12 relations: Enzyme, European Journal of Inorganic Chemistry, Genetic disorder, Journal of Clinical Investigation, Kidney failure, Molybdenum cofactor deficiency, Purine, The Lancet, Uric acid, Xanthine, Xanthine dehydrogenase, Xanthine oxidase.
Enzyme
Enzymes are macromolecular biological catalysts.
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European Journal of Inorganic Chemistry
The European Journal of Inorganic Chemistry is peer-reviewed scientific journal covering inorganic chemistry.
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Genetic disorder
A genetic disorder is a genetic problem caused by one or more abnormalities in the genome.
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Journal of Clinical Investigation
The Journal of Clinical Investigation (JCI) is a peer-reviewed biomedical research journal published by the American Society for Clinical Investigation (ASCI).
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Kidney failure
Kidney failure, also known as end-stage kidney disease, is a medical condition in which the kidneys no longer work.
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Molybdenum cofactor deficiency
Molybdenum cofactor deficiency is a rare human disease in which the absence of molybdenum cofactor leads to accumulation of toxic levels of sulphite and neurological damage.
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Purine
A purine is a heterocyclic aromatic organic compound that consists of a pyrimidine ring fused to an imidazole ring.
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The Lancet
The Lancet is a weekly peer-reviewed general medical journal.
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Uric acid
Uric acid is a heterocyclic compound of carbon, nitrogen, oxygen, and hydrogen with the formula C5H4N4O3.
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Xanthine
Xanthine (or; archaically xanthic acid) (3,7-dihydropurine-2,6-dione), is a purine base found in most human body tissues and fluids and in other organisms.
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Xanthine dehydrogenase
Xanthine dehydrogenase, also known as XDH, is a protein that, in humans, is encoded by the XDH gene.
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Xanthine oxidase
Xanthine oxidase (XO, sometimes XAO) is a form of xanthine oxidoreductase, a type of enzyme that generates reactive oxygen species.
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Redirects here:
Xanthine oxidase deficiency, Xanthine oxydase deficiency.