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Cell Reports|October 31, 2019
Interaction of Axonal Chondrolectin with Collagen XIXa1 Is Necessary for Precise Neuromuscular Junction FormationAna-Maria Oprişoreanu, Hannah L Smith, Sukrat Arya, et al.
JMIR Mhealth and Uhealth|December 21, 2019
Objectively Monitoring Amyotrophic Lateral Sclerosis Patient Symptoms During Clinical Trials With Sensors: Observational StudyLuis Garcia-Gancedo, Madeline L Kelly, Arseniy Lavrov, et al.
Journal of Lipid Research|November 5, 2016
Defective cholesterol metabolism in amyotrophic lateral sclerosisJonas Abdel-Khalik, Eylan Yutuc, Peter J Crick, et al.
Acta Neuropathologica Communications|September 26, 2018
Neurodegeneration in SCA14 is associated with increased PKCγ kinase activity, mislocalization and aggregationMaggie M K Wong, Stephanie D Hoekstra, Jane Vowles, et al.
Proteomics|November 10, 2018
UFLC-Derived CSF Extracellular Vesicle Origin and ProteomeAlexander G Thompson, Elizabeth Gray, Imre Mager, et al.
Brain Communications|July 3, 2020
Identification of a potential non-coding RNA biomarker signature for amyotrophic lateral sclerosisGreig Joilin, Elizabeth Gray, Alexander G Thompson, et al.
Brain Communications|May 23, 2024
The cortical neurophysiological signature of amyotrophic lateral sclerosisMichael Trubshaw, Chetan Gohil, Katie Yoganathan, et al.
Neurobiology of Disease|October 6, 2018
Single-copy expression of an amyotrophic lateral sclerosis-linked TDP-43 mutation (M337V) in BAC transgenic mice leads to altered stress granule dynamics and progressive motor dysfunctionDavid Gordon, Ruxandra Dafinca, Jakub Scaber, et al.
Stem Cells (Dayton, Ohio)|December 23, 2006
Transcriptional profiling of human cord blood CD133+ and cultured bone marrow mesenchymal stem cells in response to hypoxiaEnca Martin-Rendon, Sarah J M Hale, Dacey Ryan, et al.
Molecular Therapy. Nucleic Acids|February 12, 2021
Targeting the 5' untranslated region of SMN2 as a therapeutic strategy for spinal muscular atrophyAudrey M Winkelsas, Christopher Grunseich, George G Harmison, et al.
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