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GSTM1 deletion prevalence: Approximately 4050% of individuals of European ancestry carry the GSTM1 null genotype, making it one of the most common functional gene deletions in the human genome

J Appl Physiol (1985) 2012;113(8):126066

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Researched For ARA-290 has been studied in rodent models of peripheral nerve injury, with researchers examining its interactions with small fiber neuropathy endpoints and nerve conduction parameters

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OxLDL is formed by various modifications of lipids and apolipoprotein B by the process of peroxidation of lipids