Hannes Steinkellner[Author] - Search Results

Year	Number of Results
2008	1
2009	2
2010	4
2011	3
2014	1
2015	2
2017	1
2019	1
2020	1
2022	2
2024	1

1

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. J Vis Exp. 2020 May 22;(159). doi: 10.3791/61054. J Vis Exp. 2020. PMID: 32510486

2

Expression, Purification, Characterization and Cellular Uptake of MeCP2 Variants.

Beribisky AV, Steinkellner H, Geislberger S, Huber A, Sarne V, Christodoulou J, Laccone F. Beribisky AV, et al. Among authors: steinkellner h. Protein J. 2022 Apr;41(2):345-359. doi: 10.1007/s10930-022-10054-9. Epub 2022 May 12. Protein J. 2022. PMID: 35546650 Free PMC article.

3

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: steinkellner h. 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

4

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. 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

5

An electrochemiluminescence based assay for quantitative detection of endogenous and exogenously applied MeCP2 protein variants.

Steinkellner H, Schönegger A, Etzler J, Kempaiah P, Huber A, Hahn K, Rose K, Duerr M, Christodoulou J, Beribisky AV, Neuhaus W, Laccone F. Steinkellner H, et al. Sci Rep. 2019 May 28;9(1):7929. doi: 10.1038/s41598-019-44372-3. Sci Rep. 2019. PMID: 31138832 Free PMC article.

6

No changes in heme synthesis in human Friedreich´s ataxia erythroid progenitor cells.

Steinkellner H, Singh HN, Muckenthaler MU, Goldenberg H, Moganty RR, Scheiber-Mojdehkar B, Sturm B. Steinkellner H, et al. Gene. 2017 Jul 20;621:5-11. doi: 10.1016/j.gene.2017.04.014. Epub 2017 Apr 12. Gene. 2017. PMID: 28412459

7

Hydrogen sulfide scavenges the cytotoxic lipid oxidation product 4-HNE.

Schreier SM, Muellner MK, Steinkellner H, Hermann M, Esterbauer H, Exner M, Gmeiner BM, Kapiotis S, Laggner H. Schreier SM, et al. Among authors: steinkellner h. Neurotox Res. 2010 Apr;17(3):249-56. doi: 10.1007/s12640-009-9099-9. Epub 2009 Aug 13. Neurotox Res. 2010. PMID: 19680736

8

Detection of survival motor neuron protein in buccal cells through electrochemiluminescence-based assay.

Steinkellner H, Etzler J, Gmeiner BM, Laccone F. Steinkellner H, et al. Assay Drug Dev Technol. 2015 Apr;13(3):167-73. doi: 10.1089/adt.2015.635. Epub 2015 Apr 7. Assay Drug Dev Technol. 2015. PMID: 25848917

9

Effects of erythropoietin on frataxin levels and mitochondrial function in Friedreich ataxia--a dose-response trial.

Nachbauer W, Hering S, Seifert M, Steinkellner H, Sturm B, Scheiber-Mojdehkar B, Reindl M, Strasak A, Poewe W, Weiss G, Boesch S. Nachbauer W, et al. Among authors: steinkellner h. Cerebellum. 2011 Dec;10(4):763-9. doi: 10.1007/s12311-011-0287-9. Cerebellum. 2011. PMID: 21597884 Clinical Trial.

10

Neurological effects of recombinant human erythropoietin in Friedreich's ataxia: a clinical pilot trial.

Boesch S, Sturm B, Hering S, Scheiber-Mojdehkar B, Steinkellner H, Goldenberg H, Poewe W. Boesch S, et al. Among authors: steinkellner h. Mov Disord. 2008 Oct 15;23(13):1940-4. doi: 10.1002/mds.22294. Mov Disord. 2008. PMID: 18759345 Clinical Trial.

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