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Targeting ApoA Genetic association studies have established a clear link between apoA variation and TG metabolism (Nilsson et al., 2011

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The molecular docking results revealed the ability of both n-hexadecanoic acid and L-carnitine to activate SIRT1 and subsequent antioxidant, anti-inflammatory, and anti-apoptotic pathways

By both immunostaining and TEM, the smallest nLDs in L4 and D1 nuclei were close to the nuclear periphery, suggesting an origin at the INM (Fig 2H, quantified in Fig 2I)

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