"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
|
MeSH Number(s) |
D02.654.692.300 D02.948.594.310
|
Concept/Terms |
Ethylnitrosourea- Ethylnitrosourea
- Nitrosoethylurea
- N-Ethyl-N-nitrosourea
- N Ethyl N nitrosourea
|
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.
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Year | Major Topic | Minor Topic | Total |
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1999 | 0 | 1 | 1 |
2003 | 0 | 1 | 1 |
2004 | 0 | 2 | 2 |
2006 | 1 | 0 | 1 |
2009 | 1 | 0 | 1 |
2013 | 0 | 1 | 1 |
2015 | 0 | 1 | 1 |
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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Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms. Hum Mol Genet. 2016 07 15; 25(14):3011-3028.
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An ultra-dense library resource for rapid deconvolution of mutations that cause phenotypes in Escherichia coli. Nucleic Acids Res. 2016 Mar 18; 44(5):e41.
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An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions. PLoS One. 2013; 8(2):e57460.
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A missense mutation in LRR8 of RXFP2 is associated with cryptorchidism. Mamm Genome. 2010 Oct; 21(9-10):442-9.
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Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin. PLoS Genet. 2009 Dec; 5(12):e1000759.
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Polymorphisms of phase II xenobiotic-metabolizing and DNA repair genes and in vitro N-ethyl-N-nitrosourea-induced O6-ethylguanine levels in human lymphocytes. Mutat Res. 2007 Mar 05; 627(2):146-57.
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Point mutations in the melanocortin-4 receptor cause variable obesity in mice. Mamm Genome. 2006 Dec; 17(12):1162-71.
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l7Rn6 encodes a novel protein required for clara cell function in mouse lung development. Genetics. 2006 Jan; 172(1):389-99.
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A novel mouse model of hypogonadotrophic hypogonadism: N-ethyl-N-nitrosourea-induced gonadotropin-releasing hormone receptor gene mutation. Mol Endocrinol. 2005 Apr; 19(4):972-81.
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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.