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Scientific Reports|May 30, 2019
An electrochemiluminescence based assay for quantitative detection of endogenous and exogenously applied MeCP2 protein variantsHannes Steinkellner, Anna Schönegger, Julia Etzler, et al.Orphanet Journal of Rare Diseases|March 13, 2024
Tracheal agenesis versus tracheal atresia: anatomical conditions, pathomechanisms and causes with a possible link to a novel MAPK11 variant in one caseMateja Pfeifer, Helga Rehder, Maria Gerykova Bujalkova, et al.International Journal of Biological Macromolecules|April 23, 2022
TAT-MeCP2 protein variants rescue disease phenotypes in human and mouse models of Rett syndromeHannes Steinkellner, Prakasha Kempaiah, Alexander V Beribisky, et al.Stem Cells and Development|January 2, 2024
Generation and Characterization of a Human Neuronal In Vitro Model for Rett Syndrome Using a Direct Reprogramming MethodAnna Huber, Victoria Sarne, Alexander V Beribisky, et al.Pageof 2