Lista de obras -

A and B antigen levels acquired by group O donor-derived erythrocytes following ABO-non-identical transfusion or minor ABO-incompatible haematopoietic stem cell transplantation

artículo científico publicado en 2017

A clinically applicable method for determining the three major alleles at the Duffy (FY) blood group locus using polymerase chain reaction with allele-specific primers.

artículo científico publicado en 1998

A clue to the basis of allelic enhancement: occurrence of the Ax subgroup in the offspring of blood group O parents

artículo científico publicado en 2005

A large cohort study of the effects of Lewis, <scp>ABO</scp>, 13 other blood groups, and secretor status on <scp>COVID</scp>‐19 susceptibility, severity, and long <scp>COVID</scp>‐19

artículo científico publicado en 2022

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

scientific article published on 02 April 2019

A novel B(weak) hybrid allele lacks three enhancer repeats but generates normal ABO transcript levels

artículo científico publicado en 2011

A novel blood group B subgroup: serological and genetic studies.

artículo científico publicado en 2004

A novel mutation in the complement regulator clusterin in recurrent hemolytic uremic syndrome.

artículo científico publicado en 2009

A novel single-nucleotide substitution in the proximal ABO promoter gives rise to the B3 phenotype

artículo científico publicado en 2019

A rapid and simple ABO genotype screening method using a novel B/O2 versus A/O2 discriminating nucleotide substitution at the ABO locus

scientific article published on 01 January 1995

A simple screening assay for the most common JK*0 alleles revealed compound heterozygosity in Jk(a-b-) probands from Guam.

artículo científico publicado en 2009

A synthetic globotriaosylceramide analogue inhibits HIV-1 infection in vitro by two mechanisms.

artículo científico publicado en 2010

ABO blood type and risk of porcine bioprosthetic aortic valve degeneration: SWEDEHEART observational cohort study

artículo científico publicado en 2019

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

scientific article published on 07 December 2007

ADP acting on P2Y13 receptors is a negative feedback pathway for ATP release from human red blood cells.

artículo científico publicado en 2004

Allele-related variation in minisatellite repeats involved in the transcription of the blood group ABO gene

scientific article published on 01 September 1999

Allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT.

artículo científico publicado en 2018

Allelic variants ofPRDM9associated with high hyperdiploid childhood acute lymphoblastic leukaemia

artículo científico publicado en 2014

Alpha1-Microglobulin is Mitogenic to Human Peripheral Blood Lymphocytes. Regulation by both Enhancing and Suppressive Serum Factors ⬇️

artículo científico publicado el 1 de febrero de 1990

An Ael allele-specific nucleotide insertion at the blood group ABO locus and its detection using a sequence-specific polymerase chain reaction.

artículo científico publicado en 1995

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

artículo científico publicado en 2014

An extensive polymerase chain reaction-allele-specific polymorphism strategy for clinical ABO blood group genotyping that avoids potential errors caused by null, subgroup, and hybrid alleles

scientific article published on 01 November 2007

An update on the GLOB blood group system (and former GLOB collection)

scientific article published on 01 December 2018

An update on the GLOB blood group system and collection.

artículo científico publicado en 2013

Application of DNA analysis to the quality assurance of reagent red blood cells.

artículo científico publicado en 2007

Autologous del(20q)-positive erythroid progenitor cells, re-emerging after DLI treatment of an MDS patient relapsing after allo-SCT, can provide a normal peripheral red blood cell count.

artículo científico publicado en 2004

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

scientific article published on 30 October 2019

Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles.

artículo científico publicado en 2008

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

artículo científico publicado en 2020

Characterization of Jk(a+weak): a new blood group phenotype associated with an altered JK*01 allele ⬇️

artículo científico publicado el 1 de febrero de 2011

Characterization of Monoclonal Anti-alpha1-Microglobulin Antibodies: Binding Strength, Binding Sites, and Inhibition of Lymphocyte Stimulation ⬇️

artículo científico publicado el 1 de noviembre de 1991

Different genotypes causing indiscernible patterns of A expression on A(el) red blood cells as visualized by scanning immunogold electron microscopy

artículo científico publicado en 1998

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

artículo científico publicado en 2019

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

scientific article published on 10 May 2018

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

artículo científico publicado en 2020

Do ABO blood group antigens hamper the therapeutic efficacy of mesenchymal stromal cells?

scientific article published on 13 January 2014

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

artículo científico publicado en 2016

Erythroid urea transporter deficiency due to novel JKnull alleles.

artículo científico publicado en 2007

Evidence for a new type of O allele at the ABO locus, due to a combination of the A2 nucleotide deletion and the Ael nucleotide insertion

artículo científico publicado en 1996

Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotype.

artículo científico publicado en 2007

FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon

artículo científico publicado en 2016

Flow cytometry evaluation of red blood cells mimicking naturally occurring ABO subgroups after modification with variable amounts of function‐spacer‐lipid A and B constructs ⬇️

artículo científico publicado el 3 de agosto de 2011

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

artículo científico publicado en 2012

Frequent occurrence of a variant O1 gene at the blood group ABO locus.

artículo científico publicado en 1996

GBGT1 is allelically diverse but dispensable in humans and naturally occurring anti-FORS1 shows an ABO-restricted pattern

artículo científico publicado en 2018

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

artículo científico publicado en 2005

Genetic heterogeneity at the glycosyltransferase loci underlying the GLOB blood group system and collection.

artículo científico publicado en 2004

Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles

article by Martin L Olsson et al published 1 September 2001 in Blood

Genomic characterization of the kidd blood group gene:different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns.

artículo científico publicado en 2000

Genomic typing of the Kidd blood group locus by a single‐tube allele‐specific primer PCR technique ⬇️

artículo científico publicado el 1 de septiembre de 1998

Glycoproteomic and Phenotypic Elucidation of <i>B4GALNT2</i> Expression Variants in the SID Histo-Blood Group System

artículo científico publicado en 2022

Heterogeneity of the O alleles at the blood group ABO locus in Amerindians

artículo científico publicado en 1998

Heterogeneity of the blood group Ax allele: genetic recombination of common alleles can result in the Ax phenotype.

artículo científico publicado en 1998

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

artículo científico publicado en 2013

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

artículo científico publicado en 2020

Identification of a GH110 subfamily of alpha 1,3-galactosidases: novel enzymes for removal of the alpha 3Gal xenotransplantation antigen.

artículo científico publicado en 2008

Identification of a novel A4GALT exon reveals the genetic basis of the P1/P2 histo-blood groups.

artículo científico publicado en 2010

Identification of human glycosyltransferase genes expressed in erythroid cells predicts potential carbohydrate blood group loci

artículo científico publicado en 2018

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

artículo científico publicado en 2006

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

artículo científico publicado en 2015

International Society of Blood Transfusion Committee on Terminology for Red Cell Surface Antigens: Cape Town report.

artículo científico publicado en 2007

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

scientific article published on 12 November 2018

International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Berlin report.

artículo científico publicado en 2011

International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012).

artículo científico publicado en 2013

Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles.

artículo científico publicado en 2014

Many genetically defined ABO subgroups exhibit characteristic flow cytometric patterns

artículo científico publicado en 2009

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

artículo científico publicado en 2018

Missense mutations in the C-terminal portion of the B4GALNT2-encoded glycosyltransferase underlying the Sd(a-) phenotype

artículo científico publicado en 2019

Mixed field reactions in ABO and Rh typing chimerism likely resulting from twin haematopoiesis.

artículo científico publicado en 2014

Modifying the red cell surface: towards an ABO-universal blood supply.

artículo científico publicado en 2007

Molecular analysis of the O alleles at the blood group ABO locus in populations of different ethnic origin reveals novel crossing-over events and point mutations

scientific article published on 01 May 1997

Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus

artículo científico publicado en 2018

Noninvasive Single-Exon Fetal RHD Determination in a Routine Screening Program in Early Pregnancy ⬇️

artículo científico publicado el 1 de agosto de 2012

P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo‐blood group systems ⬇️

artículo científico publicado el 8 de agosto de 2013

P1PK: the blood group system that changed its name and expanded.

artículo científico publicado en 2013

Phenotype prediction by DNA-based typing of clinically significant blood group systems in Jordanian blood donors

scientific article published on 01 July 2002

Platelet concentrate increases bone ingrowth into porous hydroxyapatite

artículo científico publicado en 2002

Polymorphisms at the ABO locus in subgroup A individuals

artículo científico publicado en 1996

Quantitative and qualitative evaluation of plasma and urine alpha1-microglobulin in healthy donors and patients with different haemolytic disorders and haemochromatosis

artículo científico publicado en 2007

RIFINs are adhesins implicated in severe Plasmodium falciparum malaria

artículo científico publicado en 2015

Rabbit red blood cell stroma bind immunoglobulin M antibodies regardless of blood group specificity.

artículo científico publicado en 2006

Report of the First International Workshop on molecular blood group genotyping

artículo científico publicado en 2005

Report of the Fourth International Workshop on molecular blood group genotyping ⬇️

artículo científico publicado el 6 de septiembre de 2011

Report of the Second International Workshop on molecular blood group genotyping

scientific article published on 01 July 2007

Report of the third international workshop on molecular blood group genotyping

scientific article published on 10 February 2009

SMIM1 variants rs1175550 and rs143702418 independently modulate Vel blood group antigen expression.

artículo científico publicado en 2017

Sex-Discordant Blood Transfusions and Survival After Cardiac Surgery: A Nationwide Cohort Study.

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferase

artículo científico publicado en 2007

The Abantu phenotype in the ABO blood group system is due to a splice-site mutation in a hybrid between a new O1-like allelic lineage and the A2 allele.

artículo científico publicado en 2005

The Bloodgen Project of the European Union, 2003&ndash;2009 ⬇️

artículo científico publicado el 28 de mayo de 2009

The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein.

artículo científico publicado en 1998

The O2 allele: questioning the phenotypic definition of an ABO allele.

artículo científico publicado en 2008

The P1 histo-blood group antigen is present on human red blood cell glycoproteins

artículo científico publicado en 2018

The cis-AB blood group phenotype: fundamental lessons in glycobiology.

artículo científico publicado en 2006

The human P(k) histo-blood group antigen provides protection against HIV-1 infection.

artículo científico publicado en 2009

Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.

artículo científico publicado en 2017

Towards universally acceptable blood

scientific article published on 01 September 2019

Transfusion medicine: a target on the move

artículo científico publicado en 2009

Two cases of hemolytic uremic syndrome caused by Streptococcus pneumoniae serotype 3, one being a vaccine failure.

artículo científico publicado en 2012

Two previously proposed P1/P2-differentiating and nine novel polymorphisms at the A4GALT (Pk) locus do not correlate with the presence of the P1 blood group antigen.

artículo científico publicado en 2005

Universal red blood cells--enzymatic conversion of blood group A and B antigens.

artículo científico publicado en 2004

Vox Sanguinis International Forum on application of fetal blood grouping.

artículo científico publicado en 2017

Vox Sanguinis International Forum on application of fetal blood grouping: summary.

artículo científico publicado en 2017

Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.

artículo científico publicado en 2010

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

artículo científico publicado en 2009

Lista de obras de

A and B antigen levels acquired by group O donor-derived erythrocytes following ABO-non-identical transfusion or minor ABO-incompatible haematopoietic stem cell transplantation

A clinically applicable method for determining the three major alleles at the Duffy (FY) blood group locus using polymerase chain reaction with allele-specific primers.

A clue to the basis of allelic enhancement: occurrence of the Ax subgroup in the offspring of blood group O parents

A large cohort study of the effects of Lewis, <scp>ABO</scp>, 13 other blood groups, and secretor status on <scp>COVID</scp>‐19 susceptibility, severity, and long <scp>COVID</scp>‐19

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

A novel B(weak) hybrid allele lacks three enhancer repeats but generates normal ABO transcript levels

A novel blood group B subgroup: serological and genetic studies.

A novel mutation in the complement regulator clusterin in recurrent hemolytic uremic syndrome.

A novel single-nucleotide substitution in the proximal ABO promoter gives rise to the B3 phenotype

A rapid and simple ABO genotype screening method using a novel B/O2 versus A/O2 discriminating nucleotide substitution at the ABO locus

A simple screening assay for the most common JK*0 alleles revealed compound heterozygosity in Jk(a-b-) probands from Guam.

A synthetic globotriaosylceramide analogue inhibits HIV-1 infection in vitro by two mechanisms.

ABO blood type and risk of porcine bioprosthetic aortic valve degeneration: SWEDEHEART observational cohort study

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

ADP acting on P2Y13 receptors is a negative feedback pathway for ATP release from human red blood cells.

Allele-related variation in minisatellite repeats involved in the transcription of the blood group ABO gene

Allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT.

Allelic variants ofPRDM9associated with high hyperdiploid childhood acute lymphoblastic leukaemia

Alpha1-Microglobulin is Mitogenic to Human Peripheral Blood Lymphocytes. Regulation by both Enhancing and Suppressive Serum Factors ⬇️

An Ael allele-specific nucleotide insertion at the blood group ABO locus and its detection using a sequence-specific polymerase chain reaction.

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

An extensive polymerase chain reaction-allele-specific polymorphism strategy for clinical ABO blood group genotyping that avoids potential errors caused by null, subgroup, and hybrid alleles

An update on the GLOB blood group system (and former GLOB collection)

An update on the GLOB blood group system and collection.

Application of DNA analysis to the quality assurance of reagent red blood cells.

Autologous del(20q)-positive erythroid progenitor cells, re-emerging after DLI treatment of an MDS patient relapsing after allo-SCT, can provide a normal peripheral red blood cell count.

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

Blood grouping discrepancies between ABO genotype and phenotype caused by O alleles.

Characterization of GYP*Mur and novel GYP*Bun-like hybrids in Thai blood donors reveals a qualitatively altered s antigen

Characterization of Jk(a+weak): a new blood group phenotype associated with an altered JK*01 allele ⬇️

Characterization of Monoclonal Anti-alpha1-Microglobulin Antibodies: Binding Strength, Binding Sites, and Inhibition of Lymphocyte Stimulation ⬇️

Different genotypes causing indiscernible patterns of A expression on A(el) red blood cells as visualized by scanning immunogold electron microscopy

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

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

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

Do ABO blood group antigens hamper the therapeutic efficacy of mesenchymal stromal cells?

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

Erythroid urea transporter deficiency due to novel JKnull alleles.

Evidence for a new type of O allele at the ABO locus, due to a combination of the A2 nucleotide deletion and the Ael nucleotide insertion

Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotype.

FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon

Flow cytometry evaluation of red blood cells mimicking naturally occurring ABO subgroups after modification with variable amounts of function‐spacer‐lipid A and B constructs ⬇️

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

Frequent occurrence of a variant O1 gene at the blood group ABO locus.

GBGT1 is allelically diverse but dispensable in humans and naturally occurring anti-FORS1 shows an ABO-restricted pattern

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

Genetic heterogeneity at the glycosyltransferase loci underlying the GLOB blood group system and collection.

Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles

Genomic characterization of the kidd blood group gene:different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns.

Genomic typing of the Kidd blood group locus by a single‐tube allele‐specific primer PCR technique ⬇️

Glycoproteomic and Phenotypic Elucidation of <i>B4GALNT2</i> Expression Variants in the SID Histo-Blood Group System

Heterogeneity of the O alleles at the blood group ABO locus in Amerindians

Heterogeneity of the blood group Ax allele: genetic recombination of common alleles can result in the Ax phenotype.

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

Identification of a GH110 subfamily of alpha 1,3-galactosidases: novel enzymes for removal of the alpha 3Gal xenotransplantation antigen.

Identification of a novel A4GALT exon reveals the genetic basis of the P1/P2 histo-blood groups.

Identification of human glycosyltransferase genes expressed in erythroid cells predicts potential carbohydrate blood group loci

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

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

International Society of Blood Transfusion Committee on Terminology for Red Cell Surface Antigens: Cape Town report.

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

International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Berlin report.

International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012).

Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles.

Many genetically defined ABO subgroups exhibit characteristic flow cytometric patterns

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

Missense mutations in the C-terminal portion of the B4GALNT2-encoded glycosyltransferase underlying the Sd(a-) phenotype

Mixed field reactions in ABO and Rh typing chimerism likely resulting from twin haematopoiesis.

Modifying the red cell surface: towards an ABO-universal blood supply.

Molecular analysis of the O alleles at the blood group ABO locus in populations of different ethnic origin reveals novel crossing-over events and point mutations

Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus

Noninvasive Single-Exon Fetal RHD Determination in a Routine Screening Program in Early Pregnancy ⬇️

P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo‐blood group systems ⬇️

P1PK: the blood group system that changed its name and expanded.

Phenotype prediction by DNA-based typing of clinically significant blood group systems in Jordanian blood donors

Platelet concentrate increases bone ingrowth into porous hydroxyapatite

Polymorphisms at the ABO locus in subgroup A individuals

Quantitative and qualitative evaluation of plasma and urine alpha1-microglobulin in healthy donors and patients with different haemolytic disorders and haemochromatosis

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

The Bloodgen Project of the European Union, 2003–2009 ⬇️