Tropism-Modification Strategies for Targeted Gene Delivery Using Adenoviral Vectors

Achieving high efficiency, targeted gene delivery with adenoviral vectors is a long-standing goal in the field of clinical gene therapy. To achieve this, platform vectors must combine efficient retargeting strategies with detargeting modifications to ablate native receptor binding (i.e. CAR/integrin...

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Detalles Bibliográficos
Autores principales: Coughlan, Lynda, Alba, Raul, Parker, Alan L., Bradshaw, Angela C., McNeish, Iain A., Nicklin, Stuart A., Baker, Andrew H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2010
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185574/
https://www.ncbi.nlm.nih.gov/pubmed/21994621
http://dx.doi.org/10.3390/v2102290

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185574/
https://www.ncbi.nlm.nih.gov/pubmed/21994621
http://dx.doi.org/10.3390/v2102290

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