Improvement of Adenoviral Vectors for Human Gene Therapy
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-61028-8_11.pdf
Reference83 articles.
1. Alexander IE, Russel DW, Miller AD (1994) DNA-damaging agents greatly increase the transduction of nondividing cells by adeno-associated virus vectors. J Virol 68: 8282–8287
2. Anderson KP, Klessig DF (1983) Posttranscriptional block to synthesis of a human adenovirus capsid protein in abortively infected monkey cells. J Mol Applied Genet 2: 31–43
3. Anderson WF (1994) Making clinical grade gene therapy vectors. Human Gene Ther 5: 925–926
4. Babiss LE (1989) The cellular transcription factor E2f requires viral E1A and E4 gene products for increased DNA-binding activity and functions to stimulate adenovirus E2A gene expression. J Virol 63: 2709–2717
5. Bai M, Campisi L, Freimuth P (1994) Vitronectin receptor antibodies inhibit infection of HeLùa and A549 cells by adenovirus type 12 but not by adenovirus type 2. J Virol 68: 5925–5932
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