uric acid has been researched along with Gangliosidoses in 2 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.
Gangliosidoses: A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Sandhoff, K | 1 |
| Persaud, TV | 1 |
1 review available for uric acid and Gangliosidoses
| Article | Year |
|---|---|
Prenatal diagnosis and its pathologic confirmation.
Topics: alpha-Fetoproteins; Amniocentesis; Amniotic Fluid; Chromosome Aberrations; Chromosome Disorders; Cre | 1976 |
1 other study available for uric acid and Gangliosidoses
| Article | Year |
|---|---|
[Molecular bases of congenital metabolic disorders].
Topics: Ascorbic Acid Deficiency; Biological Transport; Female; Gangliosidoses; Glucose-6-Phosphatase; Hemop | 1982 |