A. Voigt

发表

Drosophila as a screening tool to study human neurodegenerative diseases

Jörg B Schulz, Peter Karsten, J. Schulz, 2013, Journal of neurochemistry.

Quantitative Interaction Proteomics of Neurodegenerative Disease Proteins

Matthias Heinig, Lars Lannfelt, Martin Ingelsson, 2015, Cell reports.

Knockdown of transactive response DNA‐binding protein (TDP‐43) downregulates histone deacetylase 6

Tobias M. Rasse, V. Baekelandt, M. Bonin, 2010, The EMBO journal.

Posthypoxic behavioral impairment and mortality of Drosophila melanogaster are associated with high temperatures, enhanced predeath activity and oxidative stress

J. Schulz, A. Voigt, Jennifer Jung, 2021, Experimental & Molecular Medicine.

Quantification of Protein Aggregates Using Bimolecular Fluorescence Complementation.

A. Voigt, Vibha Prasad, 2018, Methods in molecular biology.

Increased Post-Hypoxic Oxidative Stress and Activation of the PERK Branch of the UPR in Trap1-Deficient Drosophila melanogaster Is Abrogated by Metformin

A. Voigt, Jennifer Jung, P. Habib, 2021, International journal of molecular sciences.

The mitochondrial kinase PINK1: functions beyond mitophagy

A. Voigt, K. Winklhofer, Lena A. Berlemann, 2016, Journal of neurochemistry.

Nuclear import factor transportin and arginine methyltransferase 1 modify FUS neurotoxicity in Drosophila

Tobias M. Rasse, J. Schulz, X. Pan, 2015, Neurobiology of Disease.

Standardized hypoxia-reoxygenation protocol to assess posthypoxic neurobehavioral impairments and molecular mechanisms in Drosophila melanogaster

A. Voigt, Jennifer Jung, P. Habib, 2022, STAR protocols.

Analysis of pre-symptomatic Drosophila models for ALS and SMA reveals convergent impact on functional protein complexes linked to neuro-muscular degeneration

Francisco R. Pinto, A. Voigt, B. Flix, 2022, bioRxiv.

An engineered monomer binding-protein for α-synuclein efficiently inhibits the proliferation of amyloid fibrils

Alexander K. Buell, C. Dobson, A. Voigt, 2019, bioRxiv.

Regulation of the collagen IV network by the basement membrane protein perlecan is crucial for squamous epithelial cell morphogenesis and organ architecture.

A. Voigt, P. Thérond, S. Pisano, 2022, Matrix biology : journal of the International Society for Matrix Biology.

TRAP1 rescues PINK1 loss-of-function phenotypes.

A. Whitworth, J. Schulz, C. Haass, 2013, Human molecular genetics.

Targeted Ablation of Oligodendrocytes Triggers Axonal Damage

J. Schulz, M. Simons, Aniket Ghosh, 2011, PloS one.

Large-Scale Screen for Modifiers of Ataxin-3-Derived Polyglutamine-Induced Toxicity in Drosophila

J. Schulz, B. Adryan, M. Simons, 2012, PloS one.

Linking amyotrophic lateral sclerosis and spinal muscular atrophy through RNA‐transcriptome homeostasis: a genomics perspective

J. Schulz, J. Weis, A. Voigt, 2017, Journal of neurochemistry.

TDP-43-Mediated Neuron Loss In Vivo Requires RNA-Binding Activity

J. Schulz, T. Marquardt, Peter Karsten, 2010, PloS one.

BAG1 modulates huntingtin toxicity, aggregation, degradation, and subcellular distribution

J. Schulz, John Calvin Reed, M. Bähr, 2009, Journal of neurochemistry.

α-Synuclein enhances histone H3 lysine-9 dimethylation and H3K9me2-dependent transcriptional responses

A. Voigt, N. Sugeno, P. Kahle, 2016, Scientific Reports.

Perlecan participates in proliferation activation of quiescent Drosophila neuroblasts

H. Jäckle, A. Voigt, R. Pflanz, 2002, Developmental dynamics : an official publication of the American Association of Anatomists.

A Global In Vivo Drosophila RNAi Screen Identifies a Key Role of Ceramide Phosphoethanolamine for Glial Ensheathment of Axons

Bart R. H. Geurten, M. Göpfert, A. Shevchenko, 2013, PLoS genetics.

Impaired retrograde transport by the Dynein/Dynactin complex contributes to Tau-induced toxicity.

Tobias M. Rasse, J. Schulz, S. Lenz, 2015, Human molecular genetics.

Rab7 induces clearance of α‐synuclein aggregates

J. Schulz, A. Voigt, K. Marcus, 2016, Journal of neurochemistry.

Drosophila tao Controls Mushroom Body Development and Ethanol-Stimulated Behavior through par-1

H. Jäckle, U. Heberlein, Ian King, 2011, The Journal of Neuroscience.

Human TRMT2A methylates different components of the translation machinery and contributes to translation fidelity

T. Carell, H. Urlaub, R. Janowski, 2022 .

CDK5 protects from caspase‐induced Ataxin‐3 cleavage and neurodegeneration

J. Schulz, A. Karch, M. Bähr, 2014, Journal of neurochemistry.

Spinocerebellar ataxia type 3 (SCA3), also known as Machado–Joseph disease, is the most common dominantly inherited cerebellar ataxia caused by an abnormal expansion of the polyglutamine stretch in the protein Ataxin-3 (Schols

J. Schulz, A. Karch, M. Bähr, 2014 .

CK1BP Reduces α-Synuclein Oligomerization and Aggregation Independent of Serine 129 Phosphorylation

A. Voigt, P. Habib, P. Ziegler, 2021, Cells.

Monitoring α‐synuclein multimerization in vivo

I. Katona, J. Schulz, A. Goswami, 2018, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Metabolic activation and toxicological evaluation of polychlorinated biphenyls in Drosophila melanogaster

N. Quinete, T. Schettgen, T. Kraus, 2020, Scientific Reports.

Pre‐fibrillar α‐synuclein variants with impaired β‐structure increase neurotoxicity in Parkinson's disease models

H. Jäckle, S. Kügler, G. Braus, 2009, The EMBO journal.

Drosophila melanogaster as a versatile model organism to study genetic epilepsies: An overview

H. Koch, Y. Weber, A. Voigt, 2023, Frontiers in Molecular Neuroscience.

Cellular and molecular modifier pathways in tauopathies: the big picture from screening invertebrate models

Tobias M. Rasse, T. Jahn, A. Voigt, 2016, Journal of neurochemistry.

Drosophila melanogaster as a model organism for Alzheimer’s disease

J. Schulz, A. Voigt, Katja Prüßing, 2013, Molecular Neurodegeneration.

Drosophila gene tao-1 encodes proteins with and without a Ste20 kinase domain that affect cytoskeletal architecture and cell migration differently

H. Jäckle, A. Voigt, R. Pflanz, 2015, Open Biology.

The Evolutionary Conserved Transmembrane BAX Inhibitor Motif (TMBIM) Containing Protein Family is Essential for the Development and Survival of Drosophila Melanogaster

A. Voigt, A. Methner, Li Zhang, 2020 .

UBE2E Ubiquitin-conjugating Enzymes and Ubiquitin Isopeptidase Y Regulate TDP-43 Protein Ubiquitination*

Tobias M. Rasse, J. Schulz, A. Voigt, 2014, The Journal of Biological Chemistry.

Fas/CD95 Regulatory Protein Faim2 Is Neuroprotective after Transient Brain Ischemia

M. Endres, J. Schulz, K. Nave, 2011, The Journal of Neuroscience.

Dopamine-dependent neurodegeneration in Drosophila models of familial and sporadic Parkinson's disease

A. Voigt, J. A. Botella, S. Schneuwly, 2010, Neurobiology of Disease.

Small-molecule modulators of TRMT2A decrease PolyQ aggregation and PolyQ-induced cell death

J. Schulz, J. Metz, T. Carell, 2021, bioRxiv.

The Mitochondrial Chaperone Protein TRAP1 Mitigates α-Synuclein Toxicity

J. Schulz, E. Gerhardt, Peter Karsten, 2012, PLoS genetics.

The Evolutionary Conserved Transmembrane BAX Inhibitor Motif (TMBIM) Containing Protein Family Members 5 and 6 Are Essential for the Development and Survival of Drosophila melanogaster

A. Voigt, A. Methner, Li Zhang, 2021, Frontiers in Cell and Developmental Biology.

Analysis of dopaminergic neuronal dysfunction in genetic and toxin‐induced models of Parkinson's disease in Drosophila

A. Voigt, J. A. Botella, S. C. Yenisetti, 2014, Journal of neurochemistry.

Nuclear import factor transportin and arginine methyltransferase 1 modify FUS neurotoxicity in Drosophila

Tobias M. Rasse, J. Schulz, X. Pan, 2015, Neurobiology of Disease.

Drosophila melanogaster as a model organism for Alzheimer’s disease

J. Schulz, A. Voigt, Katja Prüßing, 2013, Molecular Neurodegeneration.