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Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|April 1, 1984
Interaction of Vicia graminea anti-N lectin with cell surface glycoproteins from erythrocytes with rare blood group antigensD Blanchard, A Asseraf, M J Prigent, et al.Bulletin De L'Academie Nationale De Medecine|July 28, 2001
[Value of RHD fetal genotyping in the prevention of anti-D immunization]Y Brossard, A Sender, J P Cartron, et al.Blood|June 1, 1996
Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in RN phenotypesC Rouillac, P Gane, J Cartron, et al.The Journal of Biological Chemistry|June 25, 1983
Primary structure of the oligosaccharide determinant of blood group Cad specificityD Blanchard, J P Cartron, B Fournet, et al.American Journal of Hematology|May 1, 1991
Erythrocyte Webb-type glycophorin C variant lacks N-glycosylation due to an asparagine to serine substitutionM J Telen, C Le Van Kim, M L Guizzo, et al.Biochemical and Biophysical Research Communications|October 24, 1998
Kx, a quantitatively minor protein from human erythrocytes, is palmitoylated in vivoF Carbonnet, C Hattab, I Callebaut, et al.British Journal of Haematology|March 1, 1997
Immunochemical analysis of the Kx protein from human red cells of different Kell phenotypes using antibodies raised against synthetic peptidesF Carbonnet, C Hattab, E Collec, et al.British Journal of Haematology|September 1, 1994
PCR-based determination of Rhc and RhE status of fetuses at risk of Rhc and RhE haemolytic diseaseC Le Van Kim, I Mouro, Y Brossard, et al.The Journal of Clinical Investigation|December 1, 1982
Surface modifications in the platelets of a patient with alpha-N-acetyl-D-galactosamine residues, the Tn-syndromeA T Nurden, D Dupuis, D Pidard, et al.British Journal of Haematology|February 1, 1995
Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genesC Rouillac, C Le Van Kim, A Blancher, et al.Pageof 42