Min-Su Han and Hyo-Jin Kim contributed equally to this work.
The cleidocranial dysplasia-related R131G mutation in the Runt-related transcription factor RUNX2 disrupts binding to DNA but not CBF-β†
Article first published online: 11 MAR 2010
Copyright © 2010 Wiley-Liss, Inc.
Journal of Cellular Biochemistry
Volume 110, Issue 1, pages 97–103, 1 May 2010
How to Cite
Han, M.-S., Kim, H.-J., Wee, H.-J., Lim, K.-E., Park, N.-R., Bae, S.-C., van Wijnen, A. J., Stein, J. L., Lian, J. B., Stein, G. S. and Choi, J.-Y. (2010), The cleidocranial dysplasia-related R131G mutation in the Runt-related transcription factor RUNX2 disrupts binding to DNA but not CBF-β. J. Cell. Biochem., 110: 97–103. doi: 10.1002/jcb.22516
- Issue published online: 16 APR 2010
- Article first published online: 11 MAR 2010
- Manuscript Accepted: 4 JAN 2010
- Manuscript Received: 31 DEC 2009
- The Korea Health 21 R&D Project (Ministry of Health, Welfare and Family Affairs). Grant Numbers: A010252, A030003
- Ministry of Education, Science and Technology (The Regional Core Research Program)
- National Institutes of Health. Grant Numbers: R01 AR49069, R01, AR39588, P01, AR48818, P01, CA82834
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