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MOTS-c, as a mitochondrial coding regulator, has endocrine-like and nuclear transcriptional regulation on muscle metabolism (10, 15), insulin sensitivity (16, 17) and body weight (18)

The qRT-PCR measurement suggested that TORC-1 was inhibited by both HS and rapamycin in the WT strain, indicated by increased transcription of TORC-1 downstream targets, including TORC-1 subunit RAGA-1
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A novel NanoBiT-based assay monitors the interaction between lipoprotein lipase and GPIHBP1 in real time
