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Proceedings of the National Academy of Sciences of the United States of America|March 1, 1982
Defective spectrin dimer-dimer association with hereditary elliptocytosisS C Liu, J Palek, J T Prchal
Transfusion|January 14, 1998
Does a patient with hereditary spherocytosis qualify for preoperative autologous blood donation?R Weinstein, R Martinez, H Hassoun, et al.
Blood|January 15, 1993
Dependence of the permanent deformation of red blood cell membranes on spectrin dimer-tetramer equilibrium: implication for permanent membrane deformation of irreversibly sickled cellsS C Liu, L H Derick, J Palek
The Journal of Cell Biology|June 1, 1977
Release of spectrin-free vesicles from human erythrocytes during ATP depletion. I. Characterization of spectrin-free vesiclesH U Lutz, S C Liu, J Palek
Blood|March 1, 1978
Metabolic dependence of protein arrangement in human erythrocyte membranes. I. Analysis of spectrin-rich complexes in ATP-depleted red cellsJ Palek, S C Liu, L M Snyder
Progress in Clinical and Biological Research|January 1, 1978
Crosslinking of the nearest membrane protein neighbors in ATP depleted, calcium enriched and irreversibly sickled red cellsJ Palek, S C Liu, P A Liu
Blood|June 1, 1995
Comparison of the ankyrin (AC)n microsatellites in genomic DNA and mRNA reveals absence of one ankyrin mRNA allele in 20% of patients with hereditary spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
The Journal of Biological Chemistry|October 5, 1985
Hemin-mediated dissociation of erythrocyte membrane skeletal proteinsS C Liu, S Zhai, J Lawler, et al.
Blood|September 1, 1987
Molecular determinants of clinical expression of hereditary elliptocytosis and pyropoikilocytosisT Coetzer, J Lawler, J T Prchal, et al.
The Journal of Clinical Investigation|March 1, 1995
A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosisP Jarolim, H L Rubin, V Brabec, et al.
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