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The substantial therapeutic effects observed following exogenous PRLM administration further reinforce their potential as promising treatment candidates for SS
In combination with the EGFR inhibitor gefitinib, crizotinib showed greater inhibition of cell survival in vitro as well as impaired wound closure and invasion
After the internalization of Au into tumor cells, the second DNA transition releases the anticancer drug at endosomal pH (~5.0)
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