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Allergic airway inflammation induces a pro-secretory epithelial ion transport phenotype in mice

The European respiratory journal, 2010-12, Vol.36 (6), p.1436-1447

2010

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In vivo monitoring of cystic fibrosis-like lung disease in mice by volumetric computed tomography

The European respiratory journal, 2011-11, Vol.38 (5), p.1060-1070

2011

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75 Role of the IL1 signaling pathway in the development of type 2 airway inflammation in juvenile Scnn1b-Tg mice

Journal of cystic fibrosis, 2017-06, Vol.16, p.S83-S83

2017

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WS04.1 Impaired mucus clearance promotes Aspergillus fumigatus-induced type 2 airway inflammation in cystic fibrosis-like lung disease in mice

Journal of cystic fibrosis, 2016-06, Vol.15, p.S6-S6

2016

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WS10.2 Hypoxic epithelial necrosis triggers neutrophilic inflammation via IL-1 receptor signaling in cystic fibrosis-like lung disease

Journal of cystic fibrosis, 2015-06, Vol.14, p.S20-S20

2015

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67 Preclinical evaluation of preventive hypertonic saline therapy for cystic fibrosis-like lung disease in mice

Journal of cystic fibrosis, 2011, Vol.10, p.S18-S18

2011

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P360 CFTR modulator therapy with elexacaftor/tezacaftor/ivacaftor increases plasma concentration of fat-soluble carotenoids in patients with cystic fibrosis

Journal of cystic fibrosis, 2024-06, Vol.23, p.S178-S178

2024

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Genetic and pharmacological evidence for critical role of macrophage elastase in emphysema formation in bENaC-overexpressing mice

Journal of cystic fibrosis, 2010, Vol.9, p.S45-S45

2010

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Allergic inflammation produces a hypersecretory airway ion transport phenotype in mice

Journal of cystic fibrosis, 2009, Vol.8, p.S54-S54

2009

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Increased susceptibility to allergic airway inflammation in a murine model of cystic fibrosis lung disease

Journal of cystic fibrosis, 2009, Vol.8, p.S53-S53

2009

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S11.4 Relationship between organoid swelling and improvement of CFTR function in patients with cystic fibrosis homozygous for the F508del mutation receiving lumacaftor-ivacaftor

Journal of cystic fibrosis, 2020-06, Vol.19, p.S19-S19

2020

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P257 Ivacaftor therapy on cystic fibrosis transmembrane conductance regulator function is evaluated in a patient with 3849 + 10kbC > T mutation

Journal of cystic fibrosis, 2019-06, Vol.18, p.S129-S129

2019

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Preventive but not late amiloride therapy reduces morbidity and mortality of cystic fibrosis-like lung disease in mice

Journal of cystic fibrosis, 2008-06, Vol.7, p.S23-S23

2008

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WS06.04 Effects of elexacaftor/tezacaftor/ivacaftor therapy on CFTR function in patients with cystic fibrosis and 1 or 2 F508del alleles

Journal of cystic fibrosis, 2022-06, Vol.21, p.S12

2022

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The novel long acting ENaC blocker P643 has therapeutic effects in chronic cystic fibrosis-like lung disease in mice

Journal of cystic fibrosis, 2009, Vol.8, p.S26-S26

2009

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Airways surface liquid depletion causes MMP-12 dependent emphysema in βENaC-overexpressing mice

Journal of cystic fibrosis, 2009, Vol.8, p.S53-S53

2009

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Hypothermia and Other Treatment Options for Neonatal Encephalopathy: An Executive Summary of the Eunice Kennedy Shriver NICHD Workshop

The Journal of pediatrics, 2011-11, Vol.159 (5), p.851-858.e1

2011

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Trial of Amitriptyline, Topiramate, and Placebo for Pediatric Migraine

The New England journal of medicine, 2017-01, Vol.376 (2), p.115-124

2017

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Effect of Levosimendan on Low Cardiac Output Syndrome in Patients With Low Ejection Fraction Undergoing Coronary Artery Bypass Grafting With Cardiopulmonary Bypass: The LICORN Randomized Clinical Trial

JAMA : the journal of the American Medical Association, 2017-08, Vol.318 (6), p.548

2017

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Fetal growth restriction and chronic lung disease among infants born before the 28th week of gestation

Pediatrics (Evanston), 2009-09, Vol.124 (3), p.e450

2009

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Impact of treating iron deficiency, diagnosed according to hepcidin quantification, on outcomes after a prolonged ICU stay compared to standard care: a multicenter, randomized, single-blinded trial

Critical care (London, England), 2021-02, Vol.25 (1), p.62-62, Article 62

2021

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Two-hit model of brain damage in the very preterm newborn: small for gestational age and postnatal systemic inflammation

Pediatric research, 2013-03, Vol.73 (3), p.362-370

2013

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CFTR Cl − channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis

Gastroenterology (New York, N.Y. 1943), 2004-10, Vol.127 (4), p.1085-1095

2004

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Patterns of respiratory disease during the first 2 postnatal weeks in extremely premature infants

Pediatrics (Evanston), 2009-04, Vol.123 (4), p.1124

2009

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EPS3.03 Effects of lumacaftor-ivacaftor therapy on CFTR function in Phe508del homozygous patients with cystic fibrosis

Journal of cystic fibrosis, 2018-06, Vol.17, p.S41-S42

2018

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Allergic airway inflammation induces a pro-secretory epithelial ion transport phenotype in mice

In vivo monitoring of cystic fibrosis-like lung disease in mice by volumetric computed tomography

75 Role of the IL1 signaling pathway in the development of type 2 airway inflammation in juvenile Scnn1b-Tg mice

WS04.1 Impaired mucus clearance promotes Aspergillus fumigatus-induced type 2 airway inflammation in cystic fibrosis-like lung disease in mice

WS10.2 Hypoxic epithelial necrosis triggers neutrophilic inflammation via IL-1 receptor signaling in cystic fibrosis-like lung disease

67 Preclinical evaluation of preventive hypertonic saline therapy for cystic fibrosis-like lung disease in mice

P360 CFTR modulator therapy with elexacaftor/tezacaftor/ivacaftor increases plasma concentration of fat-soluble carotenoids in patients with cystic fibrosis

Genetic and pharmacological evidence for critical role of macrophage elastase in emphysema formation in bENaC-overexpressing mice

Allergic inflammation produces a hypersecretory airway ion transport phenotype in mice

Increased susceptibility to allergic airway inflammation in a murine model of cystic fibrosis lung disease

S11.4 Relationship between organoid swelling and improvement of CFTR function in patients with cystic fibrosis homozygous for the F508del mutation receiving lumacaftor-ivacaftor

P257 Ivacaftor therapy on cystic fibrosis transmembrane conductance regulator function is evaluated in a patient with 3849 + 10kbC > T mutation

Preventive but not late amiloride therapy reduces morbidity and mortality of cystic fibrosis-like lung disease in mice

WS06.04 Effects of elexacaftor/tezacaftor/ivacaftor therapy on CFTR function in patients with cystic fibrosis and 1 or 2 F508del alleles

The novel long acting ENaC blocker P643 has therapeutic effects in chronic cystic fibrosis-like lung disease in mice

Airways surface liquid depletion causes MMP-12 dependent emphysema in βENaC-overexpressing mice

Hypothermia and Other Treatment Options for Neonatal Encephalopathy: An Executive Summary of the Eunice Kennedy Shriver NICHD Workshop

Trial of Amitriptyline, Topiramate, and Placebo for Pediatric Migraine

Effect of Levosimendan on Low Cardiac Output Syndrome in Patients With Low Ejection Fraction Undergoing Coronary Artery Bypass Grafting With Cardiopulmonary Bypass: The LICORN Randomized Clinical Trial

Fetal growth restriction and chronic lung disease among infants born before the 28th week of gestation

Impact of treating iron deficiency, diagnosed according to hepcidin quantification, on outcomes after a prolonged ICU stay compared to standard care: a multicenter, randomized, single-blinded trial

Two-hit model of brain damage in the very preterm newborn: small for gestational age and postnatal systemic inflammation

CFTR Cl − channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis

Patterns of respiratory disease during the first 2 postnatal weeks in extremely premature infants

EPS3.03 Effects of lumacaftor-ivacaftor therapy on CFTR function in Phe508del homozygous patients with cystic fibrosis

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