Prostasin expression is regulated by airway surface liquid volume and is increased in cystic fibrosis
MM Myerburg, EE McKenna, CJ Luke… - … of Physiology-Lung …, 2008 - journals.physiology.org
Airway surface liquid (ASL) absorption is initiated by Na+ entry via epithelial Na+ channels
(ENaC), which establishes an osmotic gradient that drives fluid from the luminal to serosal …
(ENaC), which establishes an osmotic gradient that drives fluid from the luminal to serosal …
Hypertonic saline therapy in cystic fibrosis: evidence against the proposed mechanism involving aquaporins
MH Levin, S Sullivan, D Nielson, B Yang… - Journal of Biological …, 2006 - ASBMB
Recent data indicate the clinical benefit of nebulized hypertonic saline in cystic fibrosis lung
disease, with a proposed mechanism involving sustained increase in airway surface liquid …
disease, with a proposed mechanism involving sustained increase in airway surface liquid …
Human airway ecto-adenylate kinase: a mechanism to propagate ATP signaling on airway surfaces
M Picher, RC Boucher - Journal of Biological Chemistry, 2003 - ASBMB
Mechanically induced ATP release from human airway epithelial cells regulates mucociliary
clearance through cell surface nucleotide receptors. Ectoenzymes detected on these cells …
clearance through cell surface nucleotide receptors. Ectoenzymes detected on these cells …
Rationale for hypertonic saline therapy for cystic fibrosis lung disease
R Tarran, S Donaldson… - Seminars in respiratory …, 2007 - thieme-connect.com
Cystic fibrosis (CF) is caused by alterations in the CF transmembrane conductance regulator
(CFTCR) gene. More than 1400 mutations in the CFTCR gene have been described, but the …
(CFTCR) gene. More than 1400 mutations in the CFTCR gene have been described, but the …
Role of cells and mediators in exercise-induced bronchoconstriction
TS Hallstrand, WA Altemeier… - Immunology and …, 2013 - immunology.theclinics.com
Role of Cells and Mediators in Exercise-Induced Bronchoconstriction - Immunology and Allergy
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Mathematical model reveals role of nucleotide signaling in airway surface liquid homeostasis and its dysregulation in cystic fibrosis
CI Sandefur, RC Boucher… - Proceedings of the …, 2017 - National Acad Sciences
Mucociliary clearance is composed of three components (ie, mucin secretion, airway surface
hydration, and ciliary-activity) which function coordinately to clear inhaled microbes and …
hydration, and ciliary-activity) which function coordinately to clear inhaled microbes and …
Paracellular permeability of bronchial epithelium is controlled by CFTR
N Weiser, N Molenda, K Urbanova, M Bähler… - Cellular Physiology and …, 2011 - karger.com
In normal airway epithelium, the cystic fibrosis transmembrane conductance regulator
(CFTR) transports Cl-ions to the apical surface of the epithelium paralleled by the flow of …
(CFTR) transports Cl-ions to the apical surface of the epithelium paralleled by the flow of …
Oral breathing challenge in participants with vocal attrition
M Sivasankar, KV Fisher - 2003 - ASHA
Vocal folds undergo osmotic challenge by mouth breathing during singing, exercising, and
loud speaking. Just 15 min of obligatory oral breathing, to dry the vocal folds, increases …
loud speaking. Just 15 min of obligatory oral breathing, to dry the vocal folds, increases …
RNA sequencing identifies transcriptional changes in the rabbit larynx in response to low humidity challenge
TW Bailey, AP Dos Santos, NC do Nascimento, S Xie… - BMC genomics, 2020 - Springer
Background Voice disorders are a worldwide problem impacting human health, particularly
for occupational voice users. Avoidance of surface dehydration is commonly prescribed as a …
for occupational voice users. Avoidance of surface dehydration is commonly prescribed as a …
Physiological Impact of Abnormal Lipoxin A4 Production on Cystic Fibrosis Airway Epithelium and Therapeutic Potential
G Higgins, F Ringholz, P Buchanan… - BioMed Research …, 2015 - Wiley Online Library
Lipoxin A4 has been described as a major signal for the resolution of inflammation and is
abnormally produced in the lungs of patients with cystic fibrosis (CF). In CF, the loss of …
abnormally produced in the lungs of patients with cystic fibrosis (CF). In CF, the loss of …