Xanthinuria, an inborn error (or deviation) of metabolism.
about
Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuriaDrosophila tools and assays for the study of human diseasesThe housekeeping gene xanthine oxidoreductase is necessary for milk fat droplet enveloping and secretion: gene sharing in the lactating mammary glandHeberden oration 1979: human aberrations of purine metabolism and their significance for rheumatology.Prevalence and complications of hypouricemia in a general population: A large-scale cross-sectional study in JapanTHE STUDY OF PURINE UTILIZATION AND EXCRETION IN A XANTHINURIC MANStudy of purine metabolism in a xanthinuric female.Molybdenum: an essential trace element.Drosophila provides rapid modeling of renal development, function, and diseaseComplete deficiency of adenine phosphoribosyltransferase: a third case presenting as renal stones in a young child.Integrative physiology and functional genomics of epithelial function in a genetic model organism.The treatment of gout and disorders of uric acid metabolism with allopurinol.Association between xanthine dehydrogenase tag single nucleotide polymorphisms and essential hypertension.A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle.Structural and functional insights into the catalytic inactivity of the major fraction of buffalo milk xanthine oxidoreductase.Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.Urate excretion.Isolation and examination of urinary metabolites containing an aromatic system.Uric acid production with particular reference to the role of xanthine oxidase and its inhibition.The conversion of 4-hydroxypyrazolo[3,4-d]pyrimidine (allopurinol) into 4,6-dihroxypyrazolo[3,4-d]pyrimidine (Oxipurinol) in vivo in the absence of xanthine-oxen oxidoreductase.Metabolomic profiling of Drosophila using liquid chromatography Fourier transform mass spectrometry.Xanthinuria.Allopurinol in treatment of gout.3-Hydroxyanthranilic Acid, A Carcinogen Produced by Endogenous Metabolism
P2860
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P2860
Xanthinuria, an inborn error (or deviation) of metabolism.
description
1954 nî lūn-bûn
@nan
1954 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1954 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1954年の論文
@ja
1954年論文
@yue
1954年論文
@zh-hant
1954年論文
@zh-hk
1954年論文
@zh-mo
1954年論文
@zh-tw
1954年论文
@wuu
name
Xanthinuria, an inborn error (or deviation) of metabolism.
@ast
Xanthinuria, an inborn error (or deviation) of metabolism.
@en
Xanthinuria, an inborn error (or deviation) of metabolism.
@nl
type
label
Xanthinuria, an inborn error (or deviation) of metabolism.
@ast
Xanthinuria, an inborn error (or deviation) of metabolism.
@en
Xanthinuria, an inborn error (or deviation) of metabolism.
@nl
prefLabel
Xanthinuria, an inborn error (or deviation) of metabolism.
@ast
Xanthinuria, an inborn error (or deviation) of metabolism.
@en
Xanthinuria, an inborn error (or deviation) of metabolism.
@nl
P1433
P1476
Xanthinuria, an inborn error (or deviation) of metabolism.
@en
P2093
P304
P356
10.1016/S0140-6736(54)91257-X
P407
P577
1954-01-01T00:00:00Z