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. infection. and epithelial respiratory cells and inhibits the bacterial invasion into these cells. This suggests that therapies aimed at restoring normal levels of GSH in the ASL might be beneficial to control CF lung infections
S-nitrosogluthatione is an endogenous substance, present at decreased levels in the lungs of CF pati...
The sustained imbalance between oxidant and antioxidant species contributes to lung damage in patien...
ABSTRACT Glutathione is an important antioxidant in the lungs but its concentration is low in the ai...
The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concentration of r...
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...
Defective hydration of airway surface mucosa is associated with recurrent lung infection in cystic f...
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...
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...
International audienceCystic fibrosis (CF) is caused by defective Cystic Fibrosis Transmembrane Cond...
Abstract: Cystic fibrosis (CF) is an autosomal recessive disease caused by CFTR mutations. It is cha...
Background: In cystic fibrosis (CF) the defective CF transmembrane conductance regulator protein may...
S-nitrosogluthatione is an endogenous substance, present at decreased levels in the lungs of CF pati...
The sustained imbalance between oxidant and antioxidant species contributes to lung damage in patien...
ABSTRACT Glutathione is an important antioxidant in the lungs but its concentration is low in the ai...
The airway surface liquid (ASL) of Cystic Fibrosis (CF) patients contains a lower concentration of r...
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...
Defective hydration of airway surface mucosa is associated with recurrent lung infection in cystic f...
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...
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...
International audienceCystic fibrosis (CF) is caused by defective Cystic Fibrosis Transmembrane Cond...
Abstract: Cystic fibrosis (CF) is an autosomal recessive disease caused by CFTR mutations. It is cha...
Background: In cystic fibrosis (CF) the defective CF transmembrane conductance regulator protein may...
S-nitrosogluthatione is an endogenous substance, present at decreased levels in the lungs of CF pati...
The sustained imbalance between oxidant and antioxidant species contributes to lung damage in patien...
ABSTRACT Glutathione is an important antioxidant in the lungs but its concentration is low in the ai...