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...

詳細記述

書誌詳細

出版年:	J Virol
主要な著者:	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
フォーマット:	Artigo
言語:	Inglês
出版事項:	American Society for Microbiology (ASM) 2003
主題:	Gene Therapy
オンライン･アクセス:	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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