"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 | 0 | 1 | 1 |
| 1997 | 0 | 1 | 1 |
| 1998 | 1 | 2 | 3 |
| 1999 | 1 | 3 | 4 |
| 2000 | 1 | 4 | 5 |
| 2001 | 1 | 4 | 5 |
| 2002 | 1 | 1 | 2 |
| 2003 | 6 | 0 | 6 |
| 2004 | 2 | 4 | 6 |
| 2005 | 2 | 10 | 12 |
| 2006 | 6 | 8 | 14 |
| 2007 | 4 | 8 | 12 |
| 2008 | 7 | 8 | 15 |
| 2009 | 12 | 8 | 20 |
| 2010 | 11 | 13 | 24 |
| 2011 | 12 | 8 | 20 |
| 2012 | 15 | 17 | 32 |
| 2013 | 20 | 17 | 37 |
| 2014 | 22 | 18 | 40 |
| 2015 | 24 | 26 | 50 |
| 2016 | 26 | 26 | 52 |
| 2017 | 16 | 19 | 35 |
| 2018 | 20 | 16 | 36 |
| 2019 | 9 | 18 | 27 |
| 2020 | 9 | 23 | 32 |
| 2021 | 14 | 24 | 38 |
| 2022 | 0 | 27 | 27 |
| 2023 | 0 | 8 | 8 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1. Neurology. 2023 08 29; 101(9):e879-e891.
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Predicting the pathogenicity of missense variants using features derived from AlphaFold2. Bioinformatics. 2023 05 04; 39(5).
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Mitigating age-related somatic mutation burden. Trends Mol Med. 2023 Jul; 29(7):530-540.
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Insufficient evidence for non-neutrality of synonymous mutations. Nature. 2023 04; 616(7957):E8-E9.
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Non-canonical integrin signaling activates EGFR and RAS-MAPK-ERK signaling in small cell lung cancer. Theranostics. 2023; 13(8):2384-2407.
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Biallelic variants in CRIPT cause a Rothmund-Thomson-like syndrome with increased cellular senescence. Genet Med. 2023 Jul; 25(7):100836.
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Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis. Genes (Basel). 2023 03 15; 14(3).
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KIT D816V Mast Cells Derived from Induced Pluripotent Stem Cells Recapitulate Systemic Mastocytosis Transcriptional Profile. Int J Mol Sci. 2023 Mar 09; 24(6).
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Inheritance of paternal DNA damage by histone-mediated repair restriction. Nature. 2023 01; 613(7943):365-374.
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Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations. HGG Adv. 2023 01 12; 4(1):100166.
MeSH information
