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Acta Neuropathologica Communications|March 15, 2020
CMT2Q-causing mutation in the Dhtkd1 gene lead to sensory defects, mitochondrial accumulation and altered metabolism in a knock-in mouse modelChun-Jie Luan, Wenting Guo, Lei Chen, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 17, 2025
Phosphodiesterase 4D inhibition improves the functional and molecular outcome in a mouse and human model of Charcot Marie Tooth disease 1 AMelissa Schepers, Tim Vangansewinkel, Karen Libberecht, et al.Brain : a Journal of Neurology|February 8, 2018
HDAC6 is a therapeutic target in mutant GARS-induced Charcot-Marie-Tooth diseaseVeronick Benoy, Lawrence Van Helleputte, Robert Prior, et al.Experimental & Molecular Medicine|June 2, 2024
Advances and challenges in modeling inherited peripheral neuropathies using iPSCsJonas Van Lent, Robert Prior, Gonzalo Pérez Siles, et al.Brain : a Journal of Neurology|May 14, 2024
PMP22 duplication dysregulates lipid homeostasis and plasma membrane organization in developing human Schwann cellsRobert Prior, Alessio Silva, Tim Vangansewinkel, et al.Science (New York, N.Y.)|January 29, 2021
Expansion sequencing: Spatially precise in situ transcriptomics in intact biological systemsShahar Alon, Daniel R Goodwin, Anubhav Sinha, et al.Pageof 2