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Epigenetic reprogramming of airway macrophages promotes polarization and inflammation in muco-obstructive lung disease

Nature communications, 2021-11, Vol.12 (1), p.6520-6520, Article 6520

2021

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Comparison of microbiomes from different niches of upper and lower airways in children and adolescents with cystic fibrosis

PloS one, 2015-01, Vol.10 (1), p.e0116029-e0116029

2015

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Ion mobility-tandem mass spectrometry of mucin-type O-glycans

Nature communications, 2024-03, Vol.15 (1), p.2611-2611, Article 2611

2024

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The value of chest magnetic resonance imaging compared to chest radiographs with and without additional lung ultrasound in children with complicated pneumonia

PloS one, 2020, Vol.15 (3), p.e0230252-e0230252

2020

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CFTR regulates early pathogenesis of chronic obstructive lung disease in βENaC-overexpressing mice

PloS one, 2012-08, Vol.7 (8), p.e44059-e44059

2012

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Validation of automated lobe segmentation on paired inspiratory-expiratory chest CT in 8-14 year-old children with cystic fibrosis

PloS one, 2018-04, Vol.13 (4), p.e0194557-e0194557

2018

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Airway Surface Dehydration Aggravates Cigarette Smoke-Induced Hallmarks of COPD in Mice

PloS one, 2015-06, Vol.10 (6), p.e0129897

2015

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Pulmonary emphysema in cystic fibrosis detected by densitometry on chest multidetector computed tomography

PloS one, 2013-08, Vol.8 (8), p.e73142-e73142

2013

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Corrigendum: Pseudomonas aeruginosa Modulates the Antiviral Response of Bronchial Epithelial Cells

Frontiers in immunology, 2020-07, Vol.11, p.1453-1453

2020

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The chitinase-like protein YKL-40 modulates cystic fibrosis lung disease

PloS one, 2011-09, Vol.6 (9), p.e24399-e24399

2011

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The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients

PloS one, 2011, Vol.6 (8), p.e24445-e24445

2011

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A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele

American journal of respiratory and critical care medicine, 2021-06, Vol.203 (12), p.1522-1532

2021

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BPIFB1 (LPLUNC1) is upregulated in cystic fibrosis lung disease

Histochemistry and cell biology, 2012-11, Vol.138 (5), p.749-758

2012

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Hfe deficiency impairs pulmonary neutrophil recruitment in response to inflammation

PloS one, 2012-06, Vol.7 (6), p.e39363

2012

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Echo Time‐Dependence of Observed Lung T1 in Patients With Cystic Fibrosis and Correlation With Clinical Metrics

Journal of magnetic resonance imaging, 2020-12, Vol.52 (6), p.1645-1654

2020

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Reply to Verbanck and Vanderhelst: The Respective Roles of Lung Clearance Index and Magnetic Resonance Imaging in the Clinical Management of Patients with Cystic Fibrosis

American journal of respiratory and critical care medicine, 2018-02, Vol.197 (3), p.410-411

2018

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Thiolated polyglycerol sulfate as potential mucolytic for muco-obstructive lung diseases

Biomaterials science, 2024-08, Vol.12 (17), p.4376-4385

2024

Volltextzugriff (PDF)

Authors' response: Letter to the Editor ‘Comparison of lung clearance index determined by washout of N2 and SF6 in infants and preschool children with cystic fibrosis’

Journal of cystic fibrosis, 2019-05, Vol.18 (3), p.e28-e29

2019

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The ENaC-overexpressing mouse as a model of cystic fibrosis lung disease

Journal of cystic fibrosis, 2011-06, Vol.10, p.S172-S182

2011

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Magnetic resonance imaging detects improvements of pulmonary and paranasal sinus abnormalities in response to elexacaftor/tezacaftor/ivacaftor therapy in adults with cystic fibrosis

Journal of cystic fibrosis, 2022-11, Vol.21 (6), p.1053-1060

2022

Volltextzugriff (PDF)

Macrophage PD-1 associates with neutrophilia and reduced bacterial killing in early cystic fibrosis airway disease

Journal of cystic fibrosis, 2022-11, Vol.21 (6), p.967-976

2022

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Neutrophil elastase and matrix metalloproteinase 12 in cystic fibrosis lung disease

Molecular and cellular pediatrics, 2016-07, Vol.3 (1), p.25-7, Article 25

2016

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The role of chitin, chitinases, and chitinase-like proteins in pediatric lung diseases

Molecular and cellular pediatrics, 2015-02, Vol.2 (1), p.3-8, Article 3

2015

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The Respective Roles of Lung Clearance Index and Magnetic Resonance Imaging in the Clinical Management of Patients with Cystic Fibrosis/Reply/Reply

American journal of respiratory and critical care medicine, 2018-02, Vol.197 (3), p.409-412

2018

Volltextzugriff (PDF)

Optical coherence tomography detects structural abnormalitiesof the nasal mucosa in patients with cystic fibrosis

Journal of cystic fibrosis, 2016-03, Vol.15 (2), p.216-222

2016

Volltextzugriff (PDF)

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Epigenetic reprogramming of airway macrophages promotes polarization and inflammation in muco-obstructive lung disease

Comparison of microbiomes from different niches of upper and lower airways in children and adolescents with cystic fibrosis

Ion mobility-tandem mass spectrometry of mucin-type O-glycans

The value of chest magnetic resonance imaging compared to chest radiographs with and without additional lung ultrasound in children with complicated pneumonia

CFTR regulates early pathogenesis of chronic obstructive lung disease in βENaC-overexpressing mice

Validation of automated lobe segmentation on paired inspiratory-expiratory chest CT in 8-14 year-old children with cystic fibrosis

Airway Surface Dehydration Aggravates Cigarette Smoke-Induced Hallmarks of COPD in Mice

Pulmonary emphysema in cystic fibrosis detected by densitometry on chest multidetector computed tomography

Corrigendum: Pseudomonas aeruginosa Modulates the Antiviral Response of Bronchial Epithelial Cells

The chitinase-like protein YKL-40 modulates cystic fibrosis lung disease

The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients

A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele

BPIFB1 (LPLUNC1) is upregulated in cystic fibrosis lung disease

Hfe deficiency impairs pulmonary neutrophil recruitment in response to inflammation

Echo Time‐Dependence of Observed Lung T1 in Patients With Cystic Fibrosis and Correlation With Clinical Metrics

Reply to Verbanck and Vanderhelst: The Respective Roles of Lung Clearance Index and Magnetic Resonance Imaging in the Clinical Management of Patients with Cystic Fibrosis

Thiolated polyglycerol sulfate as potential mucolytic for muco-obstructive lung diseases

Authors' response: Letter to the Editor ‘Comparison of lung clearance index determined by washout of N2 and SF6 in infants and preschool children with cystic fibrosis’

The ENaC-overexpressing mouse as a model of cystic fibrosis lung disease

Magnetic resonance imaging detects improvements of pulmonary and paranasal sinus abnormalities in response to elexacaftor/tezacaftor/ivacaftor therapy in adults with cystic fibrosis

Macrophage PD-1 associates with neutrophilia and reduced bacterial killing in early cystic fibrosis airway disease

Neutrophil elastase and matrix metalloproteinase 12 in cystic fibrosis lung disease

The role of chitin, chitinases, and chitinase-like proteins in pediatric lung diseases

The Respective Roles of Lung Clearance Index and Magnetic Resonance Imaging in the Clinical Management of Patients with Cystic Fibrosis/Reply/Reply

Optical coherence tomography detects structural abnormalitiesof the nasal mucosa in patients with cystic fibrosis

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