Associated Papers
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
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
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
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
Genetic variation of FUT2 in a Vietnamese population: identification of two novel Se enzyme-inactivating mutations.
Soejima M et al.
Transfusion, 2012
[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
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
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 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