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Article

Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis.

American journal of respiratory and critical care medicine - 15 May 2010

Bienvenu Thierry, Sermet-Gaudelus Isabelle, Burgel Pierre-Regis, Hubert Dominique, Crestani Bruno, Bassinet Laurence, Dusser Daniel, Fajac Isabelle

Abstract excerpt

RATIONALE: Although in patients with diffuse bronchiectasis (DB) and a normal sweat test the presence of one mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene is frequently observed, its pathogenic role in the development of DB remains unclear. OBJECTIVES: To evaluat...

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Source

Identifiers

PMID: 20167849
DOI: 10.1164/rccm.200909-1434OC

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20167849-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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