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uric acid and Abnormalities, Sex Chromosome

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.

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19906 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Thomson, WH1
Smith, I1
Nakajima, H1
Tajima, K1
Nakajima, T1
Iida, S1
Sumi, S1
Kono, N1
Moriwaki, K1
Nonaka, K1
Tarui, S1
Emmerson, BT1
DeMars, R1
Sarto, G1
Felix, JS1
Benke, P1
Dancis, J1
Cox, RP1
Berman, PH1
Jansen, V1
Balis, ME1
Becker, MH1
Wallin, JK1

Trials

1 trial available for uric acid and Abnormalities, Sex Chromosome

ArticleYear
X-linked recessive (Duchenne) muscular dystrophy (DMD) and purine metabolism: effects of oral allopurinol and adenylate.
    Metabolism: clinical and experimental, 1978, Volume: 27, Issue:2

    Topics: Adenosine Monophosphate; Administration, Oral; Adolescent; Allopurinol; Child; Child, Preschool; Cli

1978

Other Studies

5 other studies available for uric acid and Abnormalities, Sex Chromosome

ArticleYear
Renal hypouricaemia in a patient with 48,XXYY syndrome.
    Postgraduate medical journal, 1986, Volume: 62, Issue:725

    Topics: Adult; Humans; Kidney Diseases; Male; Sex Chromosome Aberrations; Syndrome; Uric Acid

1986
Metabolic implications of the Lesch-Nyhan syndrome.
    Australian and New Zealand journal of medicine, 1972, Volume: 2, Issue:1

    Topics: Athetosis; Gout; Humans; Intellectual Disability; Lesch-Nyhan Syndrome; Mass Screening; Purine-Pyrim

1972
Lesch-Nyhan mutation: prenatal detection with amniotic fluid cells.
    Science (New York, N.Y.), 1969, Jun-13, Volume: 164, Issue:3885

    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).
    Biochemical genetics, 1969, Volume: 3, Issue:6

    Topics: Adenine; Autoradiography; Cell Line; Culture Techniques; Female; Fibroblasts; Heterozygote; Humans;

1969
Congenital hyperuricosuria. Associated radiologic features.
    Radiologic clinics of North America, 1968, Volume: 6, Issue:2

    Topics: Cerebral Palsy; Child; Finger Injuries; Gout; Hip Dislocation; Humans; Intellectual Disability; Male

1968