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Article

Reduced exhaled NO is related to impaired nasal potential difference in patients with cystic fibrosis.

Vascular pharmacology - 1 Dec 2005

Texereau J, Fajac I, Hubert D, Coste J, Dusser D J, Bienvenu T, Dall'Ava-Santucci J, Dinh-Xuan A T

Abstract excerpt

Nitric oxide (NO) plays a central role in many airway physiological functions, and its production appears to be related with progression of lung disease in patients with cystic fibrosis (CF). However, underlying mechanisms which specifically link NO and CF-related lung disease remain unclear. Following in vitro and animal studies suggesting a role for NO in ion transport in various epithelia, this work...

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Share to Cystic Fibrosis
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16182611
DOI: 10.1016/j.vph.2005.08.004

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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