Cell-Type-Specific Gene Transfer into Human Cells with Retroviral Vectors That Display Single-Chain Antibodies

The successful application of human gene therapy protocols on a broad clinical basis will depend on the availability of in vivo cell-type-specific gene delivery systems. We have developed retroviral vector particles, derived from spleen necrosis virus (SNV), that display the antigen binding site of...

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Detalhes bibliográficos

Publicado no:	J Virol
Principais autores:	Jiang, An, Chu, Te-Hua T., Nocken, F., Cichutek, Klaus, Dornburg, Ralph
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Microbiology (ASM) 1998
Assuntos:	Gene Therapy
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC110554/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9811755/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.72.12.10148-10156.1998
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