"Acrylamide" 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 colorless, odorless, highly water soluble vinyl monomer formed from the hydration of acrylonitrile. It is primarily used in research laboratories for electrophoresis, chromatography, and electron microscopy and in the sewage and wastewater treatment industries.
MeSH Number(s)
D02.065.122.015
D02.241.081.069.094.015
Below are MeSH descriptors whose meaning is more general than "Acrylamide".
Below are MeSH descriptors whose meaning is more specific than "Acrylamide".
This graph shows the total number of publications written about "Acrylamide" by people in Harvard Catalyst Profiles by year, and whether "Acrylamide" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1991 | 0 | 2 | 2 |
| 1995 | 0 | 1 | 1 |
| 1997 | 0 | 1 | 1 |
| 2003 | 1 | 1 | 2 |
| 2004 | 1 | 1 | 2 |
| 2005 | 3 | 0 | 3 |
| 2006 | 1 | 0 | 1 |
| 2007 | 2 | 0 | 2 |
| 2008 | 3 | 0 | 3 |
| 2009 | 3 | 0 | 3 |
| 2010 | 1 | 0 | 1 |
| 2011 | 2 | 0 | 2 |
| 2013 | 2 | 0 | 2 |
| 2015 | 1 | 1 | 2 |
| 2016 | 1 | 0 | 1 |
| 2017 | 2 | 3 | 5 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2020 | 1 | 2 | 3 |
Below are the most recent publications written about "Acrylamide" by people in Profiles.
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(E)-3-Furan-2-yl-N-p-tolyl-acrylamide and its Derivative DM489 Decrease Neuropathic Pain in Mice Predominantly by a7 Nicotinic Acetylcholine Receptor Potentiation. ACS Chem Neurosci. 2020 11 04; 11(21):3603-3614.
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Elasticizing tissues for reversible shape transformation and accelerated molecular labeling. Nat Methods. 2020 06; 17(6):609-613.
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Exposure to acrylamide and reduced heart rate variability: The mediating role of transforming growth factor-ß. J Hazard Mater. 2020 08 05; 395:122677.
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pH and lipid unsaturation impact the formation of acrylamide and 5-hydroxymethylfurfural in model system at frying temperature. Food Res Int. 2019 09; 123:403-413.
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Leveraging Compound Promiscuity to Identify Targetable Cysteines within the Kinome. Cell Chem Biol. 2019 06 20; 26(6):818-829.e9.
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Dietary Acrylamide Intake and Risk of Renal Cell Carcinoma in Two Large Prospective Cohorts. Cancer Epidemiol Biomarkers Prev. 2018 08; 27(8):979-982.
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Feasibility of using urinary N7-(2-carbamoyl-2-hydroxyethyl) Guanine as a biomarker for acrylamide exposed workers. J Expo Sci Environ Epidemiol. 2018 11; 28(6):589-598.
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Selective Nascent Polymer Catch-and-Release Enables Scalable Isolation of Multi-Kilobase Single-Stranded DNA. Angew Chem Int Ed Engl. 2018 01 15; 57(3):714-718.
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Evaluation and optimization of reduction and alkylation methods to maximize peptide identification with MS-based proteomics. Mol Biosyst. 2017 Nov 21; 13(12):2574-2582.
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Isotope dilution HPLC-MS/MS for simultaneous quantification of acrylamide and 5-hydroxymethylfurfural (HMF) in thermally processed seafood. Food Chem. 2017 Oct 01; 232:633-638.