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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 28, 2011
Small heat-shock protein HSPB1 mutants stabilize microtubules in Charcot-Marie-Tooth neuropathyLeonardo Almeida-Souza, Bob Asselbergh, Constantin d'Ydewalle, et al.Neuron|December 27, 2016
The Antisense Transcript SMN-AS1 Regulates SMN Expression and Is a Novel Therapeutic Target for Spinal Muscular AtrophyConstantin d'Ydewalle, Daniel M Ramos, Noah J Pyles, 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.Molecular Neurodegeneration|April 23, 2024
Regulation of human microglial gene expression and function via RNAase-H active antisense oligonucleotides in vivo in Alzheimer's diseaseLina Vandermeulen, Ivana Geric, Laura Fumagalli, et al.American Journal of Human Genetics|November 12, 2013
A dominant mutation in FBXO38 causes distal spinal muscular atrophy with calf predominanceCharlotte J Sumner, Constantin d'Ydewalle, Joe Wooley, et al.The Journal of Clinical Investigation|October 8, 2019
Age-dependent SMN expression in disease-relevant tissue and implications for SMA treatmentDaniel M Ramos, Constantin d'Ydewalle, Vijayalakshmi Gabbeta, et al.Pageof 2