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Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections

American journal of respiratory and critical care medicine, 2017-06, Vol.195 (12), p.1617-1628

2017

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Loss of Anion Transport without Increased Sodium Absorption Characterizes Newborn Porcine Cystic Fibrosis Airway Epithelia

Cell, 2010-12, Vol.143 (6), p.911-923

2010

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Effects of Tham Nasal Alkalinization on Airway Microbial Communities: A Pilot Study in Non-CF and CF Adults

Annals of otology, rhinology & laryngology, 2022-09, Vol.131 (9), p.1013-1020

2022

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Amphotericin B induces epithelial voltage responses in people with cystic fibrosis

Journal of cystic fibrosis, 2021-05, Vol.20 (3), p.540-550

2021

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Randomized controlled study of aerosolized hypertonic xylitol versus hypertonic saline in hospitalized patients with pulmonary exacerbation of cystic fibrosis

Journal of cystic fibrosis, 2020-01, Vol.19 (1), p.108-113

2020

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

Journal of cystic fibrosis, 2014-07, Vol.13 (4), p.373-377

2014

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Enhancement of respiratory mucosal antiviral defenses by the oxidation of iodide

American journal of respiratory cell and molecular biology, 2011-10, Vol.45 (4), p.874-881

2011

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Concentration of the antibacterial precursor thiocyanate in cystic fibrosis airway secretions

Free radical biology & medicine, 2011-05, Vol.50 (9), p.1144-1150

2011

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An in vitro model of differentiated human airway epithelia. Methods for establishing primary cultures

Methods in molecular biology (Clifton, N.J.), 2002, Vol.188, p.115

2002

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Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor

International forum of allergy & rhinology, 2015-02, Vol.5 (2), p.178-181

2015

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Repurposing tromethamine as inhaled therapy to treat CF airway disease

JCI insight, 2016-06, Vol.1 (8)

2016

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Acute administration of ivacaftor to people with cystic fibrosis and a G551D-CFTR mutation reveals smooth muscle abnormalities

JCI insight, 2016-04, Vol.1 (4), p.e86183-e86183

2016

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The Osmolyte Xylitol Reduces the Salt Concentration of Airway Surface Liquid and May Enhance Bacterial Killing

Proceedings of the National Academy of Sciences - PNAS, 2000-10, Vol.97 (21), p.11614-11619

2000

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Patterns and density of early tracheal colonization in intensive care unit patients

Journal of critical care, 2009-03, Vol.24 (1), p.114-121

2009

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The effects of recombinant human hemoglobin on esophageal motor function in humans

Gastroenterology (New York, N.Y. 1943), 1995-10, Vol.109 (4), p.1241-1248

1995

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Safety assessment of inhaled xylitol in mice and healthy volunteers

Respiratory research, 2004-09, Vol.5 (1), p.13-13, Article 13

2004

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Bronchoscopic assessment of airway retention time of aerosolized xylitol

Respiratory research, 2006-02, Vol.7 (1), p.27-27, Article 27

2006

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Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation

PloS one, 2013-07, Vol.8 (7), p.e66955

2013

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Sequential magnetic resonance imaging analysis of the maxillary sinuses: implications for a model of gene therapy in cystic fibrosis

Journal of laryngology and otology, 1999-04, Vol.113 (4), p.329-335

1999

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TRACHEAL COLONIZATION IN NEWLY INTUBATED PATIENTS

Chest, 2005-10, Vol.128 (4), p.143S-143S

2005

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Safety assessment of inhaled xylitol in subjects with cystic fibrosis

Journal of cystic fibrosis, 2007-01, Vol.6 (1), p.31-34

2007

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Medical reversal of chronic rhinosinusitis in a cystic fibrosis patient with ivacaftor

International forum of allergy & rhinology, 2014-10, Vol.5 (2), p.178-181

2014

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Use of nasal potential difference and sweat chloride as outcome measures in multicenter clinical trials in subjects with cystic fibrosis

Pediatric pulmonology, 2002-02, Vol.33 (2), p.142-150

2002

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A phase I randomized, multicenter trial of CPX in adult subjects with mild cystic fibrosis

Pediatric pulmonology, 2002-02, Vol.33 (2), p.90-98

2002

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Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections

Loss of Anion Transport without Increased Sodium Absorption Characterizes Newborn Porcine Cystic Fibrosis Airway Epithelia

Effects of Tham Nasal Alkalinization on Airway Microbial Communities: A Pilot Study in Non-CF and CF Adults

Amphotericin B induces epithelial voltage responses in people with cystic fibrosis

Randomized controlled study of aerosolized hypertonic xylitol versus hypertonic saline in hospitalized patients with pulmonary exacerbation of cystic fibrosis

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

Enhancement of respiratory mucosal antiviral defenses by the oxidation of iodide

Concentration of the antibacterial precursor thiocyanate in cystic fibrosis airway secretions

An in vitro model of differentiated human airway epithelia. Methods for establishing primary cultures

Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor

Repurposing tromethamine as inhaled therapy to treat CF airway disease

Acute administration of ivacaftor to people with cystic fibrosis and a G551D-CFTR mutation reveals smooth muscle abnormalities

The Osmolyte Xylitol Reduces the Salt Concentration of Airway Surface Liquid and May Enhance Bacterial Killing

Patterns and density of early tracheal colonization in intensive care unit patients

The effects of recombinant human hemoglobin on esophageal motor function in humans

Safety assessment of inhaled xylitol in mice and healthy volunteers

Bronchoscopic assessment of airway retention time of aerosolized xylitol

Optimizing nasal potential difference analysis for CFTR modulator development: assessment of ivacaftor in CF subjects with the G551D-CFTR mutation

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

Sequential magnetic resonance imaging analysis of the maxillary sinuses: implications for a model of gene therapy in cystic fibrosis

TRACHEAL COLONIZATION IN NEWLY INTUBATED PATIENTS

Safety assessment of inhaled xylitol in subjects with cystic fibrosis

Medical reversal of chronic rhinosinusitis in a cystic fibrosis patient with ivacaftor

Use of nasal potential difference and sweat chloride as outcome measures in multicenter clinical trials in subjects with cystic fibrosis

A phase I randomized, multicenter trial of CPX in adult subjects with mild cystic fibrosis

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