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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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Cystic fibrosis

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

International edition, 2007

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Progress in gene and cell therapy for cystic fibrosis lung disease

Current pharmaceutical design, 2012-02, Vol.18 (5), p.642-662

2012

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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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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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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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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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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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Cystic Fibrosis Gene Therapy in the UK and Elsewhere

Human gene therapy, 2015-05, Vol.26 (5), p.266-275

2015

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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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Fixing lung health in the UK: accelerating respiratory research and innovation

Thorax, 2024-09, Vol.79 (9), p.809-810

2024

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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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Airway remodelling and its relationship to inflammation in cystic fibrosis

Thorax, 2011-07, Vol.66 (7), p.624-629

2011

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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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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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Genetic therapies in cystic fibrosis

Current opinion in pulmonary medicine, 2023-11, Vol.29 (6), p.615-620

2023

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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.1099-1107

2021

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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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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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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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Progress in Respiratory Gene Therapy

Human gene therapy, 2022-09, Vol.33 (17-18), p.893-912

2022

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Antipseudomonal Bacteriophage Reduces Infective Burden and Inflammatory Response in Murine Lung

Cystic fibrosis

Progress in gene and cell therapy for cystic fibrosis lung disease

Moving forward: cystic fibrosis gene therapy

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

Gene therapy in cystic fibrosis

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

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

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

Cystic Fibrosis Gene Therapy in the UK and Elsewhere

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

Fixing lung health in the UK: accelerating respiratory research and innovation

Changes in physiological, functional and structural markers of cystic fibrosis lung disease with treatment of a pulmonary exacerbation

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

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

Airway remodelling and its relationship to inflammation in cystic fibrosis

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

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

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

Genetic therapies in cystic fibrosis

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

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

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

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

Progress in Respiratory Gene Therapy

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