Small molecules enhance CRISPR/Cas9-mediated homology-directed genome editing in primary cells
Abstract CRISPR/Cas9 is an efficient customizable nuclease to generate double-strand breaks (DSBs) in the genome. This process results in knockout of the targeted gene or knock-in of a specific DNA fragment at the targeted locus in the genome of various species. However, efficiency of knock-in media...
Guardado en:
Autores principales: | Guoling Li, Xianwei Zhang, Cuili Zhong, Jianxin Mo, Rong Quan, Jie Yang, Dewu Liu, Zicong Li, Huaqiang Yang, Zhenfang Wu |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/1649ef17af0144d78c7d0017adcd1333 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Optimized design parameters for CRISPR Cas9 and Cas12a homology-directed repair
por: Mollie S. Schubert, et al.
Publicado: (2021) -
Mechanism and Applications of CRISPR/Cas-9-Mediated Genome Editing
por: Asmamaw M, et al.
Publicado: (2021) -
Efficient Editing of Malaria Parasite Genome Using the CRISPR/Cas9 System
por: Cui Zhang, et al.
Publicado: (2014) -
Editing of mouse and human immunoglobulin genes by CRISPR-Cas9 system
por: Taek-Chin Cheong, et al.
Publicado: (2016) -
Cas9 immunity creates challenges for CRISPR gene editing therapies
por: Julie M. Crudele, et al.
Publicado: (2018)