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Hannes Steinkellner

Institute of Medical Genetics,
Center for Pathobiochemistry and Genetics,
Institute of Medical Genetics, Center for Pathobiochemistry and Genetics

Medical University of Vienna (MUV)

BIOGRAPHY

Hannes Steinkellner has worked during his PhD thesis on advancement of recombinant human erythropoietin (rHuEPO) as a promising therapy for Friedreich’s ataxia. In this work, he has developed a novel tool for the measurement of frataxin protein levels in human and mouse samples. Additionally he has started collaboration with Dr. Franco Laccone on protein replacement therapy for Friedreich’s ataxia. After finishing his PhD-thesis he has joined the scientific group of Dr. Franco Laccone at the Institute of Medical Genetics headed by Prof. Dr. Markus Hengstschläger where he is still working on the development and investigation of TAT (transactivator of transcription)- fusion proteins for neurodevelopmental and neurodegenerative disorders like RETT syndrome and Spinal Muscular Atrophy. Moreover, he is interested in functional characterization of rare genetic diseases.

PUBLICATIONS

A high throughput electrochemiluminescence assay for the quantification of frataxin protein levels.

Analytica chimica acta Feb, 2010 | Pubmed ID: 20103114

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

Scientific reports 05, 2019 | Pubmed ID: 31138832

INSTITUTIONS

Medical University of Vienna (MUV)

JOVE ARTICLES

An Electrochemiluminescence-Based Assay for MeCP2 Protein Variants

Hannes Steinkellner¹,

Alexander V. Beribisky¹,

Philip Mausberg¹,

John Christodoulou²,

Barbara Scheiber-Mojdehkar³,

Anna Huber¹,

Victoria Sarne¹,

Franco Laccone¹

¹Institute of Medical Genetics, Center for Pathobiochemistry and Genetics, Medical University of Vienna (MUV),

²Murdoch Children's Research Institute and Department of Paediatrics, University of Melbourne, Discipline of Child & Adolescent Health, Sydney Medical School,

³Department of Medical Chemistry and Pathobiochemistry, Medical University of Vienna

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Hannes Steinkellner

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Institute of Medical Genetics,Center for Pathobiochemistry and Genetics,Institute of Medical Genetics, Center for Pathobiochemistry and Genetics

Medical University of Vienna (MUV)

An Electrochemiluminescence-Based Assay for MeCP2 Protein Variants

Institute of Medical Genetics,
Center for Pathobiochemistry and Genetics,
Institute of Medical Genetics, Center for Pathobiochemistry and Genetics