tyrosine has been researched along with Ornithine Carbamoyltransferase Deficiency Disease 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 |
|---|---|
| Lambert, M; Qureshi, IA; Rajalakshmi, S; Rao, PM; Sarma, DS; Vasudevan, S | 1 |
| Hoshide, R; Kato, H; Mastuda, I; Matsuura, T; Mori, M; Nishiyori, A; Tananari, Y; Yoshino, M | 1 |
| Horwich, AL | 1 |
1 review(s) available for tyrosine and Ornithine Carbamoyltransferase Deficiency Disease
| Article | Year |
|---|---|
Inherited hepatic enzyme defects as candidates for liver-directed gene therapy.
Topics: Animals; DNA; Female; Genes, Viral; Genetic Therapy; Humans; Hydrolases; Liver Diseases; Liver Transplantation; Male; Mice; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Prognosis; Tyrosine | 1991 |
2 other study(ies) available for tyrosine and Ornithine Carbamoyltransferase Deficiency Disease
| Article | Year |
|---|---|
Nucleotide pool imbalances in the livers of patients with urea cycle disorders associated with increased levels of orotic aciduria.
Topics: Adenine Nucleotides; Carbamoyl-Phosphate Synthase (Ammonia); Humans; Liver; Metabolism, Inborn Errors; Nucleotides; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Tyrosine; Uracil Nucleotides; Urea | 1995 |
Y55D mutation in ornithine transcarbamylase associated with late-onset hyperammonemia in a male.
Topics: Age of Onset; Amino Acid Substitution; Ammonia; Animals; Aspartic Acid; COS Cells; DNA; DNA Mutational Analysis; Fatal Outcome; Humans; Male; Middle Aged; Mutation; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Point Mutation; Polymorphism, Single-Stranded Conformational; RNA, Messenger; Tyrosine | 1998 |