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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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Blood Group Databases—Creating Order Out of Chaos?

Transfusion medicine reviews, 2021-04, Vol.35 (2), p.67-69

Storry, Jill R.

2021

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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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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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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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A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with Bw phenotype

Transfusion (Philadelphia, Pa.), 2022-10, Vol.62 (10), p.E55-E58

2022

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A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B w phenotype

Transfusion (Philadelphia, Pa.), 2022-10, Vol.62 (10), p.E55

2022

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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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A novel nonsense variant in RHAG underlies a Nordic Rh null phenotype

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

2023

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

Blood, 2018-07, Vol.132 (3), p.334-338

2018

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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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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

Blood Group Databases—Creating Order Out of Chaos?

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

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

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

A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with Bw phenotype

A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B w phenotype

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

A novel nonsense variant in RHAG underlies a Nordic Rh null phenotype

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

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

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

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