Rapid and tunable method to temporally control gene editing based on conditional Cas9 stabilization
CRISPR/Cas9-based genome editing enables specific deletion of target genes. Here, Senturket al. develop an inducible editing system by fusing a conditional destabilization domain to Cas9 and demonstrate temporal control of gene editing in response to a synthetic ligand.
Guardado en:
Autores principales: | Serif Senturk, Nitin H. Shirole, Dawid G. Nowak, Vincenzo Corbo, Debjani Pal, Alexander Vaughan, David A. Tuveson, Lloyd C. Trotman, Justin B. Kinney, Raffaella Sordella |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/12bf0bf4ae954de9832a7c856f71605e |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Numerical optimization of microfluidic vortex shedding for genome editing T cells with Cas9
por: Justin A. Jarrell, et al.
Publicado: (2021) -
Orthogonal Cas9–Cas9 chimeras provide a versatile platform for genome editing
por: Mehmet Fatih Bolukbasi, et al.
Publicado: (2018) -
TALEN outperforms Cas9 in editing heterochromatin target sites
por: Surbhi Jain, et al.
Publicado: (2021) -
Mechanism and Applications of CRISPR/Cas-9-Mediated Genome Editing
por: Asmamaw M, et al.
Publicado: (2021) -
Engineering of CRISPR-Cas12b for human genome editing
por: Jonathan Strecker, et al.
Publicado: (2019)