neuroepithelial cell

They arise early in development from neuroepithelial cells.

To make the switch, neuroepithelial cells begin downregulating their epithelial features.

Neuroepithelial cells are a class of stem cell and have similar characteristics, most notably the ability to self renew.

Integrin α6 anchors the neuroepithelial cells to the basal lamina.

Neuroepithelial cells give rise to radial glial cells early on during embryonic development.

During neurulation neuroepithelial cells stop expressing occludin, a tight junction protein.

It extends posteriorly from the roof of the fourth ventricle to dorsal neuroepithelial cells.

Many of the neuroepithelial cells also divide into radial glial cells, a similar, but more fate restricted cell.

During neuroepithelial cell division, interkinetic nuclear migration allows the cells to divide unrestricted while maintaining a dense packing.

Activation of the Wnt pathway in primitive neuroepithelial cells in utero results in a quite different outcome.

Expression of Tis21, an antiproliferative gene, causes the neuroepithelial cell to make the switch from proliferative division to neuronic division.

In the absence of occludin some polarity is still lost and the neuroepithelial cell gives rise to the radial glial cell.

The wall of the neural tube consists of neuroepithelial cells, which differentiate into neuroblasts, forming the mantle layer (the gray matter).

In fish, the neuroepithelial cells (NEC) have been implicated as the major oxygen sensing cells.

The progenitor cells that make up the precursors to neural tissues in the neural plate are called neuroepithelial cells.

The neuroepithelial cells undergo two different forms of mitosis: asymmetric differentiating division and symmetric prolific division.

Since neuroepithelial cells are distributed throughout the gills, they are often ideally situated to detect both arterial as well as environmental oxygen.

HES1 is expressed in both neuroepithelial cells and radial glial cells, both neural stem cells.

Brains from these transgenic embryos contained increased numbers of periventricular neuroepithelial cells because a greater number of the precursors re-entered the cell cycle after mitosis.

Neuroepithelial cells are the "stem cells" of the nervous system, deriving from actual stem cells in several different stages of neural development.

As part of this polarity, neuroepithelial cells express prominin-1 in the apical plasma membrane as well as tight junctions to maintain the cell polarity.

During the formation of the neural tube, neuroepithelial cells undergo symmetric proliferative divisions that give rise to two new neuroepithelial cells.

The neural tube begins as a single layer of pseudostratified epithelial cells, but rapid proliferation of neuroepithelial cells creates additional layers and eventually three distinct regions of growth.

At a later stage of brain development, neuroepithelial cells begin to self renew and give rise to non-stem cell progenitors, such as radial glial cells simultaneously by undergoing asymmetric division.

Another tight junction protein, PAR3, remains at the apical side of the cell co-localizing with N-cadherin and keeps the apical face of the neuroepithelial cell intact.