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“Para-retinal” Vector Administration into the Deep Vitreous Enhances Retinal Transgene Expression
Intravitreal administration for human adeno-associated vector (AAV) delivery is easier and less traumatic to ocular tissues than subretinal injection, but it gives limited retinal transduction. AAV vectors are large (about 4,000 kDa) compared with most intraocular drugs, such as ranibizumab (48 kDa)...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
American Society of Gene & Cell Therapy
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363691/ https://www.ncbi.nlm.nih.gov/pubmed/32695844 http://dx.doi.org/10.1016/j.omtm.2020.06.015 |