Cargando…
Highly efficient and safe genome editing by CRISPR-Cas12a using CRISPR RNA with a ribosyl-2′-O-methylated uridinylate-rich 3′-overhang in mouse zygotes
The CRISPR-Cas12a system has been developed to harness highly specific genome editing in eukaryotic cells. Given the relatively small sizes of Cas12a genes, the system has been suggested to be most applicable to gene therapy using AAV vector delivery. Previously, we reported that a U-rich crRNA enab...
Autores principales: | Ha, Dae-In, Lee, Jeong Mi, Lee, Nan-Ee, Kim, Daesik, Ko, Jeong-Heon, Kim, Yong-Sam |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080787/ https://www.ncbi.nlm.nih.gov/pubmed/33162553 http://dx.doi.org/10.1038/s12276-020-00521-7 |
Ejemplares similares
-
Highly efficient genome editing by CRISPR-Cpf1 using CRISPR RNA with a uridinylate-rich 3′-overhang
por: Bin Moon, Su, et al.
Publicado: (2018) -
CRISPR/Cas9-mediated gene editing in human tripronuclear zygotes
por: Liang, Puping, et al.
Publicado: (2015) -
One-Step Homology Mediated CRISPR-Cas Editing in Zygotes for Generating Genome Edited Cattle
por: Park, Ki-Eun, et al.
Publicado: (2020) -
Efficient CRISPR editing with a hypercompact Cas12f1 and engineered guide RNAs delivered by adeno-associated virus
por: Kim, Do Yon, et al.
Publicado: (2021) -
Chromosome engineering in zygotes with CRISPR/Cas9
por: Boroviak, Katharina, et al.
Publicado: (2016)