Associated Papers
Identification of novel germline mutations in FUT7 and EXT1 linked with hereditary multiple exostoses.
Peng W et al.
Oncogene, 2025
FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expression.
Puan KJ et al.
Communications Biology, 2021
Assessment of computational methods for predicting the effects of missense mutations in human cancers.
Gnad F et al.
Bmc Genomics, 2013
23819521 (PubMed )
Supplement: 1471-2164-14-S3-S7-S1.xlsx › dbSNP
Incidental medical information in whole-exome sequencing.
Solomon BD et al.
Pediatrics, 2012
Characterization of EBV-transformed B-cells established from an individual homozygously mutated (G329A) in the FUT7 alpha1,3-fucosyltransferase gene.
Bengtson P et al.
Scandinavian Journal of Immunology, 2005
Regulation of PSGL-1 interactions with L-selectin, P-selectin, and E-selectin: role of human fucosyltransferase-IV and -VII.
Martinez M et al.
The Journal of Biological Chemistry, 2005
Finding NEMO: genetic disorders of NF-[kappa]B activation.
Orange JS et al.
The Journal of Clinical Investigation, 2003
Polymorphonuclear leukocytes from individuals carrying the G329A mutation in the alpha 1,3-fucosyltransferase VII gene (FUT7) roll on E- and P-selectins.
Bengtson P et al.
Journal of Immunology (baltimore, Md. : 1950), 2002
Identification of a missense mutation (G329A;Arg(110)--> GLN) in the human FUT7 gene.
Bengtson P et al.
The Journal of Biological Chemistry, 2001
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