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Gene|April 17, 2017
No changes in heme synthesis in human Friedreich´s ataxia erythroid progenitor cellsHannes Steinkellner, Himanshu Narayan Singh, Martina U Muckenthaler, et al.
Journal of Visualized Experiments : Jove|June 9, 2020
An Electrochemiluminescence-Based Assay for MeCP2 Protein VariantsHannes Steinkellner, Alexander V Beribisky, Philip Mausberg, et al.
Biochimie|February 1, 2011
S-carbamoylation impairs the oxidant scavenging activity of cysteine: its possible impact on increased LDL modification in uraemiaSabine M Schreier, Hannes Steinkellner, Leopold Jirovetz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 22, 2011
Correlation of frataxin content in blood and skeletal muscle endorses frataxin as a biomarker in Friedreich ataxiaWolfgang Nachbauer, Julia Wanschitz, Hannes Steinkellner, et al.
Neurotoxicity Research|August 15, 2009
Hydrogen sulfide scavenges the cytotoxic lipid oxidation product 4-HNESabine M Schreier, Markus K Muellner, Hannes Steinkellner, et al.
Cerebellum (London, England)|May 21, 2011
Effects of erythropoietin on frataxin levels and mitochondrial function in Friedreich ataxia--a dose-response trialWolfgang Nachbauer, Sascha Hering, Markus Seifert, et al.
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.
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.
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