| Abstract |
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We describe the method for efficiently differentiating human embryonic stem cells to neuroepithelial cells in a chemically
defined condition. The protocol was established based on the fundamental principle of in vivo neuroectodermal development.
The temporal course, morphological transformation, and shift in gene expression of our neuroepithelial differentiation closely
resemble those occur during in vivo development. In particular, the primitive neuroepithelial cells generated by this protocol
can be further induced into neuronal and glial cells with forebrain, mid/hind brain, and spinal cord identities and targeted
transmitter phenotypes.
Affiliation(s): (3) Departments of Anatomy and Neurology, School of Medicine and Public Health, Waisman Center, University of Wisconsin, Madison, 1500 Highland Avenue, 53705 Madison, WI, USA
Series: Methods in Molecular Biology | Volume: 549 | Pub. Date: Jun-01-2009 | Page Range: 51-58 | DOI: 10.1007/978-1-60327-931-4_4
Subject: Cell Biology
Key Words: Human embryonic stem cells - Embryoid body - Neuroepithelia - Neuronal differentiation - Chemically defined condition
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