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By integrating data across trials and modeling continuous doseresponse relationships, the present analysis provides a more granular understanding of how these agents compare across the full range of clinically relevant doses
( f ) Food intake, ( g ) RER (effect of treatment F(1,10) = 6.34 p = 0.031), ( h ) energy expenditure (with ANCOVA using BW as covariate), ( i ) ambulatory activity and ( j ) body weight change of WT mice treated with VEH or acyl-GIP ( d - j , n = 6 per group
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