Strategies for targeted gene therapy

被引:57
作者
Harris, JD [1 ]
Lemoine, NR [1 ]
机构
[1] HAMMERSMITH HOSP, ROYAL POSTGRAD MED SCH, IMPERIAL CANC RES FUND, ONCOL UNIT, LONDON W12 0NN, ENGLAND
关键词
D O I
10.1016/0168-9525(96)40031-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genetic intervention for the therapy of human disease has long been a dream for scientists and clinicians alike, and the first steps towards reality have already been taken in clinical trails involving over 1000 patients around the world. The technology used in these initial experiments has limited potential for therapeutic effect and it is now appreciated that improvements in targeting gene delivery and gene expression are both required before real clinical benefit is achieved. The enormous advances made in the field of molecular genetics and molecular biology of the last few years have set the scene for their translation into novel approaches to gene transfer and control, for gene therapy applications.
引用
收藏
页码:400 / 405
页数:6
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