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Autor:
Zhou, Heshan, Zhao, Tiejun, Pastore, Lucio, Nageh, Maged, Zheng, Wendy, Rao, X. Mei, Beaudet, Arthur L.
Publikováno v:
Molecular Therapy; April 2001, Vol. 3 Issue: 4 p613-622, 10p
Autor:
Heshan Zhou, Tiejun Zhao, X. Mei Rao, Wendy Zheng, Arthur L. Beaudet, Maged F. Nageh, Lucio Pastore
Publikováno v:
Molecular Therapy. 3(4):613-622
Adenoviral vectors are attractive for the delivery of transgenes into mammalian cells because of their efficient transduction, high titer, and stability. The major concerns with using E1-deleted adenoviral vectors in gene therapy are the pathogenic p