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Biochimica Et Biophysica Acta|May 9, 1986
The rate of uptake and efflux of phosphatidylcholine from human erythrocytes depends on the fatty acyl composition of the exchanging speciesF A Kuypers, X Andriesse, P Child, et al.Biochimica Et Biophysica Acta|January 25, 1985
Acyl selectivity in the transfer of molecular species of phosphatidylcholines from human erythrocytesP Child, J J Myher, F A Kuypers, et al.Blood|February 1, 1996
Detection of altered membrane phospholipid asymmetry in subpopulations of human red blood cells using fluorescently labeled annexin VF A Kuypers, R A Lewis, M Hua, et al.Pediatric Blood & Cancer|October 24, 2009
Hemoglobin Hakkari: an autosomal dominant form of beta thalassemia with inclusion bodies arising from de novo mutation in exon 2 of beta globin geneB Kanathezhath, F K Hazard, H Guo, et al.Free Radical Biology & Medicine|January 1, 1996
Correlation of membrane lipid peroxidation with oxidation of hemoglobin variants: possibly related to the rates of hemin releaseD T Chiu, J van den Berg, F A Kuypers, et al.Biochemistry|September 5, 1995
Effects of bacterial endotoxin on human cross-linked and native hemoglobinsW Kaca, R I Roth, K D Vandegriff, et al.The Journal of Clinical Investigation|September 18, 1997
Removal of erythrocyte membrane iron in vivo ameliorates the pathobiology of murine thalassemiaP V Browne, O Shalev, F A Kuypers, et al.The Journal of Laboratory and Clinical Medicine|October 1, 1989
Qinghaosu-mediated oxidation in normal and abnormal erythrocytesM D Scott, S R Meshnick, R A Williams, et al.FEBS Letters|May 6, 1985
The phospholipid organisation in the membranes of McLeod and Leach phenotype erythrocytesF A Kuypers, M van Linde-Sibenius Trip, B Roelofsen, et al.Blood|May 30, 1998
Whole blood tissue factor procoagulant activity is elevated in patients with sickle cell diseaseN S Key, A Slungaard, L Dandelet, et al.Pageof 9