Associated Papers
A para-Bombay phenotype due to compound heterozygosity involving a novel FUT1 variant.
Brajovich ML et al.
Vox Sanguinis, 2026
Molecularly confirmed para-Bombay (Ah) secretor phenotype with FUT1 c.328G>A and FUT2 c.357C>T mutations: first case report from India.
Arivazhagan T et al.
Blood Transfusion = Trasfusione Del Sangue, 2025
Genetic analysis and protein modeling evaluation of a novel FUT1 variant c.683T>C (p.Met228Thr) in a Chinese individual with para-Bombay phenotype.
He Y et al.
Transfusion, 2025
Genetic and mechanistic evaluation of an individual with para-Bombay phenotype associated with a compound heterozygote comprising two novel FUT1 variants.
Ying Y et al.
Blood Transfusion = Trasfusione Del Sangue, 2024
Association of fucosyltransferase 2 gene polymorphism with the susceptibility to norovirus infection in Han Chinese population.
Liu S et al.
Journal of Medical Virology, 2024
A Pedigree Investigation of H-antigen Deletion Caused by Mutation of 658 C to T in the FUT1 Gene.
Li C et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion, 2024
Identification of a novel FUT1 allele with a nucleotide deletion (c.500del) responsible for para-Bombay phenotype.
Hou J
Transfusion, 2023
Molecular Genetic Analysis of Para-Bombay Phenotype in Chinese: Identification of a Novel FUT1 Allele.
Li T et al.
Clinical Laboratory, 2023
Analysis of the molecular mechanism and pedigree investigation of para-Bombay phenotype caused by combined mutations at position h649 and h768 of FUT1 gene.
Sun X et al.
Blood Transfusion = Trasfusione Del Sangue, 2022
NM_000148.4(FUT1):c.[229C>T;302C>T] with 2 missense variations in the FUT1 gene associated with a para-Bombay phenotype.
Chen Q et al.
Transfusion, 2022
Two novel alleles on Fucosyltransferase 2 from northern Thai para-Bombay family and computational prediction on mutation effect.
Anukul N et al.
Transfusion, 2021
Homozygous FUT1 Mutations Causing a Para-Bombay Phenotype: a Pedigree Investigation Report.
He Y et al.
Clinical Laboratory, 2021
A Para-Bombay Blood Group Case Associated with a Novel FUT1 Mutation c.361G>A.
Lei H et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2021
Rapid detection of phenotypes Bombay sedel and nonsecretor rs200157007 SNP (302C > T) by real-time PCR-based methods.
Soejima M et al.
Scientific Reports, 2021
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
A Study on Fucosyltransferase 2 Gene Polymorphism and Secretion Status Related to Neonatal Necrotizing Enterocolitis.
Ye Q et al.
Journal of Healthcare Engineering, 2021
FUT2 polymorphism in Latin American populations.
Soejima M et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 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
Aberrant ABO B Phenotype with Irregular Anti-B Caused by a Para-Bombay FUT1 Mutation.
Matzhold EM et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 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
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
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
Association of Fucosyltransferase 2 Gene Polymorphisms with Inflammatory Bowel Disease in Patients from Southeast China.
Wu H et al.
Gastroenterology Research and Practice, 2017
Molecular basis of Bombay phenotype in Mashhad, Iran: identification of a novel FUT1 deletion.
Zanjani DS et al.
Vox Sanguinis, 2016
Genomic analysis of para-Bombay individuals in south-eastern China: the possibility of linkage and disequilibrium between FUT1 and FUT2.
Zhang A et al.
Blood Transfusion = Trasfusione Del Sangue, 2015
Sequence analysis of the human fucosyltransferase 1 and 2 genes in Tibetan blood donors: identification of three novel alleles.
Tian L et al.
Transfusion, 2014
Genetic variation of FUT2 in a Vietnamese population: identification of two novel Se enzyme-inactivating mutations.
Soejima M et al.
Transfusion, 2012
H blood-group deficiency has a high frequency in Lahu Chinese.
Cai XH et al.
Transfusion Medicine (oxford, England), 2011
The relationship between Lewis/Secretor genotypes and serum carbohydrate antigen 19-9 levels in a Korean population.
Park HD et al.
The Korean Journal of Laboratory Medicine, 2010
Identification of 14 new alleles at the fucosyltransferase 1, 2, and 3 loci in Styrian blood donors, Austria.
Matzhold EM et al.
Transfusion, 2009
Systematic sequence analysis of the human fucosyltransferase 2 (FUT2) gene identifies novel sequence variations and alleles.
Yip SP et al.
Transfusion, 2007
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
Identification of a novel FUT1 allele derived from the alpha-(1,2)-fucosyltransferase gene through a nucleotide substitution 682A>G.
Yan LX et al.
Transfusion Medicine (oxford, England), 2006
Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes.
Storry JR et al.
Transfusion, 2006
The fusion allele of the FUT2 (secretor type alpha(1,2)-fucosyltransferase) gene at a high frequency and a new se385 allele in a Korean population.
Park KU et al.
Annals of Hematology, 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
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
Novel mutations, including a novel G659A missense mutation, of the FUT1 gene are responsible for the para-Bombay phenotype.
Sun CF et al.
Annals of Clinical and Laboratory Science, 2000
Two distinct Alu-mediated deletions of the human ABO-secretor (FUT2) locus in Samoan and Bangladeshi populations.
Pang H et al.
Human Mutation, 2000
Molecular characterization of secretor type alpha(1, 2)-fucosyltransferase gene deficiency in the Philippine population.
Peng CT et al.
Annals of Hematology, 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
Two missense mutations of H type alpha(1,2)fucosyltransferase gene (FUT1) responsible for para-Bombay phenotype.
Wang B et al.
Vox Sanguinis, 1997
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
Molecular genetic analysis of the human Lewis histo-blood group system. II. Secretor gene inactivation by a novel single missense mutation A385T in Japanese nonsecretor individuals.
Kudo T et al.
The Journal of Biological Chemistry, 1996