CRISPR/Cas9-based gene targeting using synthetic guide RNAs enables robust cell biological analyses
A key goal for cell biological analyses is to assess the phenotypes that result from eliminating a target gene. Since the early 1990s, the predominant strategy utilized in human tissue culture cells has been RNA interference (RNAi)-mediated protein depletion. However, RNAi suffers well-documented of...
Main Authors: | Su, Kuan-Chung (Author), Tsang, Mary-Jane (Author), Emans, Neil (Author), Cheeseman, Iain M (Author) |
---|---|
Other Authors: | Massachusetts Institute of Technology. Department of Biology (Contributor) |
Format: | Article |
Language: | English |
Published: |
American Society for Cell Biology (ASCB),
2020-07-10T20:38:30Z.
|
Subjects: | |
Online Access: | Get fulltext |
Similar Items
-
CRISPR/Cas9-deaminase enables robust base editing in Rhodobacter sphaeroides 2.4.1
by: Yufeng Luo, et al.
Published: (2020-04-01) -
CRISPRseek: a bioconductor package to identify target-specific guide RNAs for CRISPR-Cas9 genome-editing systems.
by: Lihua J Zhu, et al.
Published: (2014-01-01) -
CRISPRseek: A Bioconductor Package to Identify Target-Specific Guide RNAs for CRISPR-Cas9 Genome-Editing Systems
by: Zhu, Lihua J., et al.
Published: (2014) -
Suppression of unwanted CRISPR-Cas9 editing by co-administration of catalytically inactivating truncated guide RNAs
by: John C. Rose, et al.
Published: (2020-06-01) -
Synthetically modified guide RNA and donor DNA are a versatile platform for CRISPR-Cas9 engineering
by: Kunwoo Lee, et al.
Published: (2017-05-01)