A Commentary on TDP-43 and DNA Damage Response in Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis (ALS) is a devastating, motor neuron degenerative disease without any cure.About 95% of the ALS patients feature abnormalities in the RNA/DNA-binding protein, TDP-43, involving its nucleo-cytoplasmic mislocalization in Glucosamine spinal motor neurons.How TDP-43 pathology triggers neuronal apoptosis remains unclear.In