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Annals of Neurology|November 4, 2014
Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerizationJudith Eschbach, Björn von Einem, Kathrin Müller, et al.
The Journal of Experimental Medicine|January 13, 2019
Heterozygous Tbk1 loss has opposing effects in early and late stages of ALS in miceDavid Brenner, Kirsten Sieverding, Clara Bruno, et al.
Neuroscience|June 17, 2020
Enhanced Hyaluronan Signaling and Autophagy Dysfunction by VPS35 D620NAbir A Rahman, Alejandro Soto-Avellaneda, Hyun Yong Jin, et al.
BMJ Mental Health|August 21, 2025
Evidence for reduced synaptic protein SNAP-25 in cerebrospinal fluid in major depressive disorder and schizophreniaPetra Steinacker, Leonie Werner, Alexander Tarabuko, et al.
Human Molecular Genetics|January 10, 2018
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiencySarah J Brockmann, Axel Freischmidt, Patrick Oeckl, et al.
Acta Neuropathologica|February 25, 2016
Peripheral monocytes are functionally altered and invade the CNS in ALS patientsLisa Zondler, Kathrin Müller, Samira Khalaji, et al.
Brain : a Journal of Neurology|April 19, 2021
A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosisAxel Freischmidt, Anand Goswami, Katharina Limm, et al.
Acta Neuropathologica|March 18, 2015
Extracellular vesicle sorting of α-Synuclein is regulated by sumoylationMarcel Kunadt, Katrin Eckermann, Anne Stuendl, et al.
The Journal of Experimental Medicine|March 22, 2024
A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in miceDavid Brenner, Kirsten Sieverding, Jahnavi Srinidhi, et al.
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