Failure to clear mucus normally is a critical event in the pathogenesis of chronic bronchitis (CB). A unifying concept for the failure to clear mucus from airway surfaces has emerged that focuses on an abnormally high mucin-to-airway surface liquid volume ratio. At a certain level, a high mucin-to-volume ratio is associated with loss of the periciliary liquid layer and adhesion of the mucus layer to the cell surface. Adherent mucus becomes a stimulus for irritation and cough and is the nidus for bacterial infection. Therapeutic approaches for clearing mucus from CB airways should focus on restoring the balance of mucin and water. Pharmacologic blockade of the epithelial Na+ channel, which is rate-limiting for volume absorption from airway s...
Rationale: Chronic bronchitis (CB) is characterized by persistent cough and sputum production. Studi...
Rationale: Chronic bronchitis (CB) is characterized by persistent cough and sputum production. Studi...
AbstractThe pathogenesis of cystic fibrosis (CF) airways infection is unknown. Two hypotheses, “hypo...
Abnormalities in mucus production and qualitative properties such as mucus hydration are central to ...
Abnormalities in mucus production and qualitative properties such as mucus hydration are central to ...
In cystic fibrosis (CF), a defect in ion transport results in thick and dehydrated airway mucus, whi...
In cystic fibrosis (CF), a defect in ion transport results in thick and dehydrated airway mucus, whi...
In cystic fibrosis (CF), a defect in ion transport results in thick and dehydrated airway mucus, whi...
Chronic airway diseases like cystic fibrosis, chronic bronchitis, asthma, diffuse panbronchiolitis, ...
Mucoobstructive lung diseases have highlighted the importance of a proper description of the normal ...
The clearance of mucus from the airways protects the lungs from inhaled noxious and infectious mater...
The pathogenesis of cystic fibrosis (CF) airways infection is unknown. Two hypotheses, "hypotonic [l...
The pathogenesis of cystic fibrosis (CF) airways infection is unknown. Two hypotheses, "hypotonic [l...
Chronic obstructive pulmonary disease (COPD) is characterized by chronic bronchitic and emphysematou...
Inhaled hypertonic saline (HS) is an effective therapy for muco-obstructive lung diseases. However, ...
Rationale: Chronic bronchitis (CB) is characterized by persistent cough and sputum production. Studi...
Rationale: Chronic bronchitis (CB) is characterized by persistent cough and sputum production. Studi...
AbstractThe pathogenesis of cystic fibrosis (CF) airways infection is unknown. Two hypotheses, “hypo...
Abnormalities in mucus production and qualitative properties such as mucus hydration are central to ...
Abnormalities in mucus production and qualitative properties such as mucus hydration are central to ...
In cystic fibrosis (CF), a defect in ion transport results in thick and dehydrated airway mucus, whi...
In cystic fibrosis (CF), a defect in ion transport results in thick and dehydrated airway mucus, whi...
In cystic fibrosis (CF), a defect in ion transport results in thick and dehydrated airway mucus, whi...
Chronic airway diseases like cystic fibrosis, chronic bronchitis, asthma, diffuse panbronchiolitis, ...
Mucoobstructive lung diseases have highlighted the importance of a proper description of the normal ...
The clearance of mucus from the airways protects the lungs from inhaled noxious and infectious mater...
The pathogenesis of cystic fibrosis (CF) airways infection is unknown. Two hypotheses, "hypotonic [l...
The pathogenesis of cystic fibrosis (CF) airways infection is unknown. Two hypotheses, "hypotonic [l...
Chronic obstructive pulmonary disease (COPD) is characterized by chronic bronchitic and emphysematou...
Inhaled hypertonic saline (HS) is an effective therapy for muco-obstructive lung diseases. However, ...
Rationale: Chronic bronchitis (CB) is characterized by persistent cough and sputum production. Studi...
Rationale: Chronic bronchitis (CB) is characterized by persistent cough and sputum production. Studi...
AbstractThe pathogenesis of cystic fibrosis (CF) airways infection is unknown. Two hypotheses, “hypo...