Biomedical Engineering Reference
In-Depth Information
Yechoor, V and Chan, L. 2005. Gene therapy progress and prospects: gene therapy for diabetes mellitus.
Gene
Therapy
12
(2), 101-107.
Young, L.S., Searle, P.F., Onion, D., and Mautner, V. 2006. Viral gene therapy strategies: from basic science to
clinical application.
Journal of Pathology
208
(2), 299-318.
Antisense technology
Aboul-Fadt, T. 2005. Antisense oligonucleotides: the state of the art.
Current Medicinal Chemistry
12
(19),
2193-2214.
Adah, S.A., Bayly, S.F., Cramer, H., Silverman, R.H., and Torrence, P.F. 2001. Chemistry and biochemistry of
2´, 5´-oligoadenylate-based antisense strategy.
Current Medicinal Chemistry
8
(10), 1189-1212.
Akhtar, S., Hughes, M.D., Khan, A., Bibby, M., Hussain, M., Nawaz, Q., Double, J., and Sayyed, P. 2000. The
delivery of antisense therapeutics.
Advanced Drug Delivery Reviews
44
(1), 3-21.
Galderisi, U., Cipollaro, M., and Cascino, A. 2001. Antisense oligonucleotides as drugs for HIV treatment.
Expert
Opinion on Therapeutic Patents
11
(10), 1605-1611.
Hughes, M.D., Hussain, M., Nawaz, Q., Sayyed, P., and Akhtar, S. 2001. The cellular delivery of antisense
oligonucleotides and ribozymes.
Drug Discovery Today
6
(6), 303-315.
Jason, T.L.H., Koropatnick, J., and Berg, R.W. 2004. Toxicology of antisense therapeutics.
Toxicology and Applied
Pharmacology
201
(1), 66 -83.
Lebedeva, I. and Stein, C. 2001. Antisense oligonucleotides: promise and reality.
A n n u a l Re vie w o f Ph ar m a colog y
and Toxicology
41
, 403-419.
Rubenstein, M., Tsui, P., and Guinan, P. 2004. A review of antisense oligonucleotides in the treatment of human
disease.
Drugs of the Future
29
(9), 893-909.
Stein, C.A., Benimetskaya, L., and Mani, S. 2005. Antisense strategies for oncogene inactivation.
Seminars in
Oncology
32
(6), 563-572.
Vidal L., Blagden, S., Attard, G., and de Bono, J. 2005. Making sense of antisense.
European Journal of Cancer
41
(18), 2812-2818.
RNA interference
Amarzguioui, M., Rossi, J.J., and Kim, D. 2005. Approaches for chemically synthesized siRNA and vector-
mediated RNAi.
FEBS Letters
579
(26), 5974-5981.
Bagasra, O. 2005. RNAi as an antiviral therapy.
Expert Opinion on Biological Therapy
5
(11), 1463-1474.
Campbell, T. and Choy, F. 2005. RNA interference: past, present and future.
Current Issues in Molecular
Biology
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, 1-6.
Caplen, N. 2003. RNAi as a gene therapy approach.
Expert Opinion on Biological Therapy
3
(4), 575-568.
Chowdhury, D. and Novina, C. 2005. RNAi and RNA-based regulation of immune system function.
Advances in
Immunology
88
(88), 267-292.
Pai, S.I., Lin, Y.Y., Macaes, B., Meneshian, A., Hung, C.F., and Wu, T.C. 2006. Prospect of RNA interference
therapy for cancer.
Gene Therapy
13
(6), 464-477.
Uprichard, S. 2005. The therapeutic potential of RNA interference.
FEBS Letters
579
(26), 5996-6007.
Ribozymes
Alvarez-Salas, L.M., Benitez-Hess, M.L., and DiPaolo, J.A. 2003. Advances in the development of ribozymes
and antisense oligodeoxynucleotides as antiviral agents for human papillomaviruses.
Antiviral Therapy
8
(4),
265-278.
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