# Delivery strategies of the CRISPR‐Cas9 gene‐editing system for therapeutic applications

> The molecular mechanism and different strategies to edit genes using the CRISPR‐Cas9 system are introduced and the current systems that have been developed to deliver CRISpr‐ Cas9 in vitro and in vivo for various therapeutic purposes are highlighted.

## Metadata
- Authors: Chang Liu, Li Zhang, Hao Liu, K. Cheng
- Journal: Journal of Controlled Release
- Published: 2017
- DOI: https://doi.org/10.1016/j.jconrel.2017.09.012
- Citations: 485
- Source: Semantic Scholar
- Access: Open Access

## Technology Hub
- Hub: CRISPR Gene Editing
- Discipline: Biology / Genetics
- Hub URL: https://science-database.com/technology/crispr
- Hub llms.txt: https://science-database.com/technology/crispr/llms.txt

## Links
- DOI: https://doi.org/10.1016/j.jconrel.2017.09.012
- Semantic Scholar: https://www.semanticscholar.org/paper/5ee44d9fa67f9d3bd423067ca9f01ac4bb4e43c1
- PDF: https://europepmc.org/articles/pmc5723556?pdf=render
- JSON API: https://science-database.com/api/v1/technology/crispr

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Paper ID: s2-5ee44d9fa67f9d3bd423067ca9f01ac4bb4e43c1 | Hub: crispr