"Co-Repressor Proteins" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A subclass of repressor proteins that do not directly bind DNA. Instead, co-repressors generally act via their interaction with DNA-BINDING PROTEINS such as a TRANSCRIPTIONAL SILENCING FACTORS or NUCLEAR RECEPTORS.
| Descriptor ID |
D056970
|
| MeSH Number(s) |
D12.776.930.780.625
|
| Concept/Terms |
Co-Repressor Proteins- Co-Repressor Proteins
- Co Repressor Proteins
- Corepressor Proteins
- Corepressors
- Co-Repressors
- Co Repressors
Nuclear Receptor Co-Repressors- Nuclear Receptor Co-Repressors
- Co-Repressors, Nuclear Receptor
- Nuclear Receptor Co Repressors
- Receptor Co-Repressors, Nuclear
- Nuclear Receptor Corepressors
- Corepressors, Nuclear Receptor
|
Below are MeSH descriptors whose meaning is more general than "Co-Repressor Proteins".
Below are MeSH descriptors whose meaning is more specific than "Co-Repressor Proteins".
This graph shows the total number of publications written about "Co-Repressor Proteins" by people in this website by year, and whether "Co-Repressor Proteins" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2011 | 0 | 2 | 2 |
| 2017 | 0 | 1 | 1 |
| 2019 | 1 | 0 | 1 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Co-Repressor Proteins" by people in Profiles.
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Gupta RK, Rekhi B, Sharma MC, Ganga R, Ravina M, Kumar A, Sahu D. The BCOR -rearranged sarcoma involving the lung: Diagnosis with clinical outcome and literature review. Indian J Pathol Microbiol. 2024 Oct 01; 67(4):865-869.
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Yost KE, Clatterbuck Soper SF, Walker RL, Pineda MA, Zhu YJ, Ester CD, Showman S, Roschke AV, Waterfall JJ, Meltzer PS. Rapid and reversible suppression of ALT by DAXX in osteosarcoma cells. Sci Rep. 2019 03 14; 9(1):4544.
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Li J, Qian L, Dowling JP, Curcione C, Kurup D, Zhang J. Daxx plays a novel role in T cell survival but is dispensable in Fas-induced apoptosis. PLoS One. 2017; 12(3):e0174011.
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Pippa R, Espinosa L, Gundem G, Garc?a-Escudero R, Dominguez A, Orlando S, Gallastegui E, Saiz C, Besson A, Pujol MJ, L?pez-Bigas N, Paramio JM, Bigas A, Bachs O. p27Kip1 represses transcription by direct interaction with p130/E2F4 at the promoters of target genes. Oncogene. 2012 Sep 20; 31(38):4207-20.
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D'Agostino L, Giordano A. A novel dual signaling axis for NSP 5a3a induced apoptosis in head and neck carcinoma. Oncotarget. 2011 Dec; 2(12):1055-74.
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Popov VM, Zhou J, Shirley LA, Quong J, Yeow WS, Wright JA, Wu K, Rui H, Vadlamudi RK, Jiang J, Kumar R, Wang C, Pestell RG. The cell fate determination factor DACH1 is expressed in estrogen receptor-alpha-positive breast cancer and represses estrogen receptor-alpha signaling. Cancer Res. 2009 Jul 15; 69(14):5752-60.
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Zhu W, Foehr M, Jaynes JB, Hanes SD. Drosophila SAP18, a member of the Sin3/Rpd3 histone deacetylase complex, interacts with Bicoid and inhibits its activity. Dev Genes Evol. 2001 Mar; 211(3):109-17.
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Kiriakidou M, Driscoll DA, Lopez-Guisa JM, Strauss JF. Cloning and expression of primate Daxx cDNAs and mapping of the human gene to chromosome 6p21.3 in the MHC region. DNA Cell Biol. 1997 Nov; 16(11):1289-98.