A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference41 articles.
1. Molecular basis of tissue-specific gene expression mediated by the Runt domain transcription factor PEBP2/CBF
2. A New Transcription Factor Family Associated with Human Leukemias
3. Purification of a mouse nuclear factor that binds to both the A and B cores of the polyomavirus enhancer
4. PEBP2/PEA2 represents a family of transcription factors homologous to the products of the Drosophila runt gene and the human AML1 gene.
5. The cDNA cloning of the transcripts of human PEBP2αA/CBFA1 mapped to 6p12.3-p21.1, the locus for cleidocranial dysplasia
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