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Adeno-Associated Virus-Mediated Gene Transfer to Renal Tubule Cells via a Retrograde Ureteral Approach
BACKGROUND/AIMS: Gene therapy involves delivery of exogenous DNA to provide a therapeutic protein. Ideally, a gene therapy vector should be non-toxic, non-immunogenic, easy to produce, and efficient in protecting and delivering DNA into target cells. METHODS: Adeno-associated virus (AAV) offers thes...
Autores principales: | Chung, Daniel C., Fogelgren, Ben, Park, Kwon Moo, Heidenberg, Jessica, Zuo, Xiaofeng, Huang, Liwei, Bennett, Jean, Lipschutz, Joshua H. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3290852/ https://www.ncbi.nlm.nih.gov/pubmed/22470395 http://dx.doi.org/10.1159/000333071 |
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