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Advancing chimeric antigen receptor T cell therapy with CRISPR/Cas9
The clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated 9 (CRISPR/Cas9) system, an RNA-guided DNA targeting technology, is triggering a revolution in the field of biology. CRISPR/Cas9 has demonstrated great potential for genetic manipulation. In this review, we discu...
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| Veröffentlicht in: | Protein Cell |
|---|---|
| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Higher Education Press
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5563282/ https://ncbi.nlm.nih.gov/pubmed/28434148 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13238-017-0410-x |
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