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The Biochemical Journal|November 5, 1999
Identification and molecular characterization of acyl-CoA synthetase in human erythrocytes and erythroid precursorsK T Malhotra, K Malhotra, B H Lubin, et al.
The Journal of Biological Chemistry|October 15, 1990
Entrapment of purified alpha-hemoglobin chains in normal erythrocytes. A model for beta thalassemiaM D Scott, P Rouyer-Fessard, B H Lubin, et al.
Blood|May 1, 1991
NADPH, not glutathione, status modulates oxidant sensitivity in normal and glucose-6-phosphate dehydrogenase-deficient erythrocytesM D Scott, L Zuo, B H Lubin, et al.
The American Journal of Pediatric Hematology/Oncology|January 1, 1981
Aplastic anemia associated with the Shwachman syndrome. In vivo and in vitro observationsW G Woods, W Krivit, B H Lubin, et al.
Blood|September 1, 1982
A simple laboratory alternative to irreversibly sickled cell (ISC) countsM R Clark, N Mohandas, S H Embury, et al.
Pediatric Pathology & Molecular Medicine|April 4, 2003
Sibling donor cord blood banking for children with sickle cell diseaseW Reed, M Walters, E Trachtenberg, et al.
Biochemistry|February 27, 1996
Formation of vesicles by the action of acyl-CoA:1-acyllsophosphatidylcholine acyltransferase from rat liver microsomes: optimal solubilization conditions and analysis of lipid composition and enzyme activityH Fyrst, D V Pham, B H Lubin, et al.
The Journal of Laboratory and Clinical Medicine|July 1, 1991
Erythrocyte defense against hydrogen peroxide: preeminent importance of catalaseM D Scott, B H Lubin, L Zuo, et al.
Biochimica Et Biophysica Acta|October 24, 1979
Modification of hemoglobin A with dimethyl adipimidate. Contribution of individual reacted subunits to changes in oxygen affinityR Pennathur-Das, L E Vickery, W Mentzer, et al.
Clinics in Haematology|February 1, 1985
Membrane phospholipid organization and vesiculation of erythrocytes in sickle cell anaemiaG M Wagner, R S Schwartz, D T Chiu, et al.
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