1
Polarized monolayers of T84 cells were used as an intestinal epithelial model.
2
In vitro, we examined the effect of adiponectin on intestinal epithelial cells.
3
We investigated the role of miR-29a in intestinal epithelial apoptosis in UC.
4
Brush borders of intestinal epithelial cells are mandatory for nutrient uptake.
5
Adenoviral-mediated gene delivery targeted its expression mainly to intestinal epithelial cells.
6
Increased MRP1 expression was detected at the basolateral membrane of intestinal epithelial cells.
7
Occludin protein expression in intestinal epithelial cells was detected by immunohistochemistry.
8
C1q expression may mediate Wnt signaling activity and intestinal epithelial regeneration.
9
TL and CD1 are expressed specifically by murine intestinal epithelial cells.
10
Future studies are warranted to investigate the therapeutic potential of intestinal epithelial NF-kB2 inhibition.
11
The apoptosis rate of intestinal epithelial cells was also evaluated.
12
It arises from loss of intestinal epithelial homeostasis and hyperproliferation of the crypt epithelium.
13
Total oxygen consumption by isolated ruminal and intestinal epithelial cells was unaffected by treatment.
14
Methods: Wounds were created in confluent monolayers of the intestinal epithelial cell line of IEC-6.
15
Our results identify a novel pathway by which CUX1 regulates normal intestinal epithelial cell restitution.
16
The molecular mechanisms that direct intestinal epithelial cell morphogenesis and terminal differentiation are poorly understood.
