Cystic fibrosis (CF) is a disease characterized by the production of viscous mucoid secretions in multiple organs, particularly the airways. The pathological increase of proteins, mucin and biological polymers determines their arrangement into a three-dimensional polymeric network, affecting the whole mucus and impairing the muco-ciliary clearance which promotes inflammation and bacterial infection. Thus, to improve the efficacy of the drugs usually applied in CF therapy (e.g., mucolytics, anti-inflammatory and antibiotics), an in-depth understanding of the mucus nanostructure is of utmost importance. Drug diffusivity inside a gel-like system depends on the ratio between the diffusing drug molecule radius and the mesh size of the network. B...
The human tracheobronchial tree surface is covered with mucus. A healthy mucus is a heterogeneous ma...
11noPurpose: Development of a reliable, simple method to monitor lung condition in cystic fibrosis ...
Our current understanding of cystic fibrosis (CF) has revealed that the biophysical properties of mu...
14noCystic fibrosis (CF) is a disease characterized by the production of viscous mucoid secretions i...
14noCystic Fibrosis (CF), one of the most common lethal genetic diseases in people of Caucasian orig...
12noBackground: As most cystic fibrosis (CF) patients progress to respiratory failure, lung function...
AbstractBackgroundThere is conflicting evidence about the importance of airway mucins (MUC5AC and MU...
Sputum poses a critical diffusional barrier that strongly limits the efficacy of drug and gene carri...
Cystic fibrosis (CF) is an autosomal recessive, life-limiting condition characterized by progressive...
Cystic fibrosis (CF) is a recessive genetic disease that is characterised by airway mucus plugging a...
AbstractBackgroundCystic fibrosis (CF) lung disease is characterized by perpetuated neutrophilic inf...
12noUse of Rheology and portable Low-Field NMR for the monitoring of lung functions in cystic fibros...
AbstractOur current understanding of cystic fibrosis (CF) has revealed that the biophysical properti...
poster abstractIndividuals with cystic fibrosis (CF) have a life expectancy of 40 years and require ...
The host- and bacteria-derived extracellular polysaccharide coating of the lung is a considerable ch...
The human tracheobronchial tree surface is covered with mucus. A healthy mucus is a heterogeneous ma...
11noPurpose: Development of a reliable, simple method to monitor lung condition in cystic fibrosis ...
Our current understanding of cystic fibrosis (CF) has revealed that the biophysical properties of mu...
14noCystic fibrosis (CF) is a disease characterized by the production of viscous mucoid secretions i...
14noCystic Fibrosis (CF), one of the most common lethal genetic diseases in people of Caucasian orig...
12noBackground: As most cystic fibrosis (CF) patients progress to respiratory failure, lung function...
AbstractBackgroundThere is conflicting evidence about the importance of airway mucins (MUC5AC and MU...
Sputum poses a critical diffusional barrier that strongly limits the efficacy of drug and gene carri...
Cystic fibrosis (CF) is an autosomal recessive, life-limiting condition characterized by progressive...
Cystic fibrosis (CF) is a recessive genetic disease that is characterised by airway mucus plugging a...
AbstractBackgroundCystic fibrosis (CF) lung disease is characterized by perpetuated neutrophilic inf...
12noUse of Rheology and portable Low-Field NMR for the monitoring of lung functions in cystic fibros...
AbstractOur current understanding of cystic fibrosis (CF) has revealed that the biophysical properti...
poster abstractIndividuals with cystic fibrosis (CF) have a life expectancy of 40 years and require ...
The host- and bacteria-derived extracellular polysaccharide coating of the lung is a considerable ch...
The human tracheobronchial tree surface is covered with mucus. A healthy mucus is a heterogeneous ma...
11noPurpose: Development of a reliable, simple method to monitor lung condition in cystic fibrosis ...
Our current understanding of cystic fibrosis (CF) has revealed that the biophysical properties of mu...