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Article

Decreased expression of the CFTR protein in remodeled human nasal epithelium from non-cystic fibrosis patients.

Laboratory investigation; a journal of technical methods and pathology - 1 Feb 1995

Brezillon S, Dupuit F, Hinnrasky J, Marchand V, Kälin N, Tümmler B, Puchelle E

Abstract excerpt

BACKGROUND: In normal adult pseudostratified human nasal surface epithelium, the cystic fibrosis transmembrane conductance regulator (CFTR) is localized to the apical domain of the ciliated cells, whereas in cystic fibrosis (CF), the mutated delta F 508 CFTR exhibits an abnormal cytoplasmic localization. Frequent airway injuries either in CF or non-CF patients may induce a remodeling of the surface epithelium...

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Source

Identifiers

PMID: 7531792

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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Decreased expression of the CFTR protein in remodeled human nasal epithelium from non-cystic fibrosis patients.PMID 7531792Read ↗

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