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American Journal of Hematology|May 1, 1995
Leu110Pro substitution in the RhD polypeptide is responsible for the DVII category blood group phenotypeC Rouillac, C Le Van Kim, M Beolet, et al.
Vox Sanguinis|September 11, 2012
The ABCB6 mutation p.Arg192Trp is a recessive mutation causing the Lan- blood typeC Saison, V Helias, T Peyrard, et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1996
Tentative model for the mapping of D epitopes on the RhD polypeptideJ P Cartron, C Rouillac, C Le Van Kim, et al.
Human Genetics|April 1, 1995
Molecular basis and PCR-DNA typing of the Fya/fyb blood group polymorphismC Tournamille, C Le Van Kim, P Gane, et al.
Carbohydrate Research|April 10, 1992
Biosynthesis of the blood group Pk and P1 antigens by human kidney microsomesP Bailly, F Piller, B Gillard, et al.
Biological Chemistry Hoppe-Seyler|May 1, 1990
The Mz variety of the St(a+) phenotype--a variant of glycophorin A exhibiting a deletionW Dahr, D Blanchard, C Chevalier, et al.
The EMBO Journal|November 1, 1992
Erythroid-specific activity of the glycophorin B promoter requires GATA-1 mediated displacement of a repressorC Rahuel, M A Vinit, V Lemarchandel, et al.
The Journal of Biological Chemistry|April 25, 1987
Glycophorins B and C from human erythrocyte membranes. Purification and sequence analysisD Blanchard, W Dahr, M Hummel, et al.
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