Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.
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Update in Cystic Fibrosis 2014Early pulmonary inflammation and lung damage in children with cystic fibrosisRespiratory epithelial cells orchestrate pulmonary innate immunity.Airway Gland Structure and FunctionAirway hydration and COPDDifferent Stress-Induced Calcium Signatures Are Reported by Aequorin-Mediated Calcium Measurements in Living Cells of Aspergillus fumigatusSecretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacumContinuous mucociliary transport by primary human airway epithelial cells in vitro.Microstructural alterations of sputum in cystic fibrosis lung disease.Aspergillosis and the role of mucins in cystic fibrosisAllergic asthma is distinguished by sensitivity of allergen-specific CD4+ T cells and airway structural cells to type 2 inflammation.Localization of Burkholderia cepacia complex bacteria in cystic fibrosis lungs and interactions with Pseudomonas aeruginosa in hypoxic mucus.Airway Surface Dehydration Aggravates Cigarette Smoke-Induced Hallmarks of COPD in Mice.Excess Secretion of Gel-Forming Mucins and Associated Innate Defense Proteins with Defective Mucin Un-Packaging Underpin Gallbladder Mucocele Formation in Dogs.The Relationship of Mucus Concentration (Hydration) to Mucus Osmotic Pressure and Transport in Chronic BronchitisQuantitative proteomics reveals an altered cystic fibrosis in vitro bronchial epithelial secretomeEvidence and Role for Bacterial Mucin Degradation in Cystic Fibrosis Airway Disease.Transparent antifouling material for improved operative field visibility in endoscopy.The innate immune function of airway epithelial cells in inflammatory lung diseaseReduced mucociliary clearance in old mice is associated with a decrease in Muc5b mucinMucin Agarose Gel Electrophoresis: Western Blotting for High-molecular-weight Glycoproteins.Hydrator Therapies for Chronic Bronchitis. Lessons from Cystic FibrosisHyperglycaemia and Pseudomonas aeruginosa acidify cystic fibrosis airway surface liquid by elevating epithelial monocarboxylate transporter 2 dependent lactate-H+ secretion.Iron Uptake Analysis in a Set of Clinical Isolates of Pseudomonas putida.Contribution of mucus concentration and secreted mucins Muc5ac and Muc5b to the pathogenesis of muco-obstructive lung diseaseRole of IRE1α/XBP-1 in Cystic Fibrosis Airway Inflammation.Defective postsecretory maturation of MUC5B mucin in cystic fibrosis airwaysFinding new drugs to enhance anion secretion in cystic fibrosis: Toward suitable systems for better drug screening. Report on the pre-conference meeting to the 12th ECFS Basic Science Conference, Albufeira, 25-28 March 2015.The Mucus Barrier to Inhaled Gene Therapy.Airway mucus, inflammation and remodeling: emerging links in the pathogenesis of chronic lung diseases.Mucus Hyperconcentration as a Unifying Aspect of the Chronic Bronchitic Phenotype.Biosynthesis of the polymeric gel-forming mucin MUC5BAirway Mucin Concentration as a Marker of Chronic Bronchitis.MUC5AC and a Glycosylated Variant of MUC5B Alter Mucin Composition in Children With Acute Asthma.Genome-Wide Survey of Pseudomonas aeruginosa PA14 Reveals a Role for the Glyoxylate Pathway and Extracellular Proteases in the Utilization of Mucin.Direct monitoring of pulmonary disease treatment biomarkers using plasmonic gold nanorods with diffusion-sensitive OCT.Sialic acid-to-urea ratio as a measure of airway surface hydration.Pyomelanin-producing Pseudomonas aeruginosa selected during chronic infections have a large chromosomal deletion which confers resistance to pyocins.On the Pathogenesis of Acute Exacerbations of Mucoobstructive Lung Diseases.Hyperosmotic stress stimulates autophagy via polycystin-2.
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P2860
Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Cystic fibrosis airway secreti ...... nd increased osmotic pressure.
@ast
Cystic fibrosis airway secreti ...... nd increased osmotic pressure.
@en
type
label
Cystic fibrosis airway secreti ...... nd increased osmotic pressure.
@ast
Cystic fibrosis airway secreti ...... nd increased osmotic pressure.
@en
prefLabel
Cystic fibrosis airway secreti ...... nd increased osmotic pressure.
@ast
Cystic fibrosis airway secreti ...... nd increased osmotic pressure.
@en
P2093
P2860
P356
P1476
Cystic fibrosis airway secreti ...... nd increased osmotic pressure.
@en
P2093
Ashley G Henderson
Brian Button
C William Davis
Camille Ehre
Genevieve C DeMaria
Hiro Matsui
John K Sheehan
Li-Heng Cai
Lubna H Abdullah
Margaret W Leigh
P2860
P304
P356
10.1172/JCI73469
P407
P577
2014-06-02T00:00:00Z