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Site-specific integration mediated by a hybrid adenovirus/adeno-associated virus vector

Adenovirus (Ad) and adeno-associated virus (AAV) have attractive and complementary properties that can be exploited for gene transfer purposes. Ad vectors are probably the most efficient vehicles to deliver foreign genes both in vitro and in vivo. AAV exhibits the unique ability to establish latency...

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Detalhes bibliográficos
Main Authors: Recchia, Alessandra, Parks, Robin J., Lamartina, Stefania, Toniatti, Carlo, Pieroni, Luisa, Palombo, Fabio, Ciliberto, Gennaro, Graham, Frank L., Cortese, Riccardo, La Monica, Nicola, Colloca, Stefano
Formato: Artigo
Idioma:Inglês
Publicado em: The National Academy of Sciences 1999
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC15817/
https://ncbi.nlm.nih.gov/pubmed/10077559
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