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Localization and Functionality of the Inflammasome in Neutrophils

The Journal of biological chemistry, 2014-02, Vol.289 (8), p.5320-5329

2014

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Some ABCA3 mutations elevate ER stress and initiate apoptosis of lung epithelial cells

Respiratory research, 2011-01, Vol.12 (1030), p.4-4, Article 4

2011

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Flagellin induces myeloid-derived suppressor cells: implications for Pseudomonas aeruginosa infection in cystic fibrosis lung disease

The Journal of immunology (1950), 2013-02, Vol.190 (3), p.1276-1284

2013

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Ultrastructural characterization of cystic fibrosis sputum using atomic force and scanning electron microscopy

Journal of cystic fibrosis, 2012-03, Vol.11 (2), p.84-92

2012

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Free DNA in Cystic Fibrosis Airway Fluids Correlates with Airflow Obstruction

Mediators of Inflammation, 2015-01, Vol.2015 (2015), p.847-857-181

2015

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Transcriptomic profile of cystic fibrosis patients identifies type I interferon response and ribosomal stalk proteins as potential modifiers of disease severity

PloS one, 2017-08, Vol.12 (8), p.e0183526-e0183526

2017

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Anti-inflammatory role of CD11b+Ly6G+ neutrophilic cells in allergic airway inflammation in mice

Immunology letters, 2018-12, Vol.204, p.67-74

2018

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Choline Supplementation in Cystic Fibrosis-The Metabolic and Clinical Impact

Nutrients, 2019-03, Vol.11 (3), p.656

2019

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Chitinase activation in patients with fungus-associated cystic fibrosis lung disease

Journal of allergy and clinical immunology, 2016-10, Vol.138 (4), p.1183-1189.e4

2016

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Staphylococcal Enterotoxins Dose-Dependently Modulate the Generation of Myeloid-Derived Suppressor Cells

Frontiers in cellular and infection microbiology, 2018-09, Vol.8, p.321-321

2018

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RNA and imidazoquinolines are sensed by distinct TLR7/8 ectodomain sites resulting in functionally disparate signaling events

The Journal of immunology (1950), 2014-06, Vol.192 (12), p.5963-5973

2014

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Immune response, diagnosis and treatment of allergic bronchopulmonary aspergillosis in cystic fibrosis lung disease

Current pharmaceutical design, 2013-06, Vol.19 (20), p.3669-3678

2013

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Therapy of CF-Patients with Amitriptyline and Placebo - a Randomised, Double-Blind, Placebo-Controlled Phase IIb Multicenter, Cohort-Study

Cellular physiology and biochemistry, 2013-01, Vol.31 (4-5), p.505-512

2013

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Pseudomonas aeruginosa Airway Infection Recruits and Modulates Neutrophilic Myeloid-Derived Suppressor Cells

Frontiers in cellular and infection microbiology, 2016-11, Vol.6, p.167-167

2016

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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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Delayed but functional neutrophil extracellular trap formation in neonates

Blood, 2009-11, Vol.114 (23), p.4908-4911

2009

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Quality standards for managing children and adolescents with bronchiectasis: an international consensus

Breathe (Lausanne, Switzerland), 2022-09, Vol.18 (3), p.220144

2022

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Long-term follow-up and treatment of congenital alveolar proteinosis

BMC pediatrics, 2011-08, Vol.11 (1), p.72-72, Article 72

2011

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Expression, regulation and clinical significance of soluble and membrane CD14 receptors in pediatric inflammatory lung diseases

Respiratory research, 2010-03, Vol.11 (1), p.32-32, Article 32

2010

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Elexacaftor–Tezacaftor–Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele

The New England journal of medicine, 2019-11, Vol.381 (19), p.1809-1819

2019

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Dysregulation of innate immune receptors on neutrophils in chronic granulomatous disease

Journal of allergy and clinical immunology, 2008-02, Vol.121 (2), p.375-382.e9

2008

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In Vitro Inhibition of Neutrophil Elastase Activity by Inhaled Anti-Pseudomonas Antibiotics Used in Cystic Fibrosis Patients

Mediators of Inflammation, 2010-01, Vol.2010 (2010), p.1114-1118

2010

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Reply: glutathione inhalation treatments in cystic fibrosis: the interference of airway γ-glutamyltransferase

American journal of respiratory and critical care medicine, 2014-01, Vol.189 (2), p.234-235

2014

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Sensing technologies for the challenging Lunar environment

Advances in space research, 2024-10, Vol.74 (7), p.3407-3436

2024

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The surfactant protein C mutation A116D alters cellular processing, stress tolerance, surfactant lipid composition, and immune cell activation

BMC pulmonary medicine, 2012-03, Vol.12 (1), p.15-15, Article 15

2012

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Localization and Functionality of the Inflammasome in Neutrophils

Some ABCA3 mutations elevate ER stress and initiate apoptosis of lung epithelial cells

Flagellin induces myeloid-derived suppressor cells: implications for Pseudomonas aeruginosa infection in cystic fibrosis lung disease

Ultrastructural characterization of cystic fibrosis sputum using atomic force and scanning electron microscopy

Free DNA in Cystic Fibrosis Airway Fluids Correlates with Airflow Obstruction

Transcriptomic profile of cystic fibrosis patients identifies type I interferon response and ribosomal stalk proteins as potential modifiers of disease severity

Anti-inflammatory role of CD11b+Ly6G+ neutrophilic cells in allergic airway inflammation in mice

Choline Supplementation in Cystic Fibrosis-The Metabolic and Clinical Impact

Chitinase activation in patients with fungus-associated cystic fibrosis lung disease

Staphylococcal Enterotoxins Dose-Dependently Modulate the Generation of Myeloid-Derived Suppressor Cells

RNA and imidazoquinolines are sensed by distinct TLR7/8 ectodomain sites resulting in functionally disparate signaling events

Immune response, diagnosis and treatment of allergic bronchopulmonary aspergillosis in cystic fibrosis lung disease

Therapy of CF-Patients with Amitriptyline and Placebo - a Randomised, Double-Blind, Placebo-Controlled Phase IIb Multicenter, Cohort-Study

Pseudomonas aeruginosa Airway Infection Recruits and Modulates Neutrophilic Myeloid-Derived Suppressor Cells

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

Delayed but functional neutrophil extracellular trap formation in neonates

Quality standards for managing children and adolescents with bronchiectasis: an international consensus

Long-term follow-up and treatment of congenital alveolar proteinosis

Expression, regulation and clinical significance of soluble and membrane CD14 receptors in pediatric inflammatory lung diseases

Elexacaftor–Tezacaftor–Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele

Dysregulation of innate immune receptors on neutrophils in chronic granulomatous disease

In Vitro Inhibition of Neutrophil Elastase Activity by Inhaled Anti-Pseudomonas Antibiotics Used in Cystic Fibrosis Patients

Reply: glutathione inhalation treatments in cystic fibrosis: the interference of airway γ-glutamyltransferase

Sensing technologies for the challenging Lunar environment

The surfactant protein C mutation A116D alters cellular processing, stress tolerance, surfactant lipid composition, and immune cell activation

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