The Osteoblast-specific Transcription Factor Cbfa1 Contributes to the Expression of Osteoprotegerin, a Potent Inhibitor of Osteoclast Differentiation and Function* - Journal of Biological Chemistry
Cbfa1 Is a Positive Regulatory Factor in Chondrocyte Maturation - ScienceDirect
Osf2/Cbfa1: A Transcriptional Activator of Osteoblast Differentiation: Cell
![Role of Cbfa1 in bone formation (from [10]). | Download Scientific Diagram](https://www.researchgate.net/publication/326206711/figure/fig1/AS:1086456621731850@1636042852986/Role-of-Cbfa1-in-bone-formation-from-10.jpg "Role of Cbfa1 in bone formation (from [10]). | Download Scientific Diagram")
Role of Cbfa1 in bone formation (from [10]). | Download Scientific Diagram
A Novel Mutation of Gene CBFA1/RUNX2 in Cleidocranial Dysplasia
Semi-quantitative RT-PCR analysis of mRNA expression of Cbfa1 gene.... | Download Scientific Diagram
Cleidocranial dysplasia: clinical and molecular genetics | Journal of Medical Genetics
RUNX2 - Wikipedia
RUNX2 - Wikipedia
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
Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development - ScienceDirect
IJMS | Free Full-Text | Regulation of Proliferation, Differentiation and Functions of Osteoblasts by Runx2
Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia: Cell
A full-length Cbfa1 gene product perturbs T-cell development and promotes lymphomagenesis in synergy with MYC | Oncogene
Gene expression in Cbfa1-overexpressing mice. Northern blot (A) or... | Download Scientific Diagram
Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development - ScienceDirect
Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development - ScienceDirect
Cleidocranial dysplasia: Video, Anatomy & Definition | Osmosis
CBFA1: A molecular switch in osteoblast biology - Ducy - 2000 - Developmental Dynamics - Wiley Online Library
Role of Cbfa1 in bone formation. The diVerent steps of endochondral... | Download Scientific Diagram
A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic development
TGF‐β‐induced repression of CBFA1 by Smad3 decreases cbfa1 and osteocalcin expression and inhibits osteoblast differentiation | The EMBO Journal
A Novel Mutation of Gene CBFA1/RUNX2 in Cleidocranial Dysplasia
Antisense strand partial sequence of the 3′ region of the CBFA1 gene,... | Download Scientific Diagram
Cells | Free Full-Text | DLX Genes in the Development and Maintenance of the Vertebrate Skeleton: Implications for Human Pathologies
Human RUNX2/CBFA1 Antibody AF2006: R&D Systems
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
Figure 4 from Cbfa-1 (Runx-2) and Osteocalcin Expression by Human Osteoblasts in Heparin Osteoporosis in Vitro | Semantic Scholar
