carbamyl phosphate has been researched along with Inborn Urea Cycle Disorder in 3 studies
Carbamyl Phosphate: The monoanhydride of carbamic acid with PHOSPHORIC ACID. It is an important intermediate metabolite and is synthesized enzymatically by CARBAMYL-PHOSPHATE SYNTHASE (AMMONIA) and CARBAMOYL-PHOSPHATE SYNTHASE (GLUTAMINE-HYDROLYZING).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Ishikawa, R | 1 |
| Sugimoto, T | 1 |
| Abe, T | 1 |
| Ohno, N | 1 |
| Tazuma, T | 1 |
| Giga, M | 1 |
| Naito, H | 1 |
| Kono, T | 1 |
| Nomura, E | 1 |
| Hara, K | 1 |
| Yorifuji, T | 1 |
| Yamawaki, T | 1 |
| Choi, Y | 1 |
| Oh, A | 1 |
| Lee, Y | 1 |
| Kim, GH | 1 |
| Choi, JH | 1 |
| Yoo, HW | 1 |
| Lee, BH | 1 |
| Kok, CY | 1 |
| Cunningham, SC | 1 |
| Kuchel, PW | 1 |
| Alexander, IE | 1 |
3 other studies available for carbamyl phosphate and Inborn Urea Cycle Disorder
| Article | Year |
|---|---|
A 36-year-old Man with Repeated Short-term Transient Hyperammonemia and Impaired Consciousness with a Confirmed Carbamoyl Phosphate Synthase 1 Gene Monoallelic Mutation.
Topics: Adult; Carbamoyl-Phosphate Synthase (Ammonia); Carbamoyl-Phosphate Synthase I Deficiency Disease; Ca | 2022 |
Unfavorable clinical outcomes in patients with carbamoyl phosphate synthetase 1 deficiency.
Topics: Carbamoyl-Phosphate Synthase (Ammonia); Carbamoyl-Phosphate Synthase I Deficiency Disease; Carbamyl | 2022 |
Insights into Gene Therapy for Urea Cycle Defects by Mathematical Modeling.
Topics: Carbamyl Phosphate; Computer Simulation; Genetic Therapy; Humans; Models, Biological; Ornithine Carb | 2019 |