Cbfb Regulates Bone Development by Stabilizing Runx Family Proteins-Reference-Cited by-同舟云学术

Cbfb Regulates Bone Development by Stabilizing Runx Family Proteins

Published:2015-03-25 Issue:4 Volume:30 Page:706-714
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Qin Xin¹,Jiang Qing¹,Matsuo Yuki¹,Kawane Tetsuya¹,Komori Hisato¹,Moriishi Takeshi¹,Taniuchi Ichiro²,Ito Kosei³,Kawai Yosuke¹⁴,Rokutanda Satoshi¹⁵,Izumi Shinichi¹,Komori Toshihisa¹

Affiliation:

1. Department of Cell Biology, Unit of Basic Medical Sciences; Nagasaki University Graduate School of Biomedical Sciences; Nagasaki Japan

2. Laboratory for Transcriptional Regulation; RIKEN Research Center for Allergy and Immunology; Yokohama Japan

3. Department of Molecular Bone Biology, Unit of Basic Medical Sciences; Nagasaki University Graduate School of Biomedical Sciences; Nagasaki Japan

4. Department of Regenerative Oral Surgery, Unit of Translational Medicine; Nagasaki University Graduate School of Biomedical Sciences; Nagasaki Japan

5. Department of Oral and Maxillofacial Surgery, Unit of Translational Medicine; Nagasaki University Graduate School of Biomedical Sciences; Nagasaki Japan

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference33 articles.

1. Regulation of skeletal development by the Runx family of transcription factors;Komori;J Cell Biochem.,2005

2. Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts;Komori;Cell.,1997

3. Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development;Otto;Cell.,1997

4. Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia;Mundlos;Cell.,1997

5. Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia;Lee;Nat Genet.,1997

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