ABO alleles are linked with haplotypes of an erythroid cell-specific regulatory element in intron 1 with a few exceptions attributable to genetic recombination
Author:
Affiliation:
1. Department of Legal Medicine; Gunma University Graduate School of Medicine; Maebashi Japan
2. Department of Legal Medicine; Shimane University School of Medicine; Izumo Japan
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/vox.12312/fullpdf
Reference10 articles.
1. Geoff Daniels: Human Blood Groups 3rd edn West Sussex, UK Wiley-Blackwell 2013
2. http://www.ncbi.nlm.nih.gov/projects/gv/rbc/xslcgi.fcgi?cmd=bgmut/systems_info&system=abo
3. Expression of ABO blood-group genes is dependent upon an erythroid cell-specific regulatory element, which is deleted in persons with the Bm phenotype;Sano;Blood,2012
4. Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual;Nakajima;Transfusion,2013
5. Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype;Takahashi;Vox Sang,2014
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1. Review of <i>ABO</i> Expression and Variations based on Transcriptional Regulation of the ABO Blood Group Gene;Transfusion Medicine and Hemotherapy;2024
2. ELUCIDATION OF TRANSCRIPTIONAL REGULATION OF ABO BLOOD GROUP GENE WITH MOLECULAR BASIS FOR ABO ASSOCIATING PHENOMENA INCLUDING WEAK PHENOTYPES;Japanese Journal of Transfusion and Cell Therapy;2023-08-25
3. Emergence of an erythroid cell-specific regulatory region in ABO intron 1 attributable to A- or B-antigen expression on erythrocytes in Hominoidea;Scientific Reports;2023-03-27
4. Analysis of the Genomic Sequence of ABO Allele Using Next-Generation Sequencing Method;Frontiers in Immunology;2022-07-06
5. Molecular basis of weak A subgroups in the Korean population: Identification of three novel subgroup‐causing variants in the ABO regulatory regions;Transfusion;2021-11-16
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