[HTML][HTML] Chitosan in non-viral gene delivery: Role of structure, characterization methods, and insights in cancer and rare diseases therapies

B Santos-Carballal, E Fernández Fernández… - Polymers, 2018 - mdpi.com
Non-viral gene delivery vectors have lagged far behind viral ones in the current pipeline of
clinical trials of gene therapy nanomedicines. Even when non-viral nanovectors pose less …

Chronic rhinosinusitis in patients with cystic fibrosis

DL Hamilos - The Journal of Allergy and Clinical Immunology: In …, 2016 - Elsevier
Chronic rhinosinusitis (CRS) is highly prevalent in patients with cystic fibrosis (CF) and
accounts for significant morbidity and contribution to CF lung disease. Mutations of the cystic …

[HTML][HTML] Development of an airway mucus defect in the cystic fibrosis rat

SE Birket, JM Davis, CM Fernandez, KL Tuggle… - JCI insight, 2018 - ncbi.nlm.nih.gov
The mechanisms underlying the development and natural progression of the airway mucus
defect in cystic fibrosis (CF) remain largely unclear. New animal models of CF, coupled with …

[HTML][HTML] Antimicrobial peptides for tackling cystic fibrosis related bacterial infections: A review

F Bugli, C Martini, M Di Vito, M Cacaci… - Microbiological …, 2022 - Elsevier
Antibiotic resistance is a serious health and social problem that will have a substantial
impact in the coming years on the world health and economy. Thus, the increasing demand …

[HTML][HTML] Hypertonic saline suppresses NADPH oxidase-dependent neutrophil extracellular trap formation and promotes apoptosis

A Nadesalingam, JHK Chen, A Farahvash… - Frontiers in …, 2018 - frontiersin.org
Tonicity of saline (NaCl) is important in regulating cellular functions and homeostasis.
Hypertonic saline is administered to treat many inflammatory diseases, including cystic …

[HTML][HTML] Defective goblet cell exocytosis contributes to murine cystic fibrosis–associated intestinal disease

J Liu, NM Walker, A Ootani… - The Journal of …, 2015 - Am Soc Clin Investig
Cystic fibrosis (CF) intestinal disease is associated with the pathological manifestation
mucoviscidosis, which is the secretion of tenacious, viscid mucus that plugs ducts and …

Critical care of the adult patient with cystic fibrosis

CS King, AW Brown, S Aryal, K Ahmad, S Donaldson - Chest, 2019 - Elsevier
Cystic fibrosis (CF) is a multiorgan, genetic disease resulting from dysfunction of the CF
transmembrane conductance regulator. The primary clinical manifestations are …

Plasma membrane wounding and repair in pulmonary diseases

X Cong, RD Hubmayr, C Li… - American Journal of …, 2017 - journals.physiology.org
Various pathophysiological conditions such as surfactant dysfunction, mechanical
ventilation, inflammation, pathogen products, environmental exposures, and gastric acid …

[HTML][HTML] An intriguing involvement of mitochondria in cystic fibrosis

M Favia, L de Bari, A Bobba, A Atlante - Journal of Clinical Medicine, 2019 - mdpi.com
Cystic fibrosis (CF) occurs when the cystic fibrosis transmembrane conductance regulator
(CFTR) protein is not synthetized and folded correctly. The CFTR protein helps to maintain …

Salt, chloride, bleach, and innate host defense

G Wang, WM Nauseef - Journal of Leucocyte Biology, 2015 - academic.oup.com
Salt provides 2 life-essential elements: sodium and chlorine. Chloride, the ionic form of
chlorine, derived exclusively from dietary absorption and constituting the most abundant …