The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concentration of reduced glutathione (GSH) with respect to healthy people. It is not known whether this defect may favor lung colonization by opportunistic pathogens
Previous work in our laboratory has shown that glutathione (GSH) availability is linked to cellular ...
AbstractThe pathological hallmark of cystic fibrosis (CF) chronic inflammatory response is the massi...
Current anti-inflammatory strategies for the treatment of pulmonary disease in cystic fibrosis (CF) ...
The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concentration of r...
BACKGROUND: The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concen...
The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concentration of r...
AbstractCFTR mutation, which causes cystic fibrosis (CF), has also recently been identified as causi...
Background: Cystic fibrosis (CF) is an autosomal recessive disorder characterized by a chronic neutr...
AbstractBackground: Reduced glutathione (GSH) is a major antioxidant in the lung. In cystic fibrosis...
Glutathione (GSH) is decreased in cystic fibrosis (CF) airways, thus its resupply by inhalation has ...
Lung damage in cystic fibrosis (CF) patients is determined by mucus accumulation, Pseudomonas aerugi...
A number of inflammatory lung diseases have abnormally low glutathione (GSH) levels in the airway fl...
In CF patients, Glutathione (GSH), the first-line defence of lungs against oxidative stress, is seve...
Background: In cystic fibrosis (CF) the defective CF transmembrane conductance regulator protein may...
Rationale: Glutathione is the major antioxidant in the extracellular lining fluid of the lungs and d...
Previous work in our laboratory has shown that glutathione (GSH) availability is linked to cellular ...
AbstractThe pathological hallmark of cystic fibrosis (CF) chronic inflammatory response is the massi...
Current anti-inflammatory strategies for the treatment of pulmonary disease in cystic fibrosis (CF) ...
The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concentration of r...
BACKGROUND: The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concen...
The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concentration of r...
AbstractCFTR mutation, which causes cystic fibrosis (CF), has also recently been identified as causi...
Background: Cystic fibrosis (CF) is an autosomal recessive disorder characterized by a chronic neutr...
AbstractBackground: Reduced glutathione (GSH) is a major antioxidant in the lung. In cystic fibrosis...
Glutathione (GSH) is decreased in cystic fibrosis (CF) airways, thus its resupply by inhalation has ...
Lung damage in cystic fibrosis (CF) patients is determined by mucus accumulation, Pseudomonas aerugi...
A number of inflammatory lung diseases have abnormally low glutathione (GSH) levels in the airway fl...
In CF patients, Glutathione (GSH), the first-line defence of lungs against oxidative stress, is seve...
Background: In cystic fibrosis (CF) the defective CF transmembrane conductance regulator protein may...
Rationale: Glutathione is the major antioxidant in the extracellular lining fluid of the lungs and d...
Previous work in our laboratory has shown that glutathione (GSH) availability is linked to cellular ...
AbstractThe pathological hallmark of cystic fibrosis (CF) chronic inflammatory response is the massi...
Current anti-inflammatory strategies for the treatment of pulmonary disease in cystic fibrosis (CF) ...