Biology of adenovirus vectors with E1 and E4 deletions for liver-directed gene therapy.
Recombinant adenoviruses with E1 sequences deleted efficiently transfer genes into a wide variety of target cells. Antigen- and nonantigen-specific responses to the therapy lead to toxicity, loss of transgene expression, and difficulties with vector readministration. We have created new cell lines t...
Na minha lista:
| Udgivet i: | J Virol |
|---|---|
| Principais autores: | , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society for Microbiology (ASM)
1996
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC190991/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8971023/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.70.12.8934-8943.1996 |
| Tags: |
Ingen Tags, Vær først til at tagge denne postø!
|