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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… 
National Institutes of Health

Related topics

Related topics

3 relations
14q32.2Transcriptional Regulation

Broader (1)

BCL11B gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Stymulacja neurorozwojowa dziecka z zespołem Noonana z rzadką mutacją w genie RAF1 — opis przypadku
Introduction . Noonan syndrome (NS) is a genetically determined disease, inherited from autosomal dominant. About 50% of patients… 
Review
2017
Review
2017
Response to: Milosavljevic et al. “Two cases of RIT1 associated Noonan syndrome: Further delineation of the clinical phenotype and review of the literature”
1Department of Obstetrics, Gynecology, and Reproductive Sciences, McGovern Medical School at UT Health and The Fetal Center at… 
2016
2016
[RIT1: a novel gene associated with Noonan syndrome].
INTRODUCTION Noonan syndrome is the most frequent of the congenital group of malformation syndromes caused by germline mutations… 
2016
2016
RIT1: un nuevo gen causal del síndrome de Noonan
Introduccion. El sindrome de Noonan es el mas frecuente del grupo de los sindromes malformativos congenitos originados por… 
2016
2016
Compositions et procédés d'inhibition de rit1
La presente invention concerne divers composes, diverses compositions et divers procedes d'inhibition de Rit1. Dans des aspects… 
2016
2016
Zespół Noonan u noworodka z przeważającymi objawami niewydolności oddechowej oraz kardiomiopatii przerostowej i nadciśnienia płucnego
2014
2014
Régulation transcriptionnelle du virus HTLV-1: rôle fonctionnel des sites Sp1 et implication du cofacteur CTIP2 dans la latence virale
L’infection par le retrovirus complexe T-lymphotrope HTLV-1 (Human T-cell Leukemia Virus type 1), premier retrovirus humain… 
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