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

CFTR and Ca2+ signaling in cystic fibrosis

1 Jan 2011

Abstract excerpt

Among the diverse physiological functions exerted by calcium signaling in living cells, its role in the regulation of protein biogenesis and trafficking remains incompletely understood. In cystic fibrosis (CF) disease the most common CF transmembrane conductance regulator (CFTR) mutation, F508del-CFTR generates a misprocessed protein that is abnormally retained in the endoplasmic reticulum (ER) compartment,...

Read the complete abstract on PubMed

Topics

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

Share to Biochemical Analysis and Sensing Techniques
Share to Cystic Fibrosis Research Advances
Share to Respiratory and Cough-Related Research

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

Source

Identifiers

PMID: 22046162
DOI: 10.3389/fphar.2011.00067

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 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

CFTR and Ca2+ signaling in cystic fibrosisPMID 22046162Read ↗

CFTR: a hub for kinases and crosstalk of cAMP and Ca2+.Semantic proximity Read ↗

Functional Consequences of CFTR Interactions in Cystic Fibrosis.Semantic proximity Read ↗

CFTR activity and mitochondrial functionSemantic proximity Read ↗

CFTR!Semantic proximity Read ↗

The biogenesis, traffic, and function of the cystic fibrosis transmembrane conductance regulator.Semantic proximity Read ↗

Protein Processing and Inflammatory Signaling in Cystic Fibrosis: Challenges and Therapeutic StrategiesSemantic proximity Read ↗

CFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partnersSemantic proximity Read ↗

It Takes Two to Tango! Protein-Protein Interactions behind cAMP-Mediated CFTR Regulation.Semantic proximity Read ↗

Regulation of CFTR Biogenesis by the Proteostatic Network and Pharmacological Modulators.Semantic proximity Read ↗

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

Cystic fibrosis airway epithelial Ca2+ i signaling: the mechanism for the larger agonist-mediated Ca2+ i signals in human cystic fibrosis airway epithelia.Semantic proximity Read ↗

Revisiting CFTR Interactions: Old Partners and New Players.Semantic proximity Read ↗

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