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- W1975063089 endingPage "537" @default.
- W1975063089 startingPage "517" @default.
- W1975063089 abstract "Peripheral nerve cells, various endocrine and pigment cells and cranial connective tissue cells of vertebrates stem mainly from the embryonic neural crest. This originates with the central nervous system, but the crest cells detach from this tissue, via a decrease of cell-cell adhesion involving, particularly, a reduction of the adherens junction cell adhesive molecule A-CAM. This epithelio-mesenchymal transformation allows crest cells to migrate along pathways that are defined partly by the distribution of substrate adhesion molecules, the archetype being fibronectin, an extracellular matrix molecule recognized by integrin receptors on crest cells. Many other molecules, however, may act in the same way. In contrast, some molecules may define migration pathways by reducing adhesion; chpndroitin sulfate proteoglycan is a cadidate for this role. Pathways selection is most likely achieved by balanced combinations of molecules that promote and reduced adhesion. Cessation of migration, in the case of the nervous ganglia, correlated with re-expression of cell-cell adhesion molecules like A-CAM and others, consistent with an adhesive basis, although functional tests have not yet been peroformed. The development of the neural crest system provides a useful model that emphasizes the role of adhesion in morphogenesis." @default.
- W1975063089 created "2016-06-24" @default.
- W1975063089 creator A5028759832 @default.
- W1975063089 creator A5091769537 @default.
- W1975063089 date "1993-01-01" @default.
- W1975063089 modified "2023-09-26" @default.
- W1975063089 title "Adhesion molecules in neural crest development" @default.
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