Subgroup B and F Fiber Chimeras Eliminate Normal Adenovirus Type 5 Vector Transduction In Vitro and In Vivo

Altering adenovirus vector (Ad vector) targeting is an important goal for a variety of gene therapy applications and involves eliminating or reducing the normal tropism of a vector and retargeting through a distinct receptor-ligand pathway. The first step of Ad vector infection is high-affinity bind...

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Vydáno v:	J Virol
Hlavní autoři:	Schoggins, John W., Gall, Jason G. D., Falck-Pedersen, Erik
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	American Society for Microbiology (ASM) 2003
Témata:	Gene Therapy
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC140814/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12502819/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/JVI.77.2.1039-1048.2003
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