Adenoviral targeting using genetically incorporated camelid single variable domains

The unique ability of human adenovirus serotype 5 (Ad5) to accomplish efficient transduction has allowed the use of Ad5-based vectors for a range of gene therapy applications. Several strategies have been developed to alter tropism of Ad vectors to achieve a cell-specific gene delivery by employing...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaliberov, Sergey A., Kaliberova, Lyudmila N., Buggio, Maurizio, Tremblay, Jacqueline M., Shoemaker, Charles B., Curiel, David T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157633/
https://www.ncbi.nlm.nih.gov/pubmed/24933423
http://dx.doi.org/10.1038/labinvest.2014.82

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157633/
https://www.ncbi.nlm.nih.gov/pubmed/24933423
http://dx.doi.org/10.1038/labinvest.2014.82

Ejemplares similares