Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.
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pH Dependent Antimicrobial Peptides and Proteins, Their Mechanisms of Action and Potential as Therapeutic AgentsOrigins of cystic fibrosis lung diseaseA functional anatomic defect of the cystic fibrosis airway.pH modulates the activity and synergism of the airway surface liquid antimicrobials β-defensin-3 and LL-37Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor.Effects of airway surface liquid pH on host defense in cystic fibrosisCystic fibrosis lung environment and Pseudomonas aeruginosa infection.The innate immune function of airway epithelial cells in inflammatory lung diseaseAcidic pH increases airway surface liquid viscosity in cystic fibrosisElectrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense.Airway acidification initiates host defense abnormalities in cystic fibrosis mice.Acute administration of ivacaftor to people with cystic fibrosis and a G551D-CFTR mutation reveals smooth muscle abnormalitiesRepurposing tromethamine as inhaled therapy to treat CF airway disease.Lentiviral-mediated phenotypic correction of cystic fibrosis pigs.CFTR, bicarbonate, and the pathophysiology of cystic fibrosis.Epithelial Sodium Channel ENaC is a Modifier of the Long Term Non-progressive Phenotype Associated with F508del CFTR Mutations.Pseudomonas aeruginosa infection in cystic fibrosis: pathophysiological mechanisms and therapeutic approaches.Airway surface liquid pH is not acidic in children with cystic fibrosis.Cystic fibrosis respiratory tract salt concentration: An Exploratory Cohort Study.Cystic fibrosis respiratory tract salt concentration: An Exploratory Cohort Study.Nominal carbonic anhydrase activity minimizes airway-surface liquid pH changes during breathing.Influenza Hemagglutinin Protein Stability, Activation, and Pandemic Risk.Cftr Modulates Wnt/β-Catenin Signaling and Stem Cell Proliferation in Murine Intestine.Ivacaftor-induced sweat chloride reductions correlate with increases in airway surface liquid pH in cystic fibrosis
P2860
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P2860
Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.
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2014 nî lūn-bûn
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2014 թուականի Յունուարին հրատարակուած գիտական յօդուած
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2014 թվականի հունվարին 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
Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.
@ast
Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.
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type
label
Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.
@ast
Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.
@en
prefLabel
Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.
@ast
Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.
@en
P2093
P2860
P50
P1476
Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.
@en
P2093
Alison M Beer
Janice L Launspach
Michael J Welsh
Rebecca A Horan
P2860
P304
P356
10.1016/J.JCF.2013.12.006
P577
2014-01-11T00:00:00Z