Search Results - "ROSA, Raymonde"
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Corrigendum to “Evidence for the presence of a hybrid of phosphoglyceromutase/bisphosphoglyceromutase in the red cells: Partial characterization of the hybrid” [Biochem. Biophys. Res. Commun. 120 (1984) 715–720]
Published in Biochemical and biophysical research communications (11-04-2008)Get full text
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2
Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase
Published in European journal of biochemistry (01-04-1993)“…Human bisphosphoglycerate mutase (GriP2 mutase) is a trifunctional enzyme which synthesizes and degrades GriP2 in red cells. Among the amino acid residues…”
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3
A recombinant bisphosphoglycerate mutase variant with acid phosphate homology degrades 2,3-diphosphoglycerate
Published in Proceedings of the National Academy of Sciences - PNAS (26-04-1994)“…In an effort to decrease 2,3-bisphosphate (2,3-DPB) level in erythrocytes by increasing the bisphosphoglycerate mutase (BPGM) phosphatase activity, a study…”
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4
Identification of new mutations in two phosphoglycerate kinase (PGK) variants expressing different clinical syndromes : PGK Créteil and PGK Amiens
Published in Blood (01-08-1994)“…Phosphoglycerate kinase (PGK) deficiency is generally associated with chronic hemolytic anemia, although it can be accompanied by either mental retardation or…”
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5
The Enzymes of the Glycolytic Pathway in Erythrocytes Infected With Plasmodium falciparum Malaria Parasites
Published in Blood (01-12-1988)“…Enzymes of the glycolytic pathway as well as some ancillary enzymes were studied in normal red cells parasitized with Plasmodium falciparum in culture at…”
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6
Compound heterozygosity in a complete erythrocyte bisphosphoglycerate mutase deficiency
Published in Blood (15-11-1992)“…Erythrocyte bisphosphoglycerate mutase (BPGM) deficiency is a rare disease associated with a decrease in 2,3-diphosphoglycerate concentration. A complete BPGM…”
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The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families
Published in Blood cells, molecules, & diseases (1996)“…ABSTRACT In order to investigate the basis of the repeated occurrence of the 1591C mutation (TPI 1591C, 105 Glu–Asp) in multiple unrelated families throughout…”
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A Recombinant Bisphosphoglycerate Mutase Variant with Acid Phosphatase Homology Degrades 2,3-Diphosphoglycerate
Published in Proceedings of the National Academy of Sciences - PNAS (26-04-1994)“…To date no definite and undisputed treatment has been found for sickle cell anemia, which is characterized by polymerization of a deoxygenated hemoglobin…”
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9
Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutase
Published in Gene (16-07-1990)“…The human muscle-specific phosphoglycerate mutase encoding gene (PGAM-M) has been cloned from a genomic cosmid library and sequenced. The sequence…”
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10
Comparative effects of two sulfhydryl reagents on the activities of a multifunctional red cell enzyme: bisphosphoglycerate mutase
Published in Biochemical and biophysical research communications (30-06-1988)“…The effects of two sulfhydryl reagents on the three activities of bisphosphoglycerate mutase have been compared. Under N-ethylmaleimide treatment all the…”
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Crystallization and preliminary X-ray diffraction studies of the human erythrocyte bisphosphoglycerate mutase
Published in Journal of molecular biology (20-03-1991)“…Bisphosphoglycerate mutase (EC 2.7.5.4) catalyzes the synthesis and breakdown of 2,3-diphosphoglycerate in red cells. The human enzyme, cloned and expressed in…”
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The Use of Enzymopathic Human Red Cells in the Study of Malarial Parasite Glucose Metabolism
Published in Blood (01-05-1988)“…The in vitro growth of Plasmodium falciparum malaria parasites was assayed in mutant red cells deficient in either diphosphoglycerate mutase (DPGM) or…”
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13
A New Case of Phosphoglycerate Kinase Deficiency: PGK Creteil Associated With Rhabdomyolysis and Lacking Hemolytic Anemia
Published in Blood (01-07-1982)“…A new case of phosphoglycerate kinase (PGK) deficiency is described. The propositus displayed episodes of rhabdomyolysis crises and acute renal failure but did…”
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14
Hereditary triose phosphate isomerase deficiency: seven new homozygous cases
Published in Human genetics (01-11-1985)“…Seven new homozygous cases of hereditary triosephosphate isomerase (TPI) deficiency have been detected in five unrelated families. Two of the families…”
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Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34→7q22
Published in Human genetics (01-11-1987)“…A 1.1-kb cDNA clone for human 2,3-bisphosphoglycerate mutase (BPGM) (EC 2.7.5.4) was used to map the structural gene to metaphase chromosomes. In situ…”
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Purification of the M-type phosphoglyceromutase from rabbit muscle
Published in Journal of chromatography (1986)“…A new method for the purification of M-type phosphoglyceromutase from rabbit muscle involving affinity chromatography on dye ligand media in the presence of…”
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17
Evidence for three enzymatic activities in one electrophoretic band of 3-phosphoglycerate mutase from red cells
Published in Biochimie (1975)“…Electrophoresis of 3-phosphoglycerate mutase from erythrocytes of man and several animal species has been performed on cellulose acetate strips. In most cases…”
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18
Electrophoretic characterization of pyrimidine 5'-nucleotidase of human erythrocytes and its distinction from acid phosphatase
Published in Clinica chimica acta (15-08-1977)“…Electrophoresis of red cell pyrimidine 5'-nucleotidase was carried out on cellulose acetate strips. One major band of activity was found in preparations from…”
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Purification of human erythrocyte phosphoglyceromutase
Published in Journal of chromatography (01-01-1984)Get more information
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20
Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase : functional consequences of substitutions of His10, His187 and Arg89
Published in European journal of biochemistry (01-04-1993)“…Human bisphosphoglycerate mutase (GriP2 mutase) is a trifunctional enzyme which synthesizes and degrades GriP2 in red cells. Among the amino acid residues…”
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