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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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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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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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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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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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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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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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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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A large deletion spanning XG and GYG2 constitutes a genetic basis of the Xg null phenotype, underlying anti-Xg a production

Transfusion (Philadelphia, Pa.), 2019-05, Vol.59 (5), p.1843-1849

2019

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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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A large deletion spanning XG and GYG2 constitutes a genetic basis of the Xgnull phenotype, underlying anti‐Xga production

Transfusion (Philadelphia, Pa.), 2019-05, Vol.59 (5), p.1843-1849

2019

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Plasmodium falciparum Is Able To Invade Erythrocytes through a Trypsin-Resistant Pathway Independent of Glycophorin B

Infection and Immunity, 2003-12, Vol.71 (12), p.6742-6746

2003

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An age-dependent ABO discrepancy between mother and baby reveals a novel A(weak) allele

Transfusion (Philadelphia, Pa.), 2015-02, Vol.55 (2), p.422-426

2015

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Mutations in GYPB exon 5 drive the S-s-U+(var) phenotype in persons of African descent: implications for transfusion

Transfusion (Philadelphia, Pa.), 2003-12, Vol.43 (12), p.1738-1747

2003

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Erythroid urea transporter deficiency due to novel JKnull alleles

Transfusion (Philadelphia, Pa.), 2008-02, Vol.48 (2), p.365-372

2008

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The Ok blood group system: an update

Immunohematology, 2021-03, Vol.37 (1), p.18-19

Storry, J.R.

2021

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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)

2022

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The Role of [[alpha].sub.1]-Microglobulin in Erythropoiesis and Erythrocyte Homeostasis--Therapeutic Opportunities in Hemolytic Conditions

International journal of molecular sciences, 2020-10, Vol.21 (19), p.1

2020

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The first example of a paraben-dependent antibody to an Rh protein

Transfusion (Philadelphia, Pa.), 2001-03, Vol.41 (3), p.371-374

2001

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Will Genotyping Replace Serology in Future Routine Blood Grouping? - Opinion 4: Personalized versus Universal Blood Transfusions - Combining the Efforts

Transfusion medicine and hemotherapy, 2009, Vol.36 (3), p.232-233

2009

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Genetic basis of the K0 phenotype in the Swedish population

Transfusion (Philadelphia, Pa.), 2005-04, Vol.45 (4), p.545-549

2005

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A new hybrid RHCE gene (CeNR) is responsible for expression of a novel antigen

Transfusion (Philadelphia, Pa.), 2004-07, Vol.44 (7), p.1047-1051

2004

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Two new molecular bases for the Dombrock null phenotype

British journal of haematology, 2002-06, Vol.117 (3), p.765-767

2002

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Blood Group Databases—Creating Order Out of Chaos?

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

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

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

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

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

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

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

A large deletion spanning XG and GYG2 constitutes a genetic basis of the Xg null phenotype, underlying anti-Xg a production

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

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

A large deletion spanning XG and GYG2 constitutes a genetic basis of the Xgnull phenotype, underlying anti‐Xga production

Plasmodium falciparum Is Able To Invade Erythrocytes through a Trypsin-Resistant Pathway Independent of Glycophorin B

An age-dependent ABO discrepancy between mother and baby reveals a novel A(weak) allele

Mutations in GYPB exon 5 drive the S-s-U+(var) phenotype in persons of African descent: implications for transfusion

Erythroid urea transporter deficiency due to novel JKnull alleles

The Ok blood group system: an update

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

The Role of [[alpha].sub.1]-Microglobulin in Erythropoiesis and Erythrocyte Homeostasis--Therapeutic Opportunities in Hemolytic Conditions

The first example of a paraben-dependent antibody to an Rh protein

Will Genotyping Replace Serology in Future Routine Blood Grouping? - Opinion 4: Personalized versus Universal Blood Transfusions - Combining the Efforts

Genetic basis of the K0 phenotype in the Swedish population

A new hybrid RHCE gene (CeNR) is responsible for expression of a novel antigen

Two new molecular bases for the Dombrock null phenotype

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