arginine has been researched along with ethylnitrosourea in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Grosse, J; Nehls, MC; Peters, T; Popp, A; Russ, A; Schlueter, V; Sedlmeier, R; Thaete, C; Wolf, S | 1 |
| Beier, DR; Cockroft, JL; Goldowitz, D; Matera, I; Moran, JL; Pavan, WJ | 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 |
3 other study(ies) available for arginine and ethylnitrosourea
| Article | Year |
|---|---|
A mouse model for cystinuria type I.
Topics: Amino Acid Sequence; Amino Acid Transport Systems, Basic; Amino Acids; Animals; Arginine; Carrier Proteins; Chromosome Mapping; Cystine; Cystinuria; Disease Models, Animal; Ethylnitrosourea; Female; Genotype; Lysine; Male; Membrane Glycoproteins; Mice; Mice, Inbred C3H; Mice, Knockout; Molecular Sequence Data; Mutagenesis; Mutation; Ornithine; Phenotype; Sequence Homology, Amino Acid; Urinary Bladder Calculi; Urinary Calculi | 2003 |
A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 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 |
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 |