840 related articles for article (PubMed ID: 32899704)
1. Methods Favoring Homology-Directed Repair Choice in Response to CRISPR/Cas9 Induced-Double Strand Breaks.
Yang H; Ren S; Yu S; Pan H; Li T; Ge S; Zhang J; Xia N
Int J Mol Sci; 2020 Sep; 21(18):. PubMed ID: 32899704
[TBL] [Abstract][Full Text] [Related]
2. Knock-in of large reporter genes in human cells via CRISPR/Cas9-induced homology-dependent and independent DNA repair.
He X; Tan C; Wang F; Wang Y; Zhou R; Cui D; You W; Zhao H; Ren J; Feng B
Nucleic Acids Res; 2016 May; 44(9):e85. PubMed ID: 26850641
[TBL] [Abstract][Full Text] [Related]
3. Precision genome editing in the CRISPR era.
Salsman J; Dellaire G
Biochem Cell Biol; 2017 Apr; 95(2):187-201. PubMed ID: 28177771
[TBL] [Abstract][Full Text] [Related]
4. Versatile and precise gene-targeting strategies for functional studies in mammalian cell lines.
Wassef M; Luscan A; Battistella A; Le Corre S; Li H; Wallace MR; Vidaud M; Margueron R
Methods; 2017 May; 121-122():45-54. PubMed ID: 28499832
[TBL] [Abstract][Full Text] [Related]
5. CRISPR-Cas9 fusion to dominant-negative 53BP1 enhances HDR and inhibits NHEJ specifically at Cas9 target sites.
Jayavaradhan R; Pillis DM; Goodman M; Zhang F; Zhang Y; Andreassen PR; Malik P
Nat Commun; 2019 Jun; 10(1):2866. PubMed ID: 31253785
[TBL] [Abstract][Full Text] [Related]
6. Modulating DNA Repair Pathways to Improve Precision Genome Engineering.
Pawelczak KS; Gavande NS; VanderVere-Carozza PS; Turchi JJ
ACS Chem Biol; 2018 Feb; 13(2):389-396. PubMed ID: 29210569
[TBL] [Abstract][Full Text] [Related]
7. A novel Cas9 fusion protein promotes targeted genome editing with reduced mutational burden in primary human cells.
Carusillo A; Haider S; Schäfer R; Rhiel M; Türk D; Chmielewski KO; Klermund J; Mosti L; Andrieux G; Schäfer R; Cornu TI; Cathomen T; Mussolino C
Nucleic Acids Res; 2023 May; 51(9):4660-4673. PubMed ID: 37070192
[TBL] [Abstract][Full Text] [Related]
8. Genome editing using CRISPR/Cas9-based knock-in approaches in zebrafish.
Albadri S; Del Bene F; Revenu C
Methods; 2017 May; 121-122():77-85. PubMed ID: 28300641
[TBL] [Abstract][Full Text] [Related]
9. Highly efficient CRISPR/HDR-mediated knock-in for mouse embryonic stem cells and zygotes.
Wang B; Li K; Wang A; Reiser M; Saunders T; Lockey RF; Wang JW
Biotechniques; 2015 Oct; 59(4):201-2, 204, 206-8. PubMed ID: 26458548
[TBL] [Abstract][Full Text] [Related]
10. Enhancement of CRISPR-Cas9 induced precise gene editing by targeting histone H2A-K15 ubiquitination.
Bashir S; Dang T; Rossius J; Wolf J; Kühn R
BMC Biotechnol; 2020 Oct; 20(1):57. PubMed ID: 33097066
[TBL] [Abstract][Full Text] [Related]
11. A high-efficiency and versatile CRISPR/Cas9-mediated HDR-based biallelic editing system.
Li X; Sun B; Qian H; Ma J; Paolino M; Zhang Z
J Zhejiang Univ Sci B; 2022 Feb; 23(2):141-152. PubMed ID: 35187887
[TBL] [Abstract][Full Text] [Related]
12. Optimization of genome editing through CRISPR-Cas9 engineering.
Zhang JH; Adikaram P; Pandey M; Genis A; Simonds WF
Bioengineered; 2016 Apr; 7(3):166-74. PubMed ID: 27340770
[TBL] [Abstract][Full Text] [Related]
13. Target residence of Cas9-sgRNA influences DNA double-strand break repair pathway choices in CRISPR/Cas9 genome editing.
Liu SC; Feng YL; Sun XN; Chen RD; Liu Q; Xiao JJ; Zhang JN; Huang ZC; Xiang JF; Chen GQ; Yang Y; Lou C; Li HD; Cai Z; Xu SM; Lin H; Xie AY
Genome Biol; 2022 Aug; 23(1):165. PubMed ID: 35915475
[TBL] [Abstract][Full Text] [Related]
14. Systematic quantification of HDR and NHEJ reveals effects of locus, nuclease, and cell type on genome-editing.
Miyaoka Y; Berman JR; Cooper SB; Mayerl SJ; Chan AH; Zhang B; Karlin-Neumann GA; Conklin BR
Sci Rep; 2016 Mar; 6():23549. PubMed ID: 27030102
[TBL] [Abstract][Full Text] [Related]
15. Increasing CRISPR/Cas9-mediated homology-directed DNA repair by histone deacetylase inhibitors.
Li G; Zhang X; Wang H; Liu D; Li Z; Wu Z; Yang H
Int J Biochem Cell Biol; 2020 Aug; 125():105790. PubMed ID: 32534122
[TBL] [Abstract][Full Text] [Related]
16. Proximal binding of dCas9 at a DNA double strand break stimulates homology-directed repair as a local inhibitor of classical non-homologous end joining.
Feng YL; Liu SC; Chen RD; Sun XN; Xiao JJ; Xiang JF; Xie AY
Nucleic Acids Res; 2023 Apr; 51(6):2740-2758. PubMed ID: 36864759
[TBL] [Abstract][Full Text] [Related]
17. DNA Repair Pathway Choices in CRISPR-Cas9-Mediated Genome Editing.
Xue C; Greene EC
Trends Genet; 2021 Jul; 37(7):639-656. PubMed ID: 33896583
[TBL] [Abstract][Full Text] [Related]
18. Generation of genetically modified rat models via the CRISPR/Cas9 technology.
Liu MZ; Wang LR; Li YM; Ma XY; Han HH; Li DL
Yi Chuan; 2023 Jan; 45(1):78-87. PubMed ID: 36927640
[TBL] [Abstract][Full Text] [Related]
19. Target binding and residence: a new determinant of DNA double-strand break repair pathway choice in CRISPR/Cas9 genome editing.
Feng Y; Liu S; Chen R; Xie A
J Zhejiang Univ Sci B; 2021 Jan; 22(1):73-86. PubMed ID: 33448189
[TBL] [Abstract][Full Text] [Related]
20. Gene Disruption Using CRISPR-Cas9 Technology.
Hu N; Malek SN
Methods Mol Biol; 2019; 1881():201-209. PubMed ID: 30350208
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
