These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 9454778)

  • 1. 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; 91(4):1458-63. PubMed ID: 9454778
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 92(5):1776-84. PubMed ID: 9716608
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The human Rh50 glycoprotein gene. Structural organization and associated splicing defect resulting in Rh(null) disease.
    Huang CH
    J Biol Chem; 1998 Jan; 273(4):2207-13. PubMed ID: 9442063
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. 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; 92(2):664-71. PubMed ID: 9657769
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 92(7):2535-40. PubMed ID: 9746795
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 64(1):108-17. PubMed ID: 9915949
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 12(2):168-73. PubMed ID: 8563755
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 92(2):639-46. PubMed ID: 9657766
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 62(Pt 2):107-13. PubMed ID: 9759472
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 62(1):25-32. PubMed ID: 10467273
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 243(1):233-40. PubMed ID: 9473510
    [TBL] [Abstract][Full Text] [Related]  

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

  • 14. Structure and expression of the RH locus in the Rh-deficiency syndrome.
    Chérif-Zahar B; Raynal V; Le Van Kim C; D'Ambrosio AM; Bailly P; Cartron JP; Colin Y
    Blood; 1993 Jul; 82(2):656-62. PubMed ID: 8329719
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 249(1):78-85. PubMed ID: 9705835
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expression of the Rh-related glycoprotein (Rh50).
    Suyama K; Lunn R; Smith BL; Haller S
    Acta Haematol; 1998; 100(4):181-6. PubMed ID: 9973639
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 287 ( Pt 1)(Pt 1):223-8. PubMed ID: 1417776
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evolutionary history of the Rh blood group-related genes in vertebrates.
    Kitano T; Saitou N
    Immunogenetics; 2000 Aug; 51(10):856-62. PubMed ID: 10970100
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 48(2):151-9. PubMed ID: 9929383
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel nonsense mutation in RHAG gene responsible for Rh
    Hou L; Yan QD; Tian L
    Transfus Apher Sci; 2017 Apr; 56(2):220-222. PubMed ID: 28063760
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.