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The Journal of Laboratory and Clinical Medicine|June 1, 1985
Red cell distribution width parallels dense red cell disappearance during painful crises in sickle cell anemiaC Lawrence, M E Fabry, R L NagelBlood|February 15, 1990
Heterogeneity in the properties of burst-forming units of erythroid lineage in sickle cell anemia: DNA synthesis and burst-promoting activity production is related to peripheral hemoglobin F levelsH Croizat, H H Billett, R L NagelMolecular and Biochemical Parasitology|September 7, 1999
Antisense oligonucleotides targeting malarial aldolase inhibit the asexual erythrocytic stages of Plasmodium falciparumC Wanidworanun, R L Nagel, H L ShearThe American Journal of Tropical Medicine and Hygiene|September 1, 1982
Plasmodium falciparum: inhibition of in vitro growth by desferrioxamineC Raventos-Suarez, S Pollack, R L NagelBlood|December 1, 1987
Deoxygenation inhibits the volume-stimulated, Cl(-)-dependent K+ efflux in SS and young AA cells: a cytosolic Mg2+ modulationM Canessa, M E Fabry, R L NagelBlood|November 8, 2001
Ameliorating effects of fluorocarbon emulsion on sickle red blood cell-induced obstruction in an ex vivo vasculatureD K Kaul, X Liu, R L NagelAmerican Journal of Hematology|September 1, 1989
Polymerase chain reaction amplification applied to the determination of beta-like globin gene cluster haplotypesM Sutton, E E Bouhassira, R L NagelBlood|October 15, 1991
The unique red cell heterogeneity of SC disease: crystal formation, dense reticulocytes, and unusual morphologyC Lawrence, M E Fabry, R L NagelBiochemical and Biophysical Research Communications|July 16, 1986
Steady-state fluorescence emission from the fluorescent probe, 5-iodoacetamidofluorescein, bound to hemoglobinR E Hirsch, R S Zukin, R L NagelPageof 24