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Conclusions In our studied population, the frequency of GSTM1 null genotypes was found deviated from Inter- and Intra-Indian ethnic groups

Structurally related to and derived from Melanotan II, it interacts with melanocortin receptors, including MC3R and MC4R, making it a compound of interest to researchers studying the melanocortin signaling pathway and its role in the central nervous system.

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Alzheimer's, Parkinson's and Huntington's diseases can be caused by mutations that enhance protein aggregation, but we still do not know enough about the molecular players of these pathways to develop treatments for these devastating diseases

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