A. Zanon - Eurac Research Affiliated Institute, University of Lübeck

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论文共 10 篇作者统计合作学者相似作者

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A Novel Human Ipsc-Based Co-Culture Model to Study Neurocardiac Interaction in Vitro

G. Cattelan,G. Gentile,C. Volani,L. S. Frommelt,A. Lavdas,L. Foco,M. De Bortoli,C. Altomare,L. Barile,S. Zacchigna,P. P. Pramstaller,I. Pichler,A. Zanon,A. Rossini

Biomedical Science and Engineeringno. 1 (2023)

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A Bio-photoelectrolytic Organic Semiconductor Platform for Measurement and Control of Proliferation and Behaviour of Living Cells Using Light Pulses

M. Ciocca, S. Marcozzi, P. Mariani, V. Lacconi, A. Di Carlo,L. Cinà, M. D. Rosato-Siri,A. Zanon, G. Cattelan, E. Avancini,P. Lugli, S. Priya, A. Camaioni,T. M. Brown

2023 IEEE Nanotechnology Materials and Devices Conference (NMDC)pp.527-528, (2023)

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SLP-2 Modulated Expression Rescues Mitochondrial Function in Alpha-Synuclein Neuropathology Models

M. Castelo,G. Gentile,A. Zanon,A. Lavdas, C. Bolduc, M. Picon,S. Laouafa,J. Soliz, M. Levesque,I. Pichler

MOVEMENT DISORDERS (2023): S638-S638

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Set-up of a Novel in Vitro Neurocardiac Cell Model for the In-Depth Study of Heart Disease

G. Cattelan,L. S. Frommelt,M. De Bortoli,K. Mackova,G. Ciucci,S. Zacchigna,P. P. Pramstaller,I Pichler,A. Zanon,A. Rossini

Cardiovascular Research（2022）

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Molecular Investigation Of Apparently Healthy Heterozygous Parkin Mutation Carriers

M. Castelo,A. Zanon, V. Gilmozzi,C. Klein,P. Pramstaller,A. Hicks,I. Pichler

MOVEMENT DISORDERS（2021）

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The role of mitochondria in modifying penetrance of Parkin gene variants

M. Castelo,J. Trinh,A. Zanon,J. Rainer,P. Bauer,K. Kandaswamy,M. Werber,A. Rolfs,A. Grunewald,M. Borsche,K. Lohmann,C. Klein,P. Pramstaller,I. Pichler,A. Hicks

MOVEMENT DISORDERS（2019）

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SLP-2 rescues PINK1 deficiency in a cellular model and in Drosophila

A. Zanon, S. Meschini,S. Kalvakuri,A. A. Lavdas,R. Bodmer,P. P. Pramstaller,A. A. Hicks,I. Pichler

EUROPEAN JOURNAL OF HUMAN GENETICS（2019）

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Parkin interacting proteins are modifiers of drosophila parkin and Pink1 mutant phenotype

A. Zanon,I. Pichler,A. Rakovic,C. Schwienbacher,C. Weichenberger,F. S. Domingues,A. A. Hicks,P. P. Pramstaller,C. Klein

MOVEMENT DISORDERS（2012）

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A rare variant near a potassium channel-related gene in familial restless legs syndrome

I. Pichler,C. Schwienbacher,A. Zanon,C. Fuchsberger, A. Serafin,F. Marroni,M. F. Facheris,C. Tellgren-Roth, U. Gyllensten,J. F. Gusella,A. A. Hicks,P. P. Pramstaller

MOVEMENT DISORDERS（2012）

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Gene ontology enrichment analysis of parkin interactants

A. Zanon,I. Pichler,A. Rakovic,C. Schwienbacher,A. A. Hicks, A. Alexa,F. S. Domingues,C. Klein,P. P. Pramstaller

MOVEMENT DISORDERS（2011）

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