Progress and prospects: gene therapy for genetic diseases with helper-dependent adenoviral vectors
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
http://www.nature.com/articles/gt200814.pdf
Reference54 articles.
1. Palmer DJ, Ng P . Helper-dependent adenoviral vectors for gene therapy. Hum Gene Ther 2005; 16: 1–16.
2. Toietta G, Mane VP, Norona WS, Finegold MJ, Ng P, McDonagh AF et al. Lifelong elimination of hyperbilirubinemia in the Gunn rat with a single injection of helper-dependent adenoviral vector. Proc Natl Acad Sci USA 2005; 102: 3930–3935.
3. Brunetti-Pierri N, Nichols TC, McCorquodale S, Merricks E, Palmer DJ, Beaudet AL et al. Sustained phenotypic correction of canine hemophilia B after systemic administration of helper-dependent adenoviral vector. Hum Gene Ther 2005; 16: 811–820.
4. McCormack Jr WM, Seiler MP, Bertin TK, Ubhayakar K, Palmer DJ, Ng P et al. Helper-dependent adenoviral gene therapy mediates long-term correction of the clotting defect in the canine hemophilia A model. J Thromb Haemost 2006; 4: 1218–1225.
5. Mian A, McCormack Jr WM, Mane V, Kleppe S, Ng P, Finegold M et al. Long-term correction of ornithine transcarbamylase deficiency by WPRE-mediated overexpression using a helper-dependent adenovirus. Mol Ther 2004; 10: 492–499.
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