1. Energy Department
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3. United States Department of Energy
4. ENERGY.GOV
5. US Department of Energy
6. USDOE
7. DOE
8. USADOE
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1. 134/1–1
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Biotechnology and Biological Sciences Research Council 10.13039/501100000268
Region: Europe
gov (National government)
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2. BBSRC UK
3. BBSRC
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1. 134/1–1
2. AR36819
Deutsche Forschungsgemeinschaft 10.13039/501100001659
Region: Europe
gov (National government)
Labels3
1. German Research Association
2. German Research Foundation
3. DFG
Awards2
1. 134/1–1
2. AR36819

BibTeX

@article{Otto_1997, title={Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development}, volume={89}, ISSN={0092-8674}, url={http://dx.doi.org/10.1016/s0092-8674(00)80259-7}, DOI={10.1016/s0092-8674(00)80259-7}, number={5}, journal={Cell}, publisher={Elsevier BV}, author={Otto, Florian and Thornell, Anders P and Crompton, Tessa and Denzel, Angela and Gilmour, Kimberly C and Rosewell, Ian R and Stamp, Gordon W.H and Beddington, Rosa S.P and Mundlos, Stefan and Olsen, Bjorn R and Selby, Paul B and Owen, Michael J}, year={1997}, month=may, pages={765–771} }

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