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Targeted inhibition of immunodeficiency virus replication in lymphocytes through retroviral mediated gene transfer
To test the feasibility of gene therapy for AIDS patients, an animal model is needed to evaluate the efficacy and safety of this approach. Antiviral genes (encoding antisense RNA or viral protein) derived from Simian immunodeficiency virus (SIV) were efficiently targeted into CD4+ lymphocytes throug...
Guardat en:
| Publicat a: | Arch Virol |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer-Verlag
1993
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7086800/ https://ncbi.nlm.nih.gov/pubmed/7504917 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/BF01313779 |
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