HSC70 Heat-Shock Proteins
"HSC70 Heat-Shock 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 constitutively expressed subfamily of the HSP70 heat-shock proteins. They preferentially bind and release hydrophobic peptides by an ATP-dependent process and are involved in post-translational PROTEIN TRANSLOCATION.
| Descriptor ID |
D050883
|
| MeSH Number(s) |
D12.776.580.216.375.200
|
| Concept/Terms |
HSC70 Heat-Shock Proteins- HSC70 Heat-Shock Proteins
- HSC70 Heat Shock Proteins
- Heat-Shock Proteins, HSC70
- Hsc70 Protein
- Heat-Shock Cognate 70 Protein
- Heat Shock Cognate 70 Protein
- Clathrin Uncoating Protein
- Uncoating Protein, Clathrin
- 70 kDa Heat-Shock Cognate Protein
- 70 kDa Heat Shock Cognate Protein
|
Below are MeSH descriptors whose meaning is more general than "HSC70 Heat-Shock Proteins".
Below are MeSH descriptors whose meaning is more specific than "HSC70 Heat-Shock Proteins".
This graph shows the total number of publications written about "HSC70 Heat-Shock Proteins" by people in this website by year, and whether "HSC70 Heat-Shock Proteins" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
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Below are the most recent publications written about "HSC70 Heat-Shock Proteins" by people in Profiles.
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CDK-dependent Hsp70 Phosphorylation controls G1 cyclin abundance and cell-cycle progression. Cell. 2012 Dec 07; 151(6):1308-18.
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Loss of specific chaperones involved in membrane glycoprotein biosynthesis during the maturation of human erythroid progenitor cells. J Biol Chem. 2009 May 22; 284(21):14547-57.
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Thermal preconditioning and heat-shock protein 72 preserve synaptic transmission during thermal stress. J Neurosci. 2002 Jan 01; 22(1):RC193.
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Purification of multiple heat shock proteins from a single tumor sample. J Immunol Methods. 2000 Apr 03; 237(1-2):119-30.