The effect of oxidized glutathione (GSSG) on human erythrocyte hexokinase activity.
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Adenosine Triphosphate↗
Biomedical subjects
E Beutler
Publications and source records attributed to E Beutler.
G-6PD Bangkok: a new variant found in congenital nonspherocytic hemolytic disease (CNHD).
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Anemia, Hemolytic, Congenital↗
Response of the fever of Hodgkin's disease to nitrogen mustard (NSC-762): an evaluation of its significance.
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Adolescent↗
The in vivo regeneration of red cell 2,3 diphosphoglyceric acid (DPG) after transfusion of stored blood.
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Anemia↗
Accurate measurement of oxidized glutathione content of human, rabbit, and rat red blood cells and tissues.
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Alkylation↗
Oxidized glutathione levels in erythrocytes of glucose-6-phosphate-dehydrogenase-deficient subjects.
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Alkylation↗
Electrophoretic abnormality in triosephosphate isomerase deficiency.
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Deficiency Diseases↗
Prolonged remissions in acute myelocytic leukemia in adults.
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Adolescent↗
Electrophoretic study of glutathione reductase in human erythrocytes and leucocytes.
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Dihydrolipoamide Dehydrogenase↗
Hexokinase isoenzymes in human erythrocytes.
The electrophoretic mobility of hexokinase from human erythrocytes and other tissues was studied with a new method that depends on the fluorescence of reduced nicotinamide-adenine dinucleotide phosphate for detecting enzyme activity on starch gel. The hexokinase of cord-blood erythrocytes has slightly different electrophoretic properties from that of adult red cells. Type I enzyme is split into type I(A) and type I(F); the latter is more intense in cord blood; in hemolyzates of adult blood, the activity of the two bands is usually about equal. No type II enzyme was found in cord blood. The double type I band was present in red cells from adult rabbits.
Animals↗
Hallmarks of hypochromic anemias.
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Adolescent↗
Abnormalities of glycolysis (HMP shunt).
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Adenosine Triphosphate↗
Permeability of normal and cataractous rabbit lenses to glutathione.
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Animals↗
The utilization of glucose by normal glucose-6-phosphate dehydrogenase and by glucose-6-phosphate dehydrogenase Mediterranean.
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Bicarbonates↗
Special modifications of the fluorescent screening method for glucose-6-phosphate dehydrogenase deficiency.
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Buffers↗
Galactosemia in a 24-year-old man; detection by enzyme studies.
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Adult↗
Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital nonspherocytic hemolytic disease.
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Adolescent↗