Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview
Nadia Rouatbi, Tasneem McGlynn, Khuloud T. Al‐Jamal
Abstract
Non-viral delivery technologies for efficient in vivo Clustered Regulatory Interspaced Short Palindromic Repeats (CRISPR/Cas9) gene editing.
Topics & Concepts
CRISPRGenome editingComputational biologyBiologyGeneIn vivoCas9VirologyGeneticsCRISPR and Genetic EngineeringVirus-based gene therapy researchViral Infectious Diseases and Gene Expression in Insects