Figure 5From: Identification of novel androgen-responsive genes by sequencing of LongSAGE librariesAndrogen regulation of genes in the in vivo Hollow Fibre model of prostate cancer. Levels of transcripts in LNCaP cells from the Hollow Fibre model were analyzed by qRT-PCR. Cx, castrated mice, 10 days post castration, n = 12; Pre-Cx, pre-castration, day 0 of castration, n = 15. Exception: LRIG1 gene expression in Cx samples was represented by 11 mice. Fold-change was calculated by normalizing the mean normalized expression (MNE) of transcripts in the Pre-Cx sample to the castrate sample. In doing this, the Cx sample fold-change became one and standard deviation (SD) zero. Error bars represent ± SD. [*] Asterisks indicate the significant differential gene expression with respect to Cx according to the Two-Sample Student's T-test (p ≤ 0.05) for unequal variance.Back to article page