Cargando…
CRISPR/Cas9 – Mediated Precise Targeted Integration In Vivo Using a Double Cut Donor with Short Homology Arms
Precisely targeted genome editing is highly desired for clinical applications. However, the widely used homology-directed repair (HDR)-based genome editing strategies remain inefficient for certain in vivo applications. We here demonstrate a microhomology-mediated end-joining (MMEJ)-based strategy f...
Autores principales: | Yao, Xuan, Wang, Xing, Liu, Junlai, Hu, Xinde, Shi, Linyu, Shen, Xiaowen, Ying, Wenqin, Sun, Xinyao, Wang, Xin, Huang, Pengyu, Yang, Hui |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478232/ https://www.ncbi.nlm.nih.gov/pubmed/28527830 http://dx.doi.org/10.1016/j.ebiom.2017.05.015 |
Ejemplares similares
-
Homology-mediated end joining-based targeted integration using CRISPR/Cas9
por: Yao, Xuan, et al.
Publicado: (2017) -
Efficient precise knockin with a double cut HDR donor after CRISPR/Cas9-mediated double-stranded DNA cleavage
por: Zhang, Jian-Ping, et al.
Publicado: (2017) -
CRISPR/Cas9-mediated targeted chromosome elimination
por: Zuo, Erwei, et al.
Publicado: (2017) -
The Convenience of Single Homology Arm Donor DNA
and CRISPR/Cas9-Nickase for Targeted Insertion
of Long DNA Fragment
por: Basiri, Mohsen, et al.
Publicado: (2017) -
Genome Editing With TALEN, CRISPR-Cas9 and CRISPR-Cas12a in Combination With AAV6 Homology Donor Restores T Cell Function for XLP
por: Houghton, Benjamin C., et al.
Publicado: (2022)