Investigating CRISPR/Cas9 system as gene-editing therapy targeting the current known molecular mechanism of HIV-1 infection.
Describe how current knowledge of the virus genetics enabled application of CRISPR/Cas9 nuclease to HIV-1, what is its current development against HIV-1 and its importance.
Present a detailed analysis of CRISPR/Cas9 gene editing targets based on studies related to the molecular mechanism of HIV-1 infection .
Describe the limitations and or benefits of using CRISPR/Cas9 as a gene-editing therapy for HIv-1. Where to go next from it?.