Associated Papers
Determination of CD177 (human neutrophil antigen 2) polymorphisms using nanopore sequencing.
Kløve-Mogensen K et al.
Vox Sanguinis, 2025
The CD177 c.1291A Allele Leads to a Loss of Membrane Expression and Mimics a CD177-Null Phenotype.
Traum A et al.
International Journal of Molecular Sciences, 2024
An accurate genetic assay to identify human neutrophil antigen 2 deficiency.
Li Y et al.
Transfusion Medicine (oxford, England), 2023
Human neutrophil antigen 2 sequence-based typing: Joining the hunt for the CD177 answer.
Browne T et al.
Vox Sanguinis, 2022
Decreased CD177pos neutrophils in myeloid neoplasms is associated with NPM1, RUNX1, TET2, and U2AF1 S34F mutations.
Alayed K et al.
Leukemia Research, 2022
Multicenter Study on Differential Human Neutrophil Antigen 2 Expression and Underlying Molecular Mechanisms.
Flesch BK et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020
A novel nonsense mutation found in the CD177 gene of Thai individuals with the HNA-2 null phenotype.
Siriphanthong K et al.
Transfusion Medicine (oxford, England), 2020
The nonconservative CD177 single-nucleotide polymorphism c.1291G>A is a genetic determinant for human neutrophil antigen-2 atypical/low expression and deficiency.
Wu J et al.
Transfusion, 2019
Towards a Regional Registry of Extended Typed Blood Donors: Molecular Typing for Blood Group, Platelet and Granulocyte Antigens.
Portegys J et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2018
A sequence-specific polymerase chain reaction method for HNA-2 genotyping: homozygous c.843A>T mutation predicts the absence of CD177.
Bayat B et al.
Transfusion, 2016
Heterogeneity of Human Neutrophil CD177 Expression Results from CD177P1 Pseudogene Conversion.
Wu Z et al.
Plos Genetics, 2016
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