Deverman, Benjamin E. and Simpson, Bryan and Pravdo, Piers and Banerjee, Abhik and Patterson, Paul H. (2014) Engineering Recombinant AAV Vectors for More Efficient and Restricted Gene Expression in the CNS after Systemic Administration. Molecular Therapy, 22 (S1). S118. ISSN 1525-0016. https://resolver.caltech.edu/CaltechAUTHORS:20140717-151830932
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Abstract
We previously demonstrated that delivery of the cytokine leukemia inhibitory factor (LIF) to the brain by recombinant adenovirus enhances oligodendrocyte progenitor cell proliferation and remyelination in a mouse model of multiple sclerosis (MS).
| Item Type: | Article | ||||||||||||
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| Additional Information: | © 2014 American Society of Gene & Cell Therapy. | ||||||||||||
| Issue or Number: | S1 | ||||||||||||
| Record Number: | CaltechAUTHORS:20140717-151830932 | ||||||||||||
| Persistent URL: | https://resolver.caltech.edu/CaltechAUTHORS:20140717-151830932 | ||||||||||||
| Official Citation: | Mol Ther 22: S307-S320; doi:10.1038/mt.2014.66 | ||||||||||||
| Usage Policy: | No commercial reproduction, distribution, display or performance rights in this work are provided. | ||||||||||||
| ID Code: | 47306 | ||||||||||||
| Collection: | CaltechAUTHORS | ||||||||||||
| Deposited By: | Ruth Sustaita | ||||||||||||
| Deposited On: | 17 Jul 2014 23:59 | ||||||||||||
| Last Modified: | 03 Oct 2019 06:52 |
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