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ABO blood group system: a review of molecular aspects

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Vengelen-Tyler V, ed. Technical manual. 12th ed. Bethesda,MD:American Association of Blood Banks, 1999.Search in Google Scholar

Ogasawara K, Yabe R, Uchikawa M, et al. Molecular genetic analysis of variant phenotypes of the ABO blood group system. Blood 1996;88:2732–7.10.1182/blood.V88.7.2732.bloodjournal8872732Search in Google Scholar

Olsson ML, Chester MA. Frequent occurrence of a variant O1 gene at the blood group A BO locus. Vox Sang 1996;70:26–30.Search in Google Scholar

Grunnet N, Steffensen R, Bennett EP, Clausen H. Evaluation of histo-blood group ABO genotyping in a Danish population: frequency of a novel O allele defined as O2. Vox Sang 1994;67:210–5.10.1111/j.1423-0410.1994.tb01662.xSearch in Google Scholar

Olsson ML, Chester MA. Evidence for a new type of O allele at the AB O locus, due to a combination of the A2 nucleotide deletion and the Ael nucleotide insertion. Vox Sang 1996;71:113–7.Search in Google Scholar

Suzuki K, Iwata M, Tsuji H, et al. A de novo recombination in the AB O blood group gene and evidence for the occurrence of recombination products. Hum Genet 1997;99:454–61.10.1007/s004390050388Search in Google Scholar

Olsson ML, Guerreiro JF, Zago MA, Chester MA. Molecular analysis of the O alleles at the blood group AB O locus in populations of different ethnic origin reveals novel crossing-over events and point mutations. Biochem Biophys Res Commun 1997; 234:779–82.10.1006/bbrc.1997.6713Search in Google Scholar

Yamamoto F, McNeill PD, Hakomori S. Human histo- blood group A2 transferase coded by A2 allele, one of the A subtypes, is characterized by a single base deletion in the coding sequence, which results in an additional domain at the carboxyl terminal. Bio- chem Biophys Res Commun 1992;187:366–74.10.1016/S0006-291X(05)81502-5Search in Google Scholar

Yamamoto F, McNeill PD, Yamamoto M, et al. Molecular genetic analysis of the ABO blood group system. I. Weak subgroups: A3 and B3 alleles. Vox Sang 1993;64:116–9.Search in Google Scholar

Yamamoto F, McNeill PD, Kominato Y, et al.Molecular genetic analysis of the ABO blood group system. II. c i s- AB alleles. Vox Sang 1993;64:120-3.10.1111/j.1423-0410.1993.tb02529.xSearch in Google Scholar

Yoshida A, Yamaguchi H, Okubo Y. Genetic mechanism of ci s - A B inheritance. I. A case associated withunequal chromosomal crossing over. Am J Hum Genet 1980;32:332–8.Search in Google Scholar

Yoshida A, Yamaguchi H, Okubo Y. Genetic mechanism of c is - A B inheritance. II.Cases associated with structural mutation of blood group glycosyltransferase. Am J Hum Genet 1980;32:645–50.Search in Google Scholar

Yu L-C, Yang Y-H, Broadberry RE, Chen Y-H, Lin M. Heterogeneity of the human H blood group α (1,2) fucosyltransferase gene among para-Bombay individuals. Vox Sang 1997;72:36–40.10.1159/000461955Search in Google Scholar

Kaneko M, Nishihara S, Shinya N, et al. Wide variety of point mutations in the Hgene of Bombay and paraBombay individuals that inactivate the H enzyme. Blood 1997;90:839–49.10.1182/blood.V90.2.839Search in Google Scholar

Kelly RJ, Ernst LK, Larsen RD, Bryant JG, Robinson JS, Lowe JB. Molecular basis for H blood group deficiency in Bombay (Oh) and para- Bombay individuals. Proc Natl Acad Sci USA 1994;91:5843–7.10.1073/pnas.91.13.5843Search in Google Scholar

Clausen H, White T, Takio K, et al. Isolation to homogeneity and partial characterization of a histo-blood group A defined Fucα1÷2Galα1÷3-N-acetylgalac- tosaminyltransferase from human lung tissue. J Biol Chem 1990;265:1139–45.10.1016/S0021-9258(19)40169-5Search in Google Scholar

Yamamoto F, Marken J, Tsuji T, White T, Clausen H, Hakomori S. Cloning and characterization of DNA complementary to human UDP-GalNAc: Fucα1>2Galα1>3GalNAc transferase (histo-blood group A transferase) mRNA. J Biol Chem 1990; 265:1146–51.10.1016/S0021-9258(19)40170-1Search in Google Scholar

Yamamoto F, Clausen H, White T, Marken J, Hakomori S. Molecular genetic basis of the histo-blood group ABO system. Nature 1990;345:229–35.10.1038/345229a0Search in Google Scholar

Ogasawara K, Bannai M, Saitou N, et al. Extensive polymorphism of AB O blood group gene: three major lineages of the alleles for the common ABO phenotypes. Hum Genet 1996;97:777–83.10.1007/BF02346189Search in Google Scholar

Olsson ML, Chester MA. A rapid and simple ABO genotype screening method using a novel B/ O 2 versus A /O 2 discriminating nucleotide substitution at the AB O locus. Vox Sang 1995;69:242–7.Search in Google Scholar

Stroncek DF, Konz R, Clay ME, Houchins JP, McCullough J. Determination of AB O glycosyltransferase genotypes by use of polymerase chain reaction and restriction enzymes. Transfusion 1995;35:231–40.10.1046/j.1537-2995.1995.35395184280.xSearch in Google Scholar

Yamamoto F, Hakomori S. Sugar-nucleotide donor specificity of histo-blood group A and B transferases is based on amino acid substitutions. J Biol Chem 1990;265:19257–62.10.1016/S0021-9258(17)30652-XSearch in Google Scholar

Gassner C, SchmardaA, Nussbaumer W, Schönitzer D. ABO glycosyltransferase genotyping by polymerase chain reaction using sequence-specific primers. Blood 1996;88:1852–6.10.1182/blood.V88.5.1852.1852Search in Google Scholar

Wang BJ, Koda Y, Soejima M, Kimura H. Two missense mutations of H type α(1, 2)fucosyltransferase gene (FU T1) responsible for para-Bombay phenotype. Vox Sang 1997;72:31–5.10.1159/000461954Search in Google Scholar

Larsen RD, Ernst LK, Nair RP, Lowe JB. Molecular cloning, sequence, and expression of a human GDP- L-fucose:beta-D-galactoside 2-alpha-L-fucosyltrans- ferase cDNA that can form the H blood group antigen. Proc Natl Acad Sci USA 1990;87:6674–8.10.1073/pnas.87.17.6674545992118655Search in Google Scholar

Wagner Fīţ Flegel WA. Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles. Transfusion 1997;37:284–90.10.1046/j.1537-2995.1997.37397240210.x9122901Search in Google Scholar

Yoshida A. The existence of atypical blood group galactosyltransferase which causes an expression of A2 character in A1B red blood cells. Am J Hum Genet 19283;35:1117–251.Search in Google Scholar

Yoshida A, Dave V, Hamilton HB. Imbalance of blood group A subtypes and the existence of superactive B gene in Japanese in Hiroshima and Nagasaki. Am J Hum Genet 1988;43:422–8.Search in Google Scholar

Ogasawara K, Yabe R, Uchikawa M, et al. Di fferent alleles cause an imbalance in A2and A2B phenotypes of the ABO blood group. Vox Sang 1998;74:242–7.10.1046/j.1423-0410.1998.7440242.xSearch in Google Scholar

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Medizin, Klinische Medizin, Laboratoriumsmedizin