Associated Papers
Characterisation of the ABO Blood Group Phenotypes Using Third-Generation Sequencing.
Mobegi FM et al.
International Journal of Molecular Sciences, 2025
Truncated glycosyltransferase coding regions in novel ABO alleles give rise to weak A or B blood group expression and discrepant typing results.
Ricci Hagman J et al.
Transfusion, 2023
A c.1046_1048delAGG deletion causes a novel O allele on an ABO*O.01.04 allele in a Chinese Han blood donor.
Zhang X et al.
Transfusion, 2023
Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants.
Gueuning M et al.
Blood Advances, 2023
ABO blood group antigens and differential glycan expression: Perspective on the evolution of common human enzyme deficiencies.
Jajosky RP et al.
Iscience, 2023
ABO gene editing for the conversion of blood type A to universal type O in Rhnull donor-derived human-induced pluripotent stem cells.
Petazzi P et al.
Clinical and Translational Medicine, 2022
Analysis of the Genomic Sequence of ABO Allele Using Next-Generation Sequencing Method.
He Y et al.
Frontiers in Immunology, 2022
A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O.
Matzhold EM et al.
Transfusion, 2020
Hematopoietic Chimera in a Male Blood Donor and His Dizygotic Twin Sister.
Miola MP et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2019
Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.
Möller M et al.
Vox Sanguinis, 2018
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