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RUNX2 wt Allele

Known as: PEBP2A2, PEBP2aA1, CCD 
Human RUNX2 wild-type allele is located in the vicinity of 6p21 and is approximately 223 kb in length. This allele, which encodes runt-related… 
National Institutes of Health

Papers overview

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2020
2020
Case Report Cleidocranial dysplasia (CCD) it is an autosomal dominant skeletal dysplasia caused by mutation in CBFA1 (Core… 
2011
2011
A disostose cleidocraniana e uma sindrome relativamente rara, congenita, que se caracteriza por apresentar anomalias esqueleticas… 
2010
2010
We observed the effect of Cbfa1 on bone regeneration and microvessel density (MVD) in the process of avascular necrosis of… 
2008
2008
Background: Runt-related transcription factor 3 (RUNX3) is a novel tumor suppressor gene that is frequently silenced by promoter… 
2004
2004
The retinoblastoma (Rb) protein is a key regulator of cell proliferation, differentiation, and tumorigenesis. Initial studies of… 
2003
2003
We have recently demonstrated that all-trans retinoic acid (RA), the active metabolite of vitamin A, is an efficient alternative… 
2003
2003
INTRODUCTION: Both Demineralized Bone Powder (DBP) and BMP-2 stimulate endochondral osteogenesis in vivo. Nevertheless, the… 
2003
2003
INTRODUCTION: Endochondral bone formation processes through cartilage formation and replacement of mineralizin g growth plate… 
2001
2001
Unfavorable biological characteristics and host-related factors adversely affect the prognosis of acute myeloid leukemia (AML) in…