"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.
Proteins which are synthesized in eukaryotic organisms and bacteria in response to hyperthermia and other environmental stresses. They increase thermal tolerance and perform functions essential to cell survival under these conditions.
Descriptor ID |
D006360
|
MeSH Number(s) |
D12.776.580.216
|
Concept/Terms |
Heat-Shock Proteins- Heat-Shock Proteins
- Heat Shock Proteins
- Stress Proteins
- Heat-Shock Protein
- Heat Shock Protein
|
Below are MeSH descriptors whose meaning is more general than "Heat-Shock Proteins".
Below are MeSH descriptors whose meaning is more specific than "Heat-Shock Proteins".
This graph shows the total number of publications written about "Heat-Shock Proteins" by people in this website by year, and whether "Heat-Shock 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 |
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1995 | 0 | 1 | 1 |
1998 | 0 | 1 | 1 |
2003 | 0 | 1 | 1 |
2004 | 1 | 0 | 1 |
2005 | 0 | 1 | 1 |
2006 | 0 | 1 | 1 |
2007 | 1 | 0 | 1 |
2009 | 1 | 0 | 1 |
2010 | 0 | 1 | 1 |
2013 | 0 | 1 | 1 |
2016 | 0 | 1 | 1 |
2017 | 7 | 6 | 13 |
2018 | 8 | 5 | 13 |
2019 | 2 | 0 | 2 |
2020 | 3 | 1 | 4 |
2021 | 2 | 2 | 4 |
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Below are the most recent publications written about "Heat-Shock Proteins" by people in Profiles.
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Pneumocytes are distinguished by highly elevated expression of the ER stress biomarker GRP78, a co-receptor for SARS-CoV-2, in COVID-19 autopsies. Cell Stress Chaperones. 2021 09; 26(5):859-868.
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Mucormycosis and glucose-regulated protein 78 in COVID-19: Amenable to statin treatment? J Intern Med. 2021 10; 290(4):931-933.
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Evaluation of vertical transmission of SARS-CoV-2 in utero: Nine pregnant women and their newborns. Placenta. 2021 08; 111:91-96.
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Innate immunity, inflammation activation and heat-shock protein in COVID-19 pathogenesis. J Neuroimmunol. 2021 09 15; 358:577632.
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Recognition through GRP78 is enhanced in the UK, South African, and Brazilian variants of SARS-CoV-2; An in silico perspective. Biochem Biophys Res Commun. 2021 07 12; 562:89-93.
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Glucose-regulated protein (GRP78) is an important cell surface receptor for viral invasion, cancers, and neurological disorders. IUBMB Life. 2021 06; 73(6):843-854.
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The chaperone GRP78 is a host auxiliary factor for SARS-CoV-2 and GRP78 depleting antibody blocks viral entry and infection. J Biol Chem. 2021 Jan-Jun; 296:100759.
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Human gene polymorphisms and their possible impact on the clinical outcome of SARS-CoV-2 infection. Arch Virol. 2021 Aug; 166(8):2089-2108.
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Evaluation and characterization of HSPA5 (GRP78) expression profiles in normal individuals and cancer patients with COVID-19. Int J Biol Sci. 2021; 17(3):897-910.
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First Virtual International Congress on Cellular and Organismal Stress Responses, November 5-6, 2020. Cell Stress Chaperones. 2021 03; 26(2):289-295.