Third generation of double-data-rate synchronous dynamic random-access memory.
1Similar effects were achieved when RANK expression was knocked down in PC3 cells.
2BMSC-CM was collected to evaluate its effect on PC3 cell migration.
3PC3 cells preferred to migrate toward BMSC-CM than toward the control.
4Over-expressing INH alpha in LNCaP and PC3 cells demonstrated two different and cell-type-specific responses.
5Transfected PC3 cells were transplanted into nude mice, and the tumor growth curves were determined.
6Western blotting of PC3 cell media confirmed the presence of the FS288 isoform.
7We examined the effect of EGCG on cell survival and apoptosis in the prostate cancer cell line PC3.
8The addition of rmWnt5a improved the migration capacity of PC3 cells in a concentration-dependent manner.
9Measurements of freezing behavior mainly loaded on PC3, and this component separated rats of different genetic groups from each other.
10In addition, loss of RalA in the metastatic PC3 cell line inhibited bone metastasis but did not affect subcutaneous tumor growth.
11Primary transcription was delayed by 6 to 8 h in PC3 cells relative to LNCaP cells.
12Loss of bone volume did not slow with treatment, attributed to the highly aggressive and osteolytic nature of the PC3 cell line.
13We report herein a high-throughput DELFIA assay to quantify H3K27me3 in the prostate cancer cell line, PC3.
14The goal of these studies was to identify the step(s) of the viral replication cycle that is inhibited in PC3 cells.
15Methods: To investigate the role of ERG, LNCaP and PC3 cells were transfected with ERG and gene expression and metabolic profile were analyzed.
16In addition, in PC3 cells Aurora B expression is accompanied the by the phosphorylation of the histone H3.