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BCL11B wt Allele

Known as: CTIP-2, hRIT1-alpha, CTIP2 
Human BCL11B wild-type allele is located in the vicinity of 14q32.2 and is approximately 102 kb in length. This allele, which encodes B-cell lymphoma… Expand
National Institutes of Health

Papers overview

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Review
2016
Review
2016
Purpose:Noonan syndrome (NS) is an autosomal-dominant disorder characterized by craniofacial dysmorphism, growth retardation… Expand
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2016
2016
To the Editor: We read with great interest the article by Kouz et al.1 reporting on genotype–phenotype correlations of patients… Expand
Review
2016
Review
2016
Mutations in RIT1, involved in the RAS‐MAPK pathway, have recently been identified as a cause for Noonan syndrome. We present two… Expand
2015
2015
RIT1, (Ras-like without CAAX1), the founding member of a novel branch of the Ras subfamily, mediates a wide variety of cellular… Expand
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2014
2014
Noonan syndrome (NS) is an autosomal dominant disorder consisting of short stature, short and/or webbed neck, distinctive facial… Expand
Review
2014
Review
2014
CTIP2 is a key transcriptional regulator involved in numerous physiological functions. Initial works have shown the importance of… Expand
2009
2009
Background We have demonstrated earlier that CTIP2 is highly expressed in mouse skin during embryogenesis and in adulthood. CTIP2… Expand
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2009
2009
Abstract:  Chicken ovalbumin upstream promoter‐transcription factor‐interacting protein 2 (CTIP2) is a transcriptional regulator… Expand
Highly Cited
2004
Highly Cited
2004
Chicken ovalbumin upstream promoter transcription factor-interacting proteins 1 and 2 (CTIP1 and CTIP2) are related… Expand
Highly Cited
2003
Highly Cited
2003
Allelic loss (LOH) mapping and sequence analysis were conducted for gamma-ray induced mouse thymic lymphomas and a novel tumor… Expand