Associated Papers
Nuclear pore complex dysfunction drives TDP-43 pathology in ALS.
Ramírez-Núñez O et al.
Redox Biology, 2025
40819564 (PubMed )
Supplement: mmc2.docx
Unraveling the impact of disrupted nucleocytoplasmic transport systems in C9orf72-associated ALS.
McGoldrick P et al.
Frontiers in Cellular Neuroscience, 2023
Amyotrophic Lateral Sclerosis Genes in Drosophila melanogaster.
Layalle S et al.
International Journal of Molecular Sciences, 2021
Nuclear localization of human SOD1 and mutant SOD1-specific disruption of survival motor neuron protein complex in transgenic amyotrophic lateral sclerosis mice.
Gertz B et al.
Journal of Neuropathology and Experimental Neurology, 2012
Mutational analysis of conserved amino acids in the influenza A virus nucleoprotein.
Li Z et al.
Journal of Virology, 2009
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