Delivery Systems for Gene Transfer - Genomics: Essential Methods - page 272

3. Riddell, S.R., Elliott, M., Lewinsohn, D.A. et al . (1996) T-cell mediated rejection of
gene-modified HIV-specific cytotoxic T lymphocytes in HIV-infected patients. Nature

Medicine , 2 (2), 216-223.

4. Apparailly, F., Millet, V., Noel, D. et al . (2002) Tetracycline-inducible interleukin-10 gene trans-
fer mediated by an adeno-associated virus: application to experimental arthritis. Human Gene
Therapy , 13 (10), 1179-1188.

5. Modlich, U., Pugh, C.W. and Bicknell, R. (2000) Increasing endothelial cell specific expression
by the use of heterologous hypoxic and cytokine-inducible enhancers. Gene Therapy , 7 (10),
896-902.
6. Morgenstern, J.P. and Land, H. (1990) Advanced mammalian gene transfer: high titre retroviral
vectors with multiple drug selection markers and a complementary helper-free packaging cell
line. Nucleic Acids Research , 18 (12), 3587-3596. Describes the pBABE retroviral vectors and
eukaryotic packaging cell lines.

7. Chen, P., Tian, J., Kovesdi, I. and Bruder, J.T. (2007) Promoters influence the kinetics of
transgene expression following adenovector gene delivery. Journal of Gene Medicine , 10 (2),
123-131.
8. Chuah, M.K., Schiedner, G., Thorrez, L. et al . (2003) Therapeutic factor VIII levels and negligible
toxicity in mouse and dog models of hemophilia A following gene therapy with high-capacity
adenoviral vectors. Blood , 101 (5), 1734-1743.

9. Sadeghi, H. and Hitt, M.M. (2005) Transcriptionally targeted adenovirus vectors. Current Gene
Therapy , 5 (4), 411-427.
10. Gruh, I., Wunderlich, S., Winkler, M. et al . (2008) Human CMV immediate-early enhancer:
a useful tool to enhance cell-type-specific expression from lentiviral vectors. Journal of Gene
Medicine , 10 (1), 21-32.
11. Lewandoski, M. (2001) Conditional control of gene expression in the mouse. Nature Reviews
Genetics , 2 (10), 743-755.

12. Gossen, M. and Bujard, H. (1992) Tight control of gene expression in mammalian cells by
tetracycline-responsive promoters. Proceedings of the National Academy of Sciences of the United
States of America , 89 (12), 5547-5551.
13. Miyazaki, S., Miyazaki, T., Tashiro, F. et al . (2005) Development of a single-cassette system for
spatiotemporal gene regulation in mice. Biochemical and Biophysical Research Communications ,
338 (2), 1083-1088.

14. Pluta, K., Diehl, W., Zhang, X.Y., et al . (2007) Lentiviral vectors encoding tetracycline-dependent
repressors and transactivators for reversible knockdown of gene expression: a comparative
study. BMC Biotechnology , 7 , 41.
15. Semple-Rowland, S.L., Eccles, K.S. and Humberstone, E.J. (2007) Targeted expression of two
proteins in neural retina using self-inactivating, insulated lentiviral vectors carrying two internal
independent promoters. Molecular Vision , 13 , 2001-2011.

16. Gonzalez-Nicolini, V., Sanchez-Bustamante, C.D., Hartenbach, S. and Fussenegger, M. (2006)
Adenoviral vector platform for transduction of constitutive and regulated tricistronic or
triple-transcript transgene expression in mammalian cells and microtissues. Journal of Gene
Medicine , 8 (10), 1208-1222. Describes the use of IRES to drive transcription of more than
one gene from a viral promoter.

17. Lawson, C. (2006) Strategies for gene transfer to solid organs: viral vectors. Methods in Molec-
ular Biology 333 , 175-200.