"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 | 24 | 47 |
| 1999 | 21 | 52 | 73 |
| 2000 | 19 | 54 | 73 |
| 2001 | 18 | 48 | 66 |
| 2002 | 22 | 68 | 90 |
| 2003 | 33 | 74 | 107 |
| 2004 | 32 | 73 | 105 |
| 2005 | 33 | 88 | 121 |
| 2006 | 26 | 81 | 107 |
| 2007 | 41 | 85 | 126 |
| 2008 | 38 | 70 | 108 |
| 2009 | 39 | 71 | 110 |
| 2010 | 30 | 73 | 103 |
| 2011 | 41 | 99 | 140 |
| 2012 | 40 | 83 | 123 |
| 2013 | 36 | 102 | 138 |
| 2014 | 68 | 99 | 167 |
| 2015 | 69 | 112 | 181 |
| 2016 | 78 | 93 | 171 |
| 2017 | 69 | 120 | 189 |
| 2018 | 70 | 125 | 195 |
| 2019 | 56 | 130 | 186 |
| 2020 | 38 | 155 | 193 |
| 2021 | 37 | 123 | 160 |
| 2022 | 2 | 120 | 122 |
| 2023 | 2 | 97 | 99 |
| 2024 | 29 | 79 | 108 |
| 2025 | 12 | 34 | 46 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Characterization and treatment outcomes of malignant histiocytoses in a retrospective series of 141 cases in France. Blood Adv. 2025 May 27; 9(10):2530-2541.
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New genetic tools to define the pathophysiology of inborn errors of cobalamin metabolism impacting mammalian development. Differentiation. 2025 May-Jun; 143:100868.
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Association between Locoregional Failure and NFE2L2/KEAP1/CUL3 Mutations in NRG/RTOG 9512: A Randomized Trial of Radiation Fractionation in T2N0 Glottic Cancer. Clin Cancer Res. 2025 May 01; 31(9):1615-1624.
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Identification of Hepatic-like EPO as a Cause of Polycythemia. N Engl J Med. 2025 May 01; 392(17):1684-1697.
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ESR1 Y537S and D538G Mutations Drive Resistance to CDK4/6 Inhibitors in Estrogen Receptor-Positive Breast Cancer. Clin Cancer Res. 2025 May 01; 31(9):1667-1675.
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A highly conserved ABCG transporter mediates root-soil cohesion in Arabidopsis. Plant Physiol. 2025 Apr 30; 198(1).
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Selective inhibition of canonical STAT3 signaling suppresses K-ras mutant lung tumorigenesis and reinvigorates anti-tumor immunity. Front Immunol. 2025; 16:1575181.
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IDH status dictates oHSV mediated metabolic reprogramming affecting anti-tumor immunity. Nat Commun. 2025 Apr 24; 16(1):3874.
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Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation. Am J Hum Genet. 2025 May 01; 112(5):1139-1157.
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KRAS mutation detection by liquid biopsy for pancreatic ductal adenocarcinoma. J Hematol Oncol. 2025 Apr 17; 18(1):44.