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Blood|August 26, 1998
Targeted inactivation of murine band 3 (AE1) gene produces a hypercoagulable state causing widespread thrombosis in vivoH Hassoun, Y Wang, J Vassiliadis, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
cDNA sequence for human erythrocyte ankyrinS Lambert, H Yu, J T Prchal, 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.Biochemistry|August 5, 1997
Red cell membranes of ankyrin-deficient nb/nb mice lack band 3 tetramers but contain normal membrane skeletonsS J Yi, S C Liu, L H Derick, et al.The New England Journal of Medicine|November 29, 1990
Molecular defect of the band 3 protein in southeast Asian ovalocytosisS C Liu, S Zhai, J Palek, et al.The Journal of Clinical Investigation|January 1, 1996
Red cell membrane remodeling in sickle cell anemia. Sequestration of membrane lipids and proteins in Heinz bodiesS C Liu, S J Yi, J R Mehta, et al.The Journal of Clinical Investigation|December 1, 1995
Molecular basis of spectrin deficiency in beta spectrin Durham. A deletion within beta spectrin adjacent to the ankyrin-binding site precludes spectrin attachment to the membrane in hereditary spherocytosisH Hassoun, J N Vassiliadis, J Murray, et al.Blood|July 1, 1997
Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiencyH Hassoun, J N Vassiliadis, J Murray, et al.Proceedings of the National Academy of Sciences of the United States of America|December 15, 1991
Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosisP Jarolim, J Palek, D Amato, et al.Pageof 10