Status of gene therapy for cystic fibrosis lung disease
Open Access
- 15 February 1999
- journal article
- editorial
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 103 (4), 441-445
- https://doi.org/10.1172/jci6330
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- The genesis of cystic fibrosis lung diseaseJournal of Clinical Investigation, 1999
- EnhancedIn VivoAirway Gene Transfer via Transient Modification of Host Barrier Properties with a Surface-Active AgentHuman Gene Therapy, 1998
- Gene transfer vectors derived from equine infectious anemia virusGene Therapy, 1998
- Lentiviral Vectors for Gene Therapy of Cystic FibrosisHuman Gene Therapy, 1997
- In Vivo Gene Delivery and Stable Transduction of Nondividing Cells by a Lentiviral VectorScience, 1996
- Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosisNature Genetics, 1994
- Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosisCell, 1993
- Submucosal glands are the predominant site of CFTR expression in the human bronchusNature Genetics, 1992
- Efficiency of gene transfer for restoration of normal airway epithelial function in cystic fibrosisNature Genetics, 1992
- Abnormal apical cell membrane in cystic fibrosis respiratory epithelium. An in vitro electrophysiologic analysis.Journal of Clinical Investigation, 1987