Expression of Runx2/Cbfa1/Pebp2αA During Angiogenesis in Postnatal Rodent and Fetal Human Orofacial Tissues-Reference-Cited by-同舟云学术

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Expression of Runx2/Cbfa1/Pebp2αA During Angiogenesis in Postnatal Rodent and Fetal Human Orofacial Tissues

Published:2004-11-29 Issue:3 Volume:20 Page:428-437
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Bronckers Antonius LJJ,Sasaguri Kenichi,Cavender Adriana C,D'Souza Rena N,Engelse Marten A

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference48 articles.

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

2. Targeted disruption of cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts;Komori;Cell,1997

3. A cbfa1-dependent genetic pathway controls bone formation beyond embryonic development;Ducy;Genes Dev,1999

4. Cbfa1;Ducy;A molecular switch in osteoblast biology. Dev Dyn,2000

5. Maturational disturbance of chondrocytes in Cbfa1 deficient mice;Inada;Dev Dyn,1999

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