Page last updated: 2024-10-20

uric acid and Genetic Diseases

uric acid has been researched along with Genetic Diseases 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 Excerpts

ExcerptRelevanceReference
"The content of uric acid was measured in the blood of patients suffering from retinitis pigmentosa, as well as in the blood, retina, brain, liver and urine of rats with inherited retinal degeneration in the course of postnatal development."7.66[Changes in the blood uric acid levels in patients with retinitis pigmentosa and in rats with hereditary retinal degeneration]. ( Chusova, GG; Eliseeva, RF; Ostapenko, IA; Shabanova, ME, 1982)
"The content of uric acid was measured in the blood of patients suffering from retinitis pigmentosa, as well as in the blood, retina, brain, liver and urine of rats with inherited retinal degeneration in the course of postnatal development."3.66[Changes in the blood uric acid levels in patients with retinitis pigmentosa and in rats with hereditary retinal degeneration]. ( Chusova, GG; Eliseeva, RF; Ostapenko, IA; Shabanova, ME, 1982)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19905 (83.33)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Krysiak, R1
Kowalcze, K1
Okopień, B1
Vinay, P1
Gattereau, A1
Moulin, B1
Gougoux, A1
Lemieux, G1
Laskarzewski, PM1
Khoury, P1
Morrison, JA1
Kelly, K1
Glueck, CJ1
Chusova, GG1
Ostapenko, IA1
Shabanova, ME1
Eliseeva, RF1
Stefanovich, V1
Dipalma, JR1

Other Studies

6 other studies available for uric acid and Genetic Diseases

ArticleYear
Cardiometabolic profile of young women with hypoprolactinemia.
    Endocrine, 2022, Volume: 78, Issue:1

    Topics: C-Reactive Protein; Cabergoline; Cardiovascular Diseases; Carotid Intima-Media Thickness; Female; Fi

2022
Normal urate transport into erythrocytes in familial renal hypouricemia and in the Dalmatian dog.
    Canadian Medical Association journal, 1983, Mar-01, Volume: 128, Issue:5

    Topics: Animals; Biological Transport; Carrier Proteins; Dogs; Erythrocyte Membrane; Erythrocytes; Genetic D

1983
Familial hyper- and hypouricemias in random and hyperlipidemic recall cohorts: the Princeton School District Family Study.
    Metabolism: clinical and experimental, 1983, Volume: 32, Issue:3

    Topics: Adolescent; Adult; Age Factors; Aged; Child; Child, Preschool; Female; Genetic Diseases, Inborn; Hum

1983
[Changes in the blood uric acid levels in patients with retinitis pigmentosa and in rats with hereditary retinal degeneration].
    Biulleten' eksperimental'noi biologii i meditsiny, 1982, Volume: 94, Issue:11

    Topics: Animals; Brain; Disease Models, Animal; Genetic Diseases, Inborn; Genetic Testing; Humans; Liver; Ra

1982
The role of biochemistry in drug research.
    Current medical research and opinion, 1980, Volume: 6, Issue:7

    Topics: Biochemical Phenomena; Biochemistry; Biology; Brain; Carbon Radioisotopes; Deoxyglucose; Drug Indust

1980
Pharmacogenetics.
    American family physician, 1974, Volume: 9, Issue:4

    Topics: Abnormalities, Drug-Induced; Allopurinol; Barbiturates; Chromosome Aberrations; Drug-Related Side Ef

1974