Genetically Targeted Adenovirus Vector Directed to CD40-Expressing Cells

The success of gene therapy depends on the specificity of transgene delivery by therapeutic vectors. The present study describes the use of an adenovirus (Ad) fiber replacement strategy for genetic targeting of the virus to human CD40, which is expressed by a variety of diseased tissues. The tropism...

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Hlavní autoři: Belousova, Natalya, Korokhov, Nikolay, Krendelshchikova, Valentina, Simonenko, Vera, Mikheeva, Galina, Triozzi, Pierre L., Aldrich, Wayne A., Banerjee, Papia T., Gillies, Stephen D., Curiel, David T., Krasnykh, Victor
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Microbiology 2003
Témata:
Gene Therapy
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC229360/
https://ncbi.nlm.nih.gov/pubmed/14557622
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JVI.77.21.11367-11377.2003
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