Nuclear Receptor Co-Repressor 1
"Nuclear Receptor Co-Repressor 1" 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 nuclear protein that regulates the expression of genes involved in a diverse array of processes related to metabolism and reproduction. The protein contains three nuclear receptor interaction domains and three repressor domains and is closely-related in structure to NUCLEAR RECEPTOR CO-REPRESSOR 2.
| Descriptor ID |
D056971
|
| MeSH Number(s) |
D12.776.930.780.625.374
|
| Concept/Terms |
Nuclear Receptor Co-Repressor 1- Nuclear Receptor Co-Repressor 1
- Nuclear Receptor Co Repressor 1
- RIP140 Repressor
- Nuclear Factor RIP140
- Receptor Interacting Protein 140
- Retinoid X Receptor-Interacting Protein 13
- Retinoid X Receptor Interacting Protein 13
- Nuclear Receptor Co-Repressor RIP140
- Nuclear Receptor Co Repressor RIP140
|
Below are MeSH descriptors whose meaning is more general than "Nuclear Receptor Co-Repressor 1".
Below are MeSH descriptors whose meaning is more specific than "Nuclear Receptor Co-Repressor 1".
This graph shows the total number of publications written about "Nuclear Receptor Co-Repressor 1" by people in this website by year, and whether "Nuclear Receptor Co-Repressor 1" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 0 | 1 | 1 |
| 1998 | 0 | 2 | 2 |
| 1999 | 0 | 1 | 1 |
| 2003 | 0 | 3 | 3 |
| 2004 | 0 | 1 | 1 |
| 2005 | 0 | 2 | 2 |
| 2006 | 0 | 1 | 1 |
| 2007 | 0 | 1 | 1 |
| 2008 | 0 | 1 | 1 |
| 2009 | 0 | 3 | 3 |
| 2010 | 1 | 0 | 1 |
| 2011 | 2 | 2 | 4 |
| 2012 | 2 | 0 | 2 |
| 2013 | 3 | 1 | 4 |
| 2014 | 2 | 0 | 2 |
| 2016 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2019 | 2 | 0 | 2 |
| 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Nuclear Receptor Co-Repressor 1" by people in Profiles.
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Cohesin Subunit RAD21 Regulates the Differentiation and Self-Renewal of Hematopoietic Stem and Progenitor Cells. Stem Cells. 2023 10 08; 41(10):971-985.
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Genetic and Pharmacological Targeting of Transcriptional Repression in Resistance to Thyroid Hormone Alpha. Thyroid. 2019 05; 29(5):726-734.
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Loss of function of NCOR1 and NCOR2 impairs memory through a novel GABAergic hypothalamus-CA3 projection. Nat Neurosci. 2019 02; 22(2):205-217.
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NCoR1-independent mechanism plays a role in the action of the unliganded thyroid hormone receptor. Proc Natl Acad Sci U S A. 2017 10 03; 114(40):E8458-E8467.
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Exosomes from Glioma-Associated Mesenchymal Stem Cells Increase the Tumorigenicity of Glioma Stem-like Cells via Transfer of miR-1587. Cancer Res. 2017 11 01; 77(21):5808-5819.
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Integrated omics approaches to characterize a nuclear receptor corepressor-associated histone deacetylase in mouse skeletal muscle. Mol Cell Endocrinol. 2018 08 15; 471:22-32.
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USP44 Is an Integral Component of N-CoR that Contributes to Gene Repression by Deubiquitinating Histone H2B. Cell Rep. 2016 11 22; 17(9):2382-2393.
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MeCP2 co-ordinates liver lipid metabolism with the NCoR1/HDAC3 corepressor complex. Hum Mol Genet. 2016 07 15; 25(14):3029-3041.
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Nuclear Receptor Corepressor 1 Expression and Output Declines with Prostate Cancer Progression. Clin Cancer Res. 2016 08 01; 22(15):3937-49.
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NCoR1 and SMRT play unique roles in thyroid hormone action in vivo. Mol Cell Biol. 2015 Feb; 35(3):555-65.