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Huntington’s

Staufen1 Overabundance and the Consequent mTOR Hyperactivity in Amyotrophic Lateral Sclerosis, Spinocerebellar Ataxia Type 2, Alzheimer’s, Parkinson’s, and Huntington’s Diseases

Mechanisms of Neurodegeneration: Neuroinflammation and microglial activation

Mechanisms of Neurodegeneration: Mitochondrial Dysfunction and Oxidative Stress

Mechanisms of Neurodegeneration: Protein aggregation and failure of autophagy