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

Cystic fibrosis and formes frustes of CFTR-related disease.

Respiration; international review of thoracic diseases - 1 Jan 2007

Southern Kevin W

Abstract excerpt

Cystic fibrosis (CF) is the commonest genetic cause of bronchiectasis in the Caucasian population. Since identification of the putative gene in 1989, the molecular basis of the condition has become clearer with characterisation of the unique pathophysiology. The small airways are the primary site...

Read the complete abstract on PubMed

Topics

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

Share to Bronchiectasis
Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Lung Diseases

Share to Phenotype

Share to Vas Deferens

Share to White People

Source

Identifiers

PMID: 17534127
DOI: 10.1159/000102068

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17534127-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cystic fibrosis and formes frustes of CFTR-related disease.PMID 17534127Read ↗

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

Cystic fibrosis: terminology and diagnostic algorithms.Semantic proximity Read ↗

Atypical cystic fibrosis and CFTR-related diseases.Semantic proximity Read ↗

[Cystic fibrosis in 2008].Semantic proximity Read ↗

Cystic fibrosis.Semantic proximity Read ↗

Clinical Phenotypes of Cystic Fibrosis Carriers.Semantic proximity Read ↗

Beyond Bacteria and Fungi: Cystic Fibrosis and Possible Association with Intestinal Parasitic DiseasesSemantic proximity Read ↗

The phenotypic consequences of CFTR mutations.Semantic proximity Read ↗

Clinical characteristics and genetic analysis of cystic fibrosis transmembrane conductance reseptor-related disease.Semantic proximity Read ↗

Multisystem Imaging Findings of Cystic Fibrosis in Adults: Recognizing Typical and Atypical Patterns of Disease.Semantic proximity Read ↗

Atypical CF and CF related diseases.Semantic proximity Read ↗

Genotypes and phenotypes in cystic fibrosis and cystic fibrosis transmembrane regulator-related disorders.Semantic proximity Read ↗

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