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AAV's Anatomy: Roadmap for Optimizing Vectors for Translational Success

Adeno-Associated Virus based vectors (rAAV) are advantageous for human gene therapy due to low inflammatory responses, lack of toxicity, natural persistence, and ability to transencapsidate the genome allowing large variations in vector biology and tropism. Over sixty clinical trials have been condu...

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Detalhes bibliográficos
Main Authors: Mitchell, Angela M., Nicolson, Sarah C., Warischalk, Jayme K., Samulski, R. Jude
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3920455/
https://ncbi.nlm.nih.gov/pubmed/20712583
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