American Society for Microbiology, Journal of Virology, 23(95), 2021
DOI: 10.1128/jvi.01358-21
Full text: Download
The excision of HIV-1 provirus from the host cell genome has proven feasiblein vitroand, to some extent,in vivo. Among the different approaches, CRISPR/Cas9 is the most promising tool for gene editing.