Results 121 to 130 of about 3,031 (182)
ZOOLOGICAL SCIENCE, 1998 The developmental and the tissue-specific expression of glucosephosphate isomerase (GPI), lactate dehydrogenase (LDH) and malate dehydrogenase (MDH) multilocus isozymes were analyzed in samples of Leuciscus cephalus and the adult patterns compared with those of 8 additional Italian cyprinid species: Alburnus alburnus alborella, Chondrostoma genei, L ...
S, Manaresi, B, Mantovani, F, Zaccanti
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Comparative Biochemistry and Physiology Part B: Comparative Biochemistry, 1989 1. The isozymes of lactate dehydrogenase (LDH), malate dehydrogenase (MDH) and glucose-phosphate isomerase (GPI) of three species of Italian ictalurids: Ictalurus sp., I. nebulosus marmoratus, and I. punctatus, were analyzed. 2. Isoelectric focusing (IEF) was applied to polyacrylamide gel plates, and the isozymes revealed by means of specific ...
Fulvia Basaglia
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Comparative Biochemistry and Physiology Part B: Comparative Biochemistry, 1989 1. The present paper reports some aspects of the isozymes of LDH, MDH and GPI in fish. 2. In Petromyzontiformes LDH is encoded by a single Ldh-A gene locus. In Myxiniformes and in most vertebrates LDH is encoded by two gene loci, A and B. A third Ldh-C locus is characteristic of the bony fishes Actinopterygii. 3.
Fulvia Basaglia
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British Journal of Haematology, 1971 Summary. A new haemolytic syndrome associated with the combination of genetically determined glucosephosphate isomerase and glucose‐6‐phosphate dehydrogenase deficiency of the erythrocytes was demonstrated in a German family. The propositus (a male), homozygous for the glucosephosphate isomerase deficiency and hemizygous for the glucose‐6‐phosphate ...
W, Schröter +4 more
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Blood Cells, Molecules, and Diseases, 2003 Glucosephosphate isomerase (GPI) deficiency in humans is an autosomal recessive disorder, which results in nonspherocytic hemolytic anemia of variable clinical expression. A 4-year-old female with severe congenital hemolytic anemia had low red cell GPI activity of 15.5 IU/g Hb (50% of normal mean) indicating GPI deficiency.
Julia L, Clarke +9 more
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Arkhiv anatomii, gistologii i embriologii, 1977 A high intensity of the reactions to lactate dehydrogenase and glucous-6-phosphate dehydrogenase was demonstrated histochemically in the neural anlage of the chick embryos after 15, 20, 24, 30, 44, 48 and 72 hours of incubation. At early stages of the development cranio-caudal gradient of enzymatic reactions was distinctly traced.
R M Markov
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Human Genetics, 1981 A severe hemolytic crisis was observed in a 5-year-old boy of Italian origin. Analysis of his hemolysate revealed a hemizygous deficiency of glucose-6-phosphate dehydrogenase (G6PD) and a heterozygous deficiency of glucosephosphate isomerase (GPI). According to the literature this is the fourth family with a combined deficiency of these two enzymes ...
H, Arnold +3 more
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[Kinetic properties of partially purified glucosephosphate dehydrogenase of human erythrocytes].
Voprosy meditsinskoi khimii, 1977 Partially purified glucose-6-phosphate dehydrogenase was isolated from small amounts of human erythrocytes (15-20 ml). The Km value for glucose-6-phosphate was 35.0 +/- 3.0 micronM, the Km for NADP was 4.27 +/- 0.3 micronM. The optimal activity of the enzyme was at pH 9.0.
A I, Batishchev +2 more
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Comparative Biochemistry and Physiology Part B: Comparative Biochemistry, 1989 1. The expression of alleles encoding the enzymes sorbitol dehydrogenase (SDH; EC 1.1.1.14) and glucosephosphate isomerase (GPI; EC 5.3.1.9) was investigated in Oryzias melastigma, O. javanicus and in O. melastigma female x O. javanicus male hybrids by acrylamide gel electrophoresis. 2. It was not possible to investigate the expression of SDH or GPI in
Jack S. Frankel
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