"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 | 14 | 26 | 40 |
| 1996 | 15 | 19 | 34 |
| 1997 | 17 | 37 | 54 |
| 1998 | 23 | 26 | 49 |
| 1999 | 21 | 52 | 73 |
| 2000 | 19 | 55 | 74 |
| 2001 | 18 | 48 | 66 |
| 2002 | 22 | 68 | 90 |
| 2003 | 32 | 73 | 105 |
| 2004 | 32 | 70 | 102 |
| 2005 | 33 | 87 | 120 |
| 2006 | 26 | 80 | 106 |
| 2007 | 40 | 84 | 124 |
| 2008 | 38 | 69 | 107 |
| 2009 | 39 | 73 | 112 |
| 2010 | 30 | 74 | 104 |
| 2011 | 40 | 99 | 139 |
| 2012 | 40 | 83 | 123 |
| 2013 | 36 | 102 | 138 |
| 2014 | 69 | 99 | 168 |
| 2015 | 69 | 113 | 182 |
| 2016 | 76 | 93 | 169 |
| 2017 | 66 | 121 | 187 |
| 2018 | 70 | 124 | 194 |
| 2019 | 55 | 127 | 182 |
| 2020 | 38 | 150 | 188 |
| 2021 | 38 | 118 | 156 |
| 2022 | 1 | 120 | 121 |
| 2023 | 2 | 98 | 100 |
| 2024 | 29 | 72 | 101 |
| 2025 | 7 | 16 | 23 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Impact of Co-mutations and Transcriptional Signatures in Non-Small Cell Lung Cancer Patients Treated with Adagrasib in the KRYSTAL-1 Trial. Clin Cancer Res. 2025 Mar 17; 31(6):1069-1081.
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Lasalocid A selectively induces the degradation of MYD88 in lymphomas harboring the MYD88 L265P mutation. Blood. 2025 Mar 06; 145(10):1047-1060.
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The common HAQ STING allele prevents clinical penetrance of COPA syndrome. J Exp Med. 2025 Apr 07; 222(4).
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Regulation of Mutant Huntingtin Mitochondrial Toxicity by Phosphomimetic Mutations within Its N-Terminal Region. J Neurosci. 2025 Feb 19; 45(8).
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Clinical Activity of Selpercatinib in RET-mutant Pheochromocytoma. J Clin Endocrinol Metab. 2025 Feb 18; 110(3):e600-e606.
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Integration of multiomic data identifies core-module of inherited-retinal diseases. Hum Mol Genet. 2025 Feb 17; 34(5):454-465.
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Next-Generation Sequencing-Based MSI Scoring Predicts Benefit in Mismatch Repair-Deficient Tumors Treated with Nivolumab: Follow-up on NCI-MATCH Arm Z1D. Clin Cancer Res. 2025 Feb 17; 31(4):667-677.
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Unprecedented female mutation bias in the aye-aye, a highly unusual lemur from Madagascar. PLoS Biol. 2025 Feb; 23(2):e3003015.
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Oncogenic KRAS Mutations Confer a Unique Mechanotransduction Response to Peristalsis in Colorectal Cancer Cells. Mol Cancer Res. 2025 02 06; 23(2):128-142.
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Improving Individualized Rhabdomyosarcoma Prognosis Predictions Using Somatic Molecular Biomarkers. JCO Precis Oncol. 2025 Feb; 9:e2400556.