Gene Therapy for Cystic Fibrosis Using Cationic Liposome Mediated Gene Transfer: A Phase I Trial of Safety and Efficacy in the Nasal Airway. University of Alabama at Birmingham, Birmingham, Alabama
- 1 October 1994
- journal article
- clinical trial
- Published by Mary Ann Liebert Inc in Human Gene Therapy
- Vol. 5 (10), 1259-1277
- https://doi.org/10.1089/hum.1994.5.10-1259
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- Systemic Gene Expression After Intravenous DNA Delivery into Adult MiceScience, 1993
- Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapyNature, 1993
- Aerosol gene delivery in vivo.Proceedings of the National Academy of Sciences, 1992
- Expression of the human cystic fibrosis transmembrane conductance regulator gene in the mouse lung afterin vivointratracheal plasmid-mediated gene transferNucleic Acids Research, 1992
- Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus OocytesScience, 1991
- Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductanceCell, 1991
- Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cellsNature, 1990
- Identification of the Cystic Fibrosis Gene: Chromosome Walking and JumpingScience, 1989
- Identification of the Cystic Fibrosis Gene: Genetic AnalysisScience, 1989
- Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNAScience, 1989