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Redox system expression in the motor neurons in amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS, superoxide dismutase 1 (SOD1)-mutated familial ALS, and SOD1-mutated ALS animal models
Two decades-long journey from riluzole to edaravone: revisiting the clinical pharmacokinetics of the only two amyotrophic lateral sclerosis therapeutics
Regular use helps to cleanse the liver and support its function
Peptide mechanism elucidation : The structural features of Dihexa make it a valuable probe for dissecting peptide-receptor interactions and downstream signaling pathways
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