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Biological aspects of ceramide-enriched membrane domains

Progress in lipid research, 2007-05, Vol.46 (3), p.161-170

2007

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Chemically modified hCFTR mRNAs recuperate lung function in a mouse model of cystic fibrosis

Scientific reports, 2018-11, Vol.8 (1), p.16776-14, Article 16776

2018

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Acid sphingomyelinase inhibitors normalize pulmonary ceramide and inflammation in cystic fibrosis

American journal of respiratory cell and molecular biology, 2010-06, Vol.42 (6), p.716-724

2010

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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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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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Plasma Phosphatidylcholine Alterations in Cystic Fibrosis Patients: Impaired Metabolism and Correlation with Lung Function and Inflammation

Cellular physiology and biochemistry, 2015-01, Vol.35 (4), p.1437-1453

2015

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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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Sequential Inhalational Tobramycin-Colistin-Combination in CF-Patients with Chronic P. Aeruginosa Colonization - an Observational Study

Cellular physiology and biochemistry, 2016-01, Vol.39 (3), p.1141-1151

2016

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Ceramide accumulation mediates inflammation, cell death and infection susceptibility in cystic fibrosis

Nature medicine, 2008-04, Vol.14 (4), p.382-391

2008

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Invasion of human epithelial cells by Pseudomonas aeruginosa involves src-like tyrosine kinases p60Src and p59Fyn

Infection and immunity, 2001, Vol.69 (1), p.281-287

2001

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Gaseous nitric oxide to treat antibiotic resistant bacterial and fungal lung infections in patients with cystic fibrosis: a phase I clinical study

Infection, 2016-08, Vol.44 (4), p.513-520

2016

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Safety and Tolerance of Donor-Derived Mesenchymal Stem Cells in Pediatric Living-Donor Liver Transplantation: The MYSTEP1 Study

Stem Cells International, 2017-01, Vol.2017 (2017), p.1-11-037

2017

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Sinonasal inhalation of tobramycin vibrating aerosol in cystic fibrosis patients with upper airway Pseudomonas aeruginosa colonization: results of a randomized, double-blind, placebo-controlled pilot study

Drug design, development and therapy, 2014-01, Vol.8 (default), p.209-217

2014

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β1-Integrin Accumulates in Cystic Fibrosis Luminal Airway Epithelial Membranes and Decreases Sphingosine, Promoting Bacterial Infections

Cell host & microbe, 2017-06, Vol.21 (6), p.707-718.e8

2017

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Relative contribution of Prevotella intermedia and Pseudomonas aeruginosa to lung pathology in airways of patients with cystic fibrosis

Thorax, 2010-11, Vol.65 (11), p.978-984

2010

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Ceramide in cystic fibrosis

Handbook of experimental pharmacology, 2013 (216), p.265

2013

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Membrane rafts in host–pathogen interactions

Biochimica et biophysica acta, 2006-12, Vol.1758 (12), p.2139-2147

2006

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Colistin-Tobramycin Combinations Are Superior to Monotherapy Concerning the Killing of Biofilm Pseudomonas aeruginosa

The Journal of infectious diseases, 2010-11, Vol.202 (10), p.1585-1592

2010

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Sphingolipids as targets for inhalation treatment of cystic fibrosis

Advanced drug delivery reviews, 2018-08, Vol.133, p.66-75

2018

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Relative survival potential of platelets is associated with platelet CXCR4/CXCR7 surface exposure and functional recovery following STEMI

Atherosclerosis, 2018-11, Vol.278, p.269-277

2018

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Pulmonary infection of cystic fibrosis mice with Staphylococcus aureus requires expression of α-toxin

Biological chemistry, 2018-09, Vol.399 (10), p.1203-1213

2018

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Sinonasal inhalation of dornase alfa administered by vibrating aerosol to cystic fibrosis patients: A double-blind placebo-controlled cross-over trial

Journal of cystic fibrosis, 2014-07, Vol.13 (4), p.461-470

2014

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The chemokine CCL18 characterises Pseudomonas infections in cystic fibrosis lung disease

The European respiratory journal, 2014-12, Vol.44 (6), p.1608-1615

2014

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Biological aspects of ceramide-enriched membrane domains

Chemically modified hCFTR mRNAs recuperate lung function in a mouse model of cystic fibrosis

Acid sphingomyelinase inhibitors normalize pulmonary ceramide and inflammation in cystic fibrosis

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

Factors Associated with Worse Lung Function in Cystic Fibrosis Patients with Persistent Staphylococcus aureus

Choline Supplementation in Cystic Fibrosis-The Metabolic and Clinical Impact

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

Plasma Phosphatidylcholine Alterations in Cystic Fibrosis Patients: Impaired Metabolism and Correlation with Lung Function and Inflammation

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

Sequential Inhalational Tobramycin-Colistin-Combination in CF-Patients with Chronic P. Aeruginosa Colonization - an Observational Study

Ceramide accumulation mediates inflammation, cell death and infection susceptibility in cystic fibrosis

Invasion of human epithelial cells by Pseudomonas aeruginosa involves src-like tyrosine kinases p60Src and p59Fyn

Gaseous nitric oxide to treat antibiotic resistant bacterial and fungal lung infections in patients with cystic fibrosis: a phase I clinical study

Safety and Tolerance of Donor-Derived Mesenchymal Stem Cells in Pediatric Living-Donor Liver Transplantation: The MYSTEP1 Study

Sinonasal inhalation of tobramycin vibrating aerosol in cystic fibrosis patients with upper airway Pseudomonas aeruginosa colonization: results of a randomized, double-blind, placebo-controlled pilot study

β1-Integrin Accumulates in Cystic Fibrosis Luminal Airway Epithelial Membranes and Decreases Sphingosine, Promoting Bacterial Infections

Relative contribution of Prevotella intermedia and Pseudomonas aeruginosa to lung pathology in airways of patients with cystic fibrosis

Ceramide in cystic fibrosis

Membrane rafts in host–pathogen interactions

Colistin-Tobramycin Combinations Are Superior to Monotherapy Concerning the Killing of Biofilm Pseudomonas aeruginosa

Sphingolipids as targets for inhalation treatment of cystic fibrosis

Relative survival potential of platelets is associated with platelet CXCR4/CXCR7 surface exposure and functional recovery following STEMI

Pulmonary infection of cystic fibrosis mice with Staphylococcus aureus requires expression of α-toxin

Sinonasal inhalation of dornase alfa administered by vibrating aerosol to cystic fibrosis patients: A double-blind placebo-controlled cross-over trial

The chemokine CCL18 characterises Pseudomonas infections in cystic fibrosis lung disease

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