 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 | 12 | 25 | | 1992 | 14 | 23 | 37 | | 1993 | 10 | 18 | 28 | | 1994 | 12 | 34 | 46 | | 1995 | 16 | 28 | 44 | | 1996 | 24 | 23 | 47 | | 1997 | 26 | 19 | 45 | | 1998 | 25 | 40 | 65 | | 1999 | 15 | 35 | 50 | | 2000 | 28 | 43 | 71 | | 2001 | 14 | 50 | 64 | | 2002 | 20 | 53 | 73 | | 2003 | 20 | 80 | 100 | | 2004 | 19 | 61 | 80 | | 2005 | 26 | 79 | 105 | | 2006 | 25 | 76 | 101 | | 2007 | 28 | 55 | 83 | | 2008 | 26 | 60 | 86 | | 2009 | 25 | 62 | 87 | | 2010 | 33 | 66 | 99 | | 2011 | 38 | 82 | 120 | | 2012 | 44 | 72 | 116 | | 2013 | 41 | 67 | 108 | | 2014 | 41 | 80 | 121 | | 2015 | 41 | 85 | 126 | | 2016 | 36 | 89 | 125 | | 2017 | 27 | 65 | 92 | | 2018 | 28 | 82 | 110 | | 2019 | 7 | 7 | 14 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Perl AE, Martinelli G, Cortes JE, Neubauer A, Berman E, Paolini S, Montesinos P, Baer MR, Larson RA, Ustun C, Fabbiano F, Erba HP, Di Stasi A, Stuart R, Olin R, Kasner M, Ciceri F, Chou WC, Podoltsev N, Recher C, Yokoyama H, Hosono N, Yoon SS, Lee JH, Pardee T, Fathi AT, Liu C, Hasabou N, Liu X, Bahceci E, Levis MJ. Gilteritinib or Chemotherapy for Relapsed or Refractory FLT3-Mutated AML. N Engl J Med. 2019 10 31; 381(18):1728-1740.
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Mei L, Alikhan M, Mujacic I, Parilla M, Antic T. Genomic Alterations in Undifferentiated Malignant Tumors with Rhabdoid Phenotype and Loss of BRG1 Immunoexpression Identified by Fine Needle Aspirates. Acta Cytol. 2019; 63(5):438-444.
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Upadhyay U, Zhuang GZ, Diatchenko L, Parisien M, Kang Y, Sarantopoulos KD, Martin ER, Smith SB, Maixner W, Levitt RC. Profound analgesia is associated with a truncated peptide resulting from tissue specific alternative splicing of DRG CA8-204 regulated by an exon-level cis-eQTL. PLoS Genet. 2019 06; 15(6):e1008226.
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Chapman EM, Lant B, Ohashi Y, Yu B, Schertzberg M, Go C, Dogra D, Koskimäki J, Girard R, Li Y, Fraser AG, Awad IA, Abdelilah-Seyfried S, Gingras AC, Derry WB. A conserved CCM complex promotes apoptosis non-autonomously by regulating zinc homeostasis. Nat Commun. 2019 04 17; 10(1):1791.
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Fuller ZL, Berg JJ, Mostafavi H, Sella G, Przeworski M. Measuring intolerance to mutation in human genetics. Nat Genet. 2019 05; 51(5):772-776.
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Plourde SM, Amom P, Tan M, Dawes AT, Dobritsa AA. Changes in morphogen kinetics and pollen grain size are potential mechanisms of aberrant pollen aperture patterning in previously observed and novel mutants of Arabidopsis thaliana. PLoS Comput Biol. 2019 02; 15(2):e1006800.
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Henry C, Zheng NY, Huang M, Cabanov A, Rojas KT, Kaur K, Andrews SF, Palm AE, Chen YQ, Li Y, Hoskova K, Utset HA, Vieira MC, Wrammert J, Ahmed R, Holden-Wiltse J, Topham DJ, Treanor JJ, Ertl HC, Schmader KE, Cobey S, Krammer F, Hensley SE, Greenberg H, He XS, Wilson PC. Influenza Virus Vaccination Elicits Poorly Adapted B Cell Responses in Elderly Individuals. Cell Host Microbe. 2019 03 13; 25(3):357-366.e6.
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Miyauchi E, Matsuda T, Kiyotani K, Low SK, Hsu YW, Tsukita Y, Ichinose M, Sakurada A, Okada Y, Saito R, Nakamura Y. Significant differences in T cell receptor repertoires in lung adenocarcinomas with and without epidermal growth factor receptor mutations. Cancer Sci. 2019 Mar; 110(3):867-874.
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Kotsopoulos J, Lubinski J, Lynch HT, Tung N, Armel S, Senter L, Singer CF, Fruscio R, Couch F, Weitzel JN, Karlan B, Foulkes WD, Moller P, Eisen A, Ainsworth P, Neuhausen SL, Olopade O, Sun P, Gronwald J, Narod SA. Oophorectomy and risk of contralateral breast cancer among BRCA1 and BRCA2 mutation carriers. Breast Cancer Res Treat. 2019 Jun; 175(2):443-449.
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Metcalfe K, Lynch HT, Foulkes WD, Tung N, Olopade OI, Eisen A, Lerner-Ellis J, Snyder C, Kim SJ, Sun P, Narod SA. Oestrogen receptor status and survival in women with BRCA2-associated breast cancer. Br J Cancer. 2019 02; 120(4):398-403.
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