These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. TraFo-CRISPR: Enhanced Genome Engineering by Transient Foamy Virus Vector-Mediated Delivery of CRISPR/Cas9 Components. Lindel F; Dodt CR; Weidner N; Noll M; Bergemann F; Behrendt R; Fischer S; Dietrich J; Cartellieri M; Hamann MV; Lindemann D Mol Ther Nucleic Acids; 2019 Dec; 18():708-726. PubMed ID: 31726388 [TBL] [Abstract][Full Text] [Related]
7. Unbiased detection of off-target cleavage by CRISPR-Cas9 and TALENs using integrase-defective lentiviral vectors. Wang X; Wang Y; Wu X; Wang J; Wang Y; Qiu Z; Chang T; Huang H; Lin RJ; Yee JK Nat Biotechnol; 2015 Feb; 33(2):175-8. PubMed ID: 25599175 [TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 29764210 [TBL] [Abstract][Full Text] [Related]
10. Savić N; Ringnalda FC; Berk C; Bargsten K; Hall J; Jinek M; Schwank G Bio Protoc; 2019 Jan; 9(1):. PubMed ID: 30675496 [TBL] [Abstract][Full Text] [Related]
11. Driving DNA transposition by lentiviral protein transduction. Cai Y; Mikkelsen JG Mob Genet Elements; 2014; 4():e29591. PubMed ID: 25057443 [TBL] [Abstract][Full Text] [Related]
12. Transient Expression of Green Fluorescent Protein in Integrase-Defective Lentiviral Vector-Transduced 293T Cell Line. Nordin F; Hamid ZA; Chan L; Farzaneh F; Hamid MK Methods Mol Biol; 2016; 1448():159-73. PubMed ID: 27317180 [TBL] [Abstract][Full Text] [Related]
13. Choice of template delivery mitigates the genotoxic risk and adverse impact of editing in human hematopoietic stem cells. Ferrari S; Jacob A; Cesana D; Laugel M; Beretta S; Varesi A; Unali G; Conti A; Canarutto D; Albano L; Calabria A; Vavassori V; Cipriani C; Castiello MC; Esposito S; Brombin C; Cugnata F; Adjali O; Ayuso E; Merelli I; Villa A; Di Micco R; Kajaste-Rudnitski A; Montini E; Penaud-Budloo M; Naldini L Cell Stem Cell; 2022 Oct; 29(10):1428-1444.e9. PubMed ID: 36206730 [TBL] [Abstract][Full Text] [Related]
14. DNA transposition by protein transduction of the piggyBac transposase from lentiviral Gag precursors. Cai Y; Bak RO; Krogh LB; Staunstrup NH; Moldt B; Corydon TJ; Schrøder LD; Mikkelsen JG Nucleic Acids Res; 2014 Feb; 42(4):e28. PubMed ID: 24270790 [TBL] [Abstract][Full Text] [Related]
15. Detection of CRISPR/Cas9-Generated Off-Target Effect by Integration-Defective Lentiviral Vector. Wang X; Wu Y; Yee JK Methods Mol Biol; 2021; 2162():243-260. PubMed ID: 32926387 [TBL] [Abstract][Full Text] [Related]
16. Gene Therapy with CRISPR/Cas9 Coming to Age for HIV Cure. Soriano V AIDS Rev; 2017; 19(3):167-172. PubMed ID: 29019352 [TBL] [Abstract][Full Text] [Related]
17. Targeted Gene Insertion and Replacement in the Basidiomycete Ganoderma lucidum by Inactivation of Nonhomologous End Joining Using CRISPR/Cas9. Tu JL; Bai XY; Xu YL; Li N; Xu JW Appl Environ Microbiol; 2021 Nov; 87(23):e0151021. PubMed ID: 34524900 [TBL] [Abstract][Full Text] [Related]
18. Controlling Ratios of Plasmid-Based Double Cut Donor and CRISPR/Cas9 Components to Enhance Targeted Integration of Transgenes in Chinese Hamster Ovary Cells. Shin SW; Kim D; Lee JS Int J Mol Sci; 2021 Feb; 22(5):. PubMed ID: 33673701 [TBL] [Abstract][Full Text] [Related]
19. A Cas9-transcription factor fusion protein enhances homology-directed repair efficiency. Li G; Wang H; Zhang X; Wu Z; Yang H J Biol Chem; 2021; 296():100525. PubMed ID: 33689695 [TBL] [Abstract][Full Text] [Related]
20. Scaffold-mediated non-viral delivery platform for CRISPR/Cas9-based genome editing. Chin JS; Chooi WH; Wang H; Ong W; Leong KW; Chew SY Acta Biomater; 2019 May; 90():60-70. PubMed ID: 30978509 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]