ΔNp73 enhances promoter activity of TGF-β induced genes.

Figure 1 - a ) Luciferase expression induced by increasing quantities of the GH expressing vector (pc β A/msGH) in fish fibroblast cells co-transfected with a reporter vector with

(B) 293T cells were co-transfected with SuperTop reporter, pRL-CMV and b -catenin (S33Y) with or without the indicated TCF1 constructs, followed two days later by luciferase

(B) HIF-1 a cooperated with Osx to inhibit Wnt pathway activity. HEK293 cells were transfected with a Topflash reporter along with 25 ng b - catenin without or with different groups

Cells stably expressing the control shRNA or Snail1 shRNA were treated with TGF- b 1 (3 g/ml) for 6 days and expression of E-cadherin and N-cadherin were determined by qRT-PCR (E)

Total RNA was obtained from a pool of St32 eyes of control, control treated with SB43152 or TGF-β, miR-181a/b morphant, TGF-β-treated miR-181a/b morphant, MO-protector- erk2 and TGF-

TC620 cells were transfected with luciferase reporter plasmid for the early promoter, JCV E -LUC in the presence or absence of increasing amounts of Rad51 expression plasmid (0, 0.5

Fig 5. Cell lysates were immunoprecipitated with an antibody to LTBP4 and immunoblotted with an antibody to the FLAG tag on TGF β 1, TGF β 2, and TGF β 3.. Each of these

HEK293 cells stably expressing TRIM11 or control pCDH vector were inoculated with 50 ng/ml (p24 gag ) of HIV-1 Vpr 2 viruses and analyzed by qPCR for late reverse transcripts and