Загрузка...
Lentiviral Vector Design for Multiple shRNA Expression and Durable HIV-1 Inhibition
Human immunodeficiency virus type 1 (HIV-1) replication in T cells can be inhibited by RNA interference (RNAi) through short hairpin RNA (shRNA) expression from a lentiviral vector. However, for the development of a durable RNAi-based gene therapy against HIV-1, multiple shRNAs need to be expressed...
Сохранить в:
| Опубликовано в: : | Mol Ther |
|---|---|
| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
The American Society of Gene Therapy. Published by Elsevier Inc.
2008
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7172400/ https://ncbi.nlm.nih.gov/pubmed/18180777 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.mt.6300382 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|