Å. Hellberg

发表

The P1PK blood group system: revisited and resolved

L. Stenfelt, Å. Hellberg, J. S. Westman, 2020, Immunohematology.

P1PK: a blood group system with an identity crisis

Å. Hellberg, 2020, ISBT Science Series.

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

S. Teneberg, T. Peyrard, J. Storry, 2015, The Journal of Biological Chemistry.

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

T. Peyrard, Å. Hellberg, J. S. Westman, 2013, Transfusion.

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

G. Larson, L. Stenfelt, Å. Hellberg, 2019, Biochemistry and biophysics reports.

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

Å. Hellberg, M. Olsson, M. Möller, 2018, Vox sanguinis.

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

A. Walaszczyk, Å. Hellberg, M. Olsson, 2005, Transfusion medicine.

New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes

C. Levene, T. Wagner, Å. Hellberg, 2005, Transfusion.

Pre-transplantation confirmatory ABO genotyping reveals a novel non-deletional 0 allele

Carter, W. Howell, Å. Hellberg, 2008 .

Investigation into A antigen expression on O2 heterozygous group O–labeled red blood cell units

M. Palcic, M. Yazer, Å. Hellberg, 2008, Transfusion.

External quality assessment of noninvasive fetal RHD genotyping

Å. Hellberg, F. B. Clausen, 2020, Vox sanguinis.

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

M. Reid, Å. Hellberg, M. Olsson, 2008, Transfusion.

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

Å. Hellberg, M. Olsson, M. Chester, 2005, BMC Genetics.

Additional molecular bases of the clinically important p blood group phenotype

C. Levene, J. Poole, H. E. Heier, 2003, Transfusion.

Molecular basis of the globoside-deficient P(k) blood group phenotype. Identification of four inactivating mutations in the UDP-N-acetylgalactosamine: globotriaosylceramide 3-beta-N-acetylgalactosaminyltransferase gene.

J. Poole, Å. Hellberg, M. Olsson, 2002, The Journal of biological chemistry.

A multi‐centre study on the performance of the molecular genotyping platform ID RHD XT for resolving serological weak RhD phenotype in routine clinical practice

Å. Hellberg, D. Londero, Jorge Monge, 2020, Vox sanguinis.

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

L. Stenfelt, Å. Hellberg, J. S. Westman, 2018, Transfusion.

ABO zygosity, but not secretor or Fc receptor status, is a significant risk factor for IVIG-associated hemolysis.

T. Kuijpers, B. Binnington, N. Parmar, 2018, Blood.

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

K. Vidovic, S. Kjellström, L. Stenfelt, 2018, Blood.

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

B. Binnington, C. Lingwood, D. Jung, 2009, Blood.

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

B. Binnington, C. Lingwood, D. Jung, 2009 .

Novel glycolipid variations revealed by monoclonal antibody immunochemical analysis of weak ABO subgroups of A

L. Svensson, S. Henry, Å. Hellberg, 2005, Vox sanguinis.

Studies on the genetic basis of Pk, P and P1 blood group antigen expression

Å. Hellberg, 2007 .

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

M. Palcic, T. Peyrard, M. Yazer, 2010, Transfusion.

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

M. Moulds, Å. Hellberg, M. Olsson, 2001, Blood.

Molecular bases and clinical importance of the exceptional phenotypes of blood group P and PK

Å. Hellberg, M. Olsson, S. Chialina, 2008 .

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

M. Reid, V. Yahalom, J. Säfwenberg, 2004, British journal of haematology.

Noninvasive Prenatal Testing in Immunohematology—Clinical, Technical and Ethical Considerations

J. Kjeldsen-Kragh, Å. Hellberg, 2022, Journal of clinical medicine.

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

Å. Hellberg, M. Olsson, M. Chester, 2007, Transfusion.

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

Å. Hellberg, M. Olsson, N. Irshaid, 2002, Vox sanguinis.

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

William Arbuthnot Sir Lane, M. Keller, B. Veldhuisen, 2022, Vox sanguinis.

ABO exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferase

Å. Hellberg, M. Olsson, M. Chester, 2003, BMC Genetics.

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

J. Storry, Å. Hellberg, M. Olsson, 2005, Vox sanguinis.

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

Å. Hellberg, M. Olsson, A. Hult, 2019, Transfusion.

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

Y. Liew, G. Larson, J. Nilsson, 2022, International journal of molecular sciences.

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

P. Bugert, S. Thorlacius, W. Lane, 2021, Vox sanguinis.

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

P. Spruell, J. Storry, Å. Hellberg, 2009, Immunohematology.

A novel nonsense variant in RHAG underlies a Nordic Rhnull phenotype

J. Storry, Å. Hellberg, M. Olsson, 2023, Vox sanguinis.

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

Å. Hellberg, J. S. Westman, M. Olsson, 2018, Immunohematology.

P1PK: The blood group system that changed its name and expanded

Å. Hellberg, J. S. Westman, M. Olsson, 2013, Immunohematology.