"Mutation" 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.
Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations.
| Descriptor ID |
D009154
|
| MeSH Number(s) |
G05.365.590
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Mutation".
Below are MeSH descriptors whose meaning is more specific than "Mutation".
This graph shows the total number of publications written about "Mutation" by people in this website by year, and whether "Mutation" 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 |
|---|
| 1995 | 1 | 4 | 5 |
| 1996 | 1 | 5 | 6 |
| 1997 | 3 | 7 | 10 |
| 1998 | 1 | 3 | 4 |
| 1999 | 0 | 10 | 10 |
| 2000 | 3 | 11 | 14 |
| 2001 | 3 | 7 | 10 |
| 2002 | 5 | 9 | 14 |
| 2003 | 2 | 22 | 24 |
| 2004 | 5 | 19 | 24 |
| 2005 | 3 | 19 | 22 |
| 2006 | 6 | 27 | 33 |
| 2007 | 3 | 15 | 18 |
| 2008 | 3 | 15 | 18 |
| 2009 | 5 | 20 | 25 |
| 2010 | 8 | 20 | 28 |
| 2011 | 12 | 19 | 31 |
| 2012 | 7 | 21 | 28 |
| 2013 | 2 | 22 | 24 |
| 2014 | 6 | 17 | 23 |
| 2015 | 6 | 20 | 26 |
| 2016 | 18 | 20 | 38 |
| 2017 | 14 | 31 | 45 |
| 2018 | 4 | 23 | 27 |
| 2019 | 7 | 19 | 26 |
| 2020 | 9 | 29 | 38 |
| 2021 | 13 | 30 | 43 |
| 2022 | 0 | 12 | 12 |
| 2023 | 0 | 10 | 10 |
| 2024 | 3 | 5 | 8 |
| 2025 | 0 | 7 | 7 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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PIK3CB Inhibitor GSK2636771 in Cancers With PTEN Mutation/Deletion or Loss of PTEN Protein Expression: Results From the NCI-MATCH ECOG-ACRIN Trial (EAY131) Subprotocols N and P. JCO Precis Oncol. 2025 Aug; 9:e2500265.
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The low-fidelity DNA Pol IV accelerates evolution of pathogenicity genes in Pseudomonas aeruginosa. Commun Biol. 2025 Aug 02; 8(1):1148.
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Dhdds T206A and Dhdds K42E knock-in mouse models of retinitis pigmentosa 59 are phenotypically similar. Dis Model Mech. 2025 Jul 01; 18(7).
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Anisotropic diffuse growth in Arabidopsis thaliana stigma papillae. Plant Reprod. 2025 Jun 04; 38(2):13.
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Clinical and Genomic Features of Androgen Indifferent Prostate Cancer. Int J Mol Sci. 2025 Jan 15; 26(2).
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Phenotypic evolution of SARS-CoV-2 spike during the COVID-19 pandemic. Nat Microbiol. 2025 Jan; 10(1):77-93.
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Prognostic value of survival in patients with advanced non-small cell lung cancer treated with tyrosine-kinase inhibitors: Value of SUVmax or value of other factor? Clin Ter. 2025 Jan-Feb; 176(1):52-59.
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Expanding the Mutation Spectrum for Inherited Retinal Diseases. Genes (Basel). 2024 Dec 28; 16(1).
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Spontaneous mutation in 2310061I04Rik results in reduced expression of mitochondrial genes and impaired brain myelination. PLoS One. 2024; 19(12):e0290487.
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Phase II study of vemurafenib in children and young adults with tumors harboring BRAF V600 mutations: NCI-COG pediatric MATCH trial (APEC1621) Arm G. Oncologist. 2024 Aug 05; 29(8):723-e1093.