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- W4362611582 abstract "<p>Supplementary Figure 3: (A) NSCLC U-1810 cells or diploid fibroblasts WI-38 were treated with DMSO, 1 or 2 (3 microM) for 48 h. Cisplatin (20 microM, 72 h) treated U-1810 cells were used as a positive control for induction of apoptotic morphology. Nuclear morphology of cells was examined after fixation in 4 % paraformaldehyde and staining with DAPI. Pictures showing nuclear morphology (magnification 60x, the scale bar equals 25 microm). Arrows show apoptotic morphology of the cell nuclei. (B) NSCLC U-1810 cells were treated with 3 microM concentration of compound 2 and cleavage of caspase-3, caspase-9 or PARP was examined after 24, 48 and 72 h. β actin was used to visualize equal loading.</p>" @default.
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- W4362611582 date "2023-04-03" @default.
- W4362611582 modified "2023-09-27" @default.
- W4362611582 title "Supplementary Figure 3 from Marine Sponge <i>Cribrochalina vasculum</i> Compounds Activate Intrinsic Apoptotic Signaling and Inhibit Growth Factor Signaling Cascades in Non–Small Cell Lung Carcinoma" @default.
- W4362611582 doi "https://doi.org/10.1158/1535-7163.22500834" @default.
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