A Runx2 threshold for the cleidocranial dysplasia phenotype.

Lou, Yang; Javed, Amjad; Hussain, Sadiq; Colby, Jennifer; Frederick, Dana; Pratap, Jitesh; Xie, Ronglin; Gaur, Tripti; van Wijnen, Andre J; Jones, Stephen N; Stein, Gary S; Lian, Jane B; Stein, Janet L

Lou, Yang; Javed, Amjad; Hussain, Sadiq; Colby, Jennifer; Frederick, Dana; Pratap, Jitesh; Xie, Ronglin; Gaur, Tripti; van Wijnen, Andre J; Jones, Stephen N; Stein, Gary S; Lian, Jane B; Stein, Janet L.

Affiliation

Lou Y; Department of Cell Biology, Cancer Center, University of Massachusetts Medical School, Worcester, MA 01655-0106, USA.

Hum Mol Genet ; 18(3): 556-68, 2009 Feb 01.

Article in En | MEDLINE | ID: mdl-19028669

Subject(s)

Cleidocranial Dysplasia/metabolism; Core Binding Factor Alpha 1 Subunit/metabolism; Animals; Bone Development; Cells, Cultured; Clavicle/abnormalities; Clavicle/embryology; Clavicle/growth & development; Clavicle/metabolism; Cleidocranial Dysplasia/embryology; Cleidocranial Dysplasia/genetics; Core Binding Factor Alpha 1 Subunit/genetics; Female; Growth Plate/growth & development; Growth Plate/metabolism; Humans; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Osteoblasts/metabolism; Phenotype; Skull/abnormalities; Skull/embryology; Skull/growth & development; Skull/metabolism

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Full text: 1 Database: MEDLINE Main subject: Cleidocranial Dysplasia / Core Binding Factor Alpha 1 Subunit Type of study: Prognostic_studies Limits: Animals / Female / Humans / Male Language: En Year: 2009 Type: Article

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