Loading...
Overcoming the Undesirable CRISPR-Cas9 Expression in Gene Correction
The CRISPR-Cas9 system is attractive for gene therapy, as it allows for permanent genetic correction. However, as a new technology, Cas9 gene editing in clinical applications faces major challenges, such as safe delivery and gene targeting efficiency. Cas9 is a foreign protein to recipient cells; th...
Na minha lista:
| Udgivet i: | Mol Ther Nucleic Acids |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Society of Gene & Cell Therapy
2018
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6278715/ https://ncbi.nlm.nih.gov/pubmed/30513454 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.omtn.2018.10.015 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|