Associated Papers
Genome-wide association analysis identifies fucosyltransferase 2 variants associated with pancreatic intraductal papillary mucinous neoplasms.
Gaitanidis A et al.
Cancer, 2025
A novel allele of FUT2 gene containing a deletion of nine bases (c.461_469delGGACCTTCT) in a Chinese Han blood donor.
Zhou S et al.
Vox Sanguinis, 2023
Survey and characterization of nonfunctional alleles of FUT2 in a database.
Soejima M et al.
Scientific Reports, 2021
Norovirus infection and HBGA host genetic susceptibility in a birth community-cohort, Rio de Janeiro, Brazil.
Cantelli CP et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases, 2020
Rotavirus A shedding and HBGA host genetic susceptibility in a birth community-cohort, Rio de Janeiro, Brazil, 2014-2018.
Cantelli CP et al.
Scientific Reports, 2020
Fucosyltransferase Gene Polymorphisms and Lewisb-Negative Status Are Frequent in Swedish Newborns, With Implications for Infectious Disease Susceptibility and Personalized Medicine.
King JR et al.
Journal of the Pediatric Infectious Diseases Society, 2019
Genetic variation of FUT2 in a Peruvian population: identification of a novel LTR-mediated deletion and characterization of 4 nonsynonymous single-nucleotide polymorphisms.
Soejima M et al.
Transfusion, 2019
FUT2 Secretor Status Is Not Associated With Oral Poliovirus Vaccine Immunogenicity in South Indian Infants.
Parker EPK et al.
The Journal of Infectious Diseases, 2019
Distribution of Lewis and Secretor polymorphisms and corresponding CA19-9 antigen expression in a Chinese population.
Guo M et al.
Febs Open Bio, 2017
Molecular basis of Bombay phenotype in Mashhad, Iran: identification of a novel FUT1 deletion.
Zanjani DS et al.
Vox Sanguinis, 2016
Generation of human induced pluripotent stem cells from a Bombay individual: moving towards "universal-donor" red blood cells.
Seifinejad A et al.
Biochemical and Biophysical Research Communications, 2010
Infection-associated FUT2 (Fucosyltransferase 2) genetic variation and impact on functionality assessed by in vivo studies.
Silva LM et al.
Glycoconjugate Journal, 2010
Systematic sequence analysis of the human fucosyltransferase 2 (FUT2) gene identifies novel sequence variations and alleles.
Yip SP et al.
Transfusion, 2007
Two new FUT2 (fucosyltransferase 2 gene) missense polymorphisms, 739G-->A and 839T-->C, are partly responsible for non-secretor status in a Caucasian population from Northern Portugal.
Serpa J et al.
The Biochemical Journal, 2004
The polymorphisms of fucosyltransferases.
Koda Y et al.
Legal Medicine (tokyo, Japan), 2001
Two distinct Alu-mediated deletions of the human ABO-secretor (FUT2) locus in Samoan and Bangladeshi populations.
Pang H et al.
Human Mutation, 2000
Allelic diversity of the human plasma alpha(1,3)fucosyltransferase gene (FUT6).
Pang H et al.
Annals of Human Genetics, 1999
Identification of a new plasma alpha(1,3)fucosyltransferase (FUT6) allele requires an extended genotyping strategy.
Larson G et al.
Vox Sanguinis, 1996