CRISPR-Cas9 for in vivo Gene Therapy: Promise and Hurdles

Owing to its easy-to-use and multiplexing nature, the genome editing tool CRISPR-Cas9 (clustered regularly interspaced short palindromic repeats (CRISPR) associated nuclease 9) is revolutionizing many areas of medical research and one of the most amazing areas is its gene therapy potentials. Previou...

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Detalles Bibliográficos
Autores principales: Dai, Wei-Jing, Zhu, Li-Yao, Yan, Zhong-Yi, Xu, Yong, Wang, Qi-Long, Lu, Xiao-Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Commentary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023403/
https://www.ncbi.nlm.nih.gov/pubmed/28131272
http://dx.doi.org/10.1038/mtna.2016.58

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023403/
https://www.ncbi.nlm.nih.gov/pubmed/28131272
http://dx.doi.org/10.1038/mtna.2016.58

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