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Advances in Experimental Medicine and Biology|December 8, 2019
RNA Granules and Their Role in Neurodegenerative DiseasesHadjara Sidibé, Christine Vande VeldeSeminars in Cell & Developmental Biology|June 2, 2023
The implications of physiological biomolecular condensates in amyotrophic lateral sclerosisHana Fakim, Christine Vande VeldeFrontiers in Cellular Neuroscience|November 12, 2015
Alterations in stress granule dynamics driven by TDP-43 and FUS: a link to pathological inclusions in ALS?Anaïs Aulas, Christine Vande VeldeAmyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 5, 2012
Misfolded SOD1 and ALS: zeroing in on mitochondriaSarah Pickles, Christine Vande VeldeMethods in Molecular Biology (Clifton, N.J.)|February 16, 2022
Collective Learnings of Studies of Stress Granule Assembly and CompositionHadjara Sidibé, Christine Vande VeldeTrends in Neurosciences|August 25, 2021
Altered stress granule disassembly: links to neurodegenerative disease?Alicia Dubinski, Christine Vande VeldeJournal of Neurochemistry|December 22, 2020
The multi-functional RNA-binding protein G3BP1 and its potential implication in neurodegenerative diseaseHadjara Sidibé, Alicia Dubinski, Christine Vande VeldeMolecular Neurodegeneration|October 25, 2012
Endogenous TDP-43, but not FUS, contributes to stress granule assembly via G3BPAnaïs Aulas, Stéphanie Stabile, Christine Vande VeldeThe Journal of Physiology|September 17, 2016
New perspectives on amyotrophic lateral sclerosis: the role of glial cells at the neuromuscular junctionDanielle Arbour, Christine Vande Velde, Richard RobitaillePageof 8