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Thus, we speculated that the findings and the associated mechanisms as detailed in our mouse studies could likely translate to humans

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This realization set the stage for two parallel strategies that unfolded in the 1990s and 2000s: (1) development of injectable GLP-1 analogues resistant to degradation, and (2) development of DPP-4 inhibitors to protect and elevate native GLP-1 levels ( [44] )

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