ArticleBlood transfusion = Trasfusione del sangue2024
Characterization of GYP(B-A-B) hybrid glycophorins among Thai blood donors with Mi
Article in Blood transfusion = Trasfusione del sangue, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 4 citations in OpenAlex.
- Rapid Electrochemical Impedance Detection of the MiACS omega · 2026Article
- Red cell alloantibodies in 71,525 Malaysian blood donations: Predominance of anti-Mia reflects GP.Mur-associated antigenic diversity.Vox sanguinis · 2026Article
- Optimization of the antibody identification interval in a high-volume transfusion centre.Vox sanguinis · 2026Article
- Prediction of JENU-Negative Phenotype by Genotyping among Thai Patients with Multiple Transfusions.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2025Article
- Multiplex-PCR technique to predict polymorphic antigens - M, N, S and s - and associations between their alleles and MiScientific reports · 2025Article
- Frequencies and subtypes of glycophorinPeerJ · 2025Article
- Defining the breakpoints of hybrid blood group alleles.Blood transfusion = Trasfusione del sangue · 2024Article
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4 authors at 1 institution in 1 country.
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Abstract
backgroundGYPA and GYPB genes encode the antigens of the MNS blood group system carried on glycophorin A (GPA) and glycophorin B (GPB), or on a hybrid molecule of GPA and GPB. GP hybrid variants are created through unequal crossing over and gene conversion, typically from the parent genes GYPA and GYPB. In the present study, we characterized the GYP(B-A-B) hybrid variants among Thai blood donors with Mi MATERIALS AND
methodsAltogether, 1,020 samples from Thai blood donors were tested with anti-Mi
resultsAmong 1,020 blood donors, 127 (12.45%) were Mi(a+) phenotypes. The comparison Mi DISCUSSION: Regarding the hybrid GP variants, a consensus of observed prevalent GYP*Mur and GYP*Bun-like alleles, respectively, was identified in the Thai population. The introduction of our strategy has allowed us to identify the zygosity for GYP hybrid variants, particularly GYP(B-A-B) hybrid genes, when antisera are unavailable and lacking adequate phenotypic features to determine GP variants.
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