Glutamine

RUNX family transcription factor 2 ; Homo sapiens







8 Article(s)
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Title
Pub. Year
#Total Relationships
1 25852448 A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia. 2015 Feb 3
2 22741925 RUNX2 tandem repeats and the evolution of facial length in placental mammals. 2012 Jun 28 1
3 22912713 Glutamine repeat variants in human RUNX2 associated with decreased femoral neck BMD, broadband ultrasound attenuation and target gene transactivation. 2012 1
4 20407796 Common polymorphisms rather than rare genetic variants of the Runx2 gene are associated with femoral neck BMD in Spanish women. 2010 Nov 1
5 17976052 The correlated evolution of Runx2 tandem repeats, transcriptional activity, and facial length in carnivora. 2007 Nov-Dec 1
6 15193550 RUNX2 alleles associated with BMD in Scottish women; interaction of RUNX2 alleles with menopausal status and body mass index. 2004 Jun 1
7 12162506 Alleles of RUNX2/CBFA1 gene are associated with differences in bone mineral density and risk of fracture. 2002 Aug 1
8 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