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El BPC-157 y la timosina beta 4 se convirtieron en importantes objetos de investigacin debido a sus estructuras peptdicas nicas y a su amplia relevancia en la investigacin biolgica experimental

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These kinase inhibitors inhibited the BSA-PC-induced increase in tau phosphorylation at T181, S262, and PHF-1 sites without altering GSK-3 and CDK5 expression levels (Fig 5C and 5D)