Human Molecular Genetics, Vol 5, 1397-1404, Copyright © 1996 by Oxford University Press
U Blomer, L Naldini, IM Verma, D Trono and FH Gage
Gene therapy is a new method with potential for treating a broad range of
acquired and inherited neurologic diseases, where the causative gene defect
or deletion has been identified. In addition to gene replacement the
application of gene products that reduce cellular dysfunction or death
represent new therapeutic options. Gene transfer techniques to express
novel proteins using different viral vectors in vitro and in vivo, as well
as animal models and human trials will be reviewed in this article. We will
focus on a new lentiviral vector as a recent gene transfer method and
degenerative disorders of the CNS, and their related model systems.
REVIEWS
Applications of gene therapy to the CNS
Salk Institute for Biological Studies, La Jolla, CA 92037-1099, USA.
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