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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.
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|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.
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