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The conjugated double bonds in its lipid tail endow LTC 4 with photolability, and this, together with its high affinity for MRP1 ( K m app 100 nm), allows direct and highly specific photolabeling of MRP1 that is readily detected by autoradiography

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This study aims to analyze SAAM in STAD using bioinformatics, construct a prognostic and therapeutic scoring model, and identify a central SAAM gene to provide a potential therapeutic target for STAD

The changes in body composition become more dramatic and stable

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