In contrast, the BE group exhibited a modest increase (10.92%±1.11%) that did not reach statistical significance (P > 0.05), indicating a limited pro-apoptotic effect.
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Warfarin and bevacizumab suppress tumor progression in pancreatic ductal adenocarcinoma by targeting EGFR-PI3K-Akt signaling: inhibition of proliferation/migration and apoptosis induction.
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