Supramolecular Nanosubstrate-Mediated Delivery for CRISPR/Cas9 Gene Disruption and Deletion

CRISPR/Cas9 is an efficient and precise gene editing technology that offers a versatile solution for establishing treatments directed at genetic diseases. Current CRISPR/Cas9 delivery into cells relies primarily on viral vectors, which suffer from limitations in packaging capacity and safety concern...

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Publicado no:Small
Main Authors: Ban, Qian, Yang, Peng, Chou, Shih-Jie, Qiao, Li, Xia, Haidong, Xue, Jingjing, Wang, Fang, Xu, Xiaobin, Sun, Na, Zhang, Ryan Y., Zhang, Ceng, Lee, Athena, Liu, Wenfei, Lin, Ting-Yi, Ko, Yu-Ling, Antovski, Petar, Zhang, Xinyue, Chiou, Shih-Hwa, Lee, Chin-Fa, Hui, Wenqiao, Liu, Dahai, Jonas, Steven J., Weiss, Paul S., Tseng, Hsian-Rong
Formato: Artigo
Idioma:Inglês
Publicado em: 2021
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8282741/
https://ncbi.nlm.nih.gov/pubmed/34105245
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/smll.202100546
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