ethylnitrosourea has been researched along with Amino Acid Metabolism Disorders, Inborn in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, TH; Chen, YT; Huang, CC; Kao, HJ; Lin, WD; Sabbagha, NG; Tarn, WY; Tsai, FJ; Wu, JY; Yang, CF | 1 |
| Colwell, RE; Harding, CO; Lyne, PW; Pflanzer, DM; Williams, P; Wolff, JA | 1 |
| Bode, VC; Dove, WF; McDonald, JD; Shedlovsky, A | 1 |
| Bode, VC; Guenet, JL; McDonald, JD; Simon, D | 1 |
4 other study(ies) available for ethylnitrosourea and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
Alternative splicing in Acad8 resulting a mitochondrial defect and progressive hepatic steatosis in mice.
Topics: Acyl-CoA Dehydrogenase; Alternative Splicing; Amino Acid Metabolism, Inborn Errors; Animals; Base Sequence; Cold Temperature; Disease Models, Animal; Disease Progression; DNA Mutational Analysis; Ethylnitrosourea; Fatty Liver; Gene Expression Regulation, Enzymologic; Genetic Predisposition to Disease; Liver X Receptors; Male; Metabolomics; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Microscopy, Electron, Transmission; Mitochondria, Liver; Mitochondrial Swelling; Molecular Sequence Data; Mutagens; Mutation; Orphan Nuclear Receptors; Oxidoreductases Acting on CH-CH Group Donors; Phenotype; PPAR alpha; PPAR gamma; RNA, Messenger; Thermogenesis; Thermosensing | 2011 |
sar: a genetic mouse model for human sarcosinemia generated by ethylnitrosourea mutagenesis.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Ethylnitrosourea; Gas Chromatography-Mass Spectrometry; Mice; Mice, Mutant Strains; Mutagenesis; Oxidoreductases, N-Demethylating; Phenotype; Sarcosine; Sarcosine Dehydrogenase | 1992 |
The use of N-ethyl-N-nitrosourea to produce mouse models for human phenylketonuria and hyperphenylalaninemia.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Crosses, Genetic; Disease Models, Animal; Ethylnitrosourea; Female; Humans; Male; Mice; Mice, Mutant Strains; Mutation; Phenotype; Phenylalanine; Phenylketonurias | 1990 |
hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Chromosome Mapping; Crosses, Genetic; Ethylnitrosourea; Female; Genetic Linkage; Genotype; Male; Mice; Mice, Inbred Strains; Mice, Mutant Strains; Mutation; Pedigree; Phenotype; Phenylalanine | 1988 |