 Mutation
"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
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| MeSH Number(s) |
G05.365.590
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| Concept/Terms |
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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 |
|---|
| 1997 | 0 | 1 | 1 | | 1998 | 2 | 1 | 3 | | 1999 | 0 | 1 | 1 | | 2000 | 0 | 2 | 2 | | 2001 | 2 | 0 | 2 | | 2002 | 2 | 1 | 3 | | 2003 | 2 | 3 | 5 | | 2004 | 2 | 3 | 5 | | 2005 | 1 | 4 | 5 | | 2006 | 1 | 4 | 5 | | 2007 | 4 | 5 | 9 | | 2008 | 3 | 1 | 4 | | 2009 | 3 | 1 | 4 | | 2010 | 2 | 7 | 9 | | 2011 | 6 | 3 | 9 | | 2012 | 2 | 4 | 6 | | 2013 | 2 | 4 | 6 | | 2014 | 4 | 6 | 10 | | 2015 | 7 | 10 | 17 | | 2016 | 9 | 11 | 20 | | 2017 | 5 | 15 | 20 | | 2018 | 6 | 7 | 13 | | 2019 | 6 | 15 | 21 | | 2020 | 6 | 9 | 15 | | 2021 | 4 | 9 | 13 | | 2022 | 0 | 8 | 8 | | 2023 | 0 | 14 | 14 | | 2024 | 3 | 6 | 9 | | 2025 | 1 | 9 | 10 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Button EL, Dwyer E, Lewis JB, Mortensen MS, McDonald E, Butler E, Pearson F, Tang AE, Watts JL, Veal EA. The 1 -Cys peroxiredoxin, PRDX-6, suppresses an NHR-49-dependent pro-survival response, including the Flavin monooxygenase, FMO-2, that protects against fungal and bacterial infection. Redox Biol. 2026 04; 91:103992.
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Kishnani PS, Rehder C, Ozono K, P?rez-L?pez J, Del Angel G, Mowrey WR, Balasubramanian M, H?gler W, Rush ET. Revisiting the Genetics of Hypophosphatasia. J Inherit Metab Dis. 2025 Nov; 48(6):e70083.
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Mokhtari A, Charbonneau J, Miranda V, Jizi K, Delrue MA, Egerszegi P, Thiffault I, Campeau PM. Molecular Landscape in Limb Anomalies: Diagnostic Yield and New Candidate Genes. Clin Genet. 2026 Mar; 109(3):424-436.
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Matejcic M, Teer JK, Hoehn HJ, Diaz DB, Shankar K, Gong J, Nguyen NT, Loro?a NC, Coppola D, Fulmer CG, Saglam O, Jiang K, Cress WD, Mu?oz-Antonia T, Flores I, Gordi?n ER, Oliveras Torres JA, Felder SI, Sanchez J, Fleming JB, Siegel EM, Freedman JA, Dutil J, Stern MC, Fridley BL, Figueiredo JC, Schmit SL. Colorectal Tumors in Diverse Patient Populations Feature a Spectrum of Somatic Mutational Profiles. Cancer Res. 2025 May 15; 85(10):1928-1944.
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Soupir A, Ospina OE, Hampton O, Churchman M, Radmacher M, Hedges D, McKean D, Agius P, Zeeshan S, Seligson ND, Pollock R, Liebner D, Chen JL, Tinoco G, Salhia B, McCarter M, Wilky BA, Miller BJ, Cavnar MJ, Groundland JS, Schneider BP, Riedlinger G, Edge SB, Moskaluk CA, Cardona K, Naqash AR, Gonzalez RJ, Mullinax JE, Joyce DM, Binitie O, Douglas Letson G, Naghavi AO, Druta M, Reed DR, Siegel EM, Teer JK, Fridley BL, Brohl AS. Genomic, transcriptomic, and immunogenomic landscape of over 1300 sarcomas of diverse histology subtypes. Nat Commun. 2025 May 06; 16(1):4206.
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Mattioli F, Fri?riksd?ttir R, Hebert A, Bassani S, Ibrahim N, Naz S, Chrast J, Pailler-Pradeau C, Oddsson ?, Sulem P, Halldorsson GH, Melsted P, Gu?bjartsson DF, Palombo F, Pippucci T, Nouri N, Seri M, Farrow EG, Saunders CJ, Guex N, Ansar M, Stefansson K, Reymond A. Bi-allelic variants in BRF2 are associated with perinatal death and craniofacial anomalies. Genome Med. 2025 Apr 14; 17(1):38.
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Udemgba C, Pillay B, Shafer S, Alberstadt A, Abers M, Gilliaux O, Chen K, Rae W, Hanitsch L, Von Bernuth H, Neves JF, Raje N, Moens L, van Hagen PM, Bergerson J, Hartog N, Niehues T, D?ckers G, Falcone E, Keller M, Hsu A, Meyts I, Holland SM. IRF2BP2 deficiency: An important form of common variable immunodeficiency with inflammation. J Allergy Clin Immunol. 2025 Jun; 155(6):2052-2062.e5.
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Thoenen E, Ranjan A, Parrales A, Nishikawa S, Dixon DA, Oka S, Iwakuma T. Suppression of stress granule formation is a vulnerability imposed by mutant p53. Nat Commun. 2025 Mar 10; 16(1):2365.
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Duis J, Agresta L, Bennett WE, Chambers H, Clarke A, Fairhurst C, Hoover-Fong J, Murphy F, Noritz G, Schwantes S, Shreve M, Thusang K, Weidemann D, Beale R, Mehta A, Wilhelmsen A, Summerfield N. International Expert Opinion on Standard of Care for Patients With Schinzel-Giedion Syndrome: A Modified Delphi Study. Am J Med Genet A. 2025 Jun; 197(6):e64015.
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Rush ET, Del Angel G, Dong J, Bates T, Steiner RD, Cox A. Genetic characterization of a large cohort of individuals with a clinical suspicion of hypophosphatasia in the United States. Mol Genet Metab. 2025 Mar; 144(3):109046.
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