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Judith Stegmuller

Affiliations: 
Max-Planck-Institute for Experimental Medicine, Göttingen, Germany 
Area:
neurodevelopment, neurodegeneration, UPS
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"Judith Stegmuller"
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Parents

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Azad Bonni post-doc 2003-2008 Harvard Medical School

Children

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Madhuvanthi Kannan grad student 2008-2012 MPI for Experimental Medicine

Collaborators

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Camille Lancelin collaborator 2013-2015
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Publications

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Wang J, Joseph S, Vingill S, et al. (2023) Loss of the parkinsonism-associated protein FBXO7 in glutamatergic forebrain neurons in mice leads to abnormal motor behavior and synaptic defects. Journal of Neurochemistry
Wang Q, Crnković V, Preisinger C, et al. (2021) The parkinsonism-associated protein FBXO7 cooperates with the BAG6 complex in proteasome function and controls the subcellular localization of the complex. The Biochemical Journal
Kawabe H, Stegmüller J. (2021) The role of E3 ubiquitin ligases in synapse function in the healthy and diseased brain. Molecular and Cellular Neurosciences. 112: 103602
Stegmüller J. (2020) Restless in the mouse cage-A new genetic model for restless legs syndrome: An Editorial Highlight for "Deficiency of Meis1, a transcriptional regulator, in mice and worms:Neurochemical and behavioral characterizations with implications in the restless legs syndrome" on https://doi.org/10.1111/jnc.15177. Journal of Neurochemistry
Vingill S, Brockelt D, Lancelin C, et al. (2016) Loss of FBXO7 (PARK15) results in reduced proteasome activity and models a parkinsonism-like phenotype in mice. The Embo Journal
Mukherjee C, Holubowska A, Schwedhelm-Domeyer N, et al. (2015) Loss of the neuron-specific F-box protein FBXO41 models an ataxia-like phenotype in mice with neuronal migration defects and degeneration in the cerebellum. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 8701-17
Matz A, Lee SJ, Schwedhelm-Domeyer N, et al. (2015) Regulation of neuronal survival and morphology by the E3 ubiquitin ligase RNF157. Cell Death and Differentiation. 22: 626-42
Stegmüller J. (2013) The brake within: Mechanisms of intrinsic regulation of axon growth featuring the Cdh1-APC pathway Translational Neuroscience. 4
Stegmüller J, Bonni A. (2010) Destroy to create: E3 ubiquitin ligases in neurogenesis. F1000 Biology Reports. 2
Oberdoerffer P, Michan S, McVay M, et al. (2008) SIRT1 redistribution on chromatin promotes genomic stability but alters gene expression during aging. Cell. 135: 907-18
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