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Thereby, the application of NO-agents, NOS-blockade L-NAME, NO-over-activity (L-arginine, NOS-substrate) and their relationships (opposite or parallel activities, mutual counteraction or not), which can cover all essential points of NO-system, and the full spectrum of NO-system functions was combined with BPC 157 application to show its full efficacy on maintaining and/or reestablishing NO-system effects and functions [124,125]

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This mutation in mice nicely recapitulates the human vascular EDS phenotype, including thin and fragile skin, aortic aneurysm and rupture, and abnormal collagen fibrillogenesis in skin, aorta, and bowel