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Unraveling the Complex Story of Immune Responses to AAV Vectors Trial After Trial

Over the past decade, vectors derived from adeno-associated virus (AAV) have established themselves as a powerful tool for in vivo gene transfer, allowing long-lasting and safe transgene expression in a variety of human tissues. Nevertheless, clinical trials demonstrated how B and T cell immune resp...

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Detalhes bibliográficos
Publicado no:Hum Gene Ther
Main Authors: Vandamme, Céline, Adjali, Oumeya, Mingozzi, Federico
Formato: Artigo
Idioma:Inglês
Publicado em: Mary Ann Liebert, Inc. 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5649404/
https://ncbi.nlm.nih.gov/pubmed/28835127
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/hum.2017.150
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