pCMV-T7-ABEmax(7.10)-SpCas9-NG-P2A-EGFP (RTW4564) Citations (3)

Originally described in: Unconstrained genome targeting with near-PAMless engineered CRISPR-Cas9 variants.
Walton RT, Christie KA, Whittaker MN, Kleinstiver BP Science. 2020 Apr 17;368(6488):290-296. doi: 10.1126/science.aba8853. Epub 2020 Mar 26. PubMed Journal

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Articles Citing pCMV-T7-ABEmax(7.10)-SpCas9-NG-P2A-EGFP (RTW4564)

Articles
Base Editing in Human Cells to Produce Single-Nucleotide-Variant Clonal Cell Lines. Vasquez CA, Cowan QT, Komor AC. Curr Protoc Mol Biol. 2020 Dec;133(1):e129. doi: 10.1002/cpmb.129. PubMed
Functional restoration of a CFTR splicing mutation through RNA delivery of CRISPR adenine base editor. Amistadi S, Maule G, Ciciani M, Ensinck MM, De Keersmaecker L, Ramalho AS, Guidone D, Buccirossi M, Galietta LJV, Carlon MS, Cereseto A. Mol Ther. 2023 Jun 7;31(6):1647-1660. doi: 10.1016/j.ymthe.2023.03.004. Epub 2023 Mar 9. PubMed
Functional EPAS1/HIF2A missense variant is associated with hematocrit in Andean highlanders. Lawrence ES, Gu W, Bohlender RJ, Anza-Ramirez C, Cole AM, Yu JJ, Hu H, Heinrich EC, O'Brien KA, Vasquez CA, Cowan QT, Bruck PT, Mercader K, Alotaibi M, Long T, Hall JE, Moya EA, Bauk MA, Reeves JJ, Kong MC, Salem RM, Vizcardo-Galindo G, Macarlupu JL, Figueroa-Mujica R, Bermudez D, Corante N, Gaio E, Fox KP, Salomaa V, Havulinna AS, Murray AJ, Malhotra A, Powel FL, Jain M, Komor AC, Cavalleri GL, Huff CD, Villafuerte FC, Simonson TS. Sci Adv. 2024 Feb 9;10(6):eadj5661. doi: 10.1126/sciadv.adj5661. Epub 2024 Feb 9. PubMed

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