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Frontiers in Neurology|July 2, 2019
Identification of Cellular Pathogenicity Markers for SIL1 Mutations Linked to Marinesco-Sjögren SyndromeChristian Gatz, Denisa Hathazi, Ute Münchberg, et al.
Acta Neuropathologica|March 17, 2023
Spinal astrocyte dysfunction drives motor neuron loss in late-onset spinal muscular atrophyLinda-Isabell Schmitt, Christina David, Rebecca Steffen, et al.
Journal of Neuromuscular Diseases|March 8, 2021
Dysregulation of GSK3β-Target Proteins in Skin Fibroblasts of Myotonic Dystrophy Type 1 (DM1) PatientsValentina Grande, Denisa Hathazi, Emily O'Connor, et al.
Gene Therapy|May 12, 2026
A dose-escalation and safety gene therapy study in a model of CMT4C neuropathyElena Georgiou, Alexia Kagiava, Andreas Hentschel, et al.
Cells|December 10, 2025
Targeting Astrocytic Connexin 43 Mitigates Glutamate-Driven Motor Neuron Stress in Late-Onset Spinal Muscular AtrophySchahin Salmanian, Linda-Isabell Schmitt, Kai Christine Liebig, et al.
Frontiers in Physiology|March 29, 2021
Regulatory Function of Sympathetic Innervation on the Endo/Lysosomal Trafficking of Acetylcholine ReceptorTatjana Straka, Charlotte Schröder, Andreas Roos, et al.
Journal of the Peripheral Nervous System : JPNS|February 14, 2015
Inverted formin 2-related Charcot-Marie-Tooth disease: extension of the mutational spectrum and pathological findings in Schwann cells and axonsAndreas Roos, Joachim Weis, Rudolf Korinthenberg, et al.
Molecular Neurobiology|October 16, 2015
Cellular Signature of SIL1 Depletion: Disease Pathogenesis due to Alterations in Protein Composition Beyond the ER MachineryAndreas Roos, Laxmikanth Kollipara, Stephan Buchkremer, et al.
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