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

Heterologous expression of delta F508 CFTR results in decreased sialylation of membrane glycoconjugates.

The American journal of physiology - 1 Feb 1994

Dosanjh A, Lencer W, Brown D, Ausiello D A, Stow J L

Abstract excerpt

The cystic fibrosis transmembrane conductance regulator (CFTR) is commonly mutated in cystic fibrosis to the delta F508 CFTR. CFTR has been shown to function as a adenosine 3',5'-cyclic monophosphate-dependent Cl- channel at the cell surface, and there is evidence to suggest that CFTR may also have a role in transmembrane Cl- conductance in intracellular membrane compartments. Studies using cells from cystic...

Read the complete abstract on PubMed

Topics

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

Share to Cell Line, Transformed
Share to Cell Membrane
Share to Cystic Fibrosis

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

Share to Membrane Proteins

Share to Mutation

Share to Reference Values

Share to Transfection

Source

Identifiers

PMID: 7511336
DOI: 10.1152/ajpcell.1994.266.2.C360

Genes

CFTR

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

Heterologous expression of delta F508 CFTR results in decreased sialylation of membrane glycoconjugates.PMID 7511336Read ↗

Terminal sialylation is altered in airway cells with impaired CFTR-mediated chloride transport.Semantic proximity Read ↗

Terminal glycosylation of cystic fibrosis airway epithelial cells.Semantic proximity Read ↗

Altered terminal glycosylation and the pathophysiology of CF lung disease.Semantic proximity Read ↗

Terminal glycosylation in cystic fibrosis.Semantic proximity Read ↗

Terminal glycosylation in cystic fibrosis (CF): a review emphasizing the airway epithelial cell.Semantic proximity Read ↗

Molecular basis for defective glycosylation and <i>Pseudomonas</i> pathogenesis in cystic fibrosis lungSemantic proximity Read ↗

Host mucin glycosylation plays a role in bacterial adhesion in lungs of individuals with cystic fibrosis.Semantic proximity Read ↗

Alpha1,3fucosyltransferases in cystic fibrosis airway epithelial cells.Semantic proximity Read ↗

Functional cystic fibrosis transmembrane conductance regulator tagged with an epitope of the vesicular stomatis virus glycoprotein can be addressed to the apical domain of polarized cells.Semantic proximity Read ↗

Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia.Semantic proximity Read ↗

Genotypic analysis of respiratory mucous sulfation defects in cystic fibrosis.Semantic proximity Read ↗

Pseudomonas aeruginosa pili bind to asialoGM1 which is increased on the surface of cystic fibrosis epithelial cells.Semantic proximity Read ↗

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