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CRISPR/Cas9 Genome Editing to Disable the Latent HIV-1 Provirus
HIV-1 infection can be successfully controlled with anti-retroviral therapy (ART), but is not cured. A reservoir of cells harboring transcriptionally silent integrated provirus is able to reestablish replicating infection if ART is stopped. Latently HIV-1 infected cells are rare, but may persist for...
Autores principales: | Panfil, Amanda R., London, James A., Green, Patrick L., Yoder, Kristine E. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302043/ https://www.ncbi.nlm.nih.gov/pubmed/30619186 http://dx.doi.org/10.3389/fmicb.2018.03107 |
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