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uric acid and Electron Transfer Flavoprotein Alpha Subunit Deficiency

uric acid has been researched along with Electron Transfer Flavoprotein Alpha Subunit Deficiency in 1 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 (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Westermann, CM1
Dorland, L1
van Diggelen, OP1
Schoonderwoerd, K1
Bierau, J1
Waterham, HR1
van der Kolk, JH1

Other Studies

1 other study available for uric acid and Electron Transfer Flavoprotein Alpha Subunit Deficiency

ArticleYear
Decreased oxidative phosphorylation and PGAM deficiency in horses suffering from atypical myopathy associated with acquired MADD.
    Molecular genetics and metabolism, 2011, Volume: 104, Issue:3

    Topics: Animals; Aspartate Aminotransferases; Base Sequence; Creatine; Creatine Kinase; DNA Primers; Female;

2011