Page last updated: 2024-08-17

histidine and ethylnitrosourea

histidine has been researched along with ethylnitrosourea in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mandel, R; Ryser, HJ1
Ohta, T; Watanabe-Akanuma, M; Yamagata, H1
Beier, DR; Cockroft, JL; Goldowitz, D; Matera, I; Moran, JL; Pavan, WJ1
Gekakis, N; Lloyd, DJ; Wheeler, MC1

Other Studies

4 other study(ies) available for histidine and ethylnitrosourea

ArticleYear
Mechanisms of synergism in the mutagenicity of cadmium and N-methyl-N-nitrosourea in Salmonella typhimurium: the effect of pH.
    Mutation research, 1987, Volume: 176, Issue:1

    Topics: Cadmium; Dose-Response Relationship, Drug; Drug Synergism; Ethylnitrosourea; Histidine; Hydrogen-Ion Concentration; Hydrolysis; Methylnitrosourea; Mutagenicity Tests; Salmonella typhimurium

1987
A comparison of mutation spectra detected by the Escherichia coli lac(+) reversion assay and the Salmonella typhimurium his(+) reversion assay.
    Mutagenesis, 2000, Volume: 15, Issue:4

    Topics: 2-Aminopurine; 4-Nitroquinoline-1-oxide; Alkylating Agents; Azacitidine; Benzene Derivatives; Cytidine; DNA; DNA Mutational Analysis; Dose-Response Relationship, Drug; Escherichia coli; Ethylnitrosourea; Formaldehyde; Furans; Furylfuramide; Glyoxal; Histidine; Lac Operon; Methylnitronitrosoguanidine; Mutagenicity Tests; Mutagens; Oxidants; Phosmet; Plasmids; Point Mutation; Salmonella typhimurium; Sodium Azide; tert-Butylhydroperoxide; Uracil

2000
A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 3.
    Pigment cell research, 2007, Volume: 20, Issue:3

    Topics: Animals; Arginine; Chromosome Mapping; Disease Models, Animal; Endothelin-3; Ethylnitrosourea; Gene Expression Regulation; Genetic Linkage; Histidine; Humans; Mice; Mutation; Pigmentation; Point Mutation; Waardenburg Syndrome

2007
A point mutation in Sec61alpha1 leads to diabetes and hepatosteatosis in mice.
    Diabetes, 2010, Volume: 59, Issue:2

    Topics: Amino Acid Substitution; Animals; Diabetes Mellitus; DNA Primers; Ethylnitrosourea; Fatty Liver; Heterozygote; Histidine; Homozygote; Humans; Immunohistochemistry; Islets of Langerhans; Liver; Membrane Proteins; Mice; Mice, Inbred C57BL; Mutagenesis; Pancreas; Phenotype; Point Mutation; Reverse Transcriptase Polymerase Chain Reaction; Risk Factors; SEC Translocation Channels; Tyrosine

2010