Characterization of an Osteoblast-specific Enhancer Element in the CBFA1 Gene - ScienceDirect
A Novel Mutation of Gene CBFA1/RUNX2 in Cleidocranial Dysplasia
A novel mutation in the C-terminal region of RUNX2/CBFA1 distal to the DNA-binding runt domain in a Japanese patient with cleidocranial dysplasia - ScienceDirect
Cbfa1 Isoforms Exert Functional Differences in Osteoblast Differentiation - ScienceDirect
Relative positions of CBFA1 mutations in CCD patients. Nonsense and... | Download Scientific Diagram
Role of Cbfa1 in bone formation. The diVerent steps of endochondral... | Download Scientific Diagram
RUNX2 - Wikipedia
File:Cleidocranial dysplasia.webm - Wikimedia Commons
Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia: Cell
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
RUNX2/CBFA1 Antibody - BSA Free (NBP1-77461): Novus Biologicals
Model illustrating the mechanism by which Cbfa1 could regulate... | Download Scientific Diagram
A full-length Cbfa1 gene product perturbs T-cell development and promotes lymphomagenesis in synergy with MYC | Oncogene
A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic development
Regulation of the Bone-Specific Osteocalcin Gene by p300 Requires Runx2/ Cbfa1 and the Vitamin D3 Receptor but Not p300 Intrinsic Histone Acetyltransferase Activity | Molecular and Cellular Biology
A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic development
Lentiviral-Mediated RNAi Knockdown of Cbfa1 Gene Inhibits Endochondral Ossification of Antler Stem Cells in Micromass Culture | PLOS ONE
Cleidocranial dysplasia: clinical and molecular genetics | Journal of Medical Genetics
Figure 4 from Cbfa-1 (Runx-2) and Osteocalcin Expression by Human Osteoblasts in Heparin Osteoporosis in Vitro | Semantic Scholar
Antisense strand partial sequence of the 3′ region of the CBFA1 gene,... | Download Scientific Diagram
Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development: Cell
