Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study. - Wikidata - wikimedia - TriplyDB

Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.

Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.

http://www.wikidata.org/entity/Q33766585

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pH Dependent Antimicrobial Peptides and Proteins, Their Mechanisms of Action and Potential as Therapeutic Agents Origins of cystic fibrosis lung disease A 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-37 Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor.Effects of airway surface liquid pH on host defense in cystic fibrosis Cystic fibrosis lung environment and Pseudomonas aeruginosa infection.The innate immune function of airway epithelial cells in inflammatory lung disease Acidic pH increases airway surface liquid viscosity in cystic fibrosis Electrolyte 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 abnormalities Repurposing 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

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P2860

Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.

http://www.wikidata.org/entity/Q33766585

description

2014 nî lūn-bûn

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2014 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

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

@zh-hant

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.

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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.

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P356

J.JCF.2013.12.006

P1433

Journal of Cystic Fibrosis

P1476

Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.

@en

P2093

Alison M Beer

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

Janice L Launspach

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

Michael J Welsh

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Rebecca A Horan

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P2860

Safety assessment of inhaled xylitol in mice and healthy volunteers

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

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene.

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

Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia.

Abnormal surface liquid pH regulation by cultured cystic fibrosis bronchial epithelium.

Neonatal screening strategy for cystic fibrosis using immunoreactive trypsinogen and direct gene analysis.

Benign missense variations in the cystic fibrosis gene.

Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator.

Pathophysiology and management of pulmonary infections in cystic fibrosis.

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373-377

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scholarly article

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10.1016/J.JCF.2013.12.006

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4

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13

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Alejandro A Pezzulo

Mahmoud H Abou Alaiwa

Timothy D Starner

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2014-01-11T00:00:00Z

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259719573

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24418186

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cystic fibrosis

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4060428

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