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The potential of CRISPR/Cas9 genome editing for the study and treatment of intervertebral disc pathologies
The CRISPR/Cas9 system has emerged as a powerful tool for mammalian genome engineering. In basic and translational intervertebral disc (IVD) research, this technique has remarkable potential to answer fundamental questions on pathway interactions, to simulate IVD pathologies, and to promote drug dev...
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| Udgivet i: | JOR Spine |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
John Wiley & Sons, Inc.
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6686831/ https://ncbi.nlm.nih.gov/pubmed/31463435 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jsp2.1003 |
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