"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 |
|---|
| 1998 | 0 | 1 | 1 |
| 2001 | 0 | 2 | 2 |
| 2003 | 0 | 1 | 1 |
| 2004 | 0 | 4 | 4 |
| 2005 | 0 | 4 | 4 |
| 2006 | 0 | 1 | 1 |
| 2007 | 0 | 3 | 3 |
| 2008 | 0 | 6 | 6 |
| 2009 | 0 | 2 | 2 |
| 2010 | 1 | 1 | 2 |
| 2011 | 1 | 4 | 5 |
| 2012 | 3 | 4 | 7 |
| 2013 | 1 | 2 | 3 |
| 2014 | 1 | 3 | 4 |
| 2015 | 2 | 0 | 2 |
| 2017 | 1 | 1 | 2 |
| 2018 | 0 | 2 | 2 |
| 2019 | 0 | 2 | 2 |
| 2020 | 3 | 2 | 5 |
| 2021 | 2 | 3 | 5 |
| 2022 | 0 | 1 | 1 |
| 2023 | 1 | 2 | 3 |
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Below are the most recent publications written about "Co-Repressor Proteins" by people in Profiles.
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Molecular Basis for SPINDOC-Spindlin1 Engagement and Its Role in Transcriptional Attenuation. J Mol Biol. 2024 Apr 01; 436(7):168371.
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PELP1 inhibition by SMIP34 reduces endometrial cancer progression via attenuation of ribosomal biogenesis. Mol Oncol. 2024 Sep; 18(9):2136-2156.
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The histone chaperone function of Daxx is dispensable for embryonic development. Cell Death Dis. 2023 08 26; 14(8):565.
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VGLL4 and MENIN function as TEAD1 corepressors to block pancreatic ? cell proliferation. Cell Rep. 2023 01 31; 42(1):111904.
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Context matters - Daxx and Atrx are not robust tumor suppressors in the murine endocrine pancreas. Dis Model Mech. 2022 08 01; 15(8).
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RNA-driven JAZF1-SUZ12 gene fusion in human endometrial stromal cells. PLoS Genet. 2021 12; 17(12):e1009985.
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SPINDOC binds PARP1 to facilitate PARylation. Nat Commun. 2021 11 04; 12(1):6362.
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Nuclear S-nitrosylation impacts tissue regeneration in zebrafish. Nat Commun. 2021 11 01; 12(1):6282.
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You come at the misfolded proteins, you best not miss. Trends Biochem Sci. 2022 01; 47(1):1-2.
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Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects. Hum Genet. 2021 Aug; 140(8):1143-1156.