Measurement of the airway surface liquid volume with simple light refraction microscopy. - Test2 - elhamkhani - TriplyDB

Measurement of the airway surface liquid volume with simple light refraction microscopy.

Measurement of the airway surface liquid volume with simple light refraction microscopy.

http://www.wikidata.org/entity/Q35219853

about

Transgenic hCFTR expression fails to correct β-ENaC mouse lung disease Quantitative imaging of airway liquid absorption in cystic fibrosis.A functional anatomic defect of the cystic fibrosis airway.Linking increased airway hydration, ciliary beating, and mucociliary clearance through ENaC inhibition Genetic variation in genes encoding airway epithelial potassium channels is associated with chronic rhinosinusitis in a pediatric population.Tgf-beta downregulation of distinct chloride channels in cystic fibrosis-affected epithelia.Automated acquisition and analysis of airway surface liquid height by confocal microscopy Future directions in early cystic fibrosis lung disease research: an NHLBI workshop report Liquid hyper-absorption as a cause of increased DTPA clearance in the cystic fibrosis airway Human bronchial epithelial cells exposed in vitro to cigarette smoke at the air-liquid interface resemble bronchial epithelium from human smokers.Airway Hydration, Apical K(+) Secretion, and the Large-Conductance, Ca(2+)-activated and Voltage-dependent Potassium (BK) Channel.H2O2 stimulates cystic fibrosis transmembrane conductance regulator through an autocrine prostaglandin pathway, using multidrug-resistant protein-4 Water Permeability Adjusts Resorption in Lung Epithelia to Increased Apical Surface Liquid Volumes.CALHM1-Mediated ATP Release and Ciliary Beat Frequency Modulation in Nasal Epithelial Cells.Role of Smad3 and p38 Signalling in Cigarette Smoke-induced CFTR and BK dysfunction in Primary Human Bronchial Airway Epithelial Cells.IFN-γ-mediated reduction of large-conductance, Ca2+-activated, voltage-dependent K+ (BK) channel activity in airway epithelial cells leads to mucociliary dysfunction.Airway Surface Dehydration by Transforming Growth Factor β (TGF-β) in Cystic Fibrosis Is Due to Decreased Function of a Voltage-dependent Potassium Channel and Can Be Rescued by the Drug Pirfenidone.Roflumilast partially reverses smoke-induced mucociliary dysfunction.Cathepsin B contributes to Na+ hyperabsorption in cystic fibrosis airway epithelial cultures.ATP12A promotes mucus dysfunction during Type 2 airway inflammation.

P2860

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P2860

Measurement of the airway surface liquid volume with simple light refraction microscopy.

http://www.wikidata.org/entity/Q35219853

description

2011 nî lūn-bûn

@nan

2011 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年論文

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2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Measurement of the airway surface liquid volume with simple light refraction microscopy.

@ast

Measurement of the airway surface liquid volume with simple light refraction microscopy.

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type

label

Measurement of the airway surface liquid volume with simple light refraction microscopy.

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Measurement of the airway surface liquid volume with simple light refraction microscopy.

@en

prefLabel

Measurement of the airway surface liquid volume with simple light refraction microscopy.

@ast

Measurement of the airway surface liquid volume with simple light refraction microscopy.

@en

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P356

RCMB.2010-0484OC

P1433

American Journal of Respiratory Cell and Molecular Biology

P1476

Measurement of the airway surface liquid volume with simple light refraction microscopy.

@en

P2093

Mike M Myerburg

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

Peter R Harvey

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

Robert Tarran

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Stephen Garoff

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P2860

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

17beta-Estradiol inhibits Ca2+-dependent homeostasis of airway surface liquid volume in human cystic fibrosis airway epithelia.

Reduced histone deacetylase 7 activity restores function to misfolded CFTR in cystic fibrosis

Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770

Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice

Osmotic water permeabilities of cultured, well-differentiated normal and cystic fibrosis airway epithelia

INO-4995 therapeutic efficacy is enhanced with repeat dosing in cystic fibrosis knockout mice and human epithelia.

DeltaF508 CFTR processing correction and activity in polarized airway and non-airway cell monolayers.

Normal and cystic fibrosis airway surface liquid homeostasis. The effects of phasic shear stress and viral infections

Evaluation of second generation amiloride analogs as therapy for cystic fibrosis lung disease.

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592-599

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scholarly article

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10.1165/RCMB.2010-0484OC

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3

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45

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2011-01-14T00:00:00Z

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49759942

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21239602

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3175577

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