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Regression of Liver Steatosis Following Phosphatidylcholine Administration: A Review of Molecular and Metabolic Pathways Involved

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FAK-paxillin signaling and F-actin cytoskeletal organization Molecular Modulation of the NO-system, VEGFR2 signaling, growth-hormone receptor expression in fibroblasts, and interactions with dopamine- and serotonin-related neurotransmitter pathways Systemic (Preclinical) Rodent models of gastrointestinal mucosal lesions, liver injury, tendon and ligament transection, and vascular occlusion syndromes References (BPC-157): Sikiric P, et al