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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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The Role of α1-Microglobulin (A1M) in Erythropoiesis and Erythrocyte Homeostasis—Therapeutic Opportunities in Hemolytic Conditions

International journal of molecular sciences, 2020-09, Vol.21 (19), p.7234

2020

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A novel nonsense variant in RHAG underlies a Nordic Rhnull phenotype

Vox sanguinis, 2023-08, Vol.118 (8), p.690-694

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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Babesia divergens Shows Equal Predilection for Human ABO Blood Types in an In Vitro Erythrocyte Preference Assay

Pathogens (Basel), 2023-06, Vol.12 (6), p.803

2023

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Two Prevalent ∼100-kb GYPB Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S–s–U– in Black Africans

Transfusion medicine and hemotherapy, 2020-07, Vol.47 (4), p.326-336

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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Novel single nucleotide deletion in ART4 accounts for the Gy(a−) phenotype in a woman of Lebanese origin

Transfusion (Philadelphia, Pa.), 2021-05, Vol.61 (5), p.E39-E40

2021

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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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Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project

Blood advances, 2016-12, Vol.1 (3), p.240-249

2016

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Automatic for the people: a rapidly evolving movement for the future of genotyping

Transfusion (Philadelphia, Pa.), 2019-11, Vol.59 (11), p.3545-3547

2019

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Characterization of GYPMur and novel GYPBun‐like hybrids in Thai blood donors reveals a qualitatively altered s antigen

Vox sanguinis, 2020-07, Vol.115 (5), p.472-477

2020

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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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Human radical scavenger α1-microglobulin protects against hemolysis in vitro and α1-microglobulin knockout mice exhibit a macrocytic anemia phenotype

Free radical biology & medicine, 2021-01, Vol.162, p.149-159

2021

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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

Volltextzugriff (PDF)

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

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

The Role of α1-Microglobulin (A1M) in Erythropoiesis and Erythrocyte Homeostasis—Therapeutic Opportunities in Hemolytic Conditions

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

A novel nonsense variant in RHAG underlies a Nordic Rhnull phenotype

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

Babesia divergens Shows Equal Predilection for Human ABO Blood Types in an In Vitro Erythrocyte Preference Assay

Two Prevalent ∼100-kb GYPB Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S–s–U– in Black Africans

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

Novel single nucleotide deletion in ART4 accounts for the Gy(a−) phenotype in a woman of Lebanese origin

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

Erythrogene: a database for in-depth analysis of the extensive variation in 36 blood group systems in the 1000 Genomes Project

Automatic for the people: a rapidly evolving movement for the future of genotyping

Characterization of GYPMur and novel GYPBun‐like hybrids in Thai blood donors reveals a qualitatively altered s antigen

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

Human radical scavenger α1-microglobulin protects against hemolysis in vitro and α1-microglobulin knockout mice exhibit a macrocytic anemia 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

International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Basel and three virtual business meetings: Update on blood group systems

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

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