Gene editing and elimination of latent herpes simplex virus in vivo

We evaluate gene editing of HSV in a well-established mouse model, using adeno-associated virus (AAV)-delivered meganucleases, as a potentially curative approach to treat latent HSV infection. Here we show that AAV-delivered meganucleases, but not CRISPR/Cas9, mediate highly efficient gene editing o...

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Detalles Bibliográficos
Autores principales: Aubert, Martine, Strongin, Daniel E., Roychoudhury, Pavitra, Loprieno, Michelle A., Haick, Anoria K., Klouser, Lindsay M., Stensland, Laurence, Huang, Meei-Li, Makhsous, Negar, Tait, Alexander, De Silva Feelixge, Harshana S., Galetto, Roman, Duchateau, Philippe, Greninger, Alexander L., Stone, Daniel, Jerome, Keith R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435201/
https://www.ncbi.nlm.nih.gov/pubmed/32811834
http://dx.doi.org/10.1038/s41467-020-17936-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435201/
https://www.ncbi.nlm.nih.gov/pubmed/32811834
http://dx.doi.org/10.1038/s41467-020-17936-5

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