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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...

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Detalles Bibliográficos
Publicado en:Biomedicines
Main Authors: Piccolo, Pasquale, Brunetti-Pierri, Nicola
Formato: Artigo
Idioma:Inglês
Publicado: MDPI 2014
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5423471/
https://ncbi.nlm.nih.gov/pubmed/28548064
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/biomedicines2020132
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