Transcriptional Targeting of Lentiviral Vectors by Long Terminal Repeat Enhancer Replacement

Gene therapy of many genetic diseases requires permanent gene transfer into self-renewing stem cells and restriction of transgene expression to specific progenies. Human immunodeficiency virus (HIV)-derived lentiviral vectors are very effective in transducing rare, nondividing stem cell populations...

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Detalles Bibliográficos

Publicado en:	J Virol
Principais autores:	Lotti, Francesco, Menguzzato, Emilio, Rossi, Claudia, Naldini, Luigi, Ailles, Laurie, Mavilio, Fulvio, Ferrari, Giuliana
Formato:	Artigo
Idioma:	Inglês
Publicado:	American Society for Microbiology (ASM) 2002
Assuntos:	Gene Therapy
Acceso en liña:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC136069/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11907239/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/JVI.76.8.3996-4007.2002
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