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Image Search Results
Journal: American Journal of Cancer Research
Article Title: A p53-stabilizing agent, CP-31398, induces p21 expression with increased G2/M phase through the YY1 transcription factor in esophageal carcinoma defective of the p53 pathway
doi:
Figure Lengend Snippet: CP-31398-mediated augmentation of p21 and suppression of YY1 expression. Esophageal carcinoma cells treated with CP-31398 (A) at different concentrations as indicated for 48 hrs or (B) at 10 μM for different times as indicated, were subjected to Western blot analysis. Actin was used as a loading control.
Article Snippet: Cells were transfected with small interfering
Techniques: Expressing, Western Blot, Control
Journal: American Journal of Cancer Research
Article Title: A p53-stabilizing agent, CP-31398, induces p21 expression with increased G2/M phase through the YY1 transcription factor in esophageal carcinoma defective of the p53 pathway
doi:
Figure Lengend Snippet: CP-31398-mediated up-regulation of p21 was independent of p53 but associated with YY1 expression. (A) Esophageal carcinoma cells treated with CP-31398 as indicated for 48 hrs and amounts of p21 transcripts were analyzed with RT-PCR. GAPDH transcripts are shown as a control. (B, C) Cells transfected with either (B) p53-siRNA or (C) YY1-siRNA were treated with CP-31398 at 10 μM for 48 hrs and subjected to Western blot analysis. Cells transfected with control siRNA were also used as a reference. Actin was used as a loading control.
Article Snippet: Cells were transfected with small interfering
Techniques: Expressing, Reverse Transcription Polymerase Chain Reaction, Control, Transfection, Western Blot
Journal: American Journal of Cancer Research
Article Title: A p53-stabilizing agent, CP-31398, induces p21 expression with increased G2/M phase through the YY1 transcription factor in esophageal carcinoma defective of the p53 pathway
doi:
Figure Lengend Snippet: CP-31398-mediated cell cycle changes were attributable to augmented p21 expression. A. Cells transfected with p21-siRNA or control siRNA were treated with CP-31398 at 10 μM for 48 hrs and subjected to Western blot analysis. Actin was used as a loading control. B. Representative cell cycle profiles of cells treated with siRNA and/or CP-31398 at 10 μM for 48 hrs. The profiles were examined with a flow cytometry. A percentage of each fraction was shown in Table 2.
Article Snippet: Cells were transfected with small interfering
Techniques: Expressing, Transfection, Control, Western Blot, Flow Cytometry
Journal: American Journal of Cancer Research
Article Title: A p53-stabilizing agent, CP-31398, induces p21 expression with increased G2/M phase through the YY1 transcription factor in esophageal carcinoma defective of the p53 pathway
doi:
Figure Lengend Snippet: Cell cycle progression of esophageal carcinoma cells which were treated with CP-31398 and siRNA
Article Snippet: Cells were transfected with small interfering
Techniques: Control
Journal: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
Article Title: Central venous catheter-related bacteremia due to Tsukamurella species in the immunocompromised host: a case series and review of the literature.
doi: 10.1086/342561
Figure Lengend Snippet: Figure 1. Findings of DNA-DNA homology studies with solid-phase dot-blot hybridizations for Tsukamurella species. Probe and target DNAs are indicated. Strain numbers beginning with “A” are from the American Type Culture Collection system.
Article Snippet: The type strain of
Techniques: Dot Blot