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Transfusion Medicine (Oxford, England)|July 2, 2026
Identification and protein modelling analysis of a homozygous FUT1*01W.09 variant in a Thai patient with the para-Bombay phenotypePrakarn Sawatdee, Yan Quan Lee, Martin L Olsson, et al.Transfusion|August 27, 2014
An age-dependent ABO discrepancy between mother and baby reveals a novel A(weak) alleleJill R Storry, Jennifer Condon, Annika K Hult, et al.International Journal of Molecular Sciences|August 23, 2020
Association of Maternal Regulatory Single Nucleotide Polymorphic CD99 Genotype with Preeclampsia in Pregnancies Carrying Male Fetuses in Ethiopian WomenTsehayneh Kelemu, Lena Erlandsson, Daniel Seifu, et al.Transfusion|April 12, 2005
Genetic basis of the K(0) phenotype in the Swedish populationElisabet S Wester, Jill R Storry, Karin Schneider, et al.Transfusion|April 3, 2019
A large deletion spanning XG and GYG2 constitutes a genetic basis of the Xgnull phenotype, underlying anti-Xga productionYan Quan Lee, Jill R Storry, Vanja Karamatic Crew, et al.Blood|May 12, 2018
Disruption of a GATA1-binding motif upstream of XG/PBDX abolishes Xga expression and resolves the Xg blood group systemMattias Möller, Yan Quan Lee, Karina Vidovic, et al.Transfusion|November 22, 2007
Erythroid urea transporter deficiency due to novel JKnull allelesElisabet S Wester, Susan T Johnson, Tama Copeland, et al.Plos One|December 31, 2013
Energetic and molecular water permeation mechanisms of the human red blood cell urea transporter BSlim Azouzi, Marc Gueroult, Pierre Ripoche, et al.Transfusion Medicine (Oxford, England)|May 14, 2021
Platelets inhibit erythrocyte invasion by Plasmodium falciparum at physiological platelet:erythrocyte ratiosPhilaiphon Jongruamklang, Johan Rebetz, Rick Kapur, et al.The Journal of Biological Chemistry|June 10, 2015
Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient ErythrocytesJulia S Westman, John Benktander, Jill R Storry, et al.Pageof 8