Targeting AAV vectors

被引:3
作者
Baker, AH [1 ]
机构
[1] Univ Glasgow, Glasgow Cardiovasc Res Ctr, Glasgow G11 6NT, Lanark, Scotland
关键词
D O I
10.1016/S1525-0016(03)00072-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In summary, AAV vectors currently offer unique potential to treat pathologies that exploit the native tropism of the virion. Manipulation of the AAV-2 capsid by peptide insertion will broaden the range of diseases applicable to AAV-2-mediated gene therapy.
引用
收藏
页码:433 / 434
页数:2
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