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Manipulation of gene expression in developing or in mature central nervous systems (CNS) holds a promise for the resolution of many compelling neurobiological questions, including the feasibility of gene therapy to treat diseases of the brain. In this context, a number of viral vectors have been used in recent years to introduce and express genes into the CNS. This article discusses a gene transfer system based on the Herpes Simplex Virus-1 (HSV-1). We describe here the use of non-replicating, non-toxic HSV-1 vector, 8117/43, in a series of studies carried in our joint program. This vector proves further the utility of HSV-1 as a delivery vehicle to a number of distinct sites within the CNS.
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- State University of New York, 317 Farber Hall, Buffalo N.Y. 14214, USA
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Bibliografia
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- 13. Lokensgard JR, Bloom DC, Dobson AT, and Feldman LT (1994) Long-term promoter activity during herpes simplex virus latency. J Virol, 68: 7148–7158.
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- 15. Palmer JA, Branston RH, Lilley CE, Robinson MJ, Groutsi F, Smith J, Latchman DS, and Coffin RS (2000) Development and optimization of herpes simplex virus vectors for multiple long-term gene delivery to the peripheral nervous system. J Virol, 74: 5664–5618.
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Bibliografia
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