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Characterization of a 3(rd) Generation Lentiviral Vector Pseudotyped With Nipah Virus Envelope Proteins For Endothelial Cell Transduction

Lentiviruses are becoming progressively more popular as gene therapy vectors due to their ability to integrate into quiescent cells and recent clinical trial successes. Directing these vectors to specific cell types and limiting off-target transduction in vivo remains a challenge. Replacing the vira...

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Detalles Bibliográficos
Autores principales:	Witting, Scott R., Vallanda, Priya, Gamble, Aisha L.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2013
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3839624/ https://www.ncbi.nlm.nih.gov/pubmed/23698741 http://dx.doi.org/10.1038/gt.2013.23

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