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DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscle.
Hum Gene Ther. 1999 Feb 10;10(3):365-73. doi: 10.1089/10430349950018814.
Hum Gene Ther. 1999.
PMID: 10048389
Persistence in muscle of an adenoviral vector that lacks all viral genes.
Chen HH, Mack LM, Kelly R, Ontell M, Kochanek S, Clemens PR.
Chen HH, et al.
Proc Natl Acad Sci U S A. 1997 Mar 4;94(5):1645-50. doi: 10.1073/pnas.94.5.1645.
Proc Natl Acad Sci U S A. 1997.
PMID: 9050832
Free PMC article.
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Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles.
Floyd SS Jr, Clemens PR, Ontell MR, Kochanek S, Day CS, Yang J, Hauschka SD, Balkir L, Morgan J, Moreland MS, Feero GW, Epperly M, Huard J.
Floyd SS Jr, et al.
Gene Ther. 1998 Jan;5(1):19-30. doi: 10.1038/sj.gt.3300549.
Gene Ther. 1998.
PMID: 9536261
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