"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 | 12 | 18 | 30 |
| 1997 | 15 | 37 | 52 |
| 1998 | 23 | 23 | 46 |
| 1999 | 22 | 48 | 70 |
| 2000 | 19 | 53 | 72 |
| 2001 | 21 | 48 | 69 |
| 2002 | 21 | 62 | 83 |
| 2003 | 32 | 64 | 96 |
| 2004 | 30 | 68 | 98 |
| 2005 | 31 | 85 | 116 |
| 2006 | 26 | 81 | 107 |
| 2007 | 41 | 82 | 123 |
| 2008 | 36 | 65 | 101 |
| 2009 | 39 | 69 | 108 |
| 2010 | 27 | 72 | 99 |
| 2011 | 39 | 100 | 139 |
| 2012 | 44 | 82 | 126 |
| 2013 | 37 | 97 | 134 |
| 2014 | 68 | 107 | 175 |
| 2015 | 72 | 111 | 183 |
| 2016 | 79 | 97 | 176 |
| 2017 | 75 | 135 | 210 |
| 2018 | 74 | 133 | 207 |
| 2019 | 66 | 130 | 196 |
| 2020 | 43 | 165 | 208 |
| 2021 | 42 | 133 | 175 |
| 2022 | 3 | 130 | 133 |
| 2023 | 3 | 105 | 108 |
| 2024 | 34 | 90 | 124 |
| 2025 | 33 | 98 | 131 |
| 2026 | 12 | 51 | 63 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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[Loss of CHC1 or CHC2 in Arabidopsis compromises autophagy pathway and leads to enhanced disease resistance]. Sheng Wu Gong Cheng Xue Bao. 2026 May 25; 42(5):2129-2139.
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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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Mutational analysis of human norovirus VP2 elucidates critical molecular interactions for virus assembly. J Virol. 2026 02 17; 100(2):e0142025.
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EZHIP boosts neuronal-like synaptic gene programs and depresses polyamine metabolism. Acta Neuropathol Commun. 2025 11 07; 13(1):227.
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Mutant p53 variants differentially impact replication initiation and activate cGAS-STING to affect immune checkpoint inhibition. Commun Biol. 2025 Nov 05; 8(1):1522.
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Clonal hematopoiesis and subsequent venous thromboembolism among survivors of autologous transplantation for lymphoma. J Natl Cancer Inst. 2025 Nov 01; 117(11):2394-2398.
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Histiocyte Society blueprint for Langerhans cell histiocytosis research: from cell-of-origin to a more comprehensive cure. Haematologica. 2025 11 01; 110(11):2588-2602.
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Genomic determinants of the diffusely infiltrative gliomatosis cerebri phenotype. J Neurooncol. 2025 Oct 16; 176(1):19.
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Functional diversity in GII.4 norovirus entry: HBGA binding and capsid clustering dynamics. Proc Natl Acad Sci U S A. 2025 Oct 07; 122(40):e2517493122.
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Progressive respiratory failure in a term neonate with ABCA3 surfactant deficiency: Beyond the common causes of respiratory distress. J Neonatal Perinatal Med. 2026 Mar; 19(2):237-241.