Physiology and pathophysiology of human airway mucus
The mucus clearance system is the dominant mechanical host defense system of the human
lung. Mucus is cleared from the lung by cilia and airflow, including both two-phase gas-liquid …
lung. Mucus is cleared from the lung by cilia and airflow, including both two-phase gas-liquid …
Modeling mucus physiology and pathophysiology in human organs-on-chips
Z Izadifar, A Sontheimer-Phelps, BA Lubamba… - Advanced Drug Delivery …, 2022 - Elsevier
The surfaces of human internal organs are lined by a mucus layer that ensures symbiotic
relationships with commensal microbiome while protecting against potentially injurious …
relationships with commensal microbiome while protecting against potentially injurious …
Mucus-targeting therapies of defective mucus clearance for cystic fibrosis: a short review
MF Figueira, CMP Ribeiro, B Button - Current opinion in pharmacology, 2022 - Elsevier
In the lungs, defective CFTR associated with cystic fibrosis (CF) represents the nidus for
abnormal mucus clearance in the airways and consequently a progressive lung disease …
abnormal mucus clearance in the airways and consequently a progressive lung disease …
Pseudomonas aeruginosa in the Cystic Fibrosis Lung
Cystic fibrosis is a common genetically inherited, multisystem disorder caused by loss of
function of the cystic fibrosis transmembrane conductance regulator (CFTR) protein, an …
function of the cystic fibrosis transmembrane conductance regulator (CFTR) protein, an …
[PDF][PDF] Toward an optimized strategy of using various airway mucus clearance techniques to treat critically ill COVID-19 patients
M Luo, K Ni, Y Sun, J Guo, K Wen, L Deng - Biocell, 2022 - academia.edu
Toward an optimized strategy of using various airway mucus clearance techniques to treat
critically ill COVID-19 patients Page 1 Toward an optimized strategy of using various airway …
critically ill COVID-19 patients Page 1 Toward an optimized strategy of using various airway …
[HTML][HTML] Drug repurposing for cystic fibrosis: Identification of drugs that induce CFTR-independent fluid secretion in nasal organoids
LW Rodenburg, L Delpiano, V Railean… - International Journal of …, 2022 - mdpi.com
Individuals with cystic fibrosis (CF) suffer from severe respiratory disease due to a genetic
defect in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which …
defect in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, which …
[PDF][PDF] Mimicking the host and its microenvironment in vitro for studying
A Crabbé, MA Ledesma, CA Nickerson - academia.edu
Why is a healthy person protected from Pseudomonas aeruginosa infections, while
individuals with cystic fibrosis or damaged epithelium are particularly susceptible to this …
individuals with cystic fibrosis or damaged epithelium are particularly susceptible to this …
Proteomics of Pseudomonas aeruginosa cystic fibrosis isolates to understand host adaptation
KS Kamath - 2022 - figshare.mq.edu.au
Pseudomonas aeruginosa is an opportunistic bacterial pathogen commonly associated with
cystic fibrosis (CF) lung infection. Numerous studies have investigated the mechanism of …
cystic fibrosis (CF) lung infection. Numerous studies have investigated the mechanism of …