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Clinical and Laboratory Haematology|March 19, 2003
Automated detection of malaria-associated intraleucocytic haemozoin by Cell-Dyn CD4000 depolarization analysisC S Scott, D van Zyl, E Ho, et al.The Journal of Clinical Investigation|September 1, 1991
Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosisT L Coetzer, K Sahr, J Prchal, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1987
Isolation and characterization of cDNA clones for human erythrocyte beta-spectrinJ T Prchal, B J Morley, S H Yoon, et al.The Journal of Clinical Investigation|August 1, 1994
A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosisH Hassoun, T L Coetzer, J N Vassiliadis, et al.American Journal of Hematology|September 1, 1989
Severe hemolysis and red cell fragmentation caused by the combination of a spectrin mutation with a thrombotic microangiopathyP Jarolim, J Palek, T L Coetzer, et al.British Journal of Haematology|March 23, 1999
Automated malaria detection by depolarization of laser lightB V Mendelow, C Lyons, P Nhlangothi, et al.The Journal of Biological Chemistry|October 25, 1993
Spectrin cagliari. an Ala-->Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimerK E Sahr, T L Coetzer, L S Moy, et al.Pageof 2