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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...
Autores principales: | Skukan, Laura, Brezak, Matea, Ister, Rok, Klimaschewski, Lars, Vojta, Aleksandar, Zoldoš, Vlatka, Gajović, Srećko |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
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 |
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