Associated Papers
Genetic and immunological regulation of gut Microbiota: The Roles of TLRs, CLRs, and key proteins in microbial homeostasis and disease.
Ayoub M et al.
Gene, 2025
Detection of the weak-secretor rs1047781 (385A>T) single nucleotide polymorphism using an unlabeled probe high-resolution melting-based method.
Soejima M et al.
Electrophoresis, 2021
Divergence in phenotyping and genotyping analysis of the Lewis histo-blood group system.
Donta A et al.
Transfusion Medicine (oxford, England), 2021
Survey and characterization of nonfunctional alleles of FUT2 in a database.
Soejima M et al.
Scientific Reports, 2021
Genetic Manipulation of Human Intestinal Enteroids Demonstrates the Necessity of a Functional Fucosyltransferase 2 Gene for Secretor-Dependent Human Norovirus Infection.
Haga K et al.
Mbio, 2020
Association of FUT2 and ABO with Crohn's disease in Koreans.
Ye BD et al.
Journal of Gastroenterology and Hepatology, 2020
Associations between fucosyltransferase 3 gene polymorphisms and ankylosing spondylitis: A case-control study of an east Chinese population.
Jiang G et al.
Plos One, 2020
Hematopoietic Chimera in a Male Blood Donor and His Dizygotic Twin Sister.
Miola MP et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 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
Genetic Susceptibility to Norovirus GII.4 Sydney Strain Infections in Taiwanese Children.
Tu LT et al.
The Pediatric Infectious Disease Journal, 2017
Epidemiologic Association Between FUT2 Secretor Status and Severe Rotavirus Gastroenteritis in Children in the United States.
Payne DC et al.
Jama Pediatrics, 2015
The Blood Group A Genotype Determines the Level of Expression of the Blood Group A on Platelets But Not the Anti-B Isotiter.
Lehner B et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2015
Innate Susceptibility to Norovirus Infections Influenced by FUT2 Genotype in a United States Pediatric Population.
Currier RL et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America, 2015
Lewis histo-blood group system phenotyping and genotyping reveal divergence in the association of Le(a-b-) phenotype and type 1 diabetes.
Previato M et al.
Vox Sanguinis, 2015
FUT 2 polymorphism and outcome in very-low-birth-weight infants.
Demmert M et al.
Pediatric Research, 2015
Genetic variation of FUT2 in a Vietnamese population: identification of two novel Se enzyme-inactivating mutations.
Soejima M et al.
Transfusion, 2012
Susceptibility to winter vomiting disease: a sweet matter.
Rydell GE et al.
Reviews in Medical Virology, 2011
TaqMan-based real-time polymerase chain reaction for detection of FUT2 copy number variations: identification of novel Alu-mediated deletion.
Soejima M et al.
Transfusion, 2011
The G428A nonsense mutation in FUT2 provides strong but not absolute protection against symptomatic GII.4 Norovirus infection.
Carlsson B et al.
Plos One, 2009
Genetic variation of FUT2 in Ovambos, Turks, and Mongolians.
Soejima M et al.
Transfusion, 2008
[Alloimmunization to a high frequency Rh antigen].
Cotorruelo C et al.
Medicina, 2006
Novel glycolipid variations revealed by monoclonal antibody immunochemical analysis of weak ABO subgroups of A.
Svensson L et al.
Vox Sanguinis, 2005
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
Molecular analysis of mutations and polymorphisms of the Lewis secretor type alpha(1,2)-fucosyltransferase gene reveals that Taiwan aborigines are of Austronesian derivation.
Chang JG et al.
Journal of Human Genetics, 2002
Polymorphism and distribution of the Secretor alpha(1,2)-fucosyltransferase gene in various Taiwanese populations.
Yu LC et al.
Transfusion, 2001
The polymorphisms of fucosyltransferases.
Koda Y et al.
Legal Medicine (tokyo, Japan), 2001
Secretor genotyping for A385T, G428A, C571T, C628T, 685delTGG, G849A, and other mutations from a single PCR.
Svensson L et al.
Transfusion, 2000
Molecular characterization of secretor type alpha(1, 2)-fucosyltransferase gene deficiency in the Philippine population.
Peng CT et al.
Annals of Hematology, 1999
Molecular analysis of secretor type alpha(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations.
Chang JG et al.
Transfusion, 1999
The fusion gene at the ABO-secretor locus (FUT2): absence in Chinese populations.
Liu YH et al.
Journal of Human Genetics, 1999
Extensive polymorphism of the FUT2 gene in an African (Xhosa) population of South Africa.
Liu Y et al.
Human Genetics, 1998
Point mutations and deletion responsible for the Bombay H null and the Reunion H weak blood groups.
Fernandez-Mateos P et al.
Vox Sanguinis, 1998
Molecular basis for erythrocyte Le(a+ b+) and salivary ABH partial-secretor phenotypes: expression of a FUT2 secretor allele with an A-->T mutation at nucleotide 385 correlates with reduced alpha(1,2) fucosyltransferase activity.
Henry S et al.
Glycoconjugate Journal, 1996
Molecular basis for secretor type alpha(1,2)-fucosyltransferase gene deficiency in a Japanese population: a fusion gene generated by unequal crossover responsible for the enzyme deficiency.
Koda Y et al.
American Journal of Human Genetics, 1996