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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: American Society for Microbiology 2003
विषय:
Gene Therapy
ऑनलाइन पहुंच: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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