J. Zhao

Selective proapoptotic activity of a secreted recombinant antibody/AIF fusion protein in carcinomas overexpressing HER2

D. Fan, A. Yang, X. Qiu, 2006, Gene Therapy.

Lentivirus-mediated gene transfer of viral interleukin-10 delays but does not prevent cardiac allograft rejection

A. Lever, J. Bradley, G. Pettigrew, 2005, Gene Therapy.

Study of adenovirus-mediated dystrophin minigene transfer to skeletal muscle by combined microscopic display of adenoviral DNA and dystrophin.

J. Nalbantoglu, B. Massie, G. Karpati, 1997, Human gene therapy.

Impairment of force generation after adenovirus-mediated gene transfer to muscle is alleviated by adenoviral gene inactivation and host CD8+ T cell deficiency.

Hanns Lochmüller, J. Nalbantoglu, L. Yang, 1996, Human gene therapy.

Cosmid vectors for rapid genomic walking, restriction mapping, and gene transfer.

G. Wahl, G. Evans, K. Lewis, 1987, Proceedings of the National Academy of Sciences of the United States of America.

An hepatitis B virus surface antigen specific single chain of variable fragment derived from a natural immune antigen binding fragment phage display library is specifically internalized by HepG2.2.15 cells

W. Qin, L. Jia, L. Yao, 2007, Journal of viral hepatitis.

Survivin knockdown by short hairpin RNA abrogates the growth of human hepatocellular carcinoma xenografts in nude mice

T. Wang, M. Zheng, L. Yao, 2010, Cancer Gene Therapy.

Efficient muscle-specific transgene expression after adenovirus-mediated gene transfer in mice using a 1.35 kb muscle creatine kinase promoter/enhancer

H. Lochmüller, J. Nalbantoglu, Á. Jáni, 1997, Gene Therapy.

Lens-specific expression of recombinant ricin induces developmental defects in the eyes of transgenic mice.

G. Evans, D. Bok, C. Landel, 1988, Genes & development.