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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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2012
2012
Articular cartilage (AC) lacks ability to repair defects due to its avascular nature as healing process relies on cells being… 
2006
2006
This study tested the hypothesis that physiologic tendon loading modulates the fibrous connective tissue phenotype in… 
2005
2005
AML1/Runx1 is a frequent target of human leukemia-associated gene aberration and encodes a transcription factor with nonredundant… 
2002
2002
Cbfa1 is a transcription factor recognised as being involved in early osteoblast differentiation during embryonic skeletogenesis… 
2002
2002
Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal disorder exhibiting a wide clinical spectrum ranging from minimal… 
2000
2000
Collagenase‐3 expression in osteoblastic (UMR 106‐01, ROS 17/2.8) and non‐osteoblastic cell lines (BC1, NIH3T3) was examined. We… 
1997
1997
Multiagent chemotherapy regimens fail to cure more than one-half of the patients with acute myeloid leukemia (AML) because of the… 
Review
1994
Review
1994
The current treatment of acute promyelocytic leukemia (APL, also called AML3 subtype) is focused on differentiating agents such… 
Highly Cited
1992
Highly Cited
1992
The t(15;17) translocation is specifically observed in patients with promyelocytic leukemia (AML3). The chromosomal rearrangement…