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BCOR gene

Known as: FLJ20285, KIAA1575, BCL6 corepressor 
This gene plays a role in the repression of gene transcription.
National Institutes of Health

Related topics

Related topics

7 relations
BCL-6 CorepressorClear cell sarcoma of kidneyOdontogenesisPattern Formation

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BCOR wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Important Recently Characterized Non-Ewing Small Round Cell Tumors.
2018
2018
Case of the month 1-2019: CNS high-grade neuroepithelial tumor with BCOR alteration
No abstract available. 
2017
2017
Immunohistochemical analysis of NKX2.2, ETV4, and BCOR in a large series of genetically confirmed Ewing sarcoma family of tumors.
Review
2017
Review
2017
Genomic profile of a patient with triple negative essential thrombocythemia, unresponsive to therapy: A case report and literature review
2015
2015
Identification of the BRAF V600E mutation in gastroenteropancreatic neuroendocrine tumors
Genomic profiles of gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are still insufficiently understood, and the genetic… 
2014
2014
Evidence of Germline Mosaicism for a Novel BCOR Mutation in Two Indian Sisters with Oculo-Facio-Cardio-Dental Syndrome
In this study, we report on 2 sisters from India with oculo-facio-cardio-dental (OFCD) syndrome caused by a novel heterozygous… 
2013
2013
BCOR and BCORL 1 mutations in myelodysplastic syndromes and related disorders
BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders Frederik Damm, Virginie Chesnais, Yasunobu Nagata… 
2010
2010
Function analysis of mesenchymal Bcor in tooth development by using RNA interference
Teeth, an excellent model for studying organogenesis, develop from a series of epithelial–mesenchymal interactions that are… 
2009
2009
Molecular characterization of co‐occurring Duchenne muscular dystrophy and X‐linked oculo‐facio‐cardio‐dental syndrome in a girl
Duchenne muscular dystrophy is an X‐linked condition at the severe end of the spectrum of dystrophinopathies. Females with… 
2007
2007
Rybp, a polycomb complex-associated protein, is required for mouse eye development
BackgroundRybp (Ring1 and YY1 binding protein) is a zinc finger protein which interacts with the members of the mammalian… 
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