Ubiquitin-Specific Peptidase 7
"Ubiquitin-Specific Peptidase 7" 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 ubiquitinyl hydrolase that deubiquitinates several proteins with critical roles in DNA REPAIR, cell growth, and survival, including TUMOR SUPPRESSOR PROTEIN P53; MDM-2 PROTEIN; and PTEN PHOSPHOHYDROLASE. It also stabilizes herpesvirus 1 trans-acting transcriptional protein VMW110 during HSV-1 infection, contributing to its function as a TRANS-ACTIVATOR.
| Descriptor ID |
D000076084
|
| MeSH Number(s) |
D08.811.037.500.500 D08.811.037.750.750 D08.811.277.352.897.850.500 D08.811.277.656.300.887.875
|
| Concept/Terms |
Ubiquitin-Specific Peptidase 7- Ubiquitin-Specific Peptidase 7
- Peptidase 7, Ubiquitin-Specific
- Ubiquitin Specific Peptidase 7
- HAUSP Protein
- Herpesvirus-Associated Ubiquitin-Specific Peptidase
- Herpesvirus Associated Ubiquitin Specific Peptidase
- Peptidase, Herpesvirus-Associated Ubiquitin-Specific
- Ubiquitin-Specific Peptidase, Herpesvirus-Associated
- USP7 Protein
|
Below are MeSH descriptors whose meaning is more general than "Ubiquitin-Specific Peptidase 7".
Below are MeSH descriptors whose meaning is more specific than "Ubiquitin-Specific Peptidase 7".
This graph shows the total number of publications written about "Ubiquitin-Specific Peptidase 7" by people in this website by year, and whether "Ubiquitin-Specific Peptidase 7" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 1 | 1 |
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Below are the most recent publications written about "Ubiquitin-Specific Peptidase 7" by people in Profiles.
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Genome-wide discovery of genetic variants affecting tamoxifen sensitivity and their clinical and functional validation. Ann Oncol. 2013 Jul; 24(7):1867-1873.
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Overexpression of the ubiquitin-specific protease 7 resulting from transfection or mutations in the ICP0 binding site accelerates rather than depresses herpes simplex virus 1 gene expression. J Virol. 2012 Dec; 86(23):12871-8.