"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 |
|---|
| 1996 | 14 | 18 | 32 |
| 1997 | 16 | 35 | 51 |
| 1998 | 23 | 23 | 46 |
| 1999 | 22 | 51 | 73 |
| 2000 | 19 | 53 | 72 |
| 2001 | 21 | 48 | 69 |
| 2002 | 22 | 63 | 85 |
| 2003 | 32 | 69 | 101 |
| 2004 | 31 | 69 | 100 |
| 2005 | 31 | 86 | 117 |
| 2006 | 26 | 80 | 106 |
| 2007 | 42 | 83 | 125 |
| 2008 | 37 | 66 | 103 |
| 2009 | 39 | 70 | 109 |
| 2010 | 27 | 75 | 102 |
| 2011 | 39 | 98 | 137 |
| 2012 | 44 | 83 | 127 |
| 2013 | 39 | 101 | 140 |
| 2014 | 72 | 111 | 183 |
| 2015 | 76 | 116 | 192 |
| 2016 | 80 | 100 | 180 |
| 2017 | 76 | 139 | 215 |
| 2018 | 77 | 137 | 214 |
| 2019 | 65 | 132 | 197 |
| 2020 | 46 | 173 | 219 |
| 2021 | 42 | 135 | 177 |
| 2022 | 4 | 132 | 136 |
| 2023 | 3 | 106 | 109 |
| 2024 | 34 | 92 | 126 |
| 2025 | 34 | 103 | 137 |
| 2026 | 6 | 35 | 41 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Biomarker study of pembrolizumab in patients with advanced rare cancers. Cell Rep Med. 2026 Jun 16; 7(6):102827.
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Single-nucleus profiling reveals a core disease signature and cell type-specific vulnerabilities in early Rett syndrome. Sci Adv. 2026 Jun 12; 12(24):eaeb4265.
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Monoallelic PSMB8 variants cause PRAAS with immunodeficiency through impaired immunoproteasome assembly. Am J Hum Genet. 2026 Jun 04; 113(6):1214-1232.
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H3K27me3 spreading organizes canonical PRC1 chromatin architecture to regulate developmental programs. Nat Genet. 2026 Jun; 58(6):1368-1382.
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Clinicogenomic and Histopathologic Analyses of Supermassive Intrahepatic Cholangiocarcinoma and the Role of Ablative Radiotherapy. Clin Cancer Res. 2026 May 15; 32(10):2079-2087.
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Natural history of NGLY1 deficiency: motor function & clinical features. Hum Mol Genet. 2026 May 11; 35(8).
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Dolutegravir developmental toxicity is mitigated by magnesium and folate in zebrafish embryos. Dis Model Mech. 2026 05 01; 19(5).
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Genetic Characterization of First-Line Drug-Resistance Mutations in Multidrug-Resistant Mycobacterium tuberculosis. Pathogens. 2026 Apr 22; 15(5).
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Multi-site DMS probing reveals higher-order structure of RNA-protein complexes in living cells. Mol Cell. 2026 May 07; 86(9):1815-1830.e9.
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Phospho-mimic ?III-tubulin rescues microtubule and cardiac defects in Duchenne muscular dystrophy mice. J Mol Cell Cardiol. 2026 Jun; 215:6-19.