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Items: 1 to 20 of 92

1.

Correction: 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.

J Biol Chem. 2019 May 24;294(21):8348. doi: 10.1074/jbc.AAC119.009120. No abstract available.

2.

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.

J Biol Chem. 2018 May 4;293(18):6883-6892. doi: 10.1074/jbc.RA117.000347. Epub 2018 Mar 5. Erratum in: J Biol Chem. 2019 May 24;294(21):8348.

3.

Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype.

Yin H, Xue W, Chen S, Bogorad RL, Benedetti E, Grompe M, Koteliansky V, Sharp PA, Jacks T, Anderson DG.

Nat Biotechnol. 2014 Jun;32(6):551-3. doi: 10.1038/nbt.2884. Epub 2014 Mar 30. Erratum in: Nat Biotechnol. 2014 Sep;32(9):952.

4.

Precise genome-wide base editing by the CRISPR Nickase system in yeast.

Satomura A, Nishioka R, Mori H, Sato K, Kuroda K, Ueda M.

Sci Rep. 2017 May 18;7(1):2095. doi: 10.1038/s41598-017-02013-7. Erratum in: Sci Rep. 2017 Sep 27;7(1):12354.

5.

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.

Arch Pharm Res. 2018 Sep;41(9):911-920. doi: 10.1007/s12272-018-1042-2. Epub 2018 May 31.

PMID:
29855892
6.

Suppression of HBV replication by the expression of nickase- and nuclease dead-Cas9.

Kurihara T, Fukuhara T, Ono C, Yamamoto S, Uemura K, Okamoto T, Sugiyama M, Motooka D, Nakamura S, Ikawa M, Mizokami M, Maehara Y, Matsuura Y.

Sci Rep. 2017 Jul 21;7(1):6122. doi: 10.1038/s41598-017-05905-w.

7.

Development of an Efficient Genome Editing Tool in Bacillus licheniformis Using CRISPR-Cas9 Nickase.

Li K, Cai D, Wang Z, He Z, Chen S.

Appl Environ Microbiol. 2018 Mar 1;84(6). pii: e02608-17. doi: 10.1128/AEM.02608-17. Print 2018 Mar 15.

8.

Detailed phenotypic and molecular analyses of genetically modified mice generated by CRISPR-Cas9-mediated editing.

Parikh BA, Beckman DL, Patel SJ, White JM, Yokoyama WM.

PLoS One. 2015 Jan 14;10(1):e0116484. doi: 10.1371/journal.pone.0116484. eCollection 2015.

9.

CRISPR-Cas9D10A Nickase-Assisted Genome Editing in Lactobacillus casei.

Song X, Huang H, Xiong Z, Ai L, Yang S.

Appl Environ Microbiol. 2017 Oct 31;83(22). pii: e01259-17. doi: 10.1128/AEM.01259-17. Print 2017 Nov 15. Erratum in: Appl Environ Microbiol. 2018 Mar 1;84(6):.

10.

Performance of the Cas9 nickase system in Drosophila melanogaster.

Ren X, Yang Z, Mao D, Chang Z, Qiao HH, Wang X, Sun J, Hu Q, Cui Y, Liu LP, Ji JY, Xu J, Ni JQ.

G3 (Bethesda). 2014 Aug 15;4(10):1955-62. doi: 10.1534/g3.114.013821.

11.

Curative Ex Vivo Hepatocyte-Directed Gene Editing in a Mouse Model of Hereditary Tyrosinemia Type 1.

VanLith C, Guthman R, Nicolas CT, Allen K, Du Z, Joo DJ, Nyberg SL, Lillegard JB, Hickey RD.

Hum Gene Ther. 2018 Nov;29(11):1315-1326. doi: 10.1089/hum.2017.252. Epub 2018 Jun 22.

PMID:
29764210
12.

Genome editing for inborn errors of metabolism: advancing towards the clinic.

Schneller JL, Lee CM, Bao G, Venditti CP.

BMC Med. 2017 Feb 27;15(1):43. doi: 10.1186/s12916-017-0798-4. Review.

13.

Myostatin gene knockout mediated by Cas9-D10A nickase in chicken DF1 cells without off-target effect.

Lee JH, Kim SW, Park TS.

Asian-Australas J Anim Sci. 2017 May;30(5):743-748. doi: 10.5713/ajas.16.0695. Epub 2016 Oct 19.

14.

Efficient Genome Editing in Clostridium cellulolyticum via CRISPR-Cas9 Nickase.

Xu T, Li Y, Shi Z, Hemme CL, Li Y, Zhu Y, Van Nostrand JD, He Z, Zhou J.

Appl Environ Microbiol. 2015 Jul;81(13):4423-31. doi: 10.1128/AEM.00873-15. Epub 2015 Apr 24.

15.

All-in-one adeno-associated virus delivery and genome editing by Neisseria meningitidis Cas9 in vivo.

Ibraheim R, Song CQ, Mir A, Amrani N, Xue W, Sontheimer EJ.

Genome Biol. 2018 Sep 19;19(1):137. doi: 10.1186/s13059-018-1515-0.

16.

Highly multiplexed CRISPR-Cas9-nuclease and Cas9-nickase vectors for inactivation of hepatitis B virus.

Sakuma T, Masaki K, Abe-Chayama H, Mochida K, Yamamoto T, Chayama K.

Genes Cells. 2016 Nov;21(11):1253-1262. doi: 10.1111/gtc.12437. Epub 2016 Sep 23.

17.
18.

CRISPR/Cas9-Mediated Genome Editing Corrects Dystrophin Mutation in Skeletal Muscle Stem Cells in a Mouse Model of Muscle Dystrophy.

Zhu P, Wu F, Mosenson J, Zhang H, He TC, Wu WS.

Mol Ther Nucleic Acids. 2017 Jun 16;7:31-41. doi: 10.1016/j.omtn.2017.02.007. Epub 2017 Feb 28.

19.

Optimizing genome editing strategy by primer-extension-mediated sequencing.

Yin J, Liu M, Liu Y, Wu J, Gan T, Zhang W, Li Y, Zhou Y, Hu J.

Cell Discov. 2019 Mar 26;5:18. doi: 10.1038/s41421-019-0088-8. eCollection 2019.

20.

CRISPR-Cas9D10A nickase-assisted base editing in the solvent producer Clostridium beijerinckii.

Li Q, Seys FM, Minton NP, Yang J, Jiang Y, Jiang W, Yang S.

Biotechnol Bioeng. 2019 Jun;116(6):1475-1483. doi: 10.1002/bit.26949. Epub 2019 Feb 21.

PMID:
30739328

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