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Journal Abstract Search

133 related items for PubMed ID: 9746795

  • 1. 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
    [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
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  • 4. 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 23; 12(2):168-73. PubMed ID: 8563755
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  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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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  • 9. Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background.
    Huang CH, Chen Y, Reid ME, Seidl C.
    Blood; 1998 Jul 15; 92(2):664-71. PubMed ID: 9657769
    [Abstract] [Full Text] [Related]

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

  • 12. Defining the Rh blood group antigens. Biochemistry and molecular genetics.
    Cartron JP.
    Blood Rev; 1994 Dec 15; 8(4):199-212. PubMed ID: 7888828
    [Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. A splicing mutation of the RHAG gene associated with the Rhnull phenotype.
    Kawano M, Iwamoto S, Okuda H, Fukuda S, Hasegawa N, Kajii E.
    Ann Hum Genet; 1998 Mar 10; 62(Pt 2):107-13. PubMed ID: 9759472
    [Abstract] [Full Text] [Related]

  • 15. 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 10; 48(2):151-9. PubMed ID: 9929383
    [Abstract] [Full Text] [Related]

  • 16. 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 10; 76(4):247-8. PubMed ID: 10394146
    [No Abstract] [Full Text] [Related]

  • 17. 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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  • 18. Sequence, organization, and evolution of Rh50 glycoprotein genes in nonhuman primates.
    Huang CH, Liu Z, Apoil PA, Blancher A.
    J Mol Evol; 2000 Jul 15; 51(1):76-87. PubMed ID: 10903374
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. RH blood group system and molecular basis of Rh-deficiency.
    Cartron JP.
    Baillieres Best Pract Res Clin Haematol; 1999 Dec 01; 12(4):655-89. PubMed ID: 10895258
    [Abstract] [Full Text] [Related]

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