Mechanisms of Neuroprotection by Protein Disulphide Isomerase in Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease characterised by the progressive loss of motor neurons, leading to paralysis and death within several years of onset.Although protein misfolding is a key feature of ALS, the upstream triggers of disease remain elusive.Recently, endoplasmic reticulum (ER) stress was Hand