Efficient and specific generation of knockout mice using Campylobacter jejuni CRISPR/Cas9 system

[1]  H. Nakauchi,et al.  Intra-embryo Gene Cassette Knockin by CRISPR/Cas9-Mediated Genome Editing with Adeno-Associated Viral Vector , 2018, iScience.

[2]  Han-Woong Lee,et al.  Multiple sgRNAs with overlapping sequences enhance CRISPR/Cas9-mediated knock-in efficiency , 2018, Experimental & Molecular Medicine.

[3]  K. Sugiura,et al.  Efficient Generation of Genome-Modified Mice Using Campylobacter jejuni-Derived CRISPR/Cas , 2017, International journal of molecular sciences.

[4]  Hui Yang,et al.  One-step generation of complete gene knockout mice and monkeys by CRISPR/Cas9-mediated gene editing with multiple sgRNAs , 2017, Cell Research.

[5]  Takanori Nakane,et al.  Crystal Structure of the Minimal Cas9 from Campylobacter jejuni Reveals the Molecular Diversity in the CRISPR-Cas9 Systems. , 2017, Molecular cell.

[6]  Eunji Kim,et al.  In vivo genome editing with a small Cas9 orthologue derived from Campylobacter jejuni , 2017, Nature Communications.

[7]  T. Takemoto,et al.  Electroporation enables the efficient mRNA delivery into the mouse zygotes and facilitates CRISPR/Cas9-based genome editing , 2015, Scientific Reports.

[8]  I. Connerton,et al.  Campylobacter jejuni acquire new host-derived CRISPR spacers when in association with bacteriophages harboring a CRISPR-like Cas4 protein , 2015, Front. Microbiol..

[9]  Kira S. Makarova,et al.  Phylogeny of Cas9 determines functional exchangeability of dual-RNA and Cas9 among orthologous type II CRISPR-Cas systems , 2013, Nucleic acids research.