Associated Papers
Dysbiosis and Neurodegeneration in ALS: Unraveling the Gut-Brain Axis.
Sharma VK
Neuromolecular Medicine, 2025
The use of fibroblasts as a valuable strategy for studying mitochondrial impairment in neurological disorders.
Olesen MA et al.
Translational Neurodegeneration, 2022
Protein interaction networks in neurodegenerative diseases: From physiological function to aggregation.
Calabrese G et al.
The Journal of Biological Chemistry, 2022
Protein S-nitrosylation and oxidation contribute to protein misfolding in neurodegeneration.
Nakamura T et al.
Free Radical Biology & Medicine, 2021
Amyotrophic Lateral Sclerosis Genes in Drosophila melanogaster.
Layalle S et al.
International Journal of Molecular Sciences, 2021
Dynamin-related protein 1: A critical protein in the pathogenesis of neural system dysfunctions and neurodegenerative diseases.
Qi Z et al.
Journal of Cellular Physiology, 2019
Neurobiology of axonal transport defects in motor neuron diseases: Opportunities for translational research?
De Vos KJ et al.
Neurobiology of Disease, 2017
SOD1 and DJ-1 converge at Nrf2 pathway: a clue for antioxidant therapeutic potential in neurodegeneration.
Milani P et al.
Oxidative Medicine and Cellular Longevity, 2013
Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases.
Rodolfo C et al.
Expert Review of Proteomics, 2010
Mitochondrial medicine for aging and neurodegenerative diseases.
Reddy PH
Neuromolecular Medicine, 2008
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