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Cai X, Jin S, Liu X, et al. Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles. Transfusion 2013;53:2910–6. Cai X Jin S Liu X . Molecular genetic analysis of ABO blood group variations reveals 29 novel ABO subgroup alleles . Transfusion 2013 ; 53 : 2910 6 . 10.1111/trf.1216823521133 Search in Google Scholar

Vege S, Lomas-Francis C, Aeschlimann J, et al. Three novel ABO alleles and associated serologic phenotypes give insights for bioinformatics and NGS. Transfusion 2017;57(Suppl 3):44A(C52-A03H). Vege S Lomas-Francis C Aeschlimann J . Three novel ABO alleles and associated serologic phenotypes give insights for bioinformatics and NGS . Transfusion 2017 ; 57 ( Suppl 3 ): 44A(C52-A03H) . Search in Google Scholar

Sano R, Nakajima T, Takahashi Y, et al. Expression of ABO blood-group genes is dependent upon an erythroid cell– specific regulatory element that is deleted in persons with the Bm phenotype. Blood 2012;119:5301–10. Sano R Nakajima T Takahashi Y . Expression of ABO blood-group genes is dependent upon an erythroid cell– specific regulatory element that is deleted in persons with the Bm phenotype . Blood 2012 ; 119 : 5301 10 . 10.1182/blood-2011-10-38716722408256 Search in Google Scholar

Nakajima T, Sano R, Takahashi Y, et al. Mutation of the GATA site in the erythroid cell–specific regulatory element of the ABO gene in a Bm subgroup individual. Transfusion 2013;53: 2917–27. Nakajima T Sano R Takahashi Y . Mutation of the GATA site in the erythroid cell–specific regulatory element of the ABO gene in a Bm subgroup individual . Transfusion 2013 ; 53 : 2917 27 . Search in Google Scholar

Takahashi Y, Isa K, Sano R, et al. Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype. Vox Sang 2014;106:167–75. Takahashi Y Isa K Sano R . Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype . Vox Sang 2014 ; 106 : 167 75 . 10.1111/vox.1207723992526 Search in Google Scholar

Takahashi Y, Isa K, Sano R, et al. Presence of nucleotide substitutions in transcriptional regulatory elements such as the erythroid cell-specific enhancer-like element and the ABO promoter in individuals with phenotypes A3 and B3, respectively. Vox Sang 2014;107:171–80. Takahashi Y Isa K Sano R . Presence of nucleotide substitutions in transcriptional regulatory elements such as the erythroid cell-specific enhancer-like element and the ABO promoter in individuals with phenotypes A3 and B3, respectively . Vox Sang 2014 ; 107 : 171 80 . 10.1111/vox.1213624602004 Search in Google Scholar

Sano R, Kuboya E, Nakajima T, et al. A 3.0-kb deletion including an erythroid cell-specific regulatory element in intron 1 of the ABO blood group gene in an individual with the Bm phenotype. Vox Sang 2015;108:310–3. Sano R Kuboya E Nakajima T . A 3.0-kb deletion including an erythroid cell-specific regulatory element in intron 1 of the ABO blood group gene in an individual with the Bm phenotype . Vox Sang 2015 ; 108 : 310 3 . 10.1111/vox.1221625523382 Search in Google Scholar

Oda A, Isa K, Ogasawara K, et al. A novel mutation of the GATA site in the erythroid cell specific regulatory element of the ABO gene in a blood donor with the AmB phenotype. Vox Sang 2015;108:425–7. Oda A Isa K Ogasawara K . A novel mutation of the GATA site in the erythroid cell specific regulatory element of the ABO gene in a blood donor with the AmB phenotype . Vox Sang 2015 ; 108 : 425 7 . 10.1111/vox.1222925557060 Search in Google Scholar

Tao C, Xiao J, Hu Y, et al. A novel B allele with c.28+5885C>T substitution in the erythroid cell–specific regulatory element identified in an individual with phenotype B3. Transfusion 2017;57:1318–9. Tao C Xiao J Hu Y . A novel B allele with c.28+5885C>T substitution in the erythroid cell–specific regulatory element identified in an individual with phenotype B3 . Transfusion 2017 ; 57 : 1318 9 . 10.1111/trf.1406428425606 Search in Google Scholar

Ogasawara K, Miyazaki T, Ito S, et al. The B allele with a 5.8 kb deletion in intron 1 of the ABO gene is the major allele in Japanese individuals with Bm and A1Bm phenotypes. Vox Sang 2018;113:393–6. Ogasawara K Miyazaki T Ito S . The B allele with a 5.8 kb deletion in intron 1 of the ABO gene is the major allele in Japanese individuals with Bm and A1Bm phenotypes . Vox Sang 2018 ; 113 : 393 6 . 10.1111/vox.1264229473176 Search in Google Scholar

Ying Y, Hong X, Xu X, et al. A novel mutation +5904 C>T of RUNX1 site in the erythroid cell-specific regulatory element decreases the ABO antigen expression in Chinese population. Vox Sang 2018;113:594–600. Ying Y Hong X Xu X . A novel mutation +5904 C>T of RUNX1 site in the erythroid cell-specific regulatory element decreases the ABO antigen expression in Chinese population . Vox Sang 2018 ; 113 : 594 600 . 10.1111/vox.1267629978484 Search in Google Scholar

Wu PC, Lin Y-H, Tsai LF, et al. ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies. Transfusion 2018;58:2232–42. Wu PC Lin Y-H Tsai LF . ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies . Transfusion 2018 ; 58 : 2232 42 . 10.1111/trf.1465429770457 Search in Google Scholar

Ouellette K, Stephanie K, Sweeney J. Adsorption-elution in a weak B subgroup due to a polymorphism in the enhancer region of intron 1 of the B allele. Transfusion 2018;58(Suppl S2):194A(IGT86). Ouellette K Stephanie K Sweeney J . Adsorption-elution in a weak B subgroup due to a polymorphism in the enhancer region of intron 1 of the B allele . Transfusion 2018 ; 58 ( Suppl S2 ): 194A(IGT86) . Search in Google Scholar

Hult AK, Hellberg A, Hosseini-Maaf B, et al. Disrupted RUNX1 motifs in the ABO gene explain samples with A3 and B3 phenotypes. Vox Sang 2020;115(Suppl 1):15(3A-S04-03). Hult AK Hellberg A , Hosseini- Maaf B . Disrupted RUNX1 motifs in the ABO gene explain samples with A3 and B3 phenotypes . Vox Sang 2020 ; 115 ( Suppl 1 ): 15(3A-S04-03) . Search in Google Scholar

Stef M, Fennell K, Apraiz I, et al. RH genotyping by nonspecific quantitative next-generation sequencing. Transfusion 2020; 60:2691–701. Stef M Fennell K Apraiz I . RH genotyping by nonspecific quantitative next-generation sequencing . Transfusion 2020 ; 60 : 2691 701 . 10.1111/trf.1603432871036 Search in Google Scholar

Thuresson B, Hellberg A, Olsson ML. Disruption of a binding site for the erythroid transcription factor GATA-1 in intron 1 of the ABO gene in Am and Bm subgroup samples. Vox Sang 2013;105(Suppl 1):44(3C-S22-04). Thuresson B Hellberg A Olsson ML . Disruption of a binding site for the erythroid transcription factor GATA-1 in intron 1 of the ABO gene in Am and Bm subgroup samples . Vox Sang 2013 ; 105 ( Suppl 1 ): 44(3C-S22-04) . Search in Google Scholar

JASPAR. A database of transcription factor binding profiles. Available from http://jaspar.genereg.net/. Accessed 20 January 2021. JASPAR . A database of transcription factor binding profiles . Available from http://jaspar.genereg.net/. Accessed 20 January 2021 . Search in Google Scholar

eISSN:
1930-3955
Langue:
Anglais
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4 fois par an
Sujets de la revue:
Medicine, Clinical Medicine, Laboratory Medicine