Abstract
A major goal for gene therapy is to obtain targeted vectors that transfer genes efficiently to specific cell types. In theory, this can be achieved by targeting entry of the vector or by building gene expression cassettes that restrict gene expression to certain cell types. This review summarizes recent strategies to alter vector tropism for targeted gene delivery.
Original language | English (US) |
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Pages (from-to) | 448-453 |
Number of pages | 6 |
Journal | Molecular Medicine Today |
Volume | 5 |
Issue number | 10 |
DOIs | |
State | Published - Oct 1 1999 |
ASJC Scopus subject areas
- Molecular Medicine
- Genetics