Intimate Relationship Between TGF-β/BMP Signaling and Runt Domain Transcription Factor, PEBP2/CBF

This publication has 19 references indexed in Scilit:

• PEBP2αA/CBFA1 mutations in Japanese cleidocranial dysplasia patients
  Gene, 2000
• The cDNA cloning of the transcripts of human PEBP2αA/CBFA1 mapped to 6p12.3-p21.1, the locus for cleidocranial dysplasia
  Oncogene, 1997
• Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia
  Nature Genetics, 1997
• Targeted Disruption of Cbfa1 Results in a Complete Lack of Bone Formation owing to Maturational Arrest of Osteoblasts
  Published by Elsevier ,1997
• Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development
  Published by Elsevier ,1997
• Osf2/Cbfa1: A Transcriptional Activator of Osteoblast Differentiation
  Cell, 1997
• Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia
  Cell, 1997
• Bone morphogenetic protein-2 converts the differentiation pathway of C2C12 myoblasts into the osteoblast lineage [published erratum appears in J Cell Biol 1995 Feb;128(4):following 713]
  The Journal of cell biology, 1994
• PEBP2/PEA2 represents a family of transcription factors homologous to the products of the Drosophila runt gene and the human AML1 gene.
  Proceedings of the National Academy of Sciences, 1993
• Rapid detection of octamer binding proteins with ‘mini extracts’, prepared from a small number of cells
  Nucleic Acids Research, 1989