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CRISPR-Cas9: a promising tool for gene editing on induced pluripotent stem cells

Recent advances in genome editing with programmable nucleases have opened up new avenues for multiple applications, from basic research to clinical therapy. The ease of use of the technology—and particularly clustered regularly interspaced short palindromic repeats (CRISPR)—will allow us to improve...

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Dades bibliogràfiques
Publicat a:Korean J Intern Med
Autors principals: Kim, Eun Ji, Kang, Ki Ho, Ju, Ji Hyeon
Format: Artigo
Idioma:Inglês
Publicat: The Korean Association of Internal Medicine 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5214730/
https://ncbi.nlm.nih.gov/pubmed/28049282
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3904/kjim.2016.198
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