Similar articles

• Cas9-nickase-mediated genome editing corrects hereditary tyrosinemia in rats.

  Shao Y, Wang L, Guo N, Wang S, Yang L, Li Y, Wang M, Yin S, Han H, Zeng L, Zhang L, Hui L, Ding Q, Zhang J, Geng H, Liu M, Li D. Shao Y, et al. J Biol Chem. 2018 May 4;293(18):6883-6892. doi: 10.1074/jbc.RA117.000347. Epub 2018 Mar 5. J Biol Chem. 2018. PMID: 29507093 Free PMC article.
• Precise genome-wide base editing by the CRISPR Nickase system in yeast.

  Satomura A, Nishioka R, Mori H, Sato K, Kuroda K, Ueda M. Satomura A, et al. Sci Rep. 2017 May 18;7(1):2095. doi: 10.1038/s41598-017-02013-7. Sci Rep. 2017. PMID: 28522803 Free PMC article.
• Efficient genome editing by FACS enrichment of paired D10A Cas9 nickases coupled with fluorescent proteins.

  Gopalappa R, Song M, Chandrasekaran AP, Das S, Haq S, Koh HC, Ramakrishna S. Gopalappa R, et al. Arch Pharm Res. 2018 Sep;41(9):911-920. doi: 10.1007/s12272-018-1042-2. Epub 2018 May 31. Arch Pharm Res. 2018. PMID: 29855892
• Genome editing for inborn errors of metabolism: advancing towards the clinic.

  Schneller JL, Lee CM, Bao G, Venditti CP. Schneller JL, et al. BMC Med. 2017 Feb 27;15(1):43. doi: 10.1186/s12916-017-0798-4. BMC Med. 2017. PMID: 28238287 Free PMC article. Review.
• Applications of CRISPR/Cas9 for Gene Editing in Hereditary Movement Disorders.

  Im W, Moon J, Kim M. Im W, et al. J Mov Disord. 2016 Sep;9(3):136-43. doi: 10.14802/jmd.16029. Epub 2016 Sep 21. J Mov Disord. 2016. PMID: 27667185 Free PMC article. Review.