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Following neutralization with (NH) 4 HCO 3 , samples were frozen at −20 °C for 20 min, spun and supernatants measured directly

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Research has used AOD9604 in parallel with full-length hGH and GH receptor agonist and antagonist controls , characterising which aspects of GH’s metabolic biology are mediated through the C-terminal lipolytic domain versus GH receptor dimerisation, and establishing the pharmacological boundary between GH domain peptide biology and receptor-mediated intact GH pharmacology

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