We developed a MEM-based, glucose-centric media supplemented with EGF in which all four cell lines displayed continual proliferation over the 48 h C-glucose labeling period.
The mammalian intestinal mucosa undergoes a process of continual renewal, characterized by active proliferation of stem cells localized near the base of the crypts, progression of these cells up the crypt-villus axis with cessation of proliferation and subsequent differentiation into one of the four primary cell types [1].
The mammalian intestinal mucosa undergoes a process of continual renewal, characterized by active proliferation of stem cells localized near the base of the crypts, progression of these cells up the crypt villus axis with cessation of proliferation, and subsequent differentiation into one of the four primary cell types (that is, enterocytes, goblet cells, Paneth cells, and enteroendocrine cells).
These results demonstrate that inhibition of cell division during the second stage culture has no discernable effect on differentiation, a result consistent with the hypothesis that, after an initial proliferative phase, differentiation can occur in the absence of continual cell proliferation [ 33, 40- 43].
The proliferation of shanties continued.
Thus, increased proliferation of palatal mesenchyme allowed for continual growth of palatal shelves, which in turn may have disastrous effects on the subsequent palatal elevation and fusion.
Epithelial cells of the intestinal mucosa undergo a continual process of proliferation, differentiation, and apoptosis.
The intestinal mucosa undergoes a continual process of proliferation, differentiation, and apoptosis, which is regulated by multiple signaling pathways.
The proliferation of content will continue exponentially.
