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166 related items for PubMed ID: 2823938

  • 1. Delta glycophorin (glycophorin B) gene deletion in two individuals homozygous for the S--s--U-- blood group phenotype.
    Huang CH, Johe K, Moulds JJ, Siebert PD, Fukuda M, Blumenfeld OO.
    Blood; 1987 Dec; 70(6):1830-5. PubMed ID: 2823938
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  • 2. Amino acid sequence of an alpha-delta-glycophorin hybrid. A structure reciprocal to Sta delta-alpha-glycophorin hybrid.
    Johe KK, Smith AJ, Vengelen-Tyler V, Blumenfeld OO.
    J Biol Chem; 1989 Oct 15; 264(29):17486-93. PubMed ID: 2793868
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  • 7. Membrane glycophorins in Sta blood group erythrocytes.
    Blumenfeld OO, Adamany AM, Kikuchi M, Sabo B, McCreary J.
    J Biol Chem; 1986 Apr 25; 261(12):5544-52. PubMed ID: 3514617
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  • 8. A family study of multiple mutations of alpha and delta glycophorins (glycophorins A and B).
    Huang CH, Puglia KV, Bigbee WL, Guizzo ML, Hoffman M, Blumenfeld OO.
    Hum Genet; 1988 Dec 25; 81(1):26-30. PubMed ID: 3198123
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  • 16. The Mz variety of the St(a+) phenotype--a variant of glycophorin A exhibiting a deletion.
    Dahr W, Blanchard D, Chevalier C, Cartron JP, Beyreuther K, Fournet B.
    Biol Chem Hoppe Seyler; 1990 May 25; 371(5):403-10. PubMed ID: 2378678
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  • 19. Polymorphism of glycophorins in nonhuman primate erythrocytes.
    Lu YQ, Liu JF, Socha WW, Nagel RL, Blumenfeld OO.
    Biochem Genet; 1987 Aug 25; 25(7-8):477-91. PubMed ID: 3128973
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  • 20. Molecular analysis of glycophorin C deficiency in human erythrocytes.
    Winardi R, Reid M, Conboy J, Mohandas N.
    Blood; 1993 May 15; 81(10):2799-803. PubMed ID: 7683929
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