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Biochimica Et Biophysica Acta|February 14, 1975
The binding of hemoglobin to membranes of normal and sickle erythrocytesS Fischer, R L Nagel, R M Bookchin, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1977
Ligand kinetics of hemoglobin S containing erythrocytesJ P Harrington, D Elbaum, R M Bookchin, et al.
The Journal of Physiology|February 1, 1993
Inhibition of the calcium pump by high cytosolic Ca2+ in intact human red blood cellsA C Pereira, D Samellas, T Tiffert, et al.
The Journal of Biological Chemistry|October 11, 1996
A recombinant sickle hemoglobin triple mutant with independent inhibitory effects on polymerizationJ P Himanen, U A Mirza, B T Chait, et al.
The New England Journal of Medicine|July 15, 1976
Hemoglobin Beth Israel. A mutant causing clinically apparent cyanosisR L Nagel, J Lynfield, J Johnson, et al.
Blood|July 27, 2001
Characterization of the phosphatidylserine-exposing subpopulation of sickle cellsK de Jong, S K Larkin, L A Styles, et al.
FEBS Letters|August 28, 1995
Self-association of plasma membrane Ca(2+)-ATPase by volume exclusionD Kosk-Kosicka, M M Lopez, I Fomitcheva, et al.
The Journal of Physiology|May 16, 2000
Functional state of the plasma membrane Ca2+ pump in Plasmodium falciparum-infected human red blood cellsT Tiffert, H M Staines, J C Ellory, et al.
Blood|August 1, 1976
Molecular and cellular effects of antisickling concentrations of alkylureasD Elbaum, E F Roth, G Neumann, et al.
Blood|July 1, 1979
Hemoglobin Crete (beta 129 ala leads to pro): a new high-affinity variant interacting with beta o -and delta beta o -thalassemiaA Maniatis, T Bousios, R L Nagel, et al.
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