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

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

2023

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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

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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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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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Characterization of Jk(a+weak): a new blood group phenotype associated with an altered JK01 allele

Transfusion (Philadelphia, Pa.), 2011-02, Vol.51 (2), p.380-392

2011

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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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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, Vol.62 (10), p.55

2022

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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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DAK, a new low-incidence antigen in the Rh blood group system

Transfusion (Philadelphia, Pa.), 2003-10, Vol.43 (10), p.1394-1397

2003

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Molecular basis of the Dombrock null phenotype

Transfusion (Philadelphia, Pa.), 2001-11, Vol.41 (11), p.1405-1407

2001

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Evidence that Hy- RBCs express weak Joa antigen

Transfusion (Philadelphia, Pa.), 2004-02, Vol.44 (2), p.170-172

2004

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Human radical scavenger α 1 -microglobulin protects against hemolysis in vitro and α 1 -microglobulin knockout mice exhibit a macrocytic anemia phenotype

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

2021

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Use of a recombinant deacetylase to convert A 1 red blood cells to the acquired B phenotype for quality control purposes

Blood transfusion = Trasfusione del sangue, 2024-03, Vol.22 (2), p.106

2024

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Genetic basis of the K(0) phenotype in the Swedish population

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

2005

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The low-incidence MNS antigens M(v), s(D), and Mit arise from single amino acid substitutions on GPB

Transfusion (Philadelphia, Pa.), 2001-02, Vol.41 (2), p.269-275

2001

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KEL02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,−2 phenotypes

Vox sanguinis, 2010-08, Vol.99 (2), p.150-157

2010

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Blood group genotype analysis for the quality improvement of reagent test red blood cells

Vox sanguinis, 2005-05, Vol.88 (4), p.265-270

2005

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

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

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

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

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

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

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

Characterization of Jk(a+weak): a new blood group phenotype associated with an altered JK01 allele

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

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

Two new molecular bases for the Dombrock null phenotype

DAK, a new low-incidence antigen in the Rh blood group system

Molecular basis of the Dombrock null phenotype

Evidence that Hy- RBCs express weak Joa antigen

Human radical scavenger α 1 -microglobulin protects against hemolysis in vitro and α 1 -microglobulin knockout mice exhibit a macrocytic anemia phenotype

Use of a recombinant deacetylase to convert A 1 red blood cells to the acquired B phenotype for quality control purposes

Genetic basis of the K(0) phenotype in the Swedish population

The low-incidence MNS antigens M(v), s(D), and Mit arise from single amino acid substitutions on GPB

KEL02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,−2 phenotypes

Blood group genotype analysis for the quality improvement of reagent test red blood cells

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