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Targeted Adenoviral Vectors I: Transductional Targeting

Human adenovirus (Ad) has been used extensively to develop gene transfer vectors for vaccine and gene therapy applications. A major factor limiting the efficacy of the current generation of Ad vectors is their inability to accomplish specific gene delivery to the cells of interest. Transductional ta...

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Bibliografske podrobnosti
izdano v:Adenoviral Vectors for Gene Therapy
Main Authors: Dmitriev, Igor P., Kaliberov, Sergey A.
Format: Artigo
Jezik:Inglês
Izdano: 2016
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7149436/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/B978-0-12-800276-6.00009-7
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