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Blood|July 15, 1992
Asynchronous synthesis of membrane skeletal proteins during terminal maturation of murine erythroblastsM Hanspal, J S Hanspal, R Kalraiya, 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.
Blood|March 15, 1996
Hereditary spherocytosis with spectrin deficiency due to an unstable truncated beta spectrinH Hassoun, J N Vassiliadis, J Murray, et al.
Blood|January 1, 1991
Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrinM Hanspal, S H Yoon, H Yu, et al.
Blood|February 1, 1989
Viscoelastic properties of red cell membrane in hereditary elliptocytosisA Chabanel, K L Sung, J Rapiejko, et al.
Biochimica Et Biophysica Acta|October 17, 1977
Partition of catalase and its peroxidase activities in human red cell membrane: effect of ATP depletionL M Snyder, S C Liu, J Palek, et al.
Blood|September 15, 1992
Band 3 Memphis: a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG----GAG (Lys----Glu) in codon 56P Jarolim, H L Rubin, S Zhai, et al.
Blood|June 25, 1998
Temporal synthesis of band 3 oligomers during terminal maturation of mouse erythroblasts. Dimers and tetramers exist in the membrane as preformed stable speciesM Hanspal, D E Golan, Y Smockova, et al.
Blood|July 1, 1977
Effect of procaine HCLl on ATP: calcium-dependent alterations in red cell shape and deformabilityJ Palek, A Liu, D Liu, et al.
Blood|February 1, 1995
Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
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