Results 121 to 130 of about 66,671 (164)
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Measurements of uridine diphosphate glucose and uridine diphosphate galactose — an appraisal
European Journal of Pediatrics, 1995The 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.
Henry N Kirkman
exaly +3 more sources
Archives of Biochemistry and Biophysics, 1975
Abstract Rat liver microsomes showed very active uridine diphosphate-galactose pyrophosphatase activity leading to the hydrolysis of uridine diphosphate-galactose into galactose1-phosphate and finally into galactose. The activity was observed in presence of buffers with wide ranges of pH.
Sailen Mookerjea, S Mookerjea
exaly +3 more sources
Abstract Rat liver microsomes showed very active uridine diphosphate-galactose pyrophosphatase activity leading to the hydrolysis of uridine diphosphate-galactose into galactose1-phosphate and finally into galactose. The activity was observed in presence of buffers with wide ranges of pH.
Sailen Mookerjea, S Mookerjea
exaly +3 more sources
Deficit of uridine diphosphate galactose in galactosaemia
Journal of Inherited Metabolic Disease, 1989SummaryThe levels of uridine diphosphate galactose (UDPGal) and uridine diphosphate glucose (UDPGlc) have been determined in liver autopsy samples, erythrocytes and cultured skin fibroblasts from galactosaemic patients and compared to non‐galactosaemic controls.
Francine R Kaufman, Y K Xu, G N Donnell
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Prenatal determination of uridine diphosphate galactose-4-epimerase activity
Prenatal Diagnosis, 1983AbstractA prenatal diagnosis has been performed in a pregnancy at risk for uridine diphosphate galactose‐4‐epimerase deficiency, an enzyme variation causing severe symptoms in the neonatal period similar to those of classical galactosaemia. The postnatal enzyme investigation, and uneventful development of the child, indicate that the prediction of an ...
J B Holton, R Macfaul
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Clinica Chimica Acta, 1995
Abstract A high performance liquid chromatography (HPLC) method has been developed for the measurement of uridine diphosphate galactose (UDPGal) and uridine diphosphate glucose (UDPGlc) in erythrocytes and cultured skin fibroblasts of normal controls and galactosemia patients.
Francine R Kaufman, Y K Xu, Won G Ng
exaly +3 more sources
Abstract A high performance liquid chromatography (HPLC) method has been developed for the measurement of uridine diphosphate galactose (UDPGal) and uridine diphosphate glucose (UDPGlc) in erythrocytes and cultured skin fibroblasts of normal controls and galactosemia patients.
Francine R Kaufman, Y K Xu, Won G Ng
exaly +3 more sources
Erythrocyte uridine diphosphate galactose-4-epimerase deficiency identified by newborn screening for galactosemia in the United States [PDF]
Eight infants (two whites and six blacks) with erythrocyte uridine diphosphate galactose-4-epimerase (epimerase) deficiency were identified in four newborn screening programs for galactosemia in the United States.
Miriam G Blitzer, Won G Ng
exaly +2 more sources
Purification and properties of uridine diphosphate galactose-4-epimerase from yeast
Biochemistry, 1968R A, Darrow, R, Rodstrom
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Uridine Diphosphate Galactose 4-Epimerase Deficiency
Archives of Pediatrics & Adolescent Medicine, 1980In 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
openaire +2 more sources

