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RNA-seq analyses reveal that cervical spinal cords and anterior motor neurons from amyotrophic lateral sclerosis subjects show reduced expression of mitochondrial DNA-encoded respiratory genes, and rhTFAM may correct this respiratory deficiency.Brain Res. 2017 Jul 15;1667:74-83. doi: 10.1016/j.brainres.2017.05.010. Epub 2017 May 13.
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R521C and R521H mutations in FUS result in weak binding with Karyopherin2 leading to Amyotrophic lateral sclerosis: a molecular docking and dynamics study.J Biomol Struct Dyn. 2017 Aug;35(10):2169-2185. doi: 10.1080/07391102.2016.1209130. Epub 2016 Aug 8.
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Collagen XIX Alpha 1 Improves Prognosis in Amyotrophic Lateral Sclerosis.Aging Dis. 2019 Apr 1;10(2):278-292. doi: 10.14336/AD.2018.0917. eCollection 2019 Apr.
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ERCC6L2 rs591486 polymorphism and risk for amyotrophic lateral sclerosis in Greek population.Neurol Sci. 2019 Jun;40(6):1237-1244. doi: 10.1007/s10072-019-03825-3. Epub 2019 Mar 16.
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Elucidating the Contribution of Skeletal Muscle Ion Channels to Amyotrophic Lateral Sclerosis in search of new therapeutic options.Sci Rep. 2019 Feb 28;9(1):3185. doi: 10.1038/s41598-019-39676-3.
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Rare variants in MYH15 modify amyotrophic lateral sclerosis risk.Hum Mol Genet. 2019 Jul 15;28(14):2309-2318. doi: 10.1093/hmg/ddz063.
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HR23B pathology preferentially co-localizes with p62, pTDP-43 and poly-GA in C9ORF72-linked frontotemporal dementia and amyotrophic lateral sclerosis.Acta Neuropathol Commun. 2019 Mar 13;7(1):39. doi: 10.1186/s40478-019-0694-6.
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Combined Tissue-Fluid Proteomics to Unravel Phenotypic Variability in Amyotrophic Lateral Sclerosis.Sci Rep. 2019 Mar 14;9(1):4478. doi: 10.1038/s41598-019-40632-4.
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White matter changes in the perforant path area in patients with amyotrophic lateral sclerosis.Neuropathol Appl Neurobiol. 2019 Oct;45(6):570-585. doi: 10.1111/nan.12555. Epub 2019 May 14.
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The VAPB-PTPIP51 endoplasmic reticulum-mitochondria tethering proteins are present in neuronal synapses and regulate synaptic activity.Acta Neuropathol Commun. 2019 Mar 6;7(1):35. doi: 10.1186/s40478-019-0688-4.
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Network approach identifies Pacer as an autophagy protein involved in ALS pathogenesis.Mol Neurodegener. 2019 Mar 27;14(1):14. doi: 10.1186/s13024-019-0313-9.
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Sarm1 deletion suppresses TDP-43-linked motor neuron degeneration and cortical spine loss.Acta Neuropathol Commun. 2019 Oct 28;7(1):166. doi: 10.1186/s40478-019-0800-9.
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Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions.Brain. 2016 Jun;139(Pt 6):1723-34. doi: 10.1093/brain/aww061. Epub 2016 Mar 25.
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Carboxyl-terminal modulator protein regulates Akt signaling during skeletal muscle atrophy in vitro and a mouse model of amyotrophic lateral sclerosis.Sci Rep. 2019 Mar 8;9(1):3920. doi: 10.1038/s41598-019-40553-2.
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