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Journal Abstract Search

126 related items for PubMed ID: 20576012

  • 1. A novel RHCE*ce 48C, 733G allele with Nucleotide 941C in Exon 7 encodes an altered red blood cell e antigen.
    Hue-Roye K, Hipsky CH, Velliquette RW, Fuchisawa A, Lomas-Francis C, Hoppe C, Reid ME.
    Transfusion; 2011 Jan; 51(1):32-5. PubMed ID: 20576012
    [Abstract] [Full Text] [Related]

  • 2. Molecular background of RH in Bastiaan, the RH:-31,-34 index case, and two novel RHD alleles.
    Reid ME, Hipsky CH, Velliquette RW, Lomas-Francis C, Larimore K, Olsen C.
    Immunohematology; 2012 Jan; 28(3):97-103. PubMed ID: 23286557
    [Abstract] [Full Text] [Related]

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  • 4. RHCE*ceCF encodes partial c and partial e but not CELO, an antigen antithetical to Crawford.
    Hipsky CH, Lomas-Francis C, Fuchisawa A, Reid ME, Moulds M, Christensen J, Nickle P, Vege S, Westhoff C.
    Transfusion; 2011 Jan; 51(1):25-31. PubMed ID: 20609196
    [Abstract] [Full Text] [Related]

  • 5. Weakened expression of 'e' owing to concomitant occurrence of Cys16 and Val245 (VS antigen).
    Rodrigues A, Rios M, Costa FF, Saad ST, Pellegrino J, Castilho L.
    Vox Sang; 2004 Feb; 86(2):136-40. PubMed ID: 15023184
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  • 6. RHCE*ceMO is frequently in cis to RHD*DAU0 and encodes a hr(S) -, hr(B) -, RH:-61 phenotype in black persons: clinical significance.
    Westhoff CM, Vege S, Horn T, Hue-Roye K, Halter Hipsky C, Lomas-Francis C, Reid ME.
    Transfusion; 2013 Nov; 53(11 Suppl 2):2983-9. PubMed ID: 23772606
    [Abstract] [Full Text] [Related]

  • 7. New RHCE*ce variant allele in African descent holds 105C>T (silent) in cis to 48C in Exon 1 and 733G in Exon 5.
    Sippert E, Volkova E, Denomme GA, Liu M, Liu Z, Rios M.
    Transfusion; 2019 Sep; 59(9):3039-3040. PubMed ID: 31002175
    [No Abstract] [Full Text] [Related]

  • 8. DIIIa and DIII Type 5 are encoded by the same allele and are associated with altered RHCE*ce alleles: clinical implications.
    Westhoff CM, Vege S, Halter-Hipsky C, Whorley T, Hue-Roye K, Lomas-Francis C, Reid ME.
    Transfusion; 2010 Jun; 50(6):1303-11. PubMed ID: 20088832
    [Abstract] [Full Text] [Related]

  • 9. A Tutsi family harbouring two new RHCE variant alleles and a new haplotype in the Rh blood group system.
    Deleers M, Thonier V, Claes V, Daelemans C, Peyrard T, El Kenz H.
    Vox Sang; 2020 Jul; 115(5):451-455. PubMed ID: 32196693
    [Abstract] [Full Text] [Related]

  • 10. Molecular basis of the rare gene complex, DIVa(C)-, which encodes four low-prevalence antigens in the Rh blood group system.
    Hipsky CH, Hue-Roye K, Lomas-Francis C, Huang CH, Reid ME.
    Vox Sang; 2012 Feb; 102(2):167-70. PubMed ID: 21729099
    [Abstract] [Full Text] [Related]

  • 11. RHD*weak partial 4.0 is associated with an altered RHCE*ce(48C, 105T, 733G, 744C, 1025T) allele in the Tunisian population.
    Ouchari M, Polin H, Romdhane H, Abdelkefi S, Houissa B, Chakroun T, Gabriel C, Hmida S, Jemni Yacoub S.
    Transfus Med; 2013 Aug; 23(4):245-9. PubMed ID: 23742316
    [Abstract] [Full Text] [Related]

  • 12. Alloanti-c/ce in a c+ceAR/Ce patient suggests that the rare RHCE ceAR allele (ceAR) encodes a partial c antigen.
    Peyrard T, Pham BN, Poupel S, Martin-Blanc S, Auxerre C, Kappler-Gratias S, Bonin P, Rouger P, Le Pennec PY.
    Transfusion; 2009 Nov; 49(11):2406-11. PubMed ID: 19624489
    [Abstract] [Full Text] [Related]

  • 13. The low prevalence Rh antigen Be(a) (Rh36) is associated with RHCE*ce 662C>G in exon 5, which is predicted to encode Rhce 221Arg.
    Hue-Roye K, O'Shea K, Gillett R, Wadsworth LD, Hume H, Barnes J, Kinney J, Hodgins K, Fuchisawa A, Lomas-Francis C, Reid M.
    Vox Sang; 2010 Apr; 98(3 Pt 1):e263-8. PubMed ID: 19951310
    [Abstract] [Full Text] [Related]

  • 14. RHCE variants inherited with altered RHD alleles in Brazilian blood donors.
    Prisco Arnoni C, Guilhem Muniz J, de Paula Vendrame TA, de Medeiros Person R, Roche Moreira Latini F, Castilho L.
    Transfus Med; 2016 Aug; 26(4):285-90. PubMed ID: 27111588
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  • 16. Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.
    Noizat-Pirenne F, Lee K, Pennec PY, Simon P, Kazup P, Bachir D, Rouzaud AM, Roussel M, Juszczak G, Ménanteau C, Rouger P, Kotb R, Cartron JP, Ansart-Pirenne H.
    Blood; 2002 Dec 01; 100(12):4223-31. PubMed ID: 12393640
    [Abstract] [Full Text] [Related]

  • 17. RHCE*cE734C allele encodes an altered c antigen and a suppressed E antigen not detected with standard reagents.
    Silvy M, Barrault A, Velliquette RW, Lomas-Francis C, Simon S, Mortelecque R, Chiaroni J, Bierling P, Noizat-Pirenne F, Bailly P, Tournamille C.
    Transfusion; 2013 May 01; 53(5):955-61. PubMed ID: 22958092
    [Abstract] [Full Text] [Related]

  • 18. Red cells from the original JAL+ proband are also DAK+ and STEM+.
    Hue-Roye K, Reid ME, Westhoff CM, Lomas-Francis C.
    Vox Sang; 2011 Jul 01; 101(1):61-4. PubMed ID: 21477150
    [Abstract] [Full Text] [Related]

  • 19. Prevalence of RHD*DOL and RHCE*ce(818T) in two populations.
    Halter Hipsky C, da Costa DC, Omoto R, Zanette A, Castilho L, Reid ME.
    Immunohematology; 2011 Jul 01; 27(2):66-7. PubMed ID: 22356522
    [Abstract] [Full Text] [Related]

  • 20. The RHD*weak D type 4.0 allele is predominantly but not exclusively cis-associated with the altered RHCE*ce(c.48C, c.105T, c.733G, c.744C, c.1025T) allele in the French population.
    Fichou Y, Maréchal CL, Férec C.
    Transfus Med; 2014 Apr 01; 24(2):120-2. PubMed ID: 24456293
    [No Abstract] [Full Text] [Related]

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