RHD genotyping in weak D phenotypes by multiple polymerase chain reactions
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W. Mayr | M. Malekan | H. Ohto | S. Panzer | T. Legler | D. Schwartz | J. Maas | R. Lynen | M. Kohler | V. Blaschke | N. Bustami
[1] J. Cartron,et al. Specificity and sensitivity of RHD genotyping methods by PCR‐based DNA amplification , 1997, British journal of haematology.
[2] A. Borne,et al. Lower antigen site density and weak D immunogenicity cannot be explained by structural genomic abnormalities or regulatory defects of the RHD gene , 1997, Transfusion.
[3] N. Avent,et al. Molecular analysis of Rh transcripts and polypeptides from individuals expressing the DVI variant phenotype: an RHD gene deletion event does not generate All DVIccEe phenotypes. , 1997, Blood.
[4] B. Carritt,et al. A recombination hot spot in the Rh genes revealed by analysis of unrelated donors with the rare D-- phenotype. , 1996, American journal of human genetics.
[5] P. Gane,et al. Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in RN phenotypes. , 1996, Blood.
[6] W. Mayr,et al. Genotyping of the human platelet antigen systems 1 through 5 by multiplex polymerase chain reaction and ligation‐based typing , 1996, Transfusion.
[7] D. Filbey,et al. Selection of Monoclonal Antibodies for the Identification of D Variants: Ability to Detect Weak D and to Split epD2, epD5 and epD6/7 , 1996, Vox sanguinis.
[8] B. Faas,et al. The R0Har Rh:33 phenotype results from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene , 1996, British journal of haematology.
[9] B. Faas,et al. Rapid Rh D genotyping by polymerase chain reaction-based amplification of DNA. , 1995, Blood.
[10] J. Cartron,et al. Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes. , 1995, Blood.
[11] A. Blancher,et al. Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genes , 1995, British journal of haematology.
[12] A. Maddalena,et al. Molecular analysis of the Rh locus in a person with the Du phenotype , 1994, Transfusion.
[13] C. Hyland,et al. Three unrelated Rh D gene polymorphisms identified among blood donors with Rhesus CCee (r'r') phenotypes. , 1994, Blood.
[14] Y. Colin,et al. Prenatal determination of fetal RhD type by DNA amplification , 1994, The New England journal of medicine.
[15] J. Cartron,et al. Rearrangements of the blood group RhD gene associated with the DVI category phenotype. , 1994, Blood.
[16] J. Cartron,et al. Molecular genetic basis of the human Rhesus blood group system , 1993, Nature Genetics.
[17] K. Coyne,et al. Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals. , 1993, Blood.
[18] E. Kajii,et al. A cDNA Clone Encoding an Rh Polypeptide Detected in RhD‐Negative Erythroid Cells , 1993, Vox sanguinis.
[19] J. Cartron,et al. Molecular cloning and primary structure of the human blood group RhD polypeptide. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[20] M. Tanner,et al. cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expression. , 1990, The Biochemical journal.
[21] J. Cartron,et al. Molecular cloning and protein structure of a human blood group Rh polypeptide. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[22] D. Maddocks,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. , 1997, Blood.
[23] J. Cartron,et al. Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region. , 1994, Genomics.
[24] V. A. Fenger. The medical student. , 1956, World medical journal.