Associated Papers
Genetic Variations of the FUT3 Gene in Le(a-b-) Individuals and Their Association with Lewis Antibody Responses.
Nathalang O et al.
Medical Sciences (basel, Switzerland), 2025
VarMeter: a prediction method for the impact of glycogene variants.
Ohno S et al.
Journal of Human Genetics, 2025
Precision diagnostics in Transfusion Medicine: Advancing accuracy in Bombay blood group typing through molecular methods.
Shastry S et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2025
Exome sequencing reveals a rare damaging variant in GRIN2C in familial late-onset Alzheimer's disease.
Rubino E et al.
Alzheimer's Research & Therapy, 2025
Correlation Of Fut2 And Fut3 Gene Polymorphisms With Inflammatory Bowel Disease In Guangxi Zhuang Population.
Lv X et al.
International Journal of General Medicine, 2025
Genetic variation of FUT3 gene in the Han population from Northern China.
Zhou S et al.
Transfusion Medicine (oxford, England), 2024
Characterization of Blood Group Variants in an Omani Population by Comparison of Whole Genome Sequencing and Serology.
Haffener PE et al.
Biorxiv : the Preprint Server for Biology, 2024
Polymorphism of fucosyltransferase 3 gene is associated with inflammatory bowel disease: a systematic review.
Zheng J et al.
Asian Biomedicine : Research, Reviews and News, 2023
Estimation of Lewis Blood Group Status by Fluorescence Melting Curve Analysis in Simultaneous Genotyping of c.385A>T and Fusion Gene in FUT2 and c.59T>G and c.314C>T in FUT3.
Soejima M et al.
Diagnostics (basel, Switzerland), 2023
Fluorescence Melting Curve Analysis for Concurrent Genotyping of Three Tag SNPs in FUT3.
Soejima M et al.
Diagnostics (basel, Switzerland), 2022
ABO, secretor, and Lewis carbohydrate histo-blood groups are associated with autoimmune neutropenia of early childhood in Danish patients.
Kløve-Mogensen K et al.
Transfusion, 2022
Estimation of Lewis-negative alleles by high-resolution melting analysis of three tag SNPs of FUT3.
Soejima M et al.
Vox Sanguinis, 2022
Prediction of various blood group systems using Korean whole-genome sequencing data.
Hyun J et al.
Plos One, 2022
A cross-population atlas of genetic associations for 220 human phenotypes.
Sakaue S et al.
Nature Genetics, 2021
Divergence in phenotyping and genotyping analysis of the Lewis histo-blood group system.
Donta A et al.
Transfusion Medicine (oxford, England), 2021
A synergetic effect of BARD1 mutations on tumorigenesis.
Li W et al.
Nature Communications, 2021
Estimation of genetic variation in the Secretor and Lewis genes in Iranian hospitalized children.
Farahmand M et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2021
FUT2, Secretor Status and FUT3 Polymorphisms of Children with Acute Diarrhea Infected with Rotavirus and Norovirus in Brazil.
Loureiro Tonini MA et al.
Viruses, 2020
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
Systematic sequence analysis of the FUT3 gene identifies 11 novel alleles in the Sindhi and Punjabi populations from Pakistan.
Zhao M et al.
Scientific Reports, 2020
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
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
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
Genomic coordinates and continental distribution of 120 blood group variants reported by the 1000 Genomes Project.
Montemayor-Garcia C et al.
Transfusion, 2018
Distribution of Lewis and Secretor polymorphisms and corresponding CA19-9 antigen expression in a Chinese population.
Guo M et al.
Febs Open Bio, 2017
A common genetic variant of fucosyltransferase 2 correlates with serum carcinoembryonic antigen levels and affects cancer screening in patients with primary sclerosing cholangitis.
Wannhoff A et al.
United European Gastroenterology Journal, 2016
Association of elevated rotavirus-specific antibody titers with HBGA secretor status in Swedish individuals: The FUT2 gene as a putative susceptibility determinant for infection.
Günaydın G et al.
Virus Research, 2016
Association of Ulcerative Colitis with FUT2 and FUT3 Polymorphisms in Patients from Southeast China.
Hu D et al.
Plos One, 2016
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 influences on cystic fibrosis lung disease severity.
Weiler CA et al.
Frontiers in Pharmacology, 2013
The Lewis histo-blood group system: molecular analysis of the 59T>G, 508G>A, and 1067T>A polymorphisms in an Amazonian population.
Corvelo TC et al.
Plos One, 2013
Investigation of unexpected serum CA19-9 elevation in Lewis-negative cancer patients.
Hamada E et al.
Annals of Clinical Biochemistry, 2012
Polymorphisms of Lewis and Secretor genes are related to breast cancer and metastasis in axillary lymph nodes.
Teresa DB et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2010
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
Genetic variation of FUT3 in Ghanaians, Caucasians, and Mongolians.
Soejima M et al.
Transfusion, 2009
Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity.
Taylor-Cousar JL et al.
Plos One, 2009
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
Fucosyltransferase 3 polymorphism and atherothrombotic disease in the Framingham Offspring Study.
Djoussé L et al.
American Heart Journal, 2007
[FUT3 gene polymorphism associated with Lewis blood group in Chinese Zhejiang population].
Xu XG et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2006
Association of the Lewis genotype with cardiovascular risk factors and subclinical carotid atherosclerosis: the Atherosclerosis Risk in Communities (ARIC) study.
Cakir B et al.
Journal of Internal Medicine, 2004
Lewis enzyme (alpha1-3/4 fucosyltransferase) polymorphisms do not explain the Lewis phenotype in the gastric mucosa of a Portuguese population.
Serpa J et al.
Journal of Human Genetics, 2003
Distribution of Lewis (FUT3)genotype and allele: frequencies in a biethnic United States population.
Cakir B et al.
Annals of Hematology, 2002
Genetic background of Lewis negative blood group phenotype and its association with atherosclerotic disease in the NHLBI family heart study.
Salomaa V et al.
Journal of Internal Medicine, 2000
Molecular behavior of mutant Lewis enzymes in vivo.
Nishihara S et al.
Glycobiology, 1999
Typing for the human lewis blood group system by quantitative fluorescence-activated flow cytometry: large differences in antigen presentation on erythrocytes between A(1), A(2), B, O phenotypes.
Larson G et al.
Vox Sanguinis, 1999
Significance of each of three missense mutations, G484A, G667A, and G808A, present in an inactive allele of the human Lewis gene (FUT3) for alpha(1,3/1,4)fucosyltransferase inactivation.
Pang H et al.
Glycoconjugate Journal, 1998