Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Chloride Conductance, Nasal Potential Difference and Cystic Fibrosis Pathophysiology.

Lung - 1 Feb 2020

Procianoy Elenara da Fonseca Andrade, de Abreu E Silva Fernando Antônio, Maróstica Paulo José Cauduro, Quinton Paul M

Abstract excerpt

PURPOSE: Cystic fibrosis (CF) is a multisystem genetic disease caused by dysfunction of the epithelial anionic channel Cystic Fibrosis Transmembrane conductance Regulator (CFTR). Decreased mucociliary clearance because of thickened mucus is part of the pulmonary disease pathophysiology. It is controversial if the thickened airway surface liquid (ASL) is caused by the deficient chloride secretion and excessive...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chlorides
Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator

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

Share to Exocrine Pancreatic Insufficiency

Share to Membrane Potentials

Share to Nasal Mucosa

Share to Pseudomonas aeruginosa

Share to Pseudomonas Infections

Source

Identifiers

PMID: 31734731
DOI: 10.1007/s00408-019-00293-6

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Chloride Conductance, Nasal Potential Difference and Cystic Fibrosis Pathophysiology.PMID 31734731Read ↗

Correlation between nasal potential difference measurements, genotype and clinical condition in patients with cystic fibrosis.Semantic proximity Read ↗

Nasal airway ion transport is linked to the cystic fibrosis phenotype in adult patients.Semantic proximity Read ↗

Assessing accuracy of testing and diagnosis in cystic fibrosis.Semantic proximity Read ↗

[CFTR and transepithelial ionic transport abnormalities in cystic fibrosis].Semantic proximity Read ↗

Airway epithelial cells--hyperabsorption in CF?Semantic proximity Read ↗

Cystic fibrosis: basic science.Semantic proximity Read ↗

ECFS standards of care on CFTR-related disorders: Diagnostic criteria of CFTR dysfunction.Semantic proximity Read ↗

Update on pathogenesis of cystic fibrosis lung diseaseSemantic proximity Read ↗

Nasal potential difference in cystic fibrosis considering severe CFTR mutations.Semantic proximity Read ↗

Nasal potential difference measurements in patients with atypical cystic fibrosis.Semantic proximity Read ↗

Cystic fibrosis: An inherited disease affecting mucin-producing organsSemantic proximity Read ↗

Diagnostic tools and CFTR functional assays in cystic fibrosis: utility and availability in Switzerland.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.