Showing results (1-10 of 2,061) with videos related to
Sort By:
Pageof 207
Pediatric Research|April 1, 1977
Immunologic study of the age-related loss of activity of six enzymes in the red cells from newborn infants and adults--evidence for a fetal type of erythrocyte phosphofructokinaseA Kahn, C Boyer, D Cottreau, et al.Blood|November 1, 1976
Causal mechanisms of multiple acquired red cell enzyme defects in a patient with acquired dyserythropoiesisA Kahn, D Cottreau, C Boyer, et al.Biochimie|January 1, 1975
Human granulocyte 6 phosphogluconate dehydrogenase. Purification by elective elution with NADP+, immunological and kinetic propertiesD Cottreau, P Boivin, A Kahn, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 20, 1976
Mechanisms of the acquired erythrocyte enzyme deficiencies in blood diseasesA Kahn, J Marie, J F Bernard, et al.Humangenetik|October 20, 1975
Gd(--) Abrami: a deficient G-6PD variant with hemizygous expression in blood cells of a woman with primary myelofibrosisA Kahn, J F Bernard, D Cottreau, et al.Biochimica Et Biophysica Acta|March 14, 1980
Endogenous phosphorylation of soluble enzymes in human red cells. Cyclic 3',5'-AMP-dependent phosphorylation of phosphofructokinase without detectable regulatory effectJ L Lagrange, J Marie, D Cottreau, et al.Enzyme|January 1, 1976
Human platelet glucose-6-phosphate dehydrogenase. Total purification, kinetic studies and relationship with enzyme from other blood cellsD Cottreau, A Kahn, P BoivinEnzyme|January 1, 1976
Human granulocyte phosphoglycerate kinase. Purification by double affinity elution and immunological studyD Cottreau, A Kahn, P BoivinProceedings of the National Academy of Sciences of the United States of America|January 1, 1976
Modifications of purified glucose-6-phosphate dehydrogenase and other enzymes by a factor of low molecular weight abundant in some leukemic cellsA Kahn, P Boivin, H Rubinson, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|January 16, 1976
Glucose-phosphate isomerase deficiency due to a new variant (GP I Barcelona) and to a silent gene: biochemical, immunological and genetic studiesA Kahn, J L Vives, O Bertrand, et al.Pageof 207