| 发明名称 |
Gene delivery and expression in areas inaccessible to direct protein delivery |
| 摘要 |
The present invention provides novel methods for gene delivery and expression in areas that are currently inaccessible through the use of conventional direct protein delivery techniques. In particular, the methods and related products provided herein can be used in the treatment of alpha1 antitrypsin (AAT) related disorders such as respiratory syncytial virus (RSV) infection.
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| 申请公布号 |
US6365575(B1) |
申请公布日期 |
2002.04.02 |
| 申请号 |
US19970951552 |
申请日期 |
1997.10.16 |
| 申请人 |
VANDERBILT UNIVERSITY |
发明人 |
BRIGHAM KENNETH;CANONICO ANGELO;MEYRICK BARBARA;STECENKO ARLENE |
| 分类号 |
A61K48/00;A61K31/7088;A61K38/00;A61K38/43;A61K38/44;A61K38/55;A61K38/57;A61P11/00;A61P31/12;A61P43/00;(IPC1-7):A61K48/00;C12N15/12 |
主分类号 |
A61K48/00 |
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