M C Calvin - JoVE Visualize

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Blood|July 1, 1982

A new case of phosphoglycerate kinase deficiency: PGK Creteil associated with rhabdomyolysis and lacking hemolytic anemiaR Rosa, C George, M Fardeau, et al.

Human Genetics|January 1, 1985

Hereditary triose phosphate isomerase deficiency: seven new homozygous casesR Rosa, M O Prehu, M C Calvin, et al.

Journal of Molecular Biology|March 20, 1991

Crystallization and preliminary X-ray diffraction studies of the human erythrocyte bisphosphoglycerate mutaseJ Cherfils, R Rosa, M C Garel, et al.

The Journal of Biological Chemistry|May 15, 1989

Isolation, characterization, and structure of a mutant 89 Arg----Cys bisphosphoglycerate mutase. Implication of the active site in the mutationR Rosa, Y Blouquit, M C Calvin, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 26, 1994

A recombinant bisphosphoglycerate mutase variant with acid phosphatase homology degrades 2,3-diphosphoglycerateM C Garel, N Arous, M C Calvin, et al.

Biochemical and Biophysical Research Communications|May 16, 1984

Evidence for the presence of a hybrid of phosphoglyceromutase/bisphosphoglyceromutase in the red cells: partial characterization of the hybridR Rosa, M C Calvin, M O Préhu, et al.

Biochimie|May 1, 1990

Human bisphosphoglycerate mutase expressed in E coli: purification, characterization and structure studiesM C Calvin, Y Blouquit, M C Garel, et al.

The Journal of Biological Chemistry|November 15, 1988

Sequence of the human erythrocyte phosphoglycerate mutase by microsequencer and mass spectrometryY Blouquit, M C Calvin, R Rosa, et al.

Biomedica Biochimica Acta|January 1, 1990

Natural and artificial mutants of the human 2,3-bisphosphoglycerate as a tool for the evaluation of structure-function relationshipsM C Garel, V Lemarchandel, M O Prehu, et al.

European Journal of Biochemistry|April 1, 1993

Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase. Functional consequences of substitutions of His10, His187 and Arg89M C Garel, V Lemarchandel, M C Calvin, et al.

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Showing results (11-20 of 21) with videos related to

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Pageof 3

Blood|July 1, 1982

A new case of phosphoglycerate kinase deficiency: PGK Creteil associated with rhabdomyolysis and lacking hemolytic anemiaR Rosa, C George, M Fardeau, et al.

Human Genetics|January 1, 1985

Hereditary triose phosphate isomerase deficiency: seven new homozygous casesR Rosa, M O Prehu, M C Calvin, et al.

Journal of Molecular Biology|March 20, 1991

Crystallization and preliminary X-ray diffraction studies of the human erythrocyte bisphosphoglycerate mutaseJ Cherfils, R Rosa, M C Garel, et al.

The Journal of Biological Chemistry|May 15, 1989

Isolation, characterization, and structure of a mutant 89 Arg----Cys bisphosphoglycerate mutase. Implication of the active site in the mutationR Rosa, Y Blouquit, M C Calvin, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 26, 1994

A recombinant bisphosphoglycerate mutase variant with acid phosphatase homology degrades 2,3-diphosphoglycerateM C Garel, N Arous, M C Calvin, et al.

Biochemical and Biophysical Research Communications|May 16, 1984

Evidence for the presence of a hybrid of phosphoglyceromutase/bisphosphoglyceromutase in the red cells: partial characterization of the hybridR Rosa, M C Calvin, M O Préhu, et al.

Biochimie|May 1, 1990

Human bisphosphoglycerate mutase expressed in E coli: purification, characterization and structure studiesM C Calvin, Y Blouquit, M C Garel, et al.

The Journal of Biological Chemistry|November 15, 1988

Sequence of the human erythrocyte phosphoglycerate mutase by microsequencer and mass spectrometryY Blouquit, M C Calvin, R Rosa, et al.

Biomedica Biochimica Acta|January 1, 1990

Natural and artificial mutants of the human 2,3-bisphosphoglycerate as a tool for the evaluation of structure-function relationshipsM C Garel, V Lemarchandel, M O Prehu, et al.

European Journal of Biochemistry|April 1, 1993

Amino acid residues involved in the catalytic site of human erythrocyte bisphosphoglycerate mutase. Functional consequences of substitutions of His10, His187 and Arg89M C Garel, V Lemarchandel, M C Calvin, et al.

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