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Molecular Oncology|January 29, 2024
Harmony in chaos: understanding cancer through the lenses of developmental biologyJonas Van Lent, Arianna BaggioliniJournal of Neuromuscular Diseases|September 29, 2019
Defects in Axonal Transport in Inherited NeuropathiesDanique Beijer, Angela Sisto, Jonas Van Lent, et al.Iscience|May 4, 2026
Unperturbed dye-based imaging of spontaneous synchronized calcium activity in iPSC-derived neuronal culturesNina Dirkx, Bob Asselbergh, Peter Verstraelen, et al.Brain : a Journal of Neurology|December 13, 2022
Downregulation of PMP22 ameliorates myelin defects in iPSC-derived human organoid cultures of CMT1AJonas Van Lent, Leen Vendredy, Elias Adriaenssens, et al.The Journal of Gene Medicine|February 20, 2025
RNA Interference Targeting Small Heat Shock Protein B8 Failed to Improve Distal Hereditary Motor Neuropathy in the Mouse ModelLeen Vendredy, Vicky De Winter, Jonas Van Lent, et al.Brain : a Journal of Neurology|June 15, 2021
Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunctionJonas Van Lent, Peter Verstraelen, Bob Asselbergh, et al.The EMBO Journal|March 1, 2021
A weakened interface in the P182L variant of HSP27 associated with severe Charcot-Marie-Tooth neuropathy causes aberrant binding to interacting proteinsT Reid Alderson, Elias Adriaenssens, Bob Asselbergh, 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.JCI Insight|July 14, 2026
HDAC6 inhibition alleviates mitochondrial trafficking in novel models of Charcot-Marie-Tooth Disease Type 2ALydia H Jestice, Larissa Butler, Rebecca A Lea, et al.Nature Reviews. Disease Primers|June 17, 2022
Genetic pain loss disordersAnnette Lischka, Petra Lassuthova, Arman Çakar, et al.Pageof 2