uric acid has been researched along with Abnormalities, Sex Chromosome in 6 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 | 6 (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 |
---|---|
Thomson, WH | 1 |
Smith, I | 1 |
Nakajima, H | 1 |
Tajima, K | 1 |
Nakajima, T | 1 |
Iida, S | 1 |
Sumi, S | 1 |
Kono, N | 1 |
Moriwaki, K | 1 |
Nonaka, K | 1 |
Tarui, S | 1 |
Emmerson, BT | 1 |
DeMars, R | 1 |
Sarto, G | 1 |
Felix, JS | 1 |
Benke, P | 1 |
Dancis, J | 1 |
Cox, RP | 1 |
Berman, PH | 1 |
Jansen, V | 1 |
Balis, ME | 1 |
Becker, MH | 1 |
Wallin, JK | 1 |
1 trial available for uric acid and Abnormalities, Sex Chromosome
Article | Year |
---|---|
X-linked recessive (Duchenne) muscular dystrophy (DMD) and purine metabolism: effects of oral allopurinol and adenylate.
Topics: Adenosine Monophosphate; Administration, Oral; Adolescent; Allopurinol; Child; Child, Preschool; Cli | 1978 |
5 other studies available for uric acid and Abnormalities, Sex Chromosome
Article | Year |
---|---|
Renal hypouricaemia in a patient with 48,XXYY syndrome.
Topics: Adult; Humans; Kidney Diseases; Male; Sex Chromosome Aberrations; Syndrome; Uric Acid | 1986 |
Metabolic implications of the Lesch-Nyhan syndrome.
Topics: Athetosis; Gout; Humans; Intellectual Disability; Lesch-Nyhan Syndrome; Mass Screening; Purine-Pyrim | 1972 |
Lesch-Nyhan mutation: prenatal detection with amniotic fluid cells.
Topics: Amniotic Fluid; Autoradiography; Culture Techniques; Diseases in Twins; Female; Fetal Diseases; Gest | 1969 |
Cell population density and phenotypic expression of tissue culture fibroblasts from heterozygotes of Lesch-Nyhan's disease (inosinate pyrophosphorylase deficiency).
Topics: Adenine; Autoradiography; Cell Line; Culture Techniques; Female; Fibroblasts; Heterozygote; Humans; | 1969 |
Congenital hyperuricosuria. Associated radiologic features.
Topics: Cerebral Palsy; Child; Finger Injuries; Gout; Hip Dislocation; Humans; Intellectual Disability; Male | 1968 |