about
Two previously proposed P1/P2-differentiating and nine novel polymorphisms at the A4GALT (Pk) locus do not correlate with the presence of the P1 blood group antigen.Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferaseRIFINs are adhesins implicated in severe Plasmodium falciparum malariaA novel mutation in the complement regulator clusterin in recurrent hemolytic uremic syndrome.Two cases of hemolytic uremic syndrome caused by Streptococcus pneumoniae serotype 3, one being a vaccine failure.Shiga toxin-induced complement-mediated hemolysis and release of complement-coated red blood cell-derived microvesicles in hemolytic uremic syndrome.International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Berlin report.Genomic characterization of the kidd blood group gene:different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns.Universal red blood cells--enzymatic conversion of blood group A and B antigens.A synthetic globotriaosylceramide analogue inhibits HIV-1 infection in vitro by two mechanisms.An Ael allele-specific nucleotide insertion at the blood group ABO locus and its detection using a sequence-specific polymerase chain reaction.Will Genotyping Replace Serology in Future Routine Blood Grouping? - Opinion 4: Personalized versus Universal Blood Transfusions - Combining the Efforts.Genetic heterogeneity at the glycosyltransferase loci underlying the GLOB blood group system and collection.Mixed field reactions in ABO and Rh typing chimerism likely resulting from twin haematopoiesis.The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein.The cis-AB blood group phenotype: fundamental lessons in glycobiology.Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes.International Society of Blood Transfusion Committee on Terminology for Red Cell Surface Antigens: Cape Town report.Application of DNA analysis to the quality assurance of reagent red blood cells.Modifying the red cell surface: towards an ABO-universal blood supply.Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles.Do ABO blood group antigens hamper the therapeutic efficacy of mesenchymal stromal cells?The O2 allele: questioning the phenotypic definition of an ABO allele.An update on the GLOB blood group system and collection.P1PK: the blood group system that changed its name and expanded.A and B antigen levels acquired by group O donor-derived erythrocytes following ABO-non-identical transfusion or minor ABO-incompatible haematopoietic stem cell transplantation.Identification of a GH110 subfamily of alpha 1,3-galactosidases: novel enzymes for removal of the alpha 3Gal xenotransplantation antigen.Identification of a novel A4GALT exon reveals the genetic basis of the P1/P2 histo-blood groups.A clinically applicable method for determining the three major alleles at the Duffy (FY) blood group locus using polymerase chain reaction with allele-specific primers.Frequent occurrence of a variant O1 gene at the blood group ABO locus.SMIM1 variants rs1175550 and rs143702418 independently modulate Vel blood group antigen expression.International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012).Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles.A simple screening assay for the most common JK*0 alleles revealed compound heterozygosity in Jk(a-b-) probands from Guam.Homozygosity for a null allele of SMIM1 defines the Vel-negative blood group phenotype.The human P(k) histo-blood group antigen provides protection against HIV-1 infection.Autologous del(20q)-positive erythroid progenitor cells, re-emerging after DLI treatment of an MDS patient relapsing after allo-SCT, can provide a normal peripheral red blood cell count.ADP acting on P2Y13 receptors is a negative feedback pathway for ATP release from human red blood cells.Erythroid urea transporter deficiency due to novel JKnull alleles.The Abantu phenotype in the ABO blood group system is due to a splice-site mutation in a hybrid between a new O1-like allelic lineage and the A2 allele.
P50
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P50
description
researcher
@en
wetenschapper
@nl
name
M L Olsson
@en
M L Olsson
@nl
type
label
M L Olsson
@en
M L Olsson
@nl
prefLabel
M L Olsson
@en
M L Olsson
@nl
P106
P31
P496
0000-0003-1647-9610