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:
| Publicado no: | J Virol |
|---|---|
| Principais autores: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Microbiology (ASM)
1996
|
| Assuntos: | |
| Acesso em linha: | 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: |
Sem tags, seja o primeiro a adicionar uma tag!
|