Showing results (31-40 of 46) with videos related to
Sort By:
Pageof 5
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.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.Brain Communications|April 3, 2023
Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutationsMaximilian Wiesenfarth, Kornelia Günther, Kathrin Müller, et al.Journal of Neurology|August 14, 2024
Clinical characterization of common pathogenic variants of SOD1-ALS in GermanyMaximilian Wiesenfarth, Yalda Forouhideh-Wiesenfarth, Zeynep Elmas, 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.Nature Communications|January 25, 2018
Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formationMarcel Naumann, Arun Pal, Anand Goswami, et al.Brain Communications|May 24, 2023
Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosisWolfgang P Ruf, Matej Boros, Axel Freischmidt, et al.Pageof 5