"Bronchial Artery Delivery of Viral Vectors for Gene delivery in Cystic Fibrosis; Superior to Airway Delivery?"
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pulmonary and Respiratory Medicine
Link
http://link.springer.com/content/pdf/10.1186/1471-2466-2-2.pdf
Reference34 articles.
1. Bigger BW, Coutelle C: Perspectives on Gene Therapy for Cystic Fibrosis Airway Disease. BioDrugs. 2001, 15: 615-634.
2. Zabner J, Couture LA, Gregory RJ, Graham SM, Smith AE, Welsh MJ: Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis. Cell. 1993, 75: 207-16.
3. Caplen NJ, Alton EW, Middleton PG, et al: Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis [see comments] [published erratum appears in Nat Med 1995 Mar;1(3):272]. Nat.Med. 1995, 1: 39-46.
4. Crystal RG, McElvaney NG, Rosenfeld MA, et al: Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis [see comments]. Nat.Genet. 1994, 8: 42-51.
5. Boucher RC, Knowles MR, Johnson LG, et al: Gene therapy for cystic fibrosis using E1-deleted adenovirus: a phase I trial in the nasal cavity. The University of North Carolina at Chapel Hill. Hum.Gene Ther. 1994, 5: 615-39.
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1. Gene Therapy: Will the Promise of Optimizing Lung Allografts Become Reality?;Frontiers in Immunology;2022-07-01
2. Aerosolized VEGF in combination with intravenous magnetically targeted delivery of DNA–nanoparticle complex may increase efficiency of cystic fibrosis gene therapy;Medical Hypotheses;2006-01
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