Human cystic fibrosis airway epithelia have reduced Cl- conductance but not increased Na+ conductance. - Wikidata - wikimedia - TriplyDB

Human cystic fibrosis airway epithelia have reduced Cl- conductance but not increased Na+ conductance.

Human cystic fibrosis airway epithelia have reduced Cl- conductance but not increased Na+ conductance.

http://www.wikidata.org/entity/Q35064414

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Nedd4-2 and the regulation of epithelial sodium transport Transgenic hCFTR expression fails to correct β-ENaC mouse lung disease Epithelial Anion Transport as Modulator of Chemokine Signaling Characterization of defects in ion transport and tissue development in cystic fibrosis transmembrane conductance regulator (CFTR)-knockout rats CFTR Modulators: Shedding Light on Precision Medicine for Cystic Fibrosis Origins of cystic fibrosis lung disease Airway Gland Structure and Function Activation of the epithelial sodium channel (ENaC) by the alkaline protease from Pseudomonas aeruginosa Starting a lung transplant program: a roadmap for long-term excellence Marked increases in mucociliary clearance produced by synergistic secretory agonists or inhibition of the epithelial sodium channel.Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study Inter-α-inhibitor blocks epithelial sodium channel activation and decreases nasal potential differences in ΔF508 mice.A functional anatomic defect of the cystic fibrosis airway.CFTR and lung homeostasis.ENaCs and ASICs as therapeutic targets.Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.Regulation of transport in the connecting tubule and cortical collecting duct The innate immune function of airway epithelial cells in inflammatory lung disease Status of fluid and electrolyte absorption in cystic fibrosis.Inhibition of airway surface fluid absorption by cholinergic stimulation Liquid hyper-absorption as a cause of increased DTPA clearance in the cystic fibrosis airway Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense.Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies Nonantibiotic macrolides prevent human neutrophil elastase-induced mucus stasis and airway surface liquid volume depletion.Lessons learned from the cystic fibrosis pig.Reduced sodium transport with nasal administration of the prostasin inhibitor camostat in subjects with cystic fibrosis.Role of CFTR in epithelial physiology.Ion transport by pulmonary epithelia.Lactoferrin: an alternative view of its role in human biological fluids.Proteases, cystic fibrosis and the epithelial sodium channel (ENaC).Failure of respiratory defenses in the pathogenesis of bacterial pneumonia of cattle.Tailored Pig Models for Preclinical Efficacy and Safety Testing of Targeted Therapies.CFTR and Ca Signaling in Cystic Fibrosis.NVP-QBE170: an inhaled blocker of the epithelial sodium channel with a reduced potential to induce hyperkalaemia.Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators.Efficient delivery of RNA interference oligonucleotides to polarized airway epithelia in vitro The CFTR and ENaC debate: how important is ENaC in CF lung disease?The role of CFTR in transepithelial liquid transport in pig alveolar epithelia.Increased apical Na+ permeability in cystic fibrosis is supported by a quantitative model of epithelial ion transport.Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis.

P2860

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P2860

Human cystic fibrosis airway epithelia have reduced Cl- conductance but not increased Na+ conductance.

http://www.wikidata.org/entity/Q35064414

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2011 nî lūn-bûn

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2011 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2011 թվականի հունիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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name

Human cystic fibrosis airway e ...... not increased Na+ conductance.

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Human cystic fibrosis airway e ...... not increased Na+ conductance.

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type

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Human cystic fibrosis airway e ...... not increased Na+ conductance.

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Human cystic fibrosis airway e ...... not increased Na+ conductance.

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Human cystic fibrosis airway e ...... not increased Na+ conductance.

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Human cystic fibrosis airway e ...... not increased Na+ conductance.

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Proceedings of the National Academy of Sciences of the United States of America

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Human cystic fibrosis airway e ...... not increased Na+ conductance

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P2093

Jeng-Haur Chen

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Kalpaj Parekh

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Michael J Welsh

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Omar A Itani

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Philip H Karp

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Sarah Ernst

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Shaf Keshavjee

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P2860

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

Cystic Fibrosis: Lessons from the Sweat Gland

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

Cystic fibrosis

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

Structure and function of the CFTR chloride channel

Pathophysiology of gene-targeted mouse models for cystic fibrosis

Na+ transport in cystic fibrosis respiratory epithelia. Abnormal basal rate and response to adenylate cyclase activation.

ENaC-CFTR interactions: the role of electrical coupling of ion fluxes explored in an epithelial cell model.

Pathology of gastrointestinal organs in a porcine model of cystic fibrosis.

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25

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108

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Julia Klesney-Tait

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51196689

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21646513

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cystic fibrosis

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