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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]

Biochemical and biophysical research communications, 2008-04, Vol.368 (3), p.837-837

2008

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Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase

European journal of biochemistry, 1993-04, Vol.213 (1), p.493-500

1993

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A recombinant bisphosphoglycerate mutase variant with acid phosphate homology degrades 2,3-diphosphoglycerate

Proceedings of the National Academy of Sciences - PNAS, 1994-04, Vol.91 (9), p.3593

1994

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Identification of new mutations in two phosphoglycerate kinase (PGK) variants expressing different clinical syndromes : PGK Créteil and PGK Amiens

Blood, 1994-08, Vol.84 (3), p.898-903

1994

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Compound heterozygosity in a complete erythrocyte bisphosphoglycerate mutase deficiency

Blood, 1992-11, Vol.80 (10), p.2643-2649

1992

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A Recombinant Bisphosphoglycerate Mutase Variant with Acid Phosphatase Homology Degrades 2,3-Diphosphoglycerate

Proceedings of the National Academy of Sciences - PNAS, 1994-04, Vol.91 (9), p.3593-3597

1994

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The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families

Blood cells, molecules, & diseases, 1996, Vol.22 (2), p.115-125

1996

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Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutase

Gene, 1990-07, Vol.91 (2), p.225-232

1990

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Crystallization and preliminary X-ray diffraction studies of the human erythrocyte bisphosphoglycerate mutase

Journal of molecular biology, 1991-03, Vol.218 (2), p.269-270

1991

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Comparative effects of two sulfhydryl reagents on the activities of a multifunctional red cell enzyme: Bisphosphoglycerate mutase

Biochemical and biophysical research communications, 1988-06, Vol.153 (3), p.945-951

1988

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A New Case of Phosphoglycerate Kinase Deficiency: PGK Creteil Associated With Rhabdomyolysis and Lacking Hemolytic Anemia

Blood, 1982-07, Vol.60 (1), p.84-91

1982

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Cell-free translation of messenger RNA for human bisphospho-glyceromutase

Biochemical and biophysical research communications, 1984-04, Vol.120 (2), p.441-447

1984

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Hereditary triose phosphate isomerase deficiency: seven new homozygous cases

Human genetics, 1985-11, Vol.71 (3), p.235-240

1985

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Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34→7q22

Human genetics, 1987-11, Vol.77 (3), p.283-285

1987

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Electrophoretic characterization of pyrimidine 5'-nucleotidase of human erythrocytes and its distinction from acid phosphatase

Clinica chimica acta, 1977-08, Vol.79 (1), p.115-118

1977

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Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase : functional consequences of substitutions of His10, His187 and Arg89

European journal of biochemistry, 1993-04, Vol.213 (1), p.493-500

1993

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Electrophoretic and kinetic studies of human erythrocytes deficient in pyrimidine 5'-nucleotidase

Human genetics, 1977-01, Vol.38 (2), p.209-215

1977

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Hereditary pyruvate kinase abnormalities associated with erythrocytosis

American journal of hematology, 1981-01, Vol.10 (1), p.47-55

1981

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Purification of human erythrocyte phosphoglyceromutase

Journal of Chromatography A, 1984-01, Vol.285 (1), p.203-209

1984

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Evidence for the presence of a hybrid of phosphoglyceromutase/bisphosphoglyceromutase in the red cells: Partial characterization of the hybrid

Biochemical and biophysical research communications, 1984-05, Vol.120 (3), p.715-720

1984

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Comportement immunologique de la glucose-6-phosphate-deshydrogenase érythrocytaire chez des mutants déficients

Clinica chimica acta, 1970-08, Vol.29 (2), p.209-214

1970

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Purification of human erythrocyte phosphoglycerate kinase by dye ligand affinity chromatography

Journal of Chromatography A, 1983-01, Vol.258, p.213-222

1983

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An immunochemical method for detecting an inactive enzyme (bisphosphoglyceromutase) after Cellogel electrophoresis

Electrophoresis, 1985, Vol.6 (11), p.567-568

1985

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Biochemical and immunological arguments for homoology between red cell and liver phosphoglyceromutase isozymes

Biochimica et biophysica acta, Protein structure and molecular enzymology, 1984-06, Vol.787 (3), p.270-274

1984

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Characterization of 2,3-diphosphoglycerate phosphatase activity: Electrophoretic study

BBA - Enzymology, 1973-01, Vol.293 (1), p.285-289

1973

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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]

Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase

A recombinant bisphosphoglycerate mutase variant with acid phosphate homology degrades 2,3-diphosphoglycerate

Identification of new mutations in two phosphoglycerate kinase (PGK) variants expressing different clinical syndromes : PGK Créteil and PGK Amiens

Compound heterozygosity in a complete erythrocyte bisphosphoglycerate mutase deficiency

A Recombinant Bisphosphoglycerate Mutase Variant with Acid Phosphatase Homology Degrades 2,3-Diphosphoglycerate

The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families

Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutase

Crystallization and preliminary X-ray diffraction studies of the human erythrocyte bisphosphoglycerate mutase

Comparative effects of two sulfhydryl reagents on the activities of a multifunctional red cell enzyme: Bisphosphoglycerate mutase

A New Case of Phosphoglycerate Kinase Deficiency: PGK Creteil Associated With Rhabdomyolysis and Lacking Hemolytic Anemia

Cell-free translation of messenger RNA for human bisphospho-glyceromutase

Hereditary triose phosphate isomerase deficiency: seven new homozygous cases

Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34→7q22

Electrophoretic characterization of pyrimidine 5'-nucleotidase of human erythrocytes and its distinction from acid phosphatase

Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase : functional consequences of substitutions of His10, His187 and Arg89

Electrophoretic and kinetic studies of human erythrocytes deficient in pyrimidine 5'-nucleotidase

Hereditary pyruvate kinase abnormalities associated with erythrocytosis

Purification of human erythrocyte phosphoglyceromutase

Evidence for the presence of a hybrid of phosphoglyceromutase/bisphosphoglyceromutase in the red cells: Partial characterization of the hybrid

Comportement immunologique de la glucose-6-phosphate-deshydrogenase érythrocytaire chez des mutants déficients

Purification of human erythrocyte phosphoglycerate kinase by dye ligand affinity chromatography

An immunochemical method for detecting an inactive enzyme (bisphosphoglyceromutase) after Cellogel electrophoresis

Biochemical and immunological arguments for homoology between red cell and liver phosphoglyceromutase isozymes

Characterization of 2,3-diphosphoglycerate phosphatase activity: Electrophoretic study

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