Modification of Nasal Epithelial Potential Differences of Individuals with Cystic Fibrosis Consequent to Local Administration of a Normal CFTR cDNA Adenovirus Gene Transfer Vector
Author:
Publisher
Mary Ann Liebert Inc
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/hum.1995.6.11-1487
Reference42 articles.
1. Measurement of nasal potential difference in adult cystic fibrosis, Young's syndrome, and bronchiectasis.
2. Non–invasive liposome–mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice
3. Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.
4. Gene Therapy for Cystic Fibrosis Using E1-Deleted Adenovirus: A Phase I Trial in the Nasal Cavity. University of North Carolina at Chapel Hill, Chapel Hill, North Carolina
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