 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 |
|---|
| 1982 | 0 | 1 | 1 | | 1984 | 0 | 1 | 1 | | 1985 | 0 | 1 | 1 | | 1986 | 1 | 2 | 3 | | 1988 | 0 | 3 | 3 | | 1989 | 0 | 3 | 3 | | 1990 | 3 | 4 | 7 | | 1991 | 0 | 2 | 2 | | 1993 | 0 | 3 | 3 | | 1994 | 0 | 1 | 1 | | 1995 | 3 | 5 | 8 | | 1996 | 2 | 1 | 3 | | 1997 | 0 | 4 | 4 | | 1998 | 2 | 4 | 6 | | 1999 | 2 | 7 | 9 | | 2000 | 0 | 5 | 5 | | 2001 | 1 | 6 | 7 | | 2002 | 3 | 8 | 11 | | 2003 | 3 | 13 | 16 | | 2004 | 1 | 8 | 9 | | 2005 | 2 | 17 | 19 | | 2006 | 4 | 11 | 15 | | 2007 | 1 | 7 | 8 | | 2008 | 2 | 4 | 6 | | 2009 | 3 | 14 | 17 | | 2010 | 2 | 13 | 15 | | 2011 | 6 | 7 | 13 | | 2012 | 3 | 10 | 13 | | 2013 | 3 | 8 | 11 | | 2014 | 6 | 8 | 14 | | 2015 | 1 | 5 | 6 | | 2016 | 3 | 4 | 7 | | 2017 | 0 | 2 | 2 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Ishikawa H, Yoshikawa H, Izumikawa K, Miura Y, Taoka M, Nobe Y, Yamauchi Y, Nakayama H, Simpson RJ, Isobe T, Takahashi N. Poly(A)-specific ribonuclease regulates the processing of small-subunit rRNAs in human cells. Nucleic Acids Res. 2017 Apr 07; 45(6):3437-3447.
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Conley SM, Stuck MW, Watson JN, Naash MI. Rom1 converts Y141C-Prph2-associated pattern dystrophy to retinitis pigmentosa. Hum Mol Genet. 2017 Feb 01; 26(3):509-518.
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Singh K, Briggs JM. Functional Implications of the spectrum of BCL2 mutations in Lymphoma. Mutat Res Rev Mutat Res. 2016 Jul-Sep; 769:1-18.
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Ma Y, Wang J, Yu Y, Schwartz RJ. PKG-1a mediates GATA4 transcriptional activity. Cell Signal. 2016 Jun; 28(6):585-94.
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West JD, Carrier EJ, Bloodworth NC, Schroer AK, Chen P, Ryzhova LM, Gladson S, Shay S, Hutcheson JD, Merryman WD. Serotonin 2B Receptor Antagonism Prevents Heritable Pulmonary Arterial Hypertension. PLoS One. 2016; 11(2):e0148657.
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Yamamoto Y, Wang X, Bertrand D, Kern F, Zhang T, Duleba M, Srivastava S, Khor CC, Hu Y, Wilson LH, Blaszyk H, Rolshud D, Teh M, Liu J, Howitt BE, Vincent M, Crum CP, Nagarajan N, Ho KY, McKeon F, Xian W. Mutational spectrum of Barrett's stem cells suggests paths to initiation of a precancerous lesion. Nat Commun. 2016 Jan 19; 7:10380.
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Stuck MW, Conley SM, Naash MI. PRPH2/RDS and ROM-1: Historical context, current views and future considerations. Prog Retin Eye Res. 2016 05; 52:47-63.
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Stuck MW, Conley SM, Naash MI. RDS Functional Domains and Dysfunction in Disease. Adv Exp Med Biol. 2016; 854:217-22.
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Conley SM, Whalen P, Lewin AS, Naash MI. Characterization of Ribozymes Targeting a Congenital Night Blindness Mutation in Rhodopsin Mutation. Adv Exp Med Biol. 2016; 854:509-15.
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Ramcharan R, Aleksic T, Kamdoum WP, Gao S, Pfister SX, Tanner J, Bridges E, Asher R, Watson AJ, Margison GP, Woodcock M, Repapi E, Li JL, Middleton MR, Macaulay VM. IGF-1R inhibition induces schedule-dependent sensitization of human melanoma to temozolomide. Oncotarget. 2015 Nov 24; 6(37):39877-90.
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