ethylnitrosourea has been researched along with cysteine in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (33.33) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (66.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Kirk, MC; Ludlum, DB; Niu, T; Yu, D | 1 |
Furuse, T; Gondo, Y; Hattori, K; Hirose, R; Kanda, T; Kaneda, H; Kobayashi, K; Kushida, T; Masuya, H; Miura, I; Nakanishi, K; Noda, T; Seno, N; Sezutsu, H; Shibukawa, Y; Toki, S; Wada, Y; Wakana, S; Yamada, I; Yuasa, S | 1 |
Fukumura, R; Furuichi, T; Gondo, Y; Ichimura, S; Ikegawa, S; Murata, T; Sasaki, S | 1 |
3 other study(ies) available for ethylnitrosourea and cysteine
Article | Year |
---|---|
Synthesis of the prototype DNA-protein cross-link, 1-(guan-1-yl)-2-(cysteine-S-yl)ethane, and its role in the reactions of the haloethylnitrosoureas.
Topics: Cross-Linking Reagents; Cysteine; DNA; DNA Damage; Drug Interactions; Ethylnitrosourea; Guanine; Spectrophotometry, Ultraviolet | 1993 |
Phenotypic characterization of a new Grin1 mutant mouse generated by ENU mutagenesis.
Topics: Alkylating Agents; Amino Acid Sequence; Analysis of Variance; Animals; Arginine; Calcium; Carrier Proteins; Cells, Cultured; Central Nervous System Stimulants; Cerebral Cortex; Chromosome Mapping; Cysteine; Embryo, Mammalian; Ethylnitrosourea; Exploratory Behavior; Gene Expression Regulation; Male; Methylphenidate; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Transgenic; Mitogen-Activated Protein Kinase 1; Motor Activity; Mutagenesis; Mutation, Missense; N-Methylaspartate; Nerve Tissue Proteins; Neurons; Phenazines; Phenotype; Proto-Oncogene Proteins c-fos; Receptors, N-Methyl-D-Aspartate | 2010 |
An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes.
Topics: Amino Acid Substitution; Animals; Camurati-Engelmann Syndrome; Cysteine; Ethylnitrosourea; Female; Gene Library; Genetic Association Studies; HEK293 Cells; Humans; Male; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Molecular Targeted Therapy; Mutation, Missense; Phenotype; Serine; Signal Transduction; Transforming Growth Factor beta1 | 2017 |