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Therefore, detection of agonist-induced internalization of the α 2C subtype is complicated by its low surface expression
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1998 in the European Journal of Endocrinology , which established an effective dose 50 (ED50) of approximately 80 µg/kg intravenous (IV) for GH release in rats and demonstrated selectivity over cortisol and prolactin axes because the GHSR-1a receptor does not couple to the ACTH or prolactin pathways
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