Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis. - Wikidata - wikimedia - TriplyDB

Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.

Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.

http://www.wikidata.org/entity/Q42563377

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Update in Cystic Fibrosis 2014 Epithelial Anion Transport as Modulator of Chemokine Signaling New and emerging targeted therapies for cystic fibrosis Novel Roles for Chloride Channels, Exchangers, and Regulators in Chronic Inflammatory Airway Diseases The Contribution of the Airway Epithelial Cell to Host Defense Microscale imaging of cilia-driven fluid flow Claudins: Gatekeepers of lung epithelial function The pediatric microbiome and the lung NETs and CF Lung Disease: Current Status and Future Prospects The Evolution of Cystic Fibrosis Care A physiologically-motivated compartment-based model of the effect of inhaled hypertonic saline on mucociliary clearance and liquid transport in cystic fibrosis Bacterial evolution in PCD and CF patients follows the same mutational steps Origins of cystic fibrosis lung disease Understanding the development of the respiratory glands Airway Gland Structure and Function Barriers to inhaled gene therapy of obstructive lung diseases: A review Biological effects of carbon black nanoparticles are changed by surface coating with polycyclic aromatic hydrocarbons Defective goblet cell exocytosis contributes to murine cystic fibrosis-associated intestinal disease.Oxidation increases mucin polymer cross-links to stiffen airway mucus gels Microstructural alterations of sputum in cystic fibrosis lung disease.Marked increases in mucociliary clearance produced by synergistic secretory agonists or inhibition of the epithelial sodium channel.High-resolution mucociliary transport measurement in live excised large animal trachea using synchrotron X-ray imaging.Impact of CFTR Modulation on Intestinal pH, Motility, and Clinical Outcomes in Patients With Cystic Fibrosis and the G551D Mutation.Aspergillosis and the role of mucins in cystic fibrosis Gel-forming mucins form distinct morphologic structures in airways Hypertonic saline releases the attached small intestinal cystic fibrosis mucus Animal models of gastrointestinal and liver diseases. Animal models of cystic fibrosis: gastrointestinal, pancreatic, and hepatobiliary disease and pathophysiology.Hypoxic epithelial necrosis triggers neutrophilic inflammation via IL-1 receptor signaling in cystic fibrosis lung disease.Upregulation of TMEM16A Protein in Bronchial Epithelial Cells by Bacterial Pyocyanin Genetic Inhibition Of The Ubiquitin Ligase Rnf5 Attenuates Phenotypes Associated To F508del Cystic Fibrosis Mutation.Three-dimensional, three-vector-component velocimetry of cilia-driven fluid flow using correlation-based approaches in optical coherence tomography.Galactomannan and Zymosan Block the Epinephrine-Induced Particle Transport in Tracheal Epithelium.A spatial model of fluid recycling in the airways of the lung.Junctional abnormalities in human airway epithelial cells expressing F508del CFTR.A novel siderophore system is essential for the growth of Pseudomonas aeruginosa in airway mucus The innate immune function of airway epithelial cells in inflammatory lung disease Acidic pH increases airway surface liquid viscosity in cystic fibrosis Immunohistochemical Detection of Markers for Translational Studies of Lung Disease in Pigs and Humans Glandular Proteome Identifies Antiprotease Cystatin C as a Critical Modulator of Airway Hydration and Clearance.Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense.

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P2860

Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.

http://www.wikidata.org/entity/Q42563377

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name

Impaired mucus detachment disr ...... glet model of cystic fibrosis.

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Impaired mucus detachment disr ...... glet model of cystic fibrosis.

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Impaired mucus detachment disr ...... glet model of cystic fibrosis.

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Impaired mucus detachment disr ...... glet model of cystic fibrosis.

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Impaired mucus detachment disr ...... glet model of cystic fibrosis.

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Impaired mucus detachment disr ...... glet model of cystic fibrosis.

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Impaired mucus detachment disr ...... iglet model of cystic fibrosis

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Alex J Tucker

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Andrew S Michalski

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James D McMenimen

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Mark J Hoegger

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Michael J Welsh

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Thomas O Moninger

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P2860

Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

Role of epithelial HCO3⁻ transport in mucin secretion: lessons from cystic fibrosis

Bicarbonate and functional CFTR channel are required for proper mucin secretion and link cystic fibrosis with its mucus phenotype.

Assessing mucociliary transport of single particles in vivo shows variable speed and preference for the ventral trachea in newborn pigs

Airway mucus function and dysfunction.

Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth.

Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs.

Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children.

Conditions associated with the cystic fibrosis defect promote chronic Pseudomonas aeruginosa infection

Mucociliary clearance in cystic fibrosis.

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345

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Lynda S Ostedgaard

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Maged S Awadalla

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264794180

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25124441

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cystic fibrosis

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4346163

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