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Introducing targeted amino acid substitutions to the GLP1 sequence with the aim of increasing helical stability resulted in enhanced cAMP signalling and insulin release, with a lesser effect on arrestin2 recruitment which, although bias was not formally quantified in this study, again suggested that cAMPfavouring GLP1 receptor agonism is preferred for insulin release (Plisson et al., 2016)

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PWS has already taught us much about imprinting, and may have much more to teach us