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Journal Abstract Search


124 related items for PubMed ID: 9716608

  • 1. Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment.
    Huang CH, Liu Z, Cheng G, Chen Y.
    Blood; 1998 Sep 01; 92(5):1776-84. PubMed ID: 9716608
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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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  • 4. 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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  • 8. Sequence, organization, and evolution of Rh50 glycoprotein genes in nonhuman primates.
    Huang CH, Liu Z, Apoil PA, Blancher A.
    J Mol Evol; 2000 Jul 01; 51(1):76-87. PubMed ID: 10903374
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  • 9. Molecular defects of the RHCE gene in Rh-deficient individuals of the amorph type.
    Chérif-Zahar B, Matassi G, Raynal V, Gane P, Mempel W, Perez C, Cartron JP.
    Blood; 1998 Jul 15; 92(2):639-46. PubMed ID: 9657766
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  • 10. Molecular basis for Rh(null) syndrome: identification of three new missense mutations in the Rh50 glycoprotein gene.
    Huang CH, Cheng G, Liu Z, Chen Y, Reid ME, Halverson G, Okubo Y.
    Am J Hematol; 1999 Sep 15; 62(1):25-32. PubMed ID: 10467273
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  • 11. 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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  • 12. Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency.
    Cherif-Zahar B, Raynal V, Gane P, Mattei MG, Bailly P, Gibbs B, Colin Y, Cartron JP.
    Nat Genet; 1996 Feb 15; 12(2):168-73. PubMed ID: 8563755
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  • 13. 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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  • 14. A single point mutation at a splice site generates a silent RH50 gene in a composite heterozygous RHnull blood donor.
    Cowley NM, Saul A, Cartron J, Hyland CA.
    Vox Sang; 1999 Feb 04; 76(4):247-8. PubMed ID: 10394146
    [No Abstract] [Full Text] [Related]

  • 15. Organization of the human RH50A gene (RHAG) and evolution of base composition of the RH gene family.
    Matassi G, Chérif-Zahar B, Raynal V, Rouger P, Cartron JP.
    Genomics; 1998 Jan 15; 47(2):286-93. PubMed ID: 9479501
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  • 16. 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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  • 17. Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expression.
    Ridgwell K, Spurr NK, Laguda B, MacGeoch C, Avent ND, Tanner MJ.
    Biochem J; 1992 Oct 01; 287 ( Pt 1)(Pt 1):223-8. PubMed ID: 1417776
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  • 18. Defining the Rh blood group antigens. Biochemistry and molecular genetics.
    Cartron JP.
    Blood Rev; 1994 Dec 01; 8(4):199-212. PubMed ID: 7888828
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  • 19. Evolutionary history of the Rh blood group-related genes in vertebrates.
    Kitano T, Saitou N.
    Immunogenetics; 2000 Aug 01; 51(10):856-62. PubMed ID: 10970100
    [Abstract] [Full Text] [Related]

  • 20. Molecular insights into the Rh protein family and associated antigens.
    Huang CH.
    Curr Opin Hematol; 1997 Mar 01; 4(2):94-103. PubMed ID: 9107525
    [Abstract] [Full Text] [Related]


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