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pCAG-eCas9-GFP-U6-gRNA Citations (13)

Originally described in: pCAG-SpCas9-U6-gRNA
Unpublished

Articles Citing pCAG-eCas9-GFP-U6-gRNA

Articles
Somatic Depdc5 deletion recapitulates electroclinical features of human focal cortical dysplasia type IIA. Hu S, Knowlton RC, Watson BO, Glanowska KM, Murphy GG, Parent JM, Wang Y. Ann Neurol. 2018 Jul;84(1):140-146. doi: 10.1002/ana.25272. Epub 2018 Aug 6. PubMed
Functional genetic variants can mediate their regulatory effects through alteration of transcription factor binding. Johnston AD, Simoes-Pires CA, Thompson TV, Suzuki M, Greally JM. Nat Commun. 2019 Aug 2;10(1):3472. doi: 10.1038/s41467-019-11412-5. PubMed
High-efficiency genomic editing in Epstein-Barr virus-transformed lymphoblastoid B cells using a single-stranded donor oligonucleotide strategy. Johnston AD, Simoes-Pires CA, Suzuki M, Greally JM. Commun Biol. 2019 Aug 14;2:312. doi: 10.1038/s42003-019-0559-3. eCollection 2019. PubMed
CRISPR/Cas9 mediated generation of human ARID1B heterozygous knockout hESC lines to model Coffin-Siris syndrome. Boerstler T, Wend H, Krumbiegel M, Kavyanifar A, Reis A, Lie DC, Winner B, Turan S. Stem Cell Res. 2020 Jun 29;47:101889. doi: 10.1016/j.scr.2020.101889. PubMed
MiR-646 prevents proliferation and progression of human breast cancer cell lines by suppressing HDAC2 expression. Darvishi N, Rahimi K, Mansouri K, Fathi F, Menbari MN, Mohammadi G, Abdi M. Mol Cell Probes. 2020 Oct;53:101649. doi: 10.1016/j.mcp.2020.101649. Epub 2020 Aug 8. PubMed
Allele-Specific Knockout by CRISPR/Cas to Treat Autosomal Dominant Retinitis Pigmentosa Caused by the G56R Mutation in NR2E3. Diakatou M, Dubois G, Erkilic N, Sanjurjo-Soriano C, Meunier I, Kalatzis V. Int J Mol Sci. 2021 Mar 5;22(5). pii: ijms22052607. doi: 10.3390/ijms22052607. PubMed
Rpsa Signaling Regulates Cortical Neuronal Morphogenesis via Its Ligand, PEDF, and Plasma Membrane Interaction Partner, Itga6. Blazejewski SM, Bennison SA, Ha NT, Liu X, Smith TH, Dougherty KJ, Toyo-Oka K. Cereb Cortex. 2021 Aug 4. pii: 6338536. doi: 10.1093/cercor/bhab242. PubMed
Human Blood Vessel Organoids Penetrate Human Cerebral Organoids and Form a Vessel-Like System. Ahn Y, An JH, Yang HJ, Lee DG, Kim J, Koh H, Park YH, Song BS, Sim BW, Lee HJ, Lee JH, Kim SU. Cells. 2021 Aug 9;10(8). pii: cells10082036. doi: 10.3390/cells10082036. PubMed
Preparation of multiplexed control materials for cancer mutation analysis by genome editing in GM12878 cells. Lin G, Zhang K, Han Y, Peng R, Li J. J Clin Lab Anal. 2022 Jan;36(1):e24139. doi: 10.1002/jcla.24139. Epub 2021 Nov 23. PubMed
SDR enzymes oxidize specific lipidic alkynylcarbinols into cytotoxic protein-reactive species. Demange P, Joly E, Marcoux J, Zanon PRA, Listunov D, Rulliere P, Barthes C, Noirot C, Izquierdo JB, Rozie A, Pradines K, Hee R, de Brito MV, Marcellin M, Serre RF, Bouchez O, Burlet-Schiltz O, Oliveira MCF, Ballereau S, Bernardes-Genisson V, Maraval V, Calsou P, Hacker SM, Genisson Y, Chauvin R, Britton S. Elife. 2022 May 10;11. pii: 73913. doi: 10.7554/eLife.73913. PubMed

Associated Plasmids

Ligand-free mitochondria-localized mutant AR-induced cytotoxicity in spinal bulbar muscular atrophy. Feng X, Cheng XT, Zheng P, Li Y, Hakim J, Zhang SQ, Anderson SM, Linask K, Prestil R, Zou J, Sheng ZH, Blackstone C. Brain. 2023 Jan 5;146(1):278-294. doi: 10.1093/brain/awac269. PubMed
Microhomology-mediated endjoining repair mechanism enables rapid and effective indel generations in stem cells. Yadav N, Thelma BK. J Biosci. 2022;47:72. PubMed
PAXX binding to the NHEJ machinery explains functional redundancy with XLF. Seif-El-Dahan M, Kefala-Stavridi A, Frit P, Hardwick SW, Chirgadze DY, Maia De Oliviera T, Andreani J, Britton S, Barboule N, Bossaert M, Pandurangan AP, Meek K, Blundell TL, Ropars V, Calsou P, Charbonnier JB, Chaplin AK. Sci Adv. 2023 Jun 2;9(22):eadg2834. doi: 10.1126/sciadv.adg2834. Epub 2023 May 31. PubMed

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