 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 |
|---|
| 1980 | 1 | 5 | 6 | | 1981 | 0 | 5 | 5 | | 1982 | 1 | 6 | 7 | | 1983 | 3 | 7 | 10 | | 1984 | 3 | 11 | 14 | | 1985 | 5 | 13 | 18 | | 1986 | 3 | 16 | 19 | | 1987 | 6 | 10 | 16 | | 1988 | 4 | 11 | 15 | | 1989 | 13 | 13 | 26 | | 1990 | 10 | 19 | 29 | | 1991 | 13 | 11 | 24 | | 1992 | 14 | 24 | 38 | | 1993 | 10 | 17 | 27 | | 1994 | 12 | 33 | 45 | | 1995 | 16 | 28 | 44 | | 1996 | 24 | 22 | 46 | | 1997 | 26 | 20 | 46 | | 1998 | 25 | 39 | 64 | | 1999 | 15 | 36 | 51 | | 2000 | 28 | 43 | 71 | | 2001 | 15 | 52 | 67 | | 2002 | 21 | 51 | 72 | | 2003 | 22 | 77 | 99 | | 2004 | 19 | 59 | 78 | | 2005 | 25 | 80 | 105 | | 2006 | 25 | 75 | 100 | | 2007 | 29 | 56 | 85 | | 2008 | 26 | 65 | 91 | | 2009 | 25 | 66 | 91 | | 2010 | 34 | 69 | 103 | | 2011 | 39 | 85 | 124 | | 2012 | 44 | 73 | 117 | | 2013 | 41 | 74 | 115 | | 2014 | 44 | 82 | 126 | | 2015 | 46 | 91 | 137 | | 2016 | 40 | 95 | 135 | | 2017 | 30 | 72 | 102 | | 2018 | 38 | 99 | 137 | | 2019 | 48 | 65 | 113 | | 2020 | 24 | 76 | 100 | | 2021 | 7 | 40 | 47 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Shorthouse D, Hall BA. SARS-CoV-2 Variants Are Selecting for Spike Protein Mutations That Increase Protein Stability. J Chem Inf Model. 2021 09 27; 61(9):4152-4155.
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Bennett JA, Young RH, Howitt BE, Croce S, Wanjari P, Zhen C, Da Cruz Paula A, Meserve E, Schoolmeester JK, Westbom-Fremer S, Benzi E, Patil NM, Kooreman L, El-Bahrawy M, Zannoni GF, Krausz T, McCluggage WG, Weigelt B, Ritterhouse LL, Oliva E. A Distinctive Adnexal (Usually Paratubal) Neoplasm Often Associated With Peutz-Jeghers Syndrome and Characterized by STK11 Alterations (STK11 Adnexal Tumor): A Report of 22 Cases. Am J Surg Pathol. 2021 08 01; 45(8):1061-1074.
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Howard FM, Dolezal J, Kochanny S, Schulte J, Chen H, Heij L, Huo D, Nanda R, Olopade OI, Kather JN, Cipriani N, Grossman RL, Pearson AT. The impact of site-specific digital histology signatures on deep learning model accuracy and bias. Nat Commun. 2021 07 20; 12(1):4423.
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Chen D, Xia S, Zhang R, Li Y, Famulare CA, Fan H, Wu R, Wang M, Zhu AC, Elf SE, Su R, Dong L, Arellano M, Blum WG, Mao H, Lonial S, Stock W, Odenike O, Le Beau M, Boggon TJ, He C, Chen J, Gao X, Levine RL, Chen J. Lysine acetylation restricts mutant IDH2 activity to optimize transformation in AML cells. Mol Cell. 2021 09 16; 81(18):3833-3847.e11.
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Roychowdhury T, Lu H, Hornsby WE, Crone B, Wang GT, Guo DC, Sendamarai AK, Devineni P, Lin M, Zhou W, Graham SE, Wolford BN, Surakka I, Wang Z, Chang L, Zhang J, Mathis M, Brummett CM, Melendez TL, Shea MJ, Kim KM, Deeb GM, Patel HJ, Eliason J, Eagle KA, Yang B, Ganesh SK, Brumpton B, Åsvold BO, Skogholt AH, Hveem K. Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm. Am J Hum Genet. 2021 09 02; 108(9):1578-1589.
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Li S, Noor ZS, Zeng W, Stackpole ML, Ni X, Zhou Y, Yuan Z, Wong WH, Agopian VG, Dubinett SM, Alber F, Li W, Garon EB, Zhou XJ. Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis. Nat Commun. 2021 07 07; 12(1):4172.
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Elf SE. JAK out of the box: myeloproliferative neoplasms--associated JAK2 V617F mutations contribute to aortic aneurysms. Haematologica. 2021 07 01; 106(7):1783-1784.
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Lopez-Ramirez MA, Lai CC, Soliman SI, Hale P, Pham A, Estrada EJ, McCurdy S, Girard R, Verma R, Moore T, Lightle R, Hobson N, Shenkar R, Poulsen O, Haddad GG, Daneman R, Gongol B, Sun H, Lagarrigue F, Awad IA, Ginsberg MH. Astrocytes propel neurovascular dysfunction during cerebral cavernous malformation lesion formation. J Clin Invest. 2021 07 01; 131(13).
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Lee BH, Wang R, Moberg IM, Reeder SH, Amom P, Tan MH, Amstutz K, Chandna P, Helton A, Andrianova EP, Zhulin IB, Dobritsa AA. A species-specific functional module controls formation of pollen apertures. Nat Plants. 2021 07; 7(7):966-978.
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Rutsch N, Chamberlain CE, Dixon W, Spector L, Letourneau-Freiberg LR, Lwin WW, Philipson LH, Zarbock A, Saintus K, Wang J, German MS, Anderson MS, Lowell CA. Diabetes With Multiple Autoimmune and Inflammatory Conditions Linked to an Activating SKAP2 Mutation. Diabetes Care. 2021 08; 44(8):1816-1825.
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