G. Lopez

发表

Glycophorins and the MNS blood group system: a narrative review

C. Hyland, R. Flower, G. Lopez, 2021, Annals of Blood.

Frequency of Mia (MNS7) and Classification of Mia-Positive Hybrid Glycophorins in an Australian Blood Donor Population

Y. Liew, C. Hyland, R. Flower, 2019, Transfusion Medicine and Hemotherapy.

Genotyping analysis of MNS blood group GP(B‐A‐B) hybrid glycophorins in the Chinese Southern Han population using a high‐resolution melting assay

Yang Zhang, C. Hyland, R. Flower, 2018, Transfusion.

An alloantibody in a homozygous GYP*Mur individual defines JENU (MNS49), a new high‐frequency antigen on glycophorin B

Y. Liew, C. Hyland, R. Flower, 2017, Transfusion.

GYP*Kip, a novel GYP(B‐A‐B) hybrid allele, encoding the MNS48 (KIPP) antigen

C. Hyland, R. Flower, G. Luo, 2016, Transfusion.

Genotyping for Glycophorin GYP(B-A-B) Hybrid Genes Using a Single Nucleotide Polymorphism-Based Algorithm by Matrix-Assisted Laser Desorption/Ionisation, Time-of-Flight Mass Spectrometry

C. Hyland, R. Flower, G. Luo, 2016, Molecular Biotechnology.

Evaluation of targeted exome sequencing for 28 protein‐based blood group systems, including the homologous gene systems, for blood group genotyping

Y. Liew, E. Roulis, C. Hyland, 2017, Transfusion.

A D+ blood donor with a novel RHD*D‐CE(5‐6)‐D gene variant exhibits the low‐frequency antigen RH23 (DW) characteristic of the partial DVa phenotype

Y. Liew, C. Hyland, R. Flower, 2016, Transfusion.

Routine application of genotyping a step closer: direct PCR on plasma

C. Hyland, R. Flower, E. Schoeman, 2016 .

Targeted exome sequencing defines novel and rare variants in complex blood group serology cases for a red blood cell reference laboratory setting

Y. Liew, C. Hyland, R. Flower, 2018, Transfusion.

Duffy blood group phenotype–genotype correlations using high‐resolution melting analysis PCR and microarray reveal complex cases including a new null FY*A allele: the role for sequencing in genotyping algorithms

Y. Liew, R. Flower, G. Lopez, 2015, Vox sanguinis.

Molecular typing for the Indian blood group associated 252G>C single nucleotide polymorphism in a selected cohort of Australian blood donors.

Y. Liew, C. Hyland, R. Flower, 2015, Blood transfusion = Trasfusione del sangue.

A DEL phenotype attributed to RHD Exon 9 sequence deletion: slipped‐strand mispairing and blood group polymorphisms

Y. Liew, C. Hyland, R. Flower, 2018, Transfusion.

Anti‐D in a mother, hemizygous for the variant RHD*DNB gene, associated with hemolytic disease of the fetus and newborn

Y. Liew, C. Hyland, R. Flower, 2017, Transfusion.

A novel FY*A allele with the 265T and 298A SNPs formerly associated exclusively with the FY*B allele and weak Fyb antigen expression: implication for genotyping interpretative algorithms

Y. Liew, R. Flower, G. Lopez, 2015, Vox sanguinis.

Modified expression of the KEL2 (k) blood group antigen attributed to p.Leu196Val amino acid change three residues from the K/k antigen polymorphism site: implications for donor screening

Y. Liew, C. Hyland, R. Flower, 2018, Transfusion.

Identification of six new RHCE variant alleles in individuals of diverse racial origin

F. Garcia-sanchez, C. Hyland, A. Cemborain, 2016, Transfusion.

Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management

Y. Liew, C. Hyland, R. Flower, 2017, Vox sanguinis.

Clinical scale ex vivo manufacture of neutrophils from hematopoietic progenitor cells

Nicholas E. Timmins, L. Nielsen, Stefanie Dietmair, 2009, Biotechnology and bioengineering.

Non-invasive fetal RHD genotyping for RhD negative women stratified into RHD gene deletion or variant groups: comparative accuracy using two blood collection tube types.

C. Hyland, J. Hyett, R. Puddephatt, 2017, Pathology.

Hemolytic disease of the fetus and newborn caused by anti-sD antibody in a GP.Mur/Mur Thai mother and review of the prevalence of sD in Thai blood donors.

Y. Liew, C. Hyland, R. Flower, 2022, Transfusion.

GP.Mur red blood cells express variant form of s antigen (MNS4)

Y. Liew, C. Hyland, R. Flower, 2018 .

A new high‐prevalence LW antigen detected by an antibody in an Indigenous Australian homozygous for LW*A c.309C>A variant

Y. Liew, C. Hyland, R. Flower, 2022, Vox sanguinis.

A standardized immunofluorescence test method with human neutrophil antigen‐expressing cell lines to enhance antibody detection

F. Hirayama, M. Dean, Y. Fung, 2012, Vox sanguinis.

Y. Liew, G. Lopez, J. Morrison, 2015, Vox sanguinis.