Therapeutic strategies to correct malfunction of CFTRMeerana Lim, Pamela L. Zeitlin(Johns Hopkins University)Paediatric Respiratory ReviewsJune 1, 200110.1053/prrv.2000.0124Cited by 19SaveCiteExport RISWatch citationsAbstractRelated PapersDefective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosisSeng H. Cheng, Richard J. Gregory, John Marshall et al.|Cell|1990|1.8kProcessing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitiveGerene M. Denning, Matthew P. Anderson, Jane F. Amara et al.|Nature|1992|1.2kCationic liposome-mediated gene transfer.Xiang Gao, Leaf Huang|PubMed|1995|623Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutationsMatthew K. Howard, Raymond A. Frizzell, David M. Bedwell|Nature Medicine|1996|495Cationic lipid-mediated CFTR gene transfer to the lungs and nose of patients with cystic fibrosis: a double-blind placebo-controlled trialEWFW Alton, M. Stern, R Farley et al.|The Lancet|1999|432