Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure. - Wikidata - awgldk - TriplyDB

Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.

Cystic fibrosis airway secretions exhibit mucin hyperconcentration and increased osmotic pressure.

http://www.wikidata.org/entity/Q33810485

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Update in Cystic Fibrosis 2014 Early pulmonary inflammation and lung damage in children with cystic fibrosis Respiratory epithelial cells orchestrate pulmonary innate immunity.Airway Gland Structure and Function Airway hydration and COPD Different Stress-Induced Calcium Signatures Are Reported by Aequorin-Mediated Calcium Measurements in Living Cells of Aspergillus fumigatus Secretion of Proteases by an Opportunistic Fungal Pathogen Scedosporium aurantiacum Continuous 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 fibrosis Allergic 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 Bronchitis Quantitative proteomics reveals an altered cystic fibrosis in vitro bronchial epithelial secretome Evidence 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 disease Reduced mucociliary clearance in old mice is associated with a decrease in Muc5b mucin Mucin Agarose Gel Electrophoresis: Western Blotting for High-molecular-weight Glycoproteins.Hydrator Therapies for Chronic Bronchitis. Lessons from Cystic Fibrosis Hyperglycaemia 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 disease Role of IRE1α/XBP-1 in Cystic Fibrosis Airway Inflammation.Defective postsecretory maturation of MUC5B mucin in cystic fibrosis airways Finding 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 MUC5B Airway 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.

http://www.wikidata.org/entity/Q33810485

description

2014 nî lūn-bûn

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2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2014 թվականի հունիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Cystic fibrosis airway secreti ...... nd increased osmotic pressure.

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Cystic fibrosis airway secreti ...... nd increased osmotic pressure.

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Cystic fibrosis airway secreti ...... nd increased osmotic pressure.

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Cystic fibrosis airway secreti ...... nd increased osmotic pressure.

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Cystic fibrosis airway secreti ...... nd increased osmotic pressure.

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Cystic fibrosis airway secreti ...... nd increased osmotic pressure.

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P1433

Journal of Clinical Investigation

P1476

Cystic fibrosis airway secreti ...... nd increased osmotic pressure.

@en

P2093

Ashley G Henderson

http://www.w3.org/2001/XMLSchema#string

Brian Button

http://www.w3.org/2001/XMLSchema#string

C William Davis

http://www.w3.org/2001/XMLSchema#string

Camille Ehre

http://www.w3.org/2001/XMLSchema#string

Genevieve C DeMaria

http://www.w3.org/2001/XMLSchema#string

Hiro Matsui

http://www.w3.org/2001/XMLSchema#string

John K Sheehan

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Li-Heng Cai

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Lubna H Abdullah

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Margaret W Leigh

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P2860

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

Antimicrobial polypeptides in host defense of the respiratory tract

Roles of Pseudomonas aeruginosa las and rhl quorum-sensing systems in control of elastase and rhamnolipid biosynthesis genes

The nature of small-airway obstruction in chronic obstructive pulmonary disease

Characterizing mucous cell remodeling in cystic fibrosis: relationship to neutrophils

Analyzing the functions of large glycoconjugates through the dissipative properties of their absorbed layers using the gel-forming mucin MUC5B as an example.

Airway mucus function and dysfunction.

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

Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.

Serine proteases degrade airway mucins in cystic fibrosis.

P304

3047-3060

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scholarly article

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10.1172/JCI73469

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7

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124

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2014-06-02T00:00:00Z

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262816409

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24892808

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P921

cystic fibrosis

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4072023

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