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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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Pubblicato in:Protein Cell
Autori principali: Ren, Jiangtao, Zhao, Yangbing
Natura: Artigo
Lingua:Inglês
Pubblicazione: Higher Education Press 2017
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Accesso online: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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