Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development: Cell
Model illustrating the mechanism by which Cbfa1 could regulate... | Download Scientific Diagram
A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic development
A full-length Cbfa1 gene product perturbs T-cell development and promotes lymphomagenesis in synergy with MYC | Oncogene
RUNX2 - Wikipedia
Implant Surface Roughness Affects Osteoblast Gene Expression - G.B. Schneider, H. Perinpanayagam, M. Clegg, R. Zaharias, D. Seabold, J. Keller, C. Stanford, 2003
Cleidocranial dysplasia | Osmosis
A Novel Mutation of Gene CBFA1/RUNX2 in Cleidocranial Dysplasia
A Novel Mutation of Gene CBFA1/RUNX2 in Cleidocranial Dysplasia
Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development: Cell
Cbfa1 Isoforms Exert Functional Differences in Osteoblast Differentiation - ScienceDirect
Cbfa1 Contributes to the Osteoblast-specific Expression of type I collagen Genes - ScienceDirect
Lentiviral-Mediated RNAi Knockdown of Cbfa1 Gene Inhibits Endochondral Ossification of Antler Stem Cells in Micromass Culture | PLOS ONE
CBFA1: A molecular switch in osteoblast biology - Ducy - 2000 - Developmental Dynamics - Wiley Online Library
Lentiviral-Mediated RNAi Knockdown of Cbfa1 Gene Inhibits Endochondral Ossification of Antler Stem Cells in Micromass Culture | PLOS ONE
A full-length Cbfa1 gene product perturbs T-cell development and promotes lymphomagenesis in synergy with MYC | Oncogene