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The Journal of Clinical Investigation|January 1, 1986
Excessive binding of natural anti-alpha-galactosyl immunoglobin G to sickle erythrocytes may contribute to extravascular cell destructionU Galili, M R Clark, S B ShohetBlood|May 1, 1983
Osmotic gradient ektacytometry: comprehensive characterization of red cell volume and surface maintenanceM R Clark, N Mohandas, S B ShohetThe Journal of Clinical Investigation|November 1, 1982
Hydration of sickle cells using the sodium ionophore Monensin. A model for therapyM R Clark, N Mohandas, S B ShohetBlood|August 15, 1989
Membrane assembly and remodeling during reticulocyte maturationJ A Chasis, M Prenant, A Leung, et al.Blood|May 1, 1977
Abnormalities in granule formation in acute myelogenous leukemiaD F Bainton, L M Friedlander, S B ShohetBlood|December 1, 1976
Stabilization of the shape of sickled cells by calcium and A23187M R Clark, A C Greenquist, S B ShohetAmerican Journal of Hematology|January 1, 1993
Hereditary hemolytic disease with increased red blood cell phosphatidylcholine and dehydration: one, two, or many disorders?M R Clark, S B Shohet, E L GottfriedClinical and Investigative Medicine. Medecine Clinique Et Experimentale|January 1, 1983
Hereditary lecithin-cholesterol acyltransferase deficiency. Report of 2 new cases and review of the literatureA M Shojania, S K Jain, S B ShohetBlood|March 1, 1976
Lipid membrane peroxidation in beta-thalassemia majorE A Rachmilewitz, S B Shohet, B H LubinBlood|June 1, 1978
Marked reduction of spectrinin hereditary spherocytosis in the common house mouseA C Greenquist, S B Shohet, S E BernsteinPageof 13