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An Alternate Route for Adeno-associated Virus (AAV) Entry Independent of AAV Receptor
Determinants and mechanisms of cell attachment and entry steer adeno-associated virus (AAV) in its utility as a gene therapy vector. Thus far, a systematic assessment of how diverse AAV serotypes engage their proteinaceous receptor AAVR (KIAA0319L) to establish transduction has been lacking, despite...
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| Publicat a: | J Virol |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Microbiology
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5972900/ https://ncbi.nlm.nih.gov/pubmed/29343568 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JVI.02213-17 |
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