| 发明名称 |
USE OF GENETICALLY MODIFIED CELLS TO TREAT DEFECTS, DISEASE OR DAMAGE OF THE CENTRAL NERVOUS SYSTEM |
| 摘要 |
Methods of genetically modifying donor cells by gene transfer for grafting into the central nervous system to treat defective, Diseased or damaged cells are disclosed. The modified donor cells produce functional molecules that effect the recovery or improved function of cells in the CNS. Methods and vectors for carrying out gene transfer and grafting are described.
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| 申请公布号 |
CA2095300(C) |
申请公布日期 |
2002.06.25 |
| 申请号 |
CA19932095300 |
申请日期 |
1993.04.30 |
| 申请人 |
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发明人 |
GAGE, FRED;FRIEDMANN, THEODORE;ROSENBERG, MICHAEL B.;WOLFF, JON A.;SCHINSTINE, MALCOLM;KAWAJA, MICHAEL D.;RAY, JASODHARA |
| 分类号 |
A61K48/00;A61K38/00;A61K38/18;A61K38/44;C07K14/48;C12N5/10;C12N9/02;C12N9/10;C12N9/12;C12N15/09;C12N15/12;C12N15/52;C12N15/86;(IPC1-7):A61K35/12 |
主分类号 |
A61K48/00 |
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