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Currently it is believed that N-cadherin plays a role in the myelination process.
N-cadherin is critical to holding neural plate cells together.
Experimentation has shown that N-cadherin plays an important role in producing a remyelination-facilitating environment.
Mesenchymal cells usually express other cadherin types such as N-cadherin.
Fibronectin and N-cadherin are key to epithelialization in the developing embryo.
For example, cells containing N-cadherin tend to cluster with other N-cadherin-expressing cells.
Important molecules in these intercellular connections include N-cadherin, fibronectin, connexin and various integrins.
These cells are held together by cadherins (specifically E and N-cadherin), types of intercellular binding protein.
The transmembrane protein N-cadherin is often used as an indicator of in-vivo-like tissue assembly in 3D culturing.
A mouse mutant for N-cadherin suffers inflammatory bowel disease conditions and adenomas but does not develop carcinomas.
For example, the expression of N-cadherin is crucial to maintaining separation of precursor neural cells from precursor epithelial cells.
During the next stage, the development of the neural plate, N-cadherin (neural cadherin) is expressed and there is a decrease in E-cadherin.
A cell adhesion molecule known as neural cadherin (N-cadherin) is expressed predominantly in the nervous system, where it is implicated in neuronal migration during development.
Epithelial cells express high levels of E-cadherin, whereas mesenchymal cells express those of N-cadherin, fibronectin and vimentin.
The neural plate switches from E-cadherin expression to N-cadherin and N-CAM expression to recognize each other as the same tissue and close the tube.
Overexpression of an N-cadherin mutant incapable of adhesion prevents spine head expansion, demonstrating N-cadherin's essential role in this process.
The remaining somitomeres, likely driven by periodic expression of the hairy gene, begin expressing adhesion proteins such as N-cadherin and fibronectin, compact, and bud off forming somites.
In cultures of transfected MDCS cells, T-cadherin was also expressed apically, whereas N-cadherin located basolaterally corresponded to the zone of сеll contacts.
Additionally, mesenchymal-associated genes such as Snail, Slug, Zeb 1, 2, and N-cadherin were downregulated within the first 5 days post-OKSM induction.
In regenerating neural cells, neurite promoting factors play a role in adhesion of the axon and include neural cell adhesion molecule (N-CAM) and N-cadherin.
Thus, when the neural tube precursor cells begin expressing N-cadherin in the place of E-cadherin, this causes the neural tube to form and separate from the ectoderm and settle inside the embryo.
Only cells expressing the same kind of cadherin can bind to each other; since the peaks of the neural folds both express N-cadherin, they are able to merge into a continuous sheet of cells.
A characteristic of EMT is loss of the epithelial markers (E-cadherin, cytokeratins, claudin, occluding, desmoglein, desmocolin) and gain of mesenchymal markers (N-cadherin, vimentin, fibronectin) .
Glutamate binding to NMDA upregulates the production of N-cadherin's intracellular domain peptide, N-cad/CTF2, an effect blocked by the NMDA receptor antagonist, APV.
ADH-1 selectively and competitively binds to and blocks N-cadherin, which may result in disruption of tumor vasculature, inhibition of tumor cell growth, and the induction of tumor cell and endothelial cell apoptosis.