pEGFP-N1_MeCP2(WT) Citations (2)

Originally described in: Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.
Tillotson R, Selfridge J, Koerner MV, Gadalla KKE, Guy J, De Sousa D, Hector RD, Cobb SR, Bird A Nature. 2017 Oct 19;550(7676):398-401. doi: 10.1038/nature24058. Epub 2017 Oct 11. PubMed Journal

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Articles Citing pEGFP-N1_MeCP2(WT)

Articles
MeCP2 heterochromatin organization is modulated by arginine methylation and serine phosphorylation. Schmidt A, Frei J, Poetsch A, Chittka A, Zhang H, Assmann C, Lehmkuhl A, Bauer UM, Nuber UA, Cardoso MC. Front Cell Dev Biol. 2022 Sep 12;10:941493. doi: 10.3389/fcell.2022.941493. eCollection 2022. PubMed
Systemic Metabolic and Mitochondrial Defects in Rett Syndrome Models. Zlatic SA, Werner E, Surapaneni V, Lee CE, Gokhale A, Singleton K, Duong D, Crocker A, Gentile K, Middleton F, Dalloul JM, Liu WL, Patgiri A, Tarquinio D, Carpenter R, Faundez V. bioRxiv. 2023 May 28:2023.04.03.535431. doi: 10.1101/2023.04.03.535431. Preprint. PubMed

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