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- 2024
-
Mark
A Bioinformatically Initiated Approach to Evaluate GATA1 Regulatory Regions in Samples with Weak D, Del, or D- Phenotypes Despite Normal RHD Exons
2024) In Transfusion Medicine and Hemotherapy(
- Contribution to journal › Article
- 2023
-
Mark
SID : A new carbohydrate blood group system based on a well-characterized but still mysterious antigen of great pathophysiologic interest
(
- Contribution to journal › Article
-
Mark
Truncated glycosyltransferase coding regions in novel ABO alleles give rise to weak A or B blood group expression and discrepant typing results
(
- Contribution to journal › Article
-
Mark
A novel nonsense variant in RHAG underlies a Nordic Rhnull phenotype.
(
- Contribution to journal › Article
- 2022
-
Mark
Glycoproteomic and Phenotypic Elucidation of B4GALNT2 Expression Variants in the SID Histo-Blood Group System
(
- Contribution to journal › Article
-
Mark
Recommendation for validation and quality assurance of non-invasive prenatal testing for foetal blood groups and implications for IVD risk classification according to EU regulations
(
- Contribution to journal › Scientific review
-
Mark
A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B
w phenotype.
(
- Contribution to journal › Article
-
Mark
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
(
- Contribution to journal › Article
-
Mark
Novel RHD variant causing RhD negative phenotype identified in a pregnant woman
(
- Contribution to journal › Debate/Note/Editorial
- 2020
-
Mark
External quality assessment of noninvasive fetal RHD genotyping
(
- Contribution to journal › Article
-
Mark
The P1PK blood group system : revisited and resolved
(
- Contribution to journal › Article
-
Mark
A novel ABO allele with a 21-bp duplication identified in two unrelated European individuals with weak A expression
(
- Contribution to journal › Article
- 2019
-
Mark
The P1 histo-blood group antigen is present on human red blood cell glycoproteins
(
- Contribution to journal › Article
-
Mark
Missense mutations in the C-terminal portion of the B4GALNT2-encoded glycosyltransferase underlying the Sd(a−) phenotype
(
- Contribution to journal › Article
-
Mark
A novel single-nucleotide substitution in the proximal ABO promoter gives rise to the B3 phenotype
(
- Contribution to journal › Debate/Note/Editorial
- 2018
-
Mark
An update on the GLOB blood group system (and former GLOB collection)
(
- Contribution to journal › Article
-
Mark
Allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT
(
- Contribution to journal › Article
-
Mark
Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project
(
- Contribution to journal › Article
-
Mark
ABO zygosity, but not secretor or Fc receptor status, is a significant risk factor for IVIG-Associated hemolysis
(
- Contribution to journal › Letter
-
Mark
A molecular mechanism underlying the P1/P2 phenotypes: allele-selective RUNX1 binding regulates P1 blood group status by transcriptional control of A4GALT
2018) 35th international congress of the International Society of Blood Transfusion, ISBT, 2018 In Vox Sanguinis 113(S1). p.251-252(
- Contribution to journal › Published meeting abstract
- 2017
-
Mark
Unorthodox O alleles among Africans: characterization of predicted new ABO deletions
(
- Contribution to conference › Abstract
- 2016
-
Mark
A novel RHCE*02 allele, containing the single-nucleotide change c.460A>G, encodes weakened expression of C and e antigens
(
- Contribution to journal › Article
- 2015
-
Mark
Identification of the molecular and genetic basis of PX2, a glycosphingolipid blood group antigen lacking on globoside-deficient erythrocytes.
(
- Contribution to journal › Article
- 2014
-
Mark
Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null alleles.
(
- Contribution to journal › Article
- 2013
-
Mark
An update on the GLOB blood group system and collection.
(
- Contribution to journal › Article
-
Mark
P1PK: the blood group system that changed its name and expanded.
(
- Contribution to journal › Article
-
Mark
P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems.
(
- Contribution to journal › Article
- 2010
-
Mark
Novel Non-Deletional O Alleles Based on A or B Sequences Give Rise to Erroneous ABO Genotyping Results
(
- Contribution to journal › Published meeting abstract
-
Mark
Weak A Phenotypes Associated With Novel Abo Alleles Carrying The A(2)-Related 1061C Deletion And Various Missense Amino Acid Substitutions
(
- Contribution to journal › Published meeting abstract
-
Mark
Weak A phenotypes associated with novel ABO alleles carrying the A(2)-related 1061C deletion and various missense substitutions.
(
- Contribution to journal › Article
- 2009
-
Mark
The human P-k histo-blood group antigen provides protection against HIV-1 infection
(
- Contribution to journal › Article
-
Mark
A rare blood group: p phenotype
(
- Contribution to journal › Article
-
Mark
A simple screening assay for the most common JK*0 alleles revealed compound heterozygosity in Jk(a-b-) probands from Guam
(
- Contribution to journal › Article
- 2008
-
Mark
Serologic and molecular characterization of an ab individual with dual expression of a antigen - A case report
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.199-200(
- Contribution to journal › Published meeting abstract
-
Mark
Pre-transplantation confirmatory ABO genotyping reveals a novel non-deletional 0 allele
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.178-178(
- Contribution to journal › Published meeting abstract
-
Mark
Clinical aspects and molecular basis of a P phenotype individual from Argentina
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.201-202(
- Contribution to journal › Published meeting abstract
-
Mark
Investigation into A antigen expression on O-2 heterozygous group O-labeled red blood cell units
(
- Contribution to journal › Article
-
Mark
Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotype.
(
- Contribution to journal › Article
-
Mark
Bases moleculares e importancia clínica de los excepcionales fenotipos de grupo sanguíneo P y PK
(
- Contribution to journal › Scientific review
- 2007
-
Mark
Studies on the genetic basis of Pk, P and P1 blood group antigen expression
2007)(
- Thesis › Doctoral thesis (compilation)
-
Mark
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
(
- Contribution to journal › Article
- 2005
-
Mark
Blood group genotype analysis for the quality improvement of reagent test red blood cells
(
- Contribution to journal › Article
-
Mark
New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes.
(
- Contribution to journal › Article
-
Mark
Two previously proposed P-1/P-2-differentiating and nine novel polymorphisms at the A4GALT (P-k) locus do not correlate with the presence of the P1 blood group antigen
(
- Contribution to journal › Article
-
Mark
A clue to the basis of allelic enhancement: occurrence of the A subgroup in the offspring of blood group O parents.
(
- Contribution to journal › Article
-
Mark
Novel glycolipid variations revealed by monoclonal antibody immunochemical analysis of weak ABO subgroups of A
(
- Contribution to journal › Article
- 2004
-
Mark
Genetic heterogeneity at the glycosyltransferase loci underlying the GLOB blood group system and collection*.
(
- Contribution to journal › Article
-
Mark
Nordiskt referenslaboratorium for genomisk blodgruppstypning finns i Lund
(
- Contribution to journal › Article
- 2003
-
Mark
Additional molecular bases of the clinically important p blood group phenotype.
(
- Contribution to journal › Article
-
Mark
ABO exon and intron analysis in individuals with the A(weak)B phenotype reveals a novel O-1v-A(2) hybrid allele that causes four missense mutations in the A transferase
(
- Contribution to journal › Article