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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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Autori principali: Schoggins, John W., Gall, Jason G. D., Falck-Pedersen, Erik
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society for Microbiology 2003
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC140814/
https://ncbi.nlm.nih.gov/pubmed/12502819
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JVI.77.2.1039-1048.2003
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