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 as a disease of misprocessing of the cystic fibrosis transmembrane conductance regulator glycoprotein.

American journal of human genetics - 1 Jun 1999

Riordan J R

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to ATP-Binding Cassette Transporters
Share to Biological Transport
Share to Cystic Fibrosis

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

Share to Mutation

Share to Protein Processing, Post-Translational

Source

Open in PubMed Open full text

Identifiers

PMID: 10330337
DOI: 10.1086/302429
PMCID: PMC1377893

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

Cystic fibrosis as a disease of misprocessing of the cystic fibrosis transmembrane conductance regulator glycoprotein.PMID 10330337Read ↗

Molecular mechanisms of cystic fibrosis - how mutations lead to misfunction and guide therapy.Semantic proximity Read ↗

Defects in processing and trafficking of the cystic fibrosis transmembrane conductance regulator.Semantic proximity Read ↗

Proteomics uncovering possible key players in F508del-CFTR processing and trafficking.Semantic proximity Read ↗

Cystic fibrosis: premature degradation of mutant proteins as a molecular disease mechanism.Semantic proximity Read ↗

How do cystic fibrosis transmembrane conductance regulator mutations produce lung disease?Semantic proximity Read ↗

Targets for cystic fibrosis therapy: proteomic analysis and correction of mutant cystic fibrosis transmembrane conductance regulator.Semantic proximity Read ↗

Defects in processing and trafficking of cystic fibrosis transmembrane conductance regulator.Semantic proximity Read ↗

Cystic fibrosis transmembrane conductance regulator dysfunction and its treatment.Semantic proximity Read ↗

Trafficking and function of the cystic fibrosis transmembrane conductance regulator: a complex network of posttranslational modificationsSemantic proximity Read ↗

Cystic Fibrosis – a Multiorgan Protein Misfolding DiseaseSemantic proximity Read ↗

Misfolding of the cystic fibrosis transmembrane conductance regulator and disease.Semantic proximity Read ↗

CFTR structure: lassoing cystic fibrosis.Semantic proximity Read ↗

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