Cargando…
Challenges and Prospects for Helper-Dependent Adenoviral Vector-Mediated Gene Therapy
Helper-dependent adenoviral (HDAd) vectors that are devoid of all viral coding sequences are promising non-integrating vectors for gene therapy because they efficiently transduce a variety of cell types in vivo, have a large cloning capacity, and drive long-term transgene expression without chronic...
| Autores principales: | , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2014
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5423471/ https://www.ncbi.nlm.nih.gov/pubmed/28548064 http://dx.doi.org/10.3390/biomedicines2020132 |