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G.LiuH.DianoS.ShanabroughM.CaiX.et al

Well-designed randomized clinical studies are needed to systematically evaluate the evidence for the use of these hepatoprotective agents as treatment options for APAP-induced liver injury, to determine the timing of initiation of the therapy, and to further define the optimal treatment regimen

Interestingly, compared with A40, A42 is more prone to aggregation and exhibits a higher degree of neurotoxicity (El-Agnaf et al

Cell Regen 9 (1), 16

Subtype-selective antagonists of lysophosphatidic acid receptors inhibit platelet activation triggered by the lipid core of atherosclerotic plaques

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