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Chunk #24 — PRECLINICAL STUDIES

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The role of the Asn40Asp polymorphism of the mu opioid receptor gene (OPRM1) on alcoholism etiology and treatment: a critical review.
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Given the inconsistencies in the human literature described previously, as well as inconsistent results regarding the functional properties of the Asn40Asp variant in heterologous expression systems, a number of preclinical cellular and animal models have been developed to gain insight into the effect of the Asn40Asp variant in humans using controlled experimental systems. A nonhuman primate ortholog of the Asn40Asp SNP has been identified and 2 mouse models have been generated to address the effects of this polymorphism on phenotypes used to model alcoholism.