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Journal Abstract Search

101 related items for PubMed ID: 10686006

  • 1. Expression of Rh30 and Rh-related glycoproteins during erythroid differentiation in a two-phase liquid culture system.
    Suyama K, Li H, Zhu A.
    Transfusion; 2000 Feb; 40(2):214-21. PubMed ID: 10686006
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  • 3. The human Rh50 glycoprotein gene. Structural organization and associated splicing defect resulting in Rh(null) disease.
    Huang CH.
    J Biol Chem; 1998 Jan 23; 273(4):2207-13. PubMed ID: 9442063
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  • 5. Identification of 5' flanking sequence of RH50 gene and the core region for erythroid-specific expression.
    Iwamoto S, Omi T, Yamasaki M, Okuda H, Kawano M, Kajii E.
    Biochem Biophys Res Commun; 1998 Feb 04; 243(1):233-40. PubMed ID: 9473510
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  • 6. The members of the RH gene family (RH50 and RH30) followed different evolutionary pathways.
    Matassi G, Chérif-Zahar B, Pesole G, Raynal V, Cartron JP.
    J Mol Evol; 1999 Feb 04; 48(2):151-9. PubMed ID: 9929383
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  • 9. Rh-deficiency of the regulator type caused by splicing mutations in the human RH50 gene.
    Chérif-Zahar B, Matassi G, Raynal V, Gane P, Delaunay J, Arrizabalaga B, Cartron JP.
    Blood; 1998 Oct 01; 92(7):2535-40. PubMed ID: 9746795
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  • 10. Biochemical aspects of the blood group Rh (rhesus) antigens.
    Anstee DJ, Tanner MJ.
    Baillieres Clin Haematol; 1993 Jun 01; 6(2):401-22. PubMed ID: 8043932
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  • 11. Conserved evolution of the Rh50 gene compared to its homologous Rh blood group gene.
    Kitano T, Sumiyama K, Shiroishi T, Saitou N.
    Biochem Biophys Res Commun; 1998 Aug 10; 249(1):78-85. PubMed ID: 9705835
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  • 13. A novel single missense mutation identified along the RH50 gene in a composite heterozygous Rhnull blood donor of the regulator type.
    Hyland CA, Chérif-Zahar B, Cowley N, Raynal V, Parkes J, Saul A, Cartron JP.
    Blood; 1998 Feb 15; 91(4):1458-63. PubMed ID: 9454778
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  • 16. Time-course expression of polypeptides carrying blood group antigens during human erythroid differentiation.
    Bony V, Gane P, Bailly P, Cartron JP.
    Br J Haematol; 1999 Nov 15; 107(2):263-74. PubMed ID: 10583211
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  • 17. Evolutionary history of the Rh blood group-related genes in vertebrates.
    Kitano T, Saitou N.
    Immunogenetics; 2000 Aug 15; 51(10):856-62. PubMed ID: 10970100
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  • 19. In vitro generated Rh(null) red cells recapitulate the in vivo deficiency: a model for rare blood group phenotypes and erythroid membrane disorders.
    Cambot M, Mazurier C, Canoui-Poitrine F, Hebert N, Picot J, Clay D, Picard V, Ripoche P, Douay L, Dubart-Kupperschmitt A, Cartron JP.
    Am J Hematol; 2013 May 15; 88(5):343-9. PubMed ID: 23417980
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  • 20. Rhmod syndrome: a family study of the translation-initiator mutation in the Rh50 glycoprotein gene.
    Huang C, Cheng GJ, Reid ME, Chen Y.
    Am J Hum Genet; 1999 Jan 15; 64(1):108-17. PubMed ID: 9915949
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