pCAG-T3-hCasD10A-pA Citations (4)
Originally described in: Efficient generation of genome-modified mice via offset-nicking by CRISPR/Cas system.Fujii W, Onuma A, Sugiura K, Naito K Biochem Biophys Res Commun. 2014 Jan 31. pii: S0006-291X(14)00176-4. doi: 10.1016/j.bbrc.2014.01.141. PubMed Journal
Articles Citing pCAG-T3-hCasD10A-pA
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Generation of mouse model of TGFBI-R124C corneal dystrophy using CRISPR/Cas9-mediated homology-directed repair. Kitamoto K, Taketani Y, Fujii W, Inamochi A, Toyono T, Miyai T, Yamagami S, Kuroda M, Usui T, Ouchi Y. Sci Rep. 2020 Feb 6;10(1):2000. doi: 10.1038/s41598-020-58876-w. PubMed |
Autism-linked mutations of CTTNBP2 reduce social interaction and impair dendritic spine formation via diverse mechanisms. Shih PY, Hsieh BY, Tsai CY, Lo CA, Chen BE, Hsueh YP. Acta Neuropathol Commun. 2020 Nov 9;8(1):185. doi: 10.1186/s40478-020-01053-x. PubMed |
DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion. Silva-Pinheiro P, Pardo-Hernandez C, Reyes A, Tilokani L, Mishra A, Cerutti R, Li S, Rozsivalova DH, Valenzuela S, Dogan SA, Peter B, Fernandez-Silva P, Trifunovic A, Prudent J, Minczuk M, Bindoff L, Macao B, Zeviani M, Falkenberg M, Viscomi C. Nucleic Acids Res. 2021 May 21;49(9):5230-5248. doi: 10.1093/nar/gkab282. PubMed |
Activation of TrkB signaling mitigates cerebellar anomalies caused by Rbm4-Bdnf deficiency. Tsai YY, Shen CL, D D, Tsai CY, Tarn WY. Commun Biol. 2023 Sep 5;6(1):910. doi: 10.1038/s42003-023-05294-z. PubMed |
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