4.7 Review

Viral vectors: from virology to transgene expression

期刊

BRITISH JOURNAL OF PHARMACOLOGY
卷 157, 期 2, 页码 153-165

出版社

WILEY
DOI: 10.1038/bjp.2008.349

关键词

viral vectors; gene therapy; AAV; Ad; HSV; lentivectors; pseudotyping; cell targeting; transcriptional targeting; vectors production

资金

  1. INSERM, ENS Lyon
  2. Ligue Nationale Contre le Cancer, the European Community [LSHB-CT-2004-005242]
  3. Agence Nationale de Recherches sur le SIDA et les HEpatites Virales (ANRS)
  4. Association Francaise contre les Myopathies (AFM)

向作者/读者索取更多资源

In the late 1970s, it was predicted that gene therapy would be applied to humans within a decade. However, despite some success, gene therapy has still not become a routine practise in medicine. In this review, we will examine the problems, both experimental and clinical, associated with the use of viral material for transgenic insertion. We shall also discuss the development of viral vectors involving the most important vector types derived from retroviruses, adenoviruses, herpes simplex viruses and adeno-associated viruses.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据