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Elucidation of the low-expressing erythroid CR1 phenotype by bioinformatic mining of the GATA1-driven blood-group regulome

Nature communications, 2023-08, Vol.14 (1), p.5001-5001, Article 5001

2023

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Association of Maternal Regulatory Single Nucleotide Polymorphic CD99 Genotype with Preeclampsia in Pregnancies Carrying Male Fetuses in Ethiopian Women

International journal of molecular sciences, 2020-08, Vol.21 (16), p.5837

2020

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Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype

Nature communications, 2020-07, Vol.11 (1), p.3569-3569, Article 3569

2020

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A novel GYP(B‐A‐B) hybrid in a blood donor identified by a phenotyping discrepancy with different anti‐s reagents

Transfusion (Philadelphia, Pa.), 2023-01, Vol.63 (1), p.E1-E3

2023

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Evidence that CD36 is expressed on red blood cells and constitutes a novel blood group system of clinical importance

Vox sanguinis, 2024-05, Vol.119 (5), p.496-504

2024

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RIFINs are adhesins implicated in severe Plasmodium falciparum malaria

Nature medicine, 2015-04, Vol.21 (4), p.314-317

2015

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Autoantibodies against red blood cell antigens are common in a malaria endemic area

Microbes and infection, 2023-03, Vol.25 (3), p.105060-105060, Article 105060

2023

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Disruption of a GATA1-binding motif upstream of XG / PBDX abolishes Xg a expression and resolves the Xg blood group system

Blood, 2018-07, Vol.132 (3), p.334

2018

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Shiga toxin-induced complement-mediated hemolysis and release of complement-coated red blood cell-derived microvesicles in hemolytic uremic syndrome

The Journal of immunology (1950), 2015-03, Vol.194 (5), p.2309-2318

2015

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Homozygosity for a null allele of SMIM1 defines the Vel-negative blood group phenotype

Nature genetics, 2013-05, Vol.45 (5), p.537-541

2013

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More data needed to establish maternal breast milk IgG as cause for anti‐D hemolytic disease of fetus and newborn

Transfusion (Philadelphia, Pa.), 2018-03, Vol.58 (3), p.828-829

2018

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Transfusion management in the era of magrolimab (Hu5F9‐G4), an anti‐CD47 monoclonal antibody therapy

Transfusion (Philadelphia, Pa.), 2023-12, Vol.63 (12), p.2377-2383

2023

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Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes

Transfusion (Philadelphia, Pa.), 2006-12, Vol.46 (12), p.2149-2155

2006

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Nomenclature for red blood cell blood group alleles

Transfusion (Philadelphia, Pa.), 2013-11, Vol.53 (11pt2), p.2844-2846

Storry, Jill R.

2013

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4.1R-deficient human red blood cells have altered phosphatidylserine exposure pathways and are deficient in CD44 and CD47 glycoproteins

Haematologica (Roma), 2009-10, Vol.94 (10), p.1354-1361

2009

Volltextzugriff (PDF)

Genetic prediction of 33 blood group phenotypes using an existing genotype dataset

Transfusion (Philadelphia, Pa.), 2023-12, Vol.63 (12), p.2297-2310

2023

Volltextzugriff (PDF)

Matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry analysis of 36 blood group alleles among 396 Thai samples reveals region‐specific variants

Transfusion (Philadelphia, Pa.), 2018-07, Vol.58 (7), p.1752-1762

2018

Volltextzugriff (PDF)

Forssman expression on human erythrocytes: biochemical and genetic evidence of a new histo-blood group system

Blood, 2013-02, Vol.121 (8), p.1459-1468

2013

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Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes

The Journal of biological chemistry, 2015-07, Vol.290 (30), p.18505-18518

2015

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ABO transcript levels in peripheral blood and erythropoietic culture show different allele‐related patterns independent of the CBF/NF‐Y enhancer motif and multiple novel allele‐specific variations in the 5′‐ and 3′‐noncoding regions

Transfusion (Philadelphia, Pa.), 2008-03, Vol.48 (3), p.493-504

2008

Volltextzugriff (PDF)

A novel RHCE02 allele, containing the single-nucleotide change c.460A>G, encodes weakened expression of C and e antigens

Transfusion (Philadelphia, Pa.), 2016-09, Vol.56 (9), p.2391-2392

2016

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Platelets inhibit erythrocyte invasion by Plasmodium falciparum at physiological platelet:erythrocyte ratios

Transfusion medicine (Oxford, England), 2022-04, Vol.32 (2), p.168-174

2022

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Dimerization of small integral membrane protein 1 promotes cell surface presentation of the Vel blood group epitope

FEBS letters, 2020-04, Vol.594 (8), p.1261-1270

2020

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Elucidation of the low-expressing erythroid CR1 phenotype by bioinformatic mining of the GATA1-driven blood-group regulome

International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology: Report of the Dubai, Copenhagen and Toronto meetings

Association of Maternal Regulatory Single Nucleotide Polymorphic CD99 Genotype with Preeclampsia in Pregnancies Carrying Male Fetuses in Ethiopian Women

Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype

A novel GYP(B‐A‐B) hybrid in a blood donor identified by a phenotyping discrepancy with different anti‐s reagents

Evidence that CD36 is expressed on red blood cells and constitutes a novel blood group system of clinical importance

RIFINs are adhesins implicated in severe Plasmodium falciparum malaria

Autoantibodies against red blood cell antigens are common in a malaria endemic area

Disruption of a GATA1-binding motif upstream of XG / PBDX abolishes Xg a expression and resolves the Xg blood group system

Shiga toxin-induced complement-mediated hemolysis and release of complement-coated red blood cell-derived microvesicles in hemolytic uremic syndrome

Homozygosity for a null allele of SMIM1 defines the Vel-negative blood group phenotype

More data needed to establish maternal breast milk IgG as cause for anti‐D hemolytic disease of fetus and newborn

Transfusion management in the era of magrolimab (Hu5F9‐G4), an anti‐CD47 monoclonal antibody therapy

Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes

Nomenclature for red blood cell blood group alleles

4.1R-deficient human red blood cells have altered phosphatidylserine exposure pathways and are deficient in CD44 and CD47 glycoproteins

Genetic prediction of 33 blood group phenotypes using an existing genotype dataset

Matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry analysis of 36 blood group alleles among 396 Thai samples reveals region‐specific variants

Forssman expression on human erythrocytes: biochemical and genetic evidence of a new histo-blood group system

Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes

ABO transcript levels in peripheral blood and erythropoietic culture show different allele‐related patterns independent of the CBF/NF‐Y enhancer motif and multiple novel allele‐specific variations in the 5′‐ and 3′‐noncoding regions

A novel RHCE02 allele, containing the single-nucleotide change c.460A>G, encodes weakened expression of C and e antigens

ABO zygosity, but not secretor or Fc receptor status, is a significant risk factor for IVIG-associated hemolysis

Platelets inhibit erythrocyte invasion by Plasmodium falciparum at physiological platelet:erythrocyte ratios

Dimerization of small integral membrane protein 1 promotes cell surface presentation of the Vel blood group epitope

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