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For example, based on recent published data, one could envision that treatment of ex vivo hybrid Th1/17 cells with these inhibitors could increase their tumor suppressive effects [50]
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In silico molecular docking simulations suggested that Frag 176-191 may exhibit binding affinity toward proteins such as Ki-67, MiB1, and various steroid hormone receptors, including the estrogen and progesterone receptors
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