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

Characterization of mitochondrial function in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.

Journal of bioenergetics and biomembranes - 1 Jun 2016

Atlante Anna, Favia Maria, Bobba Antonella, Guerra Lorenzo, Casavola Valeria, Reshkin Stephan Joel

Abstract excerpt

Evidence supporting the occurrence of oxidative stress in Cystic Fibrosis (CF) is well established and the literature suggests that oxidative stress is inseparably linked to mitochondrial dysfunction. Here, we have characterized mitochondrial function, in particular as it regards the steps of oxidative phosphorylation and ROS production, in airway cells either homozygous for the F508del-CFTR allele or stably...

Read the complete abstract on PubMed

Topics

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

Share to Aminopyridines
Share to Benzodioxoles

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chlorides

Share to Cystic Fibrosis

Share to Cystic Fibrosis Transmembrane Conductance Regulator

Share to Energy Metabolism

Share to Mitochondrial Diseases

Share to Respiratory System

Source

Identifiers

PMID: 27146408
DOI: 10.1007/s10863-016-9663-y

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.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Characterization of mitochondrial function in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.PMID 27146408Read ↗

CFTR activity and mitochondrial functionSemantic proximity Read ↗

CFTR chloride channel activity modulates the mitochondrial morphology in cultured epithelial cells.Semantic proximity Read ↗

Multifaceted roles of mitochondria in asthmaSemantic proximity Read ↗

GSH monoethyl ester rescues mitochondrial defects in cystic fibrosis models.Semantic proximity Read ↗

Cigarette Smoke‐Induced Acquired Dysfunction of Cystic Fibrosis Transmembrane Conductance Regulator in the Pathogenesis of Chronic Obstructive Pulmonary DiseaseSemantic proximity Read ↗

Angiotensin II and cAMP signaling pathways regulate mitochondrial biogenesis and activity in human adrenocortical cellsSemantic proximity Read ↗

ETI corrector therapy suppresses mitochondrial respiration independently of CFTR mutational status.Semantic proximity Read ↗

Enhanced ROS Production in Mitochondria from Prematurely Aging mtDNA Mutator Mice.Semantic proximity Read ↗

The Mitochondrial Complex I Activity Is Reduced in Cells with Impaired Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) FunctionSemantic proximity Read ↗

A rapid membrane potential assay to monitor CFTR function and inhibition.Semantic proximity Read ↗

The possible links between COPD and lung cancer : cellular and mitochondrial function in airway epithelial cellsSemantic proximity Read ↗

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