Associated Papers
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
Two novel alleles on Fucosyltransferase 2 from northern Thai para-Bombay family and computational prediction on mutation effect.
Anukul N et al.
Transfusion, 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
A Study on Fucosyltransferase 2 Gene Polymorphism and Secretion Status Related to Neonatal Necrotizing Enterocolitis.
Ye Q et al.
Journal of Healthcare Engineering, 2021
Four Non-functional FUT1 Alleles Were Identified in Seven Chinese Individuals with Para-Bombay Phenotypes.
Liang W et al.
Iranian Journal of Public Health, 2018
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
The summary of FUT1 and FUT2 genotyping analysis in Chinese para-Bombay individuals including additional nine probands from Guangzhou in China.
Luo G et al.
Transfusion, 2013
H blood-group deficiency has a high frequency in Lahu Chinese.
Cai XH et al.
Transfusion Medicine (oxford, England), 2011
Identification of 14 new alleles at the fucosyltransferase 1, 2, and 3 loci in Styrian blood donors, Austria.
Matzhold EM et al.
Transfusion, 2009
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 genetic analysis of para-Bombay phenotypes in Chinese: a novel non-functional FUT1 allele is identified.
Yip SP et al.
Vox Sanguinis, 2002
The polymorphisms of fucosyltransferases.
Koda Y et al.
Legal Medicine (tokyo, Japan), 2001
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