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 …
A review of inflammatory mechanism in airway diseases
P Aghasafari, U George, R Pidaparti - Inflammation Research, 2019 - Springer
Background Inflammation in the lung is the body's natural response to injury. It acts to
remove harmful stimuli such as pathogens, irritants, and damaged cells and initiate the …
remove harmful stimuli such as pathogens, irritants, and damaged cells and initiate the …
Mathematical models of cystic fibrosis as a systemic disease
Cystic fibrosis (CF) is widely known as a disease of the lung, even though it is in truth a
systemic disease, whose symptoms typically manifest in gastrointestinal dysfunction first. CF …
systemic disease, whose symptoms typically manifest in gastrointestinal dysfunction first. CF …
ATP12A promotes mucus dysfunction during Type 2 airway inflammation
AT Lennox, SL Coburn, JA Leech, EM Heidrich… - Scientific reports, 2018 - nature.com
Allergic airway disease is known to cause significant morbidity due to impaired mucociliary
clearance, however the mechanism that leads to the mucus dysfunction is not entirely …
clearance, however the mechanism that leads to the mucus dysfunction is not entirely …
Towards a unified approach in the modeling of fibrosis: A review with research perspectives
MB Amar, C Bianca - Physics of life reviews, 2016 - Elsevier
Pathological fibrosis is the result of a failure in the wound healing process. The
comprehension and the related modeling of the different mechanisms that trigger fibrosis are …
comprehension and the related modeling of the different mechanisms that trigger fibrosis are …
Pseudomonas infection and mucociliary and absorptive clearance in the cystic fibrosis lung
Airway surface liquid hyperabsorption and mucus accumulation are key elements of cystic
fibrosis lung disease that can be assessed in vivo using functional imaging methods. In this …
fibrosis lung disease that can be assessed in vivo using functional imaging methods. In this …
Physiologically-based model of fluid absorption and mucociliary clearance in cystic fibrosis
Dehydration of mucus in the lungs of cystic fibrosis (CF) patients can inhibit mucociliary
clearance (MCC), resulting in mucus build-up and blockages. Prior mathematical models …
clearance (MCC), resulting in mucus build-up and blockages. Prior mathematical models …
A physiologically-motivated model of cystic fibrosis liquid and solute transport dynamics across primary human nasal epithelia
F Serrano Castillo, CA Bertrand, MM Myerburg… - … of Pharmacokinetics and …, 2019 - Springer
Cystic fibrosis (CF) disease is caused by mutations affecting the gene coding for the cystic
fibrosis transmembrane conductance regulator (CFTR), an anion channel expressed in the …
fibrosis transmembrane conductance regulator (CFTR), an anion channel expressed in the …
Systems medicine for lung diseases: phenotypes and precision medicine in cancer, infection, and allergy
Lung diseases cause an enormous socioeconomic burden. Four of them are among the ten
most important causes of deaths worldwide: Pneumonia has the highest death toll of all …
most important causes of deaths worldwide: Pneumonia has the highest death toll of all …
[PDF][PDF] Towards Personalized Medicine in Cystic Fibrosis: Patient-Specific Modeling of Mucociliary Clearance Using Physiologically-Based Flow Constraints
ME Shapiro - 2023 - d-scholarship.pitt.edu
Healthy humans have a thin layer of mucus lining the airways that protects the lungs from
inhaled particulate or pathogens. Trapped particles are conveyed up the airway tree and out …
inhaled particulate or pathogens. Trapped particles are conveyed up the airway tree and out …