[HTML][HTML] View from the Biological Property: Insight into the Functional Diversity and Complexity of the Gut Mucus
C He, H Gao, S Xin, R Hua, X Guo, Y Han… - International Journal of …, 2023 - mdpi.com
Highlights What are the main findings? Mucus, as the most widely distributed biofilm and
vital protective barrier on the surface of mucous membranes throughout the body, fulfills a …
vital protective barrier on the surface of mucous membranes throughout the body, fulfills a …
[HTML][HTML] Infection, Allergy, and Inflammation: The Role of Aspergillus fumigatus in Cystic Fibrosis
TS Poore, ET Zemanick - Microorganisms, 2023 - mdpi.com
Aspergillus fumigatus (Af) is a mold frequently detected in airway samples from people with
cystic fibrosis (pwCF). Abnormal airway mucus may allow Af to germinate, resulting in airway …
cystic fibrosis (pwCF). Abnormal airway mucus may allow Af to germinate, resulting in airway …
[HTML][HTML] An ex vivo rat trachea model reveals abnormal airway physiology and a gland secretion defect in cystic fibrosis
E Harris, M Easter, J Ren, S Krick, J Barnes, SM Rowe - Plos one, 2023 - journals.plos.org
Cystic fibrosis (CF) is a genetic disease hallmarked by aberrant ion transport that results in
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
delayed mucus clearance, chronic infection, and progressive lung function decline. Several …
[HTML][HTML] NLRP3 inflammasome mediates abnormal epithelial regeneration and distal lung remodeling in silica‑induced lung fibrosis
H Zhou, Q Zhang, C Liu, J Fan… - International …, 2024 - spandidos-publications.com
NOD-like receptor protein 3 (NLRP3) inflammasome is closely related to silica particle‑
induced chronic lung inflammation but its role in epithelial remodeling, repair and …
induced chronic lung inflammation but its role in epithelial remodeling, repair and …
CFTR dysfunction leads to defective bacterial eradication on cystic fibrosis airways
M Wu, JH Chen - Frontiers in Physiology, 2024 - frontiersin.org
Dysfunction of the cystic fibrosis transmembrane conductance regulator (CFTR) anion
channel by genetic mutations causes the inherited disease cystic fibrosis (CF). CF lung …
channel by genetic mutations causes the inherited disease cystic fibrosis (CF). CF lung …
[PDF][PDF] Lokalisation av luftvägsmucinerna MUC5AC och MUC5B i kryobiopsier
M Othman - 2023 - diva-portal.org
Introduktion: I normala luftvägar finns mucus med funktionen att rengöra lungorna från
inhalerade partiklar och skadliga ämnen genom mucociliary clearance (MCC). MCC är ett …
inhalerade partiklar och skadliga ämnen genom mucociliary clearance (MCC). MCC är ett …