Lentivirus- or AAV-mediated gene therapy interventions in ischemic stroke: A systematic review of preclinical in vivo studies

Due to the limited therapeutic options after ischemic stroke, gene therapy has emerged as a promising choice, especially with recent advances in viral vector delivery systems. Therefore, we aimed to provide the current state of the art of lentivirus (LV) and adeno-associated virus (AAV) mediated gen...

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Detalles Bibliográficos
Autores principales: Skukan, Laura, Brezak, Matea, Ister, Rok, Klimaschewski, Lars, Vojta, Aleksandar, Zoldoš, Vlatka, Gajović, Srećko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8795232/
https://www.ncbi.nlm.nih.gov/pubmed/34427147
http://dx.doi.org/10.1177/0271678X211039997

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8795232/
https://www.ncbi.nlm.nih.gov/pubmed/34427147
http://dx.doi.org/10.1177/0271678X211039997

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