Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia-Reference-Cited by-同舟云学术

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

Published:1997-07 Issue:3 Volume:16 Page:307-310
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Lee Brendan,Thirunavukkarasu Kannan,Zhou Lei,Pastore Lucio,Baldini Antonio,Hecht Jacqueline,Geoffrey Valeric,Ducy Patricia,Karsenty Gerard

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0797-307.pdf

Reference30 articles.

1. Jones, K.L. Smith's recognizable patterns of human malformation (W.B. Saunders Company, Philadelphia, 1997).

2. Gelb, B.D., Cooper, E., Shevell, M. & Desnick, R.J. Genetic mapping of the cleidocranial dysplasia (CCD) locus on chromosome band 6p21 to include a microdeletion. Am. J. Med. Genet. 58, 200–205 (1995).

3. Mundlos, S. et al. Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family. Hum. Mol. Genet. 4, 71–75 (1995).

4. Levanon, D. et al. AML1, AML2, and AML3, the human members of the runt domain gene-family: cDNA structure, expression, and chromosomal localization. Genomics 23, 425–32 (1994).

5. Ducy, P., Zhang, R., Geoffrey, V., Ridall, A.L. & Karsenty, G. Osf 2 Cbfa1: a transcriptional activator of osteoblast differentiation. Cell 89, 747–754 (1997).

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