Ethylnitrosourea
"Ethylnitrosourea" 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.
A nitrosourea compound with alkylating, carcinogenic, and mutagenic properties.
Descriptor ID |
D005038
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MeSH Number(s) |
D02.654.692.300 D02.948.594.310
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Concept/Terms |
Ethylnitrosourea- Ethylnitrosourea
- Nitrosoethylurea
- N-Ethyl-N-nitrosourea
- N Ethyl N nitrosourea
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Below are MeSH descriptors whose meaning is more general than "Ethylnitrosourea".
Below are MeSH descriptors whose meaning is more specific than "Ethylnitrosourea".
This graph shows the total number of publications written about "Ethylnitrosourea" by people in this website by year, and whether "Ethylnitrosourea" 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 |
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1983 | 1 | 0 | 1 | 1987 | 0 | 1 | 1 | 1988 | 1 | 0 | 1 | 2000 | 2 | 0 | 2 | 2001 | 1 | 0 | 1 | 2002 | 3 | 0 | 3 | 2004 | 0 | 1 | 1 | 2005 | 2 | 0 | 2 | 2010 | 0 | 1 | 1 | 2012 | 0 | 1 | 1 | 2013 | 0 | 2 | 2 | 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Ethylnitrosourea" by people in Profiles.
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Burnicka-Turek O, Steimle JD, Huang W, Felker L, Kamp A, Kweon J, Peterson M, Reeves RH, Maslen CL, Gruber PJ, Yang XH, Shendure J, Moskowitz IP. Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms. Hum Mol Genet. 2016 07 15; 25(14):3011-3028.
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Stoddart A, Wang J, Fernald AA, Karrison T, Anastasi J, Le Beau MM. Cell intrinsic and extrinsic factors synergize in mice with haploinsufficiency for Tp53, and two human del(5q) genes, Egr1 and Apc. Blood. 2014 Jan 09; 123(2):228-38.
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Traka M, Millen KJ, Collins D, Elbaz B, Kidd GJ, Gomez CM, Popko B. WDR81 is necessary for purkinje and photoreceptor cell survival. J Neurosci. 2013 Apr 17; 33(16):6834-44.
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Grdina DJ, Murley JS, Miller RC, Mauceri HJ, Sutton HG, Thirman MJ, Li JJ, Woloschak GE, Weichselbaum RR. A manganese superoxide dismutase (SOD2)-mediated adaptive response. Radiat Res. 2013 Feb; 179(2):115-24.
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Kamp A, Peterson MA, Svenson KL, Bjork BC, Hentges KE, Rajapaksha TW, Moran J, Justice MJ, Seidman JG, Seidman CE, Moskowitz IP, Beier DR. Genome-wide identification of mouse congenital heart disease loci. Hum Mol Genet. 2010 Aug 15; 19(16):3105-13.
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Douglas DS, Popko B. Mouse forward genetics in the study of the peripheral nervous system and human peripheral neuropathy. Neurochem Res. 2009 Jan; 34(1):124-37.
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Traka M, Seburn KL, Popko B. Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit. Mamm Genome. 2006 Sep; 17(9):950-5.
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Katayama K, Ueno M, Yamauchi H, Nakayama H, Doi K. Microarray analysis of genes in fetal central nervous system after ethylnitrosourea administration. Birth Defects Res B Dev Reprod Toxicol. 2005 Jun; 74(3):255-60.
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Katayama K, Ueno M, Yamauchi H, Nagata T, Nakayama H, Doi K. Ethylnitrosourea induces neural progenitor cell apoptosis after S-phase accumulation in a p53-dependent manner. Neurobiol Dis. 2005 Feb; 18(1):218-25.
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Baron BW, Anastasi J, Montag A, Huo D, Baron RM, Karrison T, Thirman MJ, Subudhi SK, Chin RK, Felsher DW, Fu YX, McKeithan TW, Baron JM. The human BCL6 transgene promotes the development of lymphomas in the mouse. Proc Natl Acad Sci U S A. 2004 Sep 28; 101(39):14198-203.
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