 Heat-Shock Proteins
"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
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| MeSH Number(s) |
D12.776.580.216
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| Concept/Terms |
Heat-Shock Proteins- Heat-Shock Proteins
- Heat Shock Proteins
- Stress Proteins
- Heat-Shock Protein
- Heat Shock Protein
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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 UAMS Profiles 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 |
|---|
| 2022 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 | | 2017 | 0 | 1 | 1 | | 2016 | 1 | 0 | 1 | | 2015 | 2 | 2 | 4 | | 2014 | 1 | 0 | 1 | | 2013 | 3 | 1 | 4 | | 2012 | 0 | 3 | 3 | | 2011 | 1 | 2 | 3 | | 2010 | 1 | 1 | 2 | | 2009 | 1 | 1 | 2 | | 2008 | 0 | 1 | 1 | | 2007 | 0 | 2 | 2 | | 2006 | 1 | 2 | 3 | | 2005 | 2 | 0 | 2 | | 2004 | 1 | 0 | 1 | | 2003 | 1 | 3 | 4 | | 2002 | 2 | 2 | 4 | | 2000 | 5 | 2 | 7 | | 1998 | 6 | 1 | 7 | | 1997 | 3 | 0 | 3 | | 1996 | 2 | 1 | 3 | | 1994 | 1 | 3 | 4 | | 1993 | 3 | 2 | 5 | | 1992 | 1 | 0 | 1 | | 1991 | 3 | 0 | 3 | | 1990 | 0 | 2 | 2 | | 1989 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Heat-Shock Proteins" by people in Profiles over the past ten years.
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Fouani M, Basset CA, Mangano GD, Leone LG, Lawand NB, Leone A, Barone R. Heat Shock Proteins Alterations in Rheumatoid Arthritis. Int J Mol Sci. 2022 Mar 03; 23(5).
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Puzyrenko A, Jacobs ER, Sun Y, Felix JC, Sheinin Y, Ge L, Lai S, Dai Q, Gantner BN, Nanchal R, North PE, Simpson PM, Rui H, Benjamin IJ. 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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Pothineni NVK, Subramany S, Kuriakose K, Shirazi LF, Romeo F, Shah PK, Mehta JL. Infections, atherosclerosis, and coronary heart disease. Eur Heart J. 2017 Nov 14; 38(43):3195-3201.
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Rasche L, Menoret E, Dubljevic V, Menu E, Vanderkerken K, Lapa C, Steinbrunn T, Chatterjee M, Knop S, Düll J, Greenwood DL, Hensel F, Rosenwald A, Einsele H, Brändlein S. A GRP78-Directed Monoclonal Antibody Recaptures Response in Refractory Multiple Myeloma with Extramedullary Involvement. Clin Cancer Res. 2016 Sep 01; 22(17):4341-9.
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Chandrika BB, Yang C, Ou Y, Feng X, Muhoza D, Holmes AF, Theus S, Deshmukh S, Haun RS, Kaushal GP. Endoplasmic Reticulum Stress-Induced Autophagy Provides Cytoprotection from Chemical Hypoxia and Oxidant Injury and Ameliorates Renal Ischemia-Reperfusion Injury. PLoS One. 2015; 10(10):e0140025.
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Wu Y, Wang M, Peng Y, Ding Y, Deng L, Fu Q. Overexpression of Arl6ip5 in osteoblast regulates RANKL subcellualr localization. Biochem Biophys Res Commun. 2015 Sep 04; 464(4):1275-1281.
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Rasche L, Duell J, Castro IC, Dubljevic V, Chatterjee M, Knop S, Hensel F, Rosenwald A, Einsele H, Topp MS, Brändlein S. GRP78-directed immunotherapy in relapsed or refractory multiple myeloma - results from a phase 1 trial with the monoclonal immunoglobulin M antibody PAT-SM6. Haematologica. 2015 Mar; 100(3):377-84.
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Dokladny K, Myers OB, Moseley PL. Heat shock response and autophagy--cooperation and control. Autophagy. 2015; 11(2):200-13.
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Zhang L, Fok JH, Davies FE. Heat shock proteins in multiple myeloma. Oncotarget. 2014 Mar 15; 5(5):1132-48.
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Wang X, Dai Y, Ding Z, Khaidakov M, Mercanti F, Mehta JL. Regulation of autophagy and apoptosis in response to angiotensin II in HL-1 cardiomyocytes. Biochem Biophys Res Commun. 2013 Nov 01; 440(4):696-700.
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Graham JW, Lei MG, Lee CY. Trapping and identification of cellular substrates of the Staphylococcus aureus ClpC chaperone. J Bacteriol. 2013 Oct; 195(19):4506-16.
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