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Uridine diphosphate glucose pyrophosphorylase. II.

open access: yesThe Journal of biological chemistry, 1969
S, Levine   +3 more
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Preparation of uridine diphosphogalactose and uridine diphosphate

Analytical Biochemistry, 1964
Abstract A procedure for the production of UDP-Gal and UDP on a preparative scale has been elaborated using a bacterial mutant which accumulates UDP-Gal in the presence of galactose. This method provides several possibilities for labeling these compounds with radioactive isotopes.
A E, SHEDLOVSKY, H A, BOYE, S, BRENNER
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Uridine diphosphate glucuronosyltransferase 1A1

Xenobiotica, 2019
The role that the phase-II reaction, glucuronidation, plays in the biotransformation of endo and xenobiotics is discussed with particular emphasis given to the UGT1A1 isoenzyme. This individual isoenzyme is responsible for both the mono and di-glucuronidation of bilirubin together with the glucuronidation of a number of xenobiotics of clinical interest
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Measurements of uridine diphosphate glucose and uridine diphosphate galactose — an appraisal

European Journal of Pediatrics, 1995
The recent disproof of a major deficiency of uridine diphosphate galactose in galactosemia should not lead investigators to assume either that enzymatic methods are unreliable for uridine sugar assays or that a defect in galactosylation in galactosemia has been excluded.
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[107] Isolation of uridine diphosphate glucose, uridine diphosphate acetylglucosamine, and guanosine diphosphate mannose

1963
Publisher Summary This chapter describes the isolation of uridine diphosphate glucose, uridine diphosphate acetylglucosamine, and guanosine diphosphate mannose. The basic principle is that alcoholic extract from toluene-autolyzed yeast is fractionated on anion-exchange columns.
Luis F. Leloir, Enrico Cabib
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Uridine Diphosphate Galactose 4-Epimerase Deficiency

Archives of Pediatrics & Adolescent Medicine, 1980
In addition to the galactosemias associated with galactose-1-phosphate uridylyltransferase and galactokinase deficiency, uridine diphosphate (UDP) galactose 4-epimerase deficiency is a third disorder of galactose metabolism characterized by the inability to epimerize UDPgalactose and UDPglucose.
Y, Ichiba, N, Namba, H, Misumi
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