Cargando…
Enriching CRISPR-Cas9 targeted cells by co-targeting the HPRT gene
The CRISPR-Cas9 system uses guide RNAs to direct the Cas9 endonuclease to cleave target sequences. It can, in theory, target essentially any sequence in a genome, but the efficiency of the predicted guide RNAs varies dramatically. If no targeted cells are obtained, it is also difficult to know why t...
Autores principales: | Liao, Shuren, Tammaro, Margaret, Yan, Hong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787791/ https://www.ncbi.nlm.nih.gov/pubmed/26130722 http://dx.doi.org/10.1093/nar/gkv675 |
Ejemplares similares
-
An easy and efficient inducible CRISPR/Cas9 platform with improved specificity for multiple gene targeting
por: Cao, Jian, et al.
Publicado: (2016) -
Targeting non-coding RNAs with the CRISPR/Cas9 system in human cell lines
por: Ho, Tsui-Ting, et al.
Publicado: (2015) -
On-target activity predictions enable improved CRISPR–dCas9 screens in bacteria
por: Calvo-Villamañán, Alicia, et al.
Publicado: (2020) -
Demonstration of CRISPR/Cas9/sgRNA-mediated targeted gene modification in Arabidopsis, tobacco, sorghum and rice
por: Jiang, Wenzhi, et al.
Publicado: (2013) -
Comparison of TALE designer transcription factors and the CRISPR/dCas9 in regulation of gene expression by targeting enhancers
por: Gao, Xuefei, et al.
Publicado: (2014)