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Article

Terminal glycosylation in cystic fibrosis (CF): a review emphasizing the airway epithelial cell.

Glycoconjugate journal - 1 Sept 2001

Rhim A D, Stoykova L, Glick M C, Scanlin T F

Abstract excerpt

Altered terminal glycosylation, with increased fucosylation and decreased sialylation is a hallmark of the cystic fibrosis (CF) glycosylation phenotype. Oligosaccharides purified from the surface membrane glycoconjugates of CF airway epithelial cells have the Lewis x, selectin ligand in terminal positions. This review is focused on the investigations of the glycoconjugates of the CF airway epithelial cell...

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Source

Identifiers

PMID: 12386452
DOI: 10.1023/a:1020815205022

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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