uric acid has been researched along with Metal Metabolism, Inborn Error in 3 studies
Uric Acid: An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
uric acid : An oxopurine that is the final oxidation product of purine metabolism.
6-hydroxy-1H-purine-2,8(7H,9H)-dione : A tautomer of uric acid having oxo groups at C-2 and C-8 and a hydroxy group at C-6.
7,9-dihydro-1H-purine-2,6,8(3H)-trione : An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Lee, HF | 1 |
| Hsu, CC | 1 |
| Chi, CS | 1 |
| Tsai, CR | 1 |
| Wu, LH | 1 |
| Jiang, Y | 1 |
| Hu, Y | 1 |
| Sass, JO | 1 |
| Kishikawa, M | 1 |
| Puttinger, R | 1 |
| Reiss, J | 1 |
| Erwa, W | 1 |
| Shimizu, A | 1 |
| Sperl, W | 1 |
3 other studies available for uric acid and Metal Metabolism, Inborn Error
| Article | Year |
|---|---|
Genotype-Phenotype Dissociation in Two Taiwanese Children with Molybdenum Cofactor Deficiency Caused by MOCS2 Mutation.
Topics: Child; Homozygote; Humans; Magnetic Resonance Imaging; Metal Metabolism, Inborn Errors; Movement Dis | 2022 |
[Molybdenum cofactor deficiency caused by
Topics: Carbon-Carbon Lyases; China; Humans; Infant, Newborn; Male; Metal Metabolism, Inborn Errors; Mutatio | 2021 |
Hypohomocysteinaemia and highly increased proportion of S-sulfonated plasma transthyretin in molybdenum cofactor deficiency.
Topics: Coenzymes; Female; Homocysteine; Humans; Infant, Newborn; Magnetic Resonance Imaging; Metal Metaboli | 2003 |