메뉴 건너뛰기




Volumn 48, Issue 1, 2013, Pages 113-116

RHD gene polymorphisms in alloimmunized RhD-negative individuals with high rate of racial admixture

Author keywords

Anti D alloantibody; PCR; Polymorphisms; RHD gene; RHD

Indexed keywords

ALLOANTIBODY; GENOMIC DNA; RHESUS D ANTIBODY;

EID: 84873204559     PISSN: 14730502     EISSN: 18781683     Source Type: Journal    
DOI: 10.1016/j.transci.2012.09.004     Document Type: Article
Times cited : (7)

References (21)
  • 1
    • 0028569107 scopus 로고
    • The Rh blood group system: additional complexities
    • Issitt P.D. The Rh blood group system: additional complexities. Immunohematology 1994, 10:109-116.
    • (1994) Immunohematology , vol.10 , pp. 109-116
    • Issitt, P.D.1
  • 2
    • 0006420405 scopus 로고    scopus 로고
    • International society of blood transfusion working party on terminology for red cell surface antigens
    • Daniels G.L., Anstee D.J., Cartron J.P., et al. International society of blood transfusion working party on terminology for red cell surface antigens. Vox Sang 2001, 80:193-196.
    • (2001) Vox Sang , vol.80 , pp. 193-196
    • Daniels, G.L.1    Anstee, D.J.2    Cartron, J.P.3
  • 3
    • 0026101085 scopus 로고
    • Localization of the human Rh blood group gene structure to chromosome region 1p34.3-1p36.1 by in situ hybridization
    • Cherif-Zahar B., Mattei M.G., Le V.C., Bailly P., Cartron J.P., Colin Y. Localization of the human Rh blood group gene structure to chromosome region 1p34.3-1p36.1 by in situ hybridization. Human Genetics 1991, 86:398-400.
    • (1991) Human Genetics , vol.86 , pp. 398-400
    • Cherif-Zahar, B.1    Mattei, M.G.2    Le, V.C.3    Bailly, P.4    Cartron, J.P.5    Colin, Y.6
  • 4
  • 6
    • 0030945033 scopus 로고    scopus 로고
    • Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene
    • Avent N.D., Martin P.G., Armstrong-Fisher S.S., et al. Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene. Blood 1997, 89:2568-2577.
    • (1997) Blood , vol.89 , pp. 2568-2577
    • Avent, N.D.1    Martin, P.G.2    Armstrong-Fisher, S.S.3
  • 7
    • 15244361715 scopus 로고    scopus 로고
    • Molecular characterization of D-Korean persons: development of a diagnostic strategy
    • Kim Jy, Kim Sy, Kim C.A., Yon G.S., Park S.S. Molecular characterization of D-Korean persons: development of a diagnostic strategy. Transfusion 2005, 45:345-352.
    • (2005) Transfusion , vol.45 , pp. 345-352
    • Kim, J.1    Kim, S.2    Kim, C.A.3    Yon, G.S.4    Park, S.S.5
  • 8
    • 0033957696 scopus 로고    scopus 로고
    • The presence of an RHD pseudogene containing a 37 bp duplication and a nonsense mutation in africans with the Rh D-negative blood group phenotype
    • Singleton B.K., Green C.A., Avent N.D., et al. The presence of an RHD pseudogene containing a 37 bp duplication and a nonsense mutation in africans with the Rh D-negative blood group phenotype. Blood 2000, 95:12-18.
    • (2000) Blood , vol.95 , pp. 12-18
    • Singleton, B.K.1    Green, C.A.2    Avent, N.D.3
  • 9
    • 0032932817 scopus 로고    scopus 로고
    • Molecular basis of weak D phenotypes
    • Wagner F.F., Flegel W.A. Molecular basis of weak D phenotypes. Blood 1999, 93:385-393.
    • (1999) Blood , vol.93 , pp. 385-393
    • Wagner, F.F.1    Flegel, W.A.2
  • 10
    • 0035716917 scopus 로고    scopus 로고
    • RHD sequencing: a new tool for decision making on transfusion therapy and provision of Rh prophylaxis
    • Legler T.J., Maas J.H., Kohler M., et al. RHD sequencing: a new tool for decision making on transfusion therapy and provision of Rh prophylaxis. Transfus Med 2001, 11:383-388.
    • (2001) Transfus Med , vol.11 , pp. 383-388
    • Legler, T.J.1    Maas, J.H.2    Kohler, M.3
  • 11
    • 39749121512 scopus 로고    scopus 로고
    • Rh discrepancies caused by variable reactivity of partial and weak D types different serologic techniques
    • Dennome G.A., Dake L.R., Vilensky D., Ramyar L., Judd W.J. Rh discrepancies caused by variable reactivity of partial and weak D types different serologic techniques. Transfusion 2008, 48:473-478.
    • (2008) Transfusion , vol.48 , pp. 473-478
    • Dennome, G.A.1    Dake, L.R.2    Vilensky, D.3    Ramyar, L.4    Judd, W.J.5
  • 12
    • 84873122673 scopus 로고    scopus 로고
    • WHO. Model standard operating procedure for blood transfusion services. Publication Geneva: World Health Organization;
    • WHO. Model standard operating procedure for blood transfusion services. Publication Geneva: World Health Organization; 2002.
    • (2002)
  • 13
    • 84873135174 scopus 로고    scopus 로고
    • German guidelines for antigen D typing 2000, 7 July 2000. .
    • Wagner FF. German guidelines for antigen D typing 2000, 7 July 2000. . http://www.uni-ulm.de/flegel/RH.
    • Wagner, F.F.1
  • 14
    • 11144354712 scopus 로고    scopus 로고
    • Guidelines for compatibility procedures in blood transfusion laboratories
    • British Committee for Standards in Haematology
    • British Committee for Standards in Haematology Guidelines for compatibility procedures in blood transfusion laboratories. Transfus Med 2004, 14:59-73.
    • (2004) Transfus Med , vol.14 , pp. 59-73
  • 15
    • 0030009496 scopus 로고    scopus 로고
    • The Rh antigen D: partial D antigens and associated low incidence antigens
    • Tippett P., Lomas-Francis C., Wallace M. The Rh antigen D: partial D antigens and associated low incidence antigens. Vox Sang 1996, 70:123-131.
    • (1996) Vox Sang , vol.70 , pp. 123-131
    • Tippett, P.1    Lomas-Francis, C.2    Wallace, M.3
  • 16
    • 84899661375 scopus 로고    scopus 로고
    • RHD antigen density and agglutination in RHD variant red cells
    • Flegel W.A., Wagner F.F. RHD antigen density and agglutination in RHD variant red cells. Transfus Clin Biol 1996, 380:5-10.
    • (1996) Transfus Clin Biol , vol.380 , pp. 5-10
    • Flegel, W.A.1    Wagner, F.F.2
  • 17
    • 0032521490 scopus 로고    scopus 로고
    • Three molecular structures cause Rhesus D category VI phenotypes with distinct immunohematologic features
    • Wagner F.F., Gassner C., Muller T.H., Schonitzer D., Schunter F., Flegel W.A. Three molecular structures cause Rhesus D category VI phenotypes with distinct immunohematologic features. Blood 1998, 91:2157-2168.
    • (1998) Blood , vol.91 , pp. 2157-2168
    • Wagner, F.F.1    Gassner, C.2    Muller, T.H.3    Schonitzer, D.4    Schunter, F.5    Flegel, W.A.6
  • 18
    • 84858796209 scopus 로고    scopus 로고
    • RHD alleles in Brazilian blood donors with weak D or D-negative phenotypes
    • Cruz B.R., Chiba A.K., Moritz E., Bordin J.O. RHD alleles in Brazilian blood donors with weak D or D-negative phenotypes. Transfus Med 2012, 22(2):84-89.
    • (2012) Transfus Med , vol.22 , Issue.2 , pp. 84-89
    • Cruz, B.R.1    Chiba, A.K.2    Moritz, E.3    Bordin, J.O.4
  • 19
    • 0031035263 scopus 로고    scopus 로고
    • Molecular background of VS and weak C expression in blacks
    • Faas B.H.W., Beckers E.A.M., Wildoer P., et al. Molecular background of VS and weak C expression in blacks. Transfusion 1997, 37:38-44.
    • (1997) Transfusion , vol.37 , pp. 38-44
    • Faas, B.H.W.1    Beckers, E.A.M.2    Wildoer, P.3
  • 20
    • 0036628978 scopus 로고    scopus 로고
    • Presence of the RHD pseudogene and the hybrid RHD-CE-D(s) gene in Brazilians with the D-negative phenotype
    • Rodrigues A., Rios M., Pellegrino J., Costa F.F., Castilho L. Presence of the RHD pseudogene and the hybrid RHD-CE-D(s) gene in Brazilians with the D-negative phenotype. Braz J Med Biol Res 2002, 35:767-773.
    • (2002) Braz J Med Biol Res , vol.35 , pp. 767-773
    • Rodrigues, A.1    Rios, M.2    Pellegrino, J.3    Costa, F.F.4    Castilho, L.5
  • 21
    • 0032762182 scopus 로고    scopus 로고
    • DAR, a new RhD variant involving exons 4, 5, and 7, often in linkage with ceAR, a new Rhce variant frequently found in african blacks
    • Hemker M.B., Ligthart P.C., Berger L., van Rhenen D.J., van der Schoot C.E., Wijk P.A. DAR, a new RhD variant involving exons 4, 5, and 7, often in linkage with ceAR, a new Rhce variant frequently found in african blacks. Blood 1999, 94:4337-4342.
    • (1999) Blood , vol.94 , pp. 4337-4342
    • Hemker, M.B.1    Ligthart, P.C.2    Berger, L.3    van Rhenen, D.J.4    van der Schoot, C.E.5    Wijk, P.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.