Review
Potensi CRISPR-Cas9 Terkonjugasi Sistem Pengantar Vesikel Ekstraseluler Berbasis Metode Genome Editing sebagai Strategi Terapeutik Penyakit HIV
The findings indicate that CRISPR-Cas9 can target multiple stages of the HIV life cycle, including disruption of viral entry coreceptors, inhibition of viral replication, and elimination of latent proviral DNA integrated within host genomes.
M. R. Hidayatullah, Salwa Adilah Ningtiyas, Adinda Nezma Meidina et al.
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