| 发明名称 |
LENTIVIRAL VECTOR-MEDIATED GENE TRANSFER AND COMPOSITION THEREFOR |
| 摘要 |
The present invention provides a means of human gene therapy for inherited or acquired proliferative ocular disease. It furnishes methods to exploit the ability of lentiviral vectors to transduce both mitotically active and inactive cells so that eye diseases may be treated.
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| 申请公布号 |
KR20100011994(A) |
申请公布日期 |
2010.02.03 |
| 申请号 |
KR20097027248 |
申请日期 |
2001.12.18 |
| 申请人 |
RESEARCH DEVELOPMENT FOUNDATION |
发明人 |
STOUT J. TIMOTHY;APPUKUTTAN BINOY |
| 分类号 |
A61K48/00;C12N15/09;A61K35/74;A61P27/02;A61P27/06;C07K14/47;C07K14/52;C12N15/867 |
主分类号 |
A61K48/00 |
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