Molecular alterations in congenital erythrocyte pyruvate kinase deficiencies
- 1 May 1976
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 68 (3) , 245-253
- https://doi.org/10.1016/0009-8981(76)90388-0
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Four New Pyruvate Kinase (PK) Variants and a Classical PK DeficiencyBritish Journal of Haematology, 1975
- Metabolie Regulation in Enzyme-Deficient Red CellsEnzyme, 1974
- Studies on Pyruvate Kinase (PK) DeficiencyThe Journal of Biochemistry, 1973
- Allosteric activation of human erythrocyte pyruvate kinase by fructose-1,6-diphosphate: Kinetic and equilibrium binding studiesBiochimie, 1972
- Multimolecular Forms of Pyruvate KinaseThe Journal of Biochemistry, 1972
- Multimolecular Forms of Pyruvate Kinase from Rat and Other Mammalian Tissues*The Journal of Biochemistry, 1972
- Déficit en congénital pyruvate kinase érythrocytaire: Étude cinétique de l'enzyme et conséquences métaboliquesClinica Chimica Acta; International Journal of Clinical Chemistry, 1972
- Les anomalies de la glycolyse au cours de l'anémie hémolytique par déficit du globule rouge en pyruvate kinaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1968
- A structurally modified liver aldolase in fructose intolerance: Immunological and kinetic evidenceBiochemical and Biophysical Research Communications, 1968
- Crystallization, Characterization and Metabolic Regulation of Two Types of Pyruvate Kinase Isolated from Rat Tissues*The Journal of Biochemistry, 1967