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. 1999 Jan 19;96(2):324-6.
doi: 10.1073/pnas.96.2.324.

Development of optimized vectors for gene therapy

Affiliations

Development of optimized vectors for gene therapy

G J Nabel. Proc Natl Acad Sci U S A. .
No abstract available

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Figures

Figure 1
Figure 1
Features of an optimized adenovirus gene therapy vector. Schematic diagram of a gutted adenoviral vector with an adenoviral packaging sequence and terminal repeats (ITR), containing a minimum of adenoviral genome sequences. The indicated regulatory sequences are intended to confer tissue-specific, regulatable gene expression and the inability to synthesize natural viral gene products.
Figure 2
Figure 2
Model of selective and inducible gene expression with ligand-regulated adenoviral vector. Gray area (Left) shows initial distribution of vector after intravenous injection. In the absence of drug treatment, vector gene expression remains minimal (Center). It is markedly increased, primarily in the liver, in a reversible fashion after drug administration (Right).

Comment on

References

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