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Article

Alpha1,3fucosyltransferases in cystic fibrosis airway epithelial cells.

Biochimie - 1 Jan 2000

Stoykova Lidia I, Liu Aihua, Scanlin Thomas F, Glick Mary Catherine

Abstract excerpt

Cystic fibrosis (CF) has a glycophenotype of aberrant sialylation and/or fucosylation. The CF glycophenotype is expressed on membrane glycoconjugates of CF airway epithelial cells as increased fucosyl residues in alpha1,3/4 linkage to N-acetyl glucosamine, decreased fucosyl residues in alpha1,2 linkage to galactose and decreased sialic acid. To define the cause of this phenotype, the enzyme activity of...

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Share to Carbohydrate Sequence
Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Galactoside 2-alpha-L-fucosyltransferase

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Source

Identifiers

PMID: 12770774
DOI: 10.1016/s0300-9084(03)00061-0

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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