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Adenovirus-mediated regulable target gene expression in vivo

To regulate expression of a transferred gene in response to an exogenous compound, we have combined a high capacity adenoviral vector devoid of all viral coding sequences with a regulatory system that can be used to express a target gene in vivo in a selected site and at a desired time. This system...

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Autores principales: Burcin, Mark M., Schiedner, Gudrun, Kochanek, Stefan, Tsai, Sophia Y., O’Malley, Bert W.
Formato: Artigo
Lenguaje:Inglês
Publicado: The National Academy of Sciences 1999
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC15140/
https://ncbi.nlm.nih.gov/pubmed/9892637
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