This review aims to provide a comprehensive overview of the pharmaceutical properties and multi-dimensional pharmacological mechanisms of GLPS from a modern scientific perspective, summarize clinical evidence across different types of liver diseases, and objectively discuss their safety profiles, thereby providing a holistic overview to support rational clinical application and guide future research (Figure 1)
IVF, In Vitro Fertilization
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Variant gp34 1-179 was the minimum ectodomain region required to maintain Fc binding of gp34 as well as retain the ability to antagonize host FcRIII activation and was therefore suitable for further studies (Fig
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Mice infected with the D39 gpoA mutant strain exhibited a significant reduction in bacterial loads across multiple tissues, including the lung, brain, liver, and spleen, relative to those infected with the wild-type strain
