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[No title available]
[No authors listed] [No authors listed] PMID: 33563932
TAT-MeCP2 protein variants rescue disease phenotypes in human and mouse models of Rett syndrome.
Steinkellner H, Kempaiah P, Beribisky AV, Pferschy S, Etzler J, Huber A, Sarne V, Neuhaus W, Kuttke M, Bauer J, Arunachalam JP, Christodoulou J, Dressel R, Mildner A, Prinz M, Laccone F. Steinkellner H, et al. Among authors: sarne v. Int J Biol Macromol. 2022 Jun 1;209(Pt A):972-983. doi: 10.1016/j.ijbiomac.2022.04.080. Epub 2022 Apr 20. Int J Biol Macromol. 2022. PMID: 35460749
An Electrochemiluminescence-Based Assay for MeCP2 Protein Variants.
Steinkellner H, Beribisky AV, Mausberg P, Christodoulou J, Scheiber-Mojdehkar B, Huber A, Sarne V, Laccone F. Steinkellner H, et al. Among authors: sarne v. J Vis Exp. 2020 May 22;(159). doi: 10.3791/61054. J Vis Exp. 2020. PMID: 32510486
Generation and Characterization of a Human Neuronal In Vitro Model for Rett Syndrome Using a Direct Reprogramming Method.
Huber A, Sarne V, Beribisky AV, Ackerbauer D, Derdak S, Madritsch S, Etzler J, Huck S, Scholze P, Gorgulu I, Christodoulou J, Studenik CR, Neuhaus W, Connor B, Laccone F, Steinkellner H. Huber A, et al. Among authors: sarne v. Stem Cells Dev. 2024 Mar;33(5-6):128-142. doi: 10.1089/scd.2023.0233. Epub 2024 Feb 22. Stem Cells Dev. 2024. PMID: 38164119
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