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M-L Olsson

Showing results (51-60 of 57) with videos related to

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Blood|July 4, 2001
Intercellular adhesion molecule-4 binds alpha(4)beta(1) and alpha(V)-family integrins through novel integrin-binding mechanismsF A Spring, S F Parsons, S Ortlepp, et al.
Blood|August 25, 2001
Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup allelesM L Olsson, N M Irshaid, B Hosseini-Maaf, et al.
British Journal of Haematology|January 14, 1999
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoproteinM L Olsson, J S Smythe, C Hansson, et al.
Vox Sanguinis|April 14, 2010
KEL*02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,-2 phenotypesE S Wester, R Steffensen, P C Ligthart, et al.
Transfusion Medicine (Oxford, England)|June 7, 2018
Multiple miscarriages in two sisters of Thai origin with the rare P<sup>k</sup> phenotype caused by a novel nonsense mutation at the B3GALNT1 locusJ Ricci Hagman, A K Hult, J S Westman, et al.
ISBT Science Series|November 3, 2017
International society of blood transfusion working party on red cell immunogenetics and terminology: report of the Seoul and London meetingsJ R Storry, L Castilho, Q Chen, et al.
Vox Sanguinis|December 31, 2013
International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012)J R Storry, L Castilho, G Daniels, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Blood|July 4, 2001
Intercellular adhesion molecule-4 binds alpha(4)beta(1) and alpha(V)-family integrins through novel integrin-binding mechanismsF A Spring, S F Parsons, S Ortlepp, et al.
Blood|August 25, 2001
Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup allelesM L Olsson, N M Irshaid, B Hosseini-Maaf, et al.
British Journal of Haematology|January 14, 1999
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoproteinM L Olsson, J S Smythe, C Hansson, et al.
Vox Sanguinis|April 14, 2010
KEL*02 alleles with alterations in and around exon 8 in individuals with apparent KEL:1,-2 phenotypesE S Wester, R Steffensen, P C Ligthart, et al.
Transfusion Medicine (Oxford, England)|June 7, 2018
Multiple miscarriages in two sisters of Thai origin with the rare P<sup>k</sup> phenotype caused by a novel nonsense mutation at the B3GALNT1 locusJ Ricci Hagman, A K Hult, J S Westman, et al.
ISBT Science Series|November 3, 2017
International society of blood transfusion working party on red cell immunogenetics and terminology: report of the Seoul and London meetingsJ R Storry, L Castilho, Q Chen, et al.
Vox Sanguinis|December 31, 2013
International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012)J R Storry, L Castilho, G Daniels, et al.
Pageof 6