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Neural Regeneration Research|August 31, 2017
Mitochondrial quality control in amyotrophic lateral sclerosis: towards a common pathway?Bilal Khalil, Jean-Charles LiévensNeuron|April 18, 2024
14-3-3θ, a novel player in TDP-43 pathophysiology: Implications for ALS/FTDBilal Khalil, Sandrine Da CruzNeurobiology of Disease|March 18, 2020
Traffic jam at the nuclear pore: All roads lead to nucleocytoplasmic transport defects in ALS/FTDClaudia Fallini, Bilal Khalil, Courtney L Smith, et al.Molecular Neurodegeneration|January 23, 2024
Nuclear-import receptors as gatekeepers of pathological phase transitions in ALS/FTDBilal Khalil, Miriam Linsenmeier, Courtney L Smith, et al.Brain Research|February 21, 2018
mRNP assembly, axonal transport, and local translation in neurodegenerative diseasesBilal Khalil, Dmytro Morderer, Phillip L Price, et al.International Journal of Ophthalmology|October 27, 2018
Association of LOXL1 gene common sequence variants in Jordanian patients with exfoliation syndrome and exfoliative glaucomaWisam Shihadeh, Omar Khabour, Mohammed Bilal Khalil, et al.Human Molecular Genetics|November 8, 2019
Sigma-1 receptor is a key genetic modulator in amyotrophic lateral sclerosisSimon Couly, Bilal Khalil, Véronique Viguier, et al.Glia|December 30, 2017
Glial lipid droplets and neurodegeneration in a Drosophila model of complex I deficiencyMarie-Jeanne Cabirol-Pol, Bilal Khalil, Thomas Rival, et al.Neurobiology of Aging|March 22, 2017
Enhancing Mitofusin/Marf ameliorates neuromuscular dysfunction in Drosophila models of TDP-43 proteinopathiesBilal Khalil, Marie-Jeanne Cabirol-Pol, Laetitia Miguel, et al.Nature Communications|November 5, 2020
Sigma-1 receptor chaperones rescue nucleocytoplasmic transport deficit seen in cellular and Drosophila ALS/FTD modelsPin-Tse Lee, Jean-Charles Liévens, Shao-Ming Wang, et al.Pageof 2