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Asa Hellberg

Showing results (1-10 of 14) with videos related to

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Vox Sanguinis|January 9, 2020
A multi-centre study on the performance of the molecular genotyping platform ID RHD XT for resolving serological weak RhD phenotype in routine clinical practiceDonatella Londero, Jorge Monge, Asa Hellberg
The Journal of Biological Chemistry|May 23, 2002
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 geneAsa Hellberg, Joyce Poole, Martin L Olsson
BMC Genetics|October 11, 2005
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 antigenAsa Hellberg, M Alan Chester, Martin L Olsson
Transfusion|October 26, 2007
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 allelesBahram Hosseini-Maaf, Asa Hellberg, M Alan Chester, et al.
Transfusion|December 11, 2007
Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotypeAsa Hellberg, Anne-Christine Schmidt-Melbye, Marion E Reid, et al.
Transfusion|January 15, 2014
Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null allelesJulia S Westman, Asa Hellberg, Thierry Peyrard, et al.
Transfusion|August 10, 2013
P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systemsJulia S Westman, Asa Hellberg, Thierry Peyrard, et al.
BMC Genetics|November 18, 2003
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 transferaseBahram Hosseini-Maaf, Asa Hellberg, Maria J Rodrigues, et al.
Transfusion|May 17, 2008
Investigation into A antigen expression on O2 heterozygous group O-labeled red blood cell unitsMark H Yazer, Annika K Hult, Asa Hellberg, et al.
Transfusion|June 26, 2003
Additional molecular bases of the clinically important p blood group phenotypeAsa Hellberg, Rudi Steffensen, Vered Yahalom, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Vox Sanguinis|January 9, 2020
A multi-centre study on the performance of the molecular genotyping platform ID RHD XT for resolving serological weak RhD phenotype in routine clinical practiceDonatella Londero, Jorge Monge, Asa Hellberg
The Journal of Biological Chemistry|May 23, 2002
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 geneAsa Hellberg, Joyce Poole, Martin L Olsson
BMC Genetics|October 11, 2005
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 antigenAsa Hellberg, M Alan Chester, Martin L Olsson
Transfusion|October 26, 2007
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 allelesBahram Hosseini-Maaf, Asa Hellberg, M Alan Chester, et al.
Transfusion|December 11, 2007
Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotypeAsa Hellberg, Anne-Christine Schmidt-Melbye, Marion E Reid, et al.
Transfusion|January 15, 2014
Large deletions involving the regulatory upstream regions of A4GALT give rise to principally novel P1PK-null allelesJulia S Westman, Asa Hellberg, Thierry Peyrard, et al.
Transfusion|August 10, 2013
P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systemsJulia S Westman, Asa Hellberg, Thierry Peyrard, et al.
BMC Genetics|November 18, 2003
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 transferaseBahram Hosseini-Maaf, Asa Hellberg, Maria J Rodrigues, et al.
Transfusion|May 17, 2008
Investigation into A antigen expression on O2 heterozygous group O-labeled red blood cell unitsMark H Yazer, Annika K Hult, Asa Hellberg, et al.
Transfusion|June 26, 2003
Additional molecular bases of the clinically important p blood group phenotypeAsa Hellberg, Rudi Steffensen, Vered Yahalom, et al.
Pageof 2