Targeted adenovirus gene transfer to endothelial and smooth muscle cells by using bispecific antibodies.

A major hurdle to adenovirus (Ad)-mediated gene transfer is that the target issue lacks sufficient levels of receptors to mediate vector attachment via its fiber coat protein. Endothelial and smooth muscle cells are primary targets in gene therapy approaches to prevent restenosis following angioplas...

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Detalhes bibliográficos

Publicado no:	J Virol
Principais autores:	Wickham, T J, Segal, D M, Roelvink, P W, Carrion, M E, Lizonova, A, Lee, G M, Kovesdi, I
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Microbiology (ASM) 1996
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC190730/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8794324/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jvi.70.10.6831-6838.1996
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