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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Autores principales: 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
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society for Microbiology 2003
Materias:
Gene Therapy
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC296051/
https://ncbi.nlm.nih.gov/pubmed/14645549
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JVI.77.24.12931-12940.2003
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