Alanine

RUNX family transcription factor 2 ; Homo sapiens







7 Article(s)
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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