We observed the expression of DAB2IP to be expressed in the prostate epithelial cells (PrEC), but not in all PCa including LNCaP, C4-2, DU-145 and PC-3.
Further, we observed the expression of FZP gene to be uniformly low throughout the development stages analyzed here.
Pozo-Guisado et al. observed the expression of caspase 3 may contribute to death of breast cancer cells [39].
Subsequently, Banerjee and Chandel (2011) also observed the expression of 43 metal homeostasis related genes in 12 rice cultivars and showed significant genotypic variation in their levels of expression.
In addition, we observed the expression of myofibroblast marker α smooth muscle actin (α-SMA), the product of Acta2, in IKKβ-null but not wild type cells (Fig. 1D).
We have also observed the expression of SALL4 in breast cancer as reported.
In addition, we observed the expression of GFP using fluorescence microscopy in CHO colonies.
We also observed the expression of both phospho-p38 and CB2 receptors in perivascular cells, suggesting that ECBs may also directly regulate p38 signaling in these cells.
We have previously characterized the gene expression profile of endothelial progenitors under pro-endothelial differentiation conditions [25], and observed the expression of members of the Notch pathway.
In this paper we observed the expression of NTS and NTS mRNA in HBEC and demonstrated that NTS is an estrogen target gene in those cells.
Joshi et al. [23] have also observed the expression of Lrp5 mRNA in both basal and luminal cells (from normal glands, separated using a different protocol).
