Associated Papers
Molecular Blood Group Screening in Donors from Arabian Countries and Iran Using High-Throughput MALDI-TOF Mass Spectrometry and PCR-SSP.
Flesch BK et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020
Next-Generation Sequencing Technologies in Blood Group Typing.
Fürst D et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020
Blood group typing from whole-genome sequencing data.
Paganini J et al.
Plos One, 2020
DO/ART4 gene sequencing in sub-Saharan cohorts and African migrants: useful data describing the diversity and spreading of rare variants.
Chapel-Fernandes S et al.
Transfusion, 2019
Sequencing of the ART4 gene in sub-Saharan cohorts reveals ethnic differences and two new DO alleles: DO*B-Ile5Thr and DO*B-Trp266Arg.
Durousseau de Coulgeans C et al.
Transfusion, 2015
Synonymous nucleotide polymorphisms influence Dombrock blood group protein expression in K562 cells.
de Coulgeans CD et al.
British Journal of Haematology, 2014
Dombrock genotyping in Brazilian blood donors reveals different regional frequencies of the HY allele.
Piassi FC et al.
Revista Brasileira De Hematologia E Hemoterapia, 2013
A PCR-based strategy for Dombrock screening in Brazilian blood donors reveals a novel allele: the DO* A-WL.
Baleotti W et al.
Journal of Clinical Laboratory Analysis, 2011
New antigen in the Dombrock blood group system, DOYA, ablates expression of Do(a) and weakens expression of Hy, Jo(a), and Gy(a) antigens.
Mayer B et al.
Transfusion, 2010
Dombrock genotyping in a native Congolese cohort reveals two novel alleles.
Chapel-Fernandes S et al.
Transfusion, 2009
Molecular studies of DO alleles reveal that JO is more prevalent than HY in Brazil, whereas HY is more prevalent in New York.
Castilho L et al.
Immunohematology, 2008
Dombrock gene analysis in Brazilian people reveals novel alleles.
Baleotti W et al.
Vox Sanguinis, 2006
Short deletion within the blood group Dombrock locus causing a Do(null) phenotype.
Lucien N et al.
Blood, 2002