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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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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
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2016
2016
INTRODUCTION Noonan syndrome is the most frequent of the congenital group of malformation syndromes caused by germline mutations… Expand
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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
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Review
2014
Review
2014
CTIP2 is a key transcriptional regulator involved in numerous physiological functions. Initial works have shown the importance of… Expand
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Review
2012
Review
2012
Noonan syndrome (NS) and NS-related disorders (cardio-facio-cutaneous syndrome, Costello syndrome, NS with multiple lentigines… Expand
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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
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Highly Cited
2004
Highly Cited
2004
Chicken ovalbumin upstream promoter transcription factor-interacting proteins 1 and 2 (CTIP1 and CTIP2) are related… Expand
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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
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