Similar articles for PMID: 27280971

Year	Number of Results
2003	1
2007	1
2009	1
2010	2
2011	10
2012	7
2013	5
2014	4
2015	12
2016	27
2017	25
2018	22
2019	19
2020	21
2021	20
2022	16
2023	7
2024	1

1

AAV Vectorization of DSB-mediated Gene Editing Technologies.

Moser RJ, Hirsch ML. Moser RJ, et al. Curr Gene Ther. 2016;16(3):207-19. doi: 10.2174/1566523216666160602213738. Curr Gene Ther. 2016. PMID: 27280971 Review.

2

High levels of AAV vector integration into CRISPR-induced DNA breaks.

Hanlon KS, Kleinstiver BP, Garcia SP, Zaborowski MP, Volak A, Spirig SE, Muller A, Sousa AA, Tsai SQ, Bengtsson NE, Lööv C, Ingelsson M, Chamberlain JS, Corey DP, Aryee MJ, Joung JK, Breakefield XO, Maguire CA, György B. Hanlon KS, et al. Nat Commun. 2019 Sep 30;10(1):4439. doi: 10.1038/s41467-019-12449-2. Nat Commun. 2019. PMID: 31570731 Free PMC article.

3

Combining Engineered Nucleases with Adeno-associated Viral Vectors for Therapeutic Gene Editing.

Epstein BE, Schaffer DV. Epstein BE, et al. Adv Exp Med Biol. 2017;1016:29-42. doi: 10.1007/978-3-319-63904-8_2. Adv Exp Med Biol. 2017. PMID: 29130152 Free PMC article. Review.

4

Versatile and efficient genome editing in human cells by combining zinc-finger nucleases with adeno-associated viral vectors.

Händel EM, Gellhaus K, Khan K, Bednarski C, Cornu TI, Müller-Lerch F, Kotin RM, Heilbronn R, Cathomen T. Händel EM, et al. Hum Gene Ther. 2012 Mar;23(3):321-9. doi: 10.1089/hum.2011.140. Epub 2011 Dec 14. Hum Gene Ther. 2012. PMID: 21980922 Free PMC article.

5

Homologous Recombination-Based Genome Editing by Clade F AAVs Is Inefficient in the Absence of a Targeted DNA Break.

Rogers GL, Chen HY, Morales H, Cannon PM. Rogers GL, et al. Mol Ther. 2019 Oct 2;27(10):1726-1736. doi: 10.1016/j.ymthe.2019.08.019. Epub 2019 Sep 9. Mol Ther. 2019. PMID: 31540849 Free PMC article.

6

CRISPR-Mediated Integration of Large Gene Cassettes Using AAV Donor Vectors.

Bak RO, Porteus MH. Bak RO, et al. Cell Rep. 2017 Jul 18;20(3):750-756. doi: 10.1016/j.celrep.2017.06.064. Cell Rep. 2017. PMID: 28723575 Free PMC article.

7

Delivery and therapeutic applications of gene editing technologies ZFNs, TALENs, and CRISPR/Cas9.

LaFountaine JS, Fathe K, Smyth HD. LaFountaine JS, et al. Int J Pharm. 2015 Oct 15;494(1):180-94. doi: 10.1016/j.ijpharm.2015.08.029. Epub 2015 Aug 13. Int J Pharm. 2015. PMID: 26278489 Review.

8

Adeno-Associated Virus-Mediated Delivery of CRISPR-Cas Systems for Genome Engineering in Mammalian Cells.

Gaj T, Schaffer DV. Gaj T, et al. Cold Spring Harb Protoc. 2016 Nov 1;2016(11):10.1101/pdb.prot086868. doi: 10.1101/pdb.prot086868. Cold Spring Harb Protoc. 2016. PMID: 27803249 Free PMC article.

9

Fishing for understanding: Unlocking the zebrafish gene editor's toolbox.

Simone BW, Martínez-Gálvez G, WareJoncas Z, Ekker SC. Simone BW, et al. Methods. 2018 Nov 1;150:3-10. doi: 10.1016/j.ymeth.2018.07.012. Epub 2018 Aug 2. Methods. 2018. PMID: 30076892 Free PMC article. Review.

10

Self-complementary AAV mediates gene targeting and enhances endonuclease delivery for double-strand break repair.

Hirsch ML, Green L, Porteus MH, Samulski RJ. Hirsch ML, et al. Gene Ther. 2010 Sep;17(9):1175-80. doi: 10.1038/gt.2010.65. Epub 2010 May 13. Gene Ther. 2010. PMID: 20463753 Free PMC article.

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