ALS Compendium
Store-operated cyclic AMP signalling mediated by STIM1
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
Growth factor-expressing human neural progenitor cell grafts protect motor neurons but do not ameliorate motor performance and survival in ALS mice
A role for motoneuron subtype-selective ER stress in disease manifestations of FALS mice
Angiogenin protects motoneurons against hypoxic injury
Mimicking aspects of frontotemporal lobar degeneration and Lou Gehrig’s disease in rats via TDP-43 overexpression
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
MicroRNA-206 delays ALS progression and promotes regeneration of neuromuscular synapses in mice
Intracellular amyloid beta interacts with SOD1 and impairs the enzymatic activity of SOD1: implications for the pathogenesis of amyotrophic lateral sclerosis
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