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Pseudomonas aeruginosa induces p38MAP kinase-dependent IL-6 and CXCL8 release from bronchial epithelial cells via a Syk kinase pathway

PloS one, 2021-02, Vol.16 (2), p.e0246050-e0246050

2021

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Progress in gene and cell therapy for cystic fibrosis lung disease

Current pharmaceutical design, 2012-02, Vol.18 (5), p.642

2012

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Gene therapy in cystic fibrosis

Archives of Disease in Childhood, 2014-05, Vol.99 (5), p.465-468

2014

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CpG-free plasmids confer reduced inflammation and sustained pulmonary gene expression

Nature biotechnology, 2008-05, Vol.26 (5), p.549-551

2008

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Antipseudomonal Bacteriophage Reduces Infective Burden and Inflammatory Response in Murine Lung

Antimicrobial agents and chemotherapy, 2016-02, Vol.60 (2), p.744-751

2016

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Distinct patterns of inflammation in the airway lumen and bronchial mucosa of children with cystic fibrosis

Thorax, 2012-02, Vol.67 (2), p.164-170

2012

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Cystic fibrosis

BMJ (British Medical Journal), 2007-12, Vol.335 (7632), p.1255-1259

International edition, 2007

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Lytic Bacteriophage Is a Promising Adjunct to Common Antibiotics across Cystic Fibrosis Clinical Strains and Culture Models of Pseudomonas aeruginosa Infection

Antibiotics (Basel), 2023-03, Vol.12 (3), p.593

2023

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Lung Clearance Index and High-Resolution Computed Tomography Scores in Primary Ciliary Dyskinesia

American journal of respiratory and critical care medicine, 2013-09, Vol.188 (5), p.545-549

2013

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Whole-Gene Sequencing of CFTR Reveals a High Prevalence of the Intronic Variant c.3874-4522A>G in Cystic Fibrosis

American journal of respiratory and critical care medicine, 2020-06, Vol.201 (11), p.1438-1441

2020

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Metabolic Phenotyping and Strain Characterisation of Pseudomonas aeruginosa Isolates from Cystic Fibrosis Patients Using Rapid Evaporative Ionisation Mass Spectrometry

Scientific reports, 2018-07, Vol.8 (1), p.10952-10, Article 10952

2018

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Assessment of F/HN-Pseudotyped Lentivirus as a Clinically Relevant Vector for Lung Gene Therapy

American journal of respiratory and critical care medicine, 2012-11, Vol.186 (9), p.846-856

2012

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Transepithelial nasal potential difference in patients with, and at risk of acute respiratory distress syndrome

Thorax, 2021-11, Vol.76 (11), p.1099

2021

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Airway remodelling in children with cystic fibrosis

Thorax, 2007-12, Vol.62 (12), p.1074-1080

2007

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Increased Airway Smooth Muscle Mass in Children with Asthma, Cystic Fibrosis, and Non-Cystic Fibrosis Bronchiectasis

American journal of respiratory and critical care medicine, 2008-04, Vol.177 (8), p.837-843

2008

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Cyanide levels found in infected cystic fibrosis sputum inhibit airway ciliary function

The European respiratory journal, 2014-11, Vol.44 (5), p.1253-1261

2014

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The murine lung as a factory to produce secreted intrapulmonary and circulatory proteins

Gene therapy, 2018-08, Vol.25 (5), p.345-358

2018

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A Phase I/IIa Safety and Efficacy Study of Nebulized Liposome-mediated Gene Therapy for Cystic Fibrosis Supports a Multidose Trial

American journal of respiratory and critical care medicine, 2015-12, Vol.192 (11), p.1389-1392

2015

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Oral contraceptives do not appear to affect cystic fibrosis disease severity

The European respiratory journal, 2013, Vol.41 (1), p.67-73

2013

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Moving forward: cystic fibrosis gene therapy

Human molecular genetics, 2013-10, Vol.22 (R1), p.R52-R58

2013

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Cystic Fibrosis Gene Therapy in the UK and Elsewhere

Human gene therapy, 2015-05, Vol.26 (5), p.266

2015

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Gene transfer to the lung: Lessons learned from more than 2 decades of CF gene therapy

Advanced drug delivery reviews, 2009-02, Vol.61 (2), p.128-139

2009

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Variability in Bacteriophage and Antibiotic Sensitivity in Serial Pseudomonas aeruginosa Isolates from Cystic Fibrosis Airway Cultures over 12 Months

Microorganisms (Basel), 2021-03, Vol.9 (3), p.660

2021

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Pseudomonas aeruginosa induces p38MAP kinase-dependent IL-6 and CXCL8 release from bronchial epithelial cells via a Syk kinase pathway

Progress in gene and cell therapy for cystic fibrosis lung disease

Gene therapy in cystic fibrosis

CpG-free plasmids confer reduced inflammation and sustained pulmonary gene expression

Antipseudomonal Bacteriophage Reduces Infective Burden and Inflammatory Response in Murine Lung

Distinct patterns of inflammation in the airway lumen and bronchial mucosa of children with cystic fibrosis

Cystic fibrosis

Lytic Bacteriophage Is a Promising Adjunct to Common Antibiotics across Cystic Fibrosis Clinical Strains and Culture Models of Pseudomonas aeruginosa Infection

Lung Clearance Index and High-Resolution Computed Tomography Scores in Primary Ciliary Dyskinesia

Whole-Gene Sequencing of CFTR Reveals a High Prevalence of the Intronic Variant c.3874-4522A>G in Cystic Fibrosis

Metabolic Phenotyping and Strain Characterisation of Pseudomonas aeruginosa Isolates from Cystic Fibrosis Patients Using Rapid Evaporative Ionisation Mass Spectrometry

Assessment of F/HN-Pseudotyped Lentivirus as a Clinically Relevant Vector for Lung Gene Therapy

Unsupervised home spirometry is not equivalent to supervised clinic spirometry in children and young people with cystic fibrosis: Results from the CLIMB‐CF study

Transepithelial nasal potential difference in patients with, and at risk of acute respiratory distress syndrome

Airway remodelling in children with cystic fibrosis

Increased Airway Smooth Muscle Mass in Children with Asthma, Cystic Fibrosis, and Non-Cystic Fibrosis Bronchiectasis

Cyanide levels found in infected cystic fibrosis sputum inhibit airway ciliary function

The murine lung as a factory to produce secreted intrapulmonary and circulatory proteins

A Phase I/IIa Safety and Efficacy Study of Nebulized Liposome-mediated Gene Therapy for Cystic Fibrosis Supports a Multidose Trial

Oral contraceptives do not appear to affect cystic fibrosis disease severity

Moving forward: cystic fibrosis gene therapy

Cystic Fibrosis Gene Therapy in the UK and Elsewhere

Gene transfer to the lung: Lessons learned from more than 2 decades of CF gene therapy

Variability in Bacteriophage and Antibiotic Sensitivity in Serial Pseudomonas aeruginosa Isolates from Cystic Fibrosis Airway Cultures over 12 Months

Preparation for a first-in-man lentivirus trial in patients with cystic fibrosis

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