"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.
Linear POLYPEPTIDES that are synthesized on RIBOSOMES and may be further modified, crosslinked, cleaved, or assembled into complex proteins with several subunits. The specific sequence of AMINO ACIDS determines the shape the polypeptide will take, during PROTEIN FOLDING, and the function of the protein.
| Descriptor ID |
D011506
|
| MeSH Number(s) |
D12.776
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Proteins".
Below are MeSH descriptors whose meaning is more specific than "Proteins".
This graph shows the total number of publications written about "Proteins" by people in this website by year, and whether "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 |
|---|
| 1994 | 1 | 0 | 1 |
| 1995 | 1 | 0 | 1 |
| 1999 | 2 | 0 | 2 |
| 2000 | 3 | 0 | 3 |
| 2001 | 4 | 1 | 5 |
| 2002 | 1 | 1 | 2 |
| 2003 | 1 | 0 | 1 |
| 2004 | 2 | 1 | 3 |
| 2005 | 0 | 2 | 2 |
| 2006 | 0 | 1 | 1 |
| 2007 | 2 | 1 | 3 |
| 2008 | 5 | 0 | 5 |
| 2009 | 2 | 3 | 5 |
| 2010 | 2 | 0 | 2 |
| 2011 | 1 | 1 | 2 |
| 2012 | 1 | 2 | 3 |
| 2013 | 5 | 2 | 7 |
| 2014 | 7 | 1 | 8 |
| 2015 | 5 | 1 | 6 |
| 2016 | 4 | 2 | 6 |
| 2017 | 2 | 0 | 2 |
| 2018 | 1 | 1 | 2 |
| 2019 | 1 | 1 | 2 |
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click here.
Below are the most recent publications written about "Proteins" by people in Profiles.
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Identification of loci of functional relevance to Barrett's esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association data. PLoS One. 2019; 14(12):e0227072.
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HE4 as a biomarker for diagnosis of lung cancer: A meta-analysis. Medicine (Baltimore). 2019 Sep; 98(39):e17198.
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Screening and identification of potential protein biomarkers for evaluating the efficacy of intensive therapy in pulmonary tuberculosis. Biochem Biophys Res Commun. 2018 09 18; 503(4):2263-2270.
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Modeling and simulating networks of interdependent protein interactions. Integr Biol (Camb). 2018 05 21; 10(5):290-305.
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WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features. Am J Hum Genet. 2017 Jul 06; 101(1):139-148.
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A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes. Sci Rep. 2017 03 10; 7:44138.
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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nat Genet. 2016 09; 48(9):1043-8.
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Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances. Epigenomics. 2016 06; 8(6):801-16.
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Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening tool. Gene. 2016 Sep 15; 590(1):1-4.
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Identification and Functional Characterization of Two Intronic NIPBL Mutations in Two Patients with Cornelia de Lange Syndrome. Biomed Res Int. 2016; 2016:8742939.
MeSH information
