| 发明名称 |
Vectors for occular transduction and use therefor for genetic therapy |
| 摘要 |
Adenovirus vector-based gene therapy methods for treating ocular disorders are provided. Adenovirus vectors for therapy of ocular diseases and methods of treatment using the vectors are provided. Compositions, kits, and methods of preparation and use of the vectors for gene therapy are provided.
|
| 申请公布号 |
US2002193327(A1) |
申请公布日期 |
2002.12.19 |
| 申请号 |
US20010847101 |
申请日期 |
2001.05.01 |
| 申请人 |
THE SCRIPPS RESEARCH INSTITUTE |
发明人 |
NEMEROW GLEN R.;VON SEGGERN DANIEL J.;FRIEDLANDER MARTIN |
| 分类号 |
C12N15/09;A61K35/76;A61K48/00;A61P9/10;A61P27/02;C12N5/10;C12N15/861;(IPC1-7):A61K48/00;C07H21/04;C12N7/00 |
主分类号 |
C12N15/09 |
| 代理机构 |
|
代理人 |
|
| 主权项 |
|
| 地址 |
|
