ALS Compendium
The mouse C9ORF72 ortholog degenerate in ALS and FTD
Functional and pathological TDP-43 aggregation
Molecular basis of UG-rich RNA recognition by the human splicing factor TDP-43
Gluthathionylation potentiates bening superoxide dismutase 1 variants to the toxic forms associated with amyotrophic lateral sclerosis
Dysregulated microRNAs in amyotrophic lateral sclerosis microglia modulate genes linked to neuroinflammation
Therapeutic modulation of eIF2 α phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models
Postnatal muscle modification by myogenicfactors modulates neuropathology and survival in an ALS mouse model
Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis
Ligand binding and aggregation of pathogenic SOD1
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