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Image Search Results
Journal: PeerJ
Article Title: Identification of a novel immune infiltration-related gene signature, MCEMP1 , for coronary artery disease
doi: 10.7717/peerj.18135
Figure Lengend Snippet: Lollipop chart for immune cell infiltration with DIRC2 (A) and MCEMP1 (B). Line graph GSEA analysis for the top five pathways of DIRC2 (C) and MCEMP1 (D).
Article Snippet: The
Techniques:
Journal: PeerJ
Article Title: Identification of a novel immune infiltration-related gene signature, MCEMP1 , for coronary artery disease
doi: 10.7717/peerj.18135
Figure Lengend Snippet: (A) The mRNA and protein expression of DIRC2 and MCEMP1 in ox-LDL-treated HUVECs by qRT‐PCR assay and Western blot assay. * p < 0.05; ** p < 0.01; *** p < 0.001. ox-LDL, oxidized low-density lipoprotein; HUVECs, human umbilical vein endothelial cells; qRT‐PCR, quantitative real‐time polymerase chain reaction.
Article Snippet: The
Techniques: Expressing, Quantitative RT-PCR, Western Blot, Real-time Polymerase Chain Reaction
Journal: Biochemistry and Biophysics Reports
Article Title: 15-deoxy-Δ 12, 14 -prostaglandin J 2 enhances anticancer activities independently of VHL status in renal cell carcinomas
doi: 10.1016/j.bbrep.2019.01.001
Figure Lengend Snippet: Effects of 15d-PGJ 2 on the anti-cancerous activities of topoisomerase inhibitors in RCC4 (-) cells . RCC4 (-) cells were treated with CPT (A), VP-16 (B), DOX (C) or 15d-PGJ 2 (D) at the indicated concentrations for 24 h. Cell viabilities were determined by MTT-reducing activity. Data are expressed as means ± SE. (n = 6). *P < 0.05, compared with control, **P < 0.01, compared with control. (E) RCC4 (-) cells were treated with 0.05 μM CPT, 20 μM VP-16 or 1 μM DOX in the absence (open column) or presence (closed column) of 20 μM 15d-PGJ 2 for 24 h. Cell viabilities were determined by MTT-reducing activity. Data are expressed as means ± SE. (n = 6). **P < 0.01, compared with control. (F) RCC4 (-) cells were treated with 0.05 μM CPT, 20 μM VP-16 or 1 μM DOX in the absence or presence of 20 μM 15d-PGJ 2 for 24 h. Morphologies were photographed by phase contrast. Scale bar = 100 µm.
Article Snippet: RCC4(+) and RCC4(
Techniques: Activity Assay, Control
Journal: Biochemistry and Biophysics Reports
Article Title: 15-deoxy-Δ 12, 14 -prostaglandin J 2 enhances anticancer activities independently of VHL status in renal cell carcinomas
doi: 10.1016/j.bbrep.2019.01.001
Figure Lengend Snippet: Effects of 15d-PGJ 2 on the anti-cancerous activities of topoisomerase inhibitors in RCC4 (+) cells. RCC4 (+) cells were treated with CPT (A), VP-16 (B), DOX (C) or 15d-PGJ 2 (D) at the indicated concentrations for 24 h. Cell viabilities were determined by MTT-reducing activity. Data are expressed as means ± SE. (n = 3). *P < 0.05, compared with control, **P < 0.01, compared with control. (E) RCC4 (+) cells were treated with 0.05 μM CPT, 20 μM VP-16 or 1 μM DOX in the absence (open column) or presence (closed column) of 20 μM 15d-PGJ 2 for 24 h. Cell viabilities were determined by MTT-reducing activity. Data are expressed as means ± SE. (n = 6). **P < 0.01, compared with control. ## P < 0.01, compared with each topoisomerase inhibitor alone. (F) RCC4 (+) cells were treated with 0.05 μM CPT, 20 μM VP-16 or 1 μM DOX in the 0.05 absence or presence of 20 μM 15d-PGJ 2 for 24 h. Morphologies were photographed by phase contrast. Scale bar = 100 µm.
Article Snippet: RCC4(+) and RCC4(
Techniques: Activity Assay, Control