7 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 26220009 | Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient. | 2016 Jan | 9 |
2 | 25852448 | A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia. | 2015 Feb | 1 |
3 | 17976052 | The correlated evolution of Runx2 tandem repeats, transcriptional activity, and facial length in carnivora. | 2007 Nov-Dec | 1 |
4 | 16613857 | Cyclin D1-cdk4 induce runx2 ubiquitination and degradation. | 2006 Jun 16 | 3 |
5 | 15193550 | RUNX2 alleles associated with BMD in Scottish women; interaction of RUNX2 alleles with menopausal status and body mass index. | 2004 Jun | 1 |
6 | 12162506 | Alleles of RUNX2/CBFA1 gene are associated with differences in bone mineral density and risk of fracture. | 2002 Aug | 1 |
7 | 9632804 | Two domains unique to osteoblast-specific transcription factor Osf2/Cbfa1 contribute to its transactivation function and its inability to heterodimerize with Cbfbeta. | 1998 Jul | 1 |