Suprachoroidal and Subretinal Injections of AAV Using Transscleral Microneedles for Retinal Gene Delivery in Nonhuman Primates

Retinal gene therapy using adeno-associated viruses (AAVs) is constrained by the mode of viral vector delivery. Intravitreal AAV injections are impeded by the internal limiting membrane barrier, while subretinal injections require invasive surgery and produce a limited region of therapeutic effect....

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Detalles Bibliográficos
Autores principales: Yiu, Glenn, Chung, Sook Hyun, Mollhoff, Iris N., Nguyen, Uyen Tu, Thomasy, Sara M., Yoo, Jesse, Taraborelli, Donna, Noronha, Glenn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005511/
https://www.ncbi.nlm.nih.gov/pubmed/32055646
http://dx.doi.org/10.1016/j.omtm.2020.01.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005511/
https://www.ncbi.nlm.nih.gov/pubmed/32055646
http://dx.doi.org/10.1016/j.omtm.2020.01.002

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