Adenoviral Gene Delivery to Solid Tumors by Recombinant Silk–Elastinlike Protein Polymers-Reference-Cited by-同舟云学术

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Adenoviral Gene Delivery to Solid Tumors by Recombinant Silk–Elastinlike Protein Polymers

Published:2007-02-17 Issue:4 Volume:24 Page:773-779
ISSN:0724-8741
Container-title:Pharmaceutical Research
language:en
Short-container-title:Pharm Res

Author:

Hatefi A.,Cappello J.,Ghandehari H.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Organic Chemistry,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biotechnology

Link

http://link.springer.com/content/pdf/10.1007/s11095-006-9200-5.pdf

Reference23 articles.

1. L. Thorrez, T. VandenDriessche, D. Collen, and M. K. Chuah. Preclinical gene therapy studies for hemophilia using adenoviral vectors. Semin. Thromb. Hemost. 30:173–183 (2004).

2. T. VandenDriessche, L. Naldini, D. Collen, and M. K. Chuah. Oncoretroviral and lentiviral vector-mediated gene therapy. Methods Enzymol. 346:573–589 (2002).

3. Y. Kawashita, H. Fujioka, A. Ohtsuru, Y. Kaneda, Y. Kamohara, Y. Kawazoe, S. Yamashita, and T. Kanematsu. The efficacy and safety of gene transfer into the porcine liver in vivo by HVJ (Sendai virus) liposome. Transplantation 80:1623–1629 (2005).

4. M. Guan, J. R. Rodriguez-Madoz, P. Alzuguren, C. Gomar, M. G. Kramer, S. Kochanek, J. Prieto, C. Smerdou, and C. Qian. Increased efficacy and safety in the treatment of experimental liver cancer with a novel adenovirus-alphavirus hybrid vector. Cancer Res. 66:1620–1629 (2006).

5. S. Worgall, G. Wolff, E. Falck-Pedersen, and R. G. Crystal. Innate immune mechanisms dominate elimination of adenoviral vectors following in vivo administration. Hum. Gene Ther. 8:37–44 (1997).

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