Associated Papers
Patient-derived models recapitulate heterogeneity of molecular signatures and drug response in pediatric high-grade glioma.
He C et al.
Nature Communications, 2021
34215733 (PubMed )
Supplement: 41467_2021_24168_MOESM5_ESM.xlsx › SD2d
Molecular basis of Bombay phenotype in Mashhad, Iran: identification of a novel FUT1 deletion.
Zanjani DS et al.
Vox Sanguinis, 2016
Infection-associated FUT2 (Fucosyltransferase 2) genetic variation and impact on functionality assessed by in vivo studies.
Silva LM et al.
Glycoconjugate Journal, 2010
Genetic variation of FUT2 in a Ghanaian population: identification of four novel mutations and inference of balancing selection.
Soejima M et al.
Annals of Hematology, 2007
DNA sequence variation of the human ABO-secretor locus ( FUT2) in New Guinean populations: possible early human migration from Africa.
Koda Y et al.
Human Genetics, 2003
Two distinct Alu-mediated deletions of the human ABO-secretor (FUT2) locus in Samoan and Bangladeshi populations.
Pang H et al.
Human Mutation, 2000
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