ATP1A1_plasmid_donor_RD Citations (1)
Originally described in: Marker-free coselection for CRISPR-driven genome editing in human cells.Agudelo D, Duringer A, Bozoyan L, Huard CC, Carter S, Loehr J, Synodinou D, Drouin M, Salsman J, Dellaire G, Laganiere J, Doyon Y Nat Methods. 2017 Apr 17. doi: 10.1038/nmeth.4265. PubMed Journal
Articles Citing ATP1A1_plasmid_donor_RD
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TDP1 mutation causing SCAN1 neurodegenerative syndrome hampers the repair of transcriptional DNA double-strand breaks. Geraud M, Cristini A, Salimbeni S, Bery N, Jouffret V, Russo M, Ajello AC, Fernandez Martinez L, Marinello J, Cordelier P, Trouche D, Favre G, Nicolas E, Capranico G, Sordet O. Cell Rep. 2024 May 28;43(5):114214. doi: 10.1016/j.celrep.2024.114214. Epub 2024 May 17. PubMed |
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