Targeting of Adenovirus via Genetic Modification of the Viral Capsid Combined with a Protein Bridge

A potential barrier to the development of genetically targeted adenovirus (Ad) vectors for cell-specific delivery of gene therapeutics lies in the fact that several types of targeting protein ligands require posttranslational modifications, such as the formation of disulfide bonds, which are not ava...

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Bibliografische Detailangaben

Veröffentlicht in:	J Virol
Hauptverfasser:	Korokhov, Nikolay, Mikheeva, Galina, Krendelshchikov, Alexander, Belousova, Natalya, Simonenko, Vera, Krendelshchikova, Valentina, Pereboev, Alexander, Kotov, Alexander, Kotova, Olga, Triozzi, Pierre L., Aldrich, Wayne A., Douglas, Joanne T., Lo, Kin-Ming, Banerjee, Papia T., Gillies, Stephen D., Curiel, David T., Krasnykh, Victor
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	American Society for Microbiology (ASM) 2003
Schlagworte:	Gene Therapy
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC296051/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/14645549/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/JVI.77.24.12931-12940.2003
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