Gene therapy for Cystic Fibrosis: Improved delivery techniques and conditioning with lysophosphatidylcholine enhance lentiviral gene transfer in mouse lung airways-Reference-Cited by-同舟云学术

Gene therapy for Cystic Fibrosis: Improved delivery techniques and conditioning with lysophosphatidylcholine enhance lentiviral gene transfer in mouse lung airways

Published:2017-11-26 Issue:9-10 Volume:43 Page:426-433
ISSN:0190-2148
Container-title:Experimental Lung Research
language:en
Short-container-title:Experimental Lung Research

Author:

Cmielewski Patricia¹²³^ORCID,Farrow Nigel¹²³,Devereux Sharnna³,Parsons David¹²³,Donnelley Martin¹²³

Affiliation:

1. Department of Respiratory and Sleep Medicine, Women's and Children's Hospital Network, North Adelaide, SA, Australia

2. Robinson Research Institute, University of Adelaide, Adelaide, SA, Australia

3. Discipline of Paediatrics, Adelaide Medical School, Faculty of Health and Medical Sciences, University of Adelaide, Adelaide, SA, Australia

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,Pulmonary and Respiratory Medicine,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/01902148.2017.1395931

Reference24 articles.

1. Recovery of Airway Cystic Fibrosis Transmembrane Conductance Regulator Function in Mice with Cystic Fibrosis After Single-Dose Lentivirus-Mediated Gene Transfer

2. Advances in Cell and Gene-based Therapies for Cystic Fibrosis Lung Disease

3. Lentiviral Vectors and Cystic Fibrosis Gene Therapy

4. Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis.

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