ethylnitrosourea has been researched along with BH4 Deficiency in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chang, TM; Safos, S | 1 |
| Blain, F; Chang, TM; Heft, R; Peevers, R; Sarkissian, CN; Scriver, CR; Shao, Z; Su, H | 1 |
| Bode, VC; Dove, WF; McDonald, JD; Shedlovsky, A | 1 |
3 other study(ies) available for ethylnitrosourea and BH4 Deficiency
| Article | Year |
|---|---|
Enzyme replacement therapy in ENU2 phenylketonuric mice using oral microencapsulated phenylalanine ammonia-lyase: a preliminary report.
Topics: Administration, Oral; Animals; Collodion; Drug Compounding; Ethylnitrosourea; Feasibility Studies; Fungal Proteins; Humans; Mice; Mice, Mutant Strains; Mutagenesis; Phenylalanine Ammonia-Lyase; Phenylalanine Hydroxylase; Phenylketonurias; Rats; Rhodotorula; Species Specificity | 1995 |
A different approach to treatment of phenylketonuria: phenylalanine degradation with recombinant phenylalanine ammonia lyase.
Topics: Animals; Basidiomycota; Cloning, Molecular; Disease Models, Animal; Escherichia coli; Ethylnitrosourea; Humans; Injections, Intraperitoneal; Mice; Phenylalanine; Phenylalanine Ammonia-Lyase; Phenylketonurias; Recombinant Proteins | 1999 |
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 |