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The Biochemical Journal|August 1, 1984
Rhnull human erythrocytes have an abnormal membrane phospholipid organizationF Kuypers, M van Linde-Sibenius-Trip, B Roelofsen, et al.Transfusion Medicine (Oxford, England)|June 3, 1999
Glycophorin A mutation Ala65 --> Pro gives rise to a novel pair of MNS alleles ENEP (MNS39) and HAG (MNS41) and altered Wrb expression: direct evidence for GPA/band 3 interaction necessary for normal Wrb expressionJ Poole, J Banks, L J Bruce, et al.Blood|December 15, 1991
Biochemical studies on red blood cells from a patient with the Inab phenotype (decay-accelerating factor deficiency)M E Reid, G Mallinson, R B Sim, et al.Transfusion|May 29, 2000
The low-frequency MNS blood group antigens Ny(a) (MNS18) and Os(a) (MNS38) are associated with GPA amino acid substitutionsG L Daniels, L J Bruce, W J Mawby, et al.Vox Sanguinis|February 1, 1980
The rare phenotype En(a-) in a French-Canadian familyV Taliano, R M Guévin, D Hébert, 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.British Journal of Haematology|January 1, 1997
Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locusE Miraglia del Giudice, A Vallier, P Maillet, et al.Blood|April 21, 2001
Glycophorin A dimerization and band 3 interaction during erythroid membrane biogenesis: in vivo studies in human glycophorin A transgenic miceI Auffray, S Marfatia, K de Jong, et al.British Journal of Haematology|April 1, 1995
A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemiaS Hayette, L Morle, M Bozon, et al.The Journal of Biological Chemistry|July 25, 1992
Localization of the C termini of the Rh (rhesus) polypeptides to the cytoplasmic face of the human erythrocyte membraneN D Avent, S K Butcher, W Liu, et al.Pageof 16