POD-1Tcf21 overexpression reduces endogenous SF-1 and StAR expression in rat adrenal cells

Since the secretory function of mesangial cells has been impli- cated in several autocrine and paracrine ac- tivities, the present study evaluated the abil- ity of mouse and

IFN- g mRNA expression was evaluated in nonstimulated peripheral blood mononuclear cells (PBMC) of HIV-infected and seronegative individuals using quantitative competitive

realizing that in this work when used only DMBA, the elementary lesion presented keratosis in nearly 50% of the sample, in the three studied times, associated with the

Differential expression of steroidogenic factor-1/adrenal 4 binding protein and liver receptor homolog-1 (LRH-1)/fetoprotein transcription factor in the rat testis: LRH-1 as

( B–C ) Quantitative RT-PCR analysis reveals robust transcription of human MyoD following H a 7-mediated fusion ( B ) of MRC-5 cells and differentiating C2C12 myotubes, whereas

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)

cells have similar levels of Stat1 mRNA (Fig. The expression levels of Mx1 in Stat1 2 / 2 cells and untreated Stat1 ind cells were below detection limits but upon treatment with

(A) miR-320a expression was decreased in SW480/ shE2A cells as shown by qRT-PCR; (B) Co-transfection of E12 or E47 into SW480/shE2A cells could normalize the expression of miR-320a;