dc.contributor.authorHeese, Klaus.
dc.date.accessioned2008-11-06T03:29:00Z
dc.date.available2008-11-06T03:29:00Z
dc.date.copyright2007en_US
dc.date.issued2007
dc.identifier.urihttp://hdl.handle.net/10356/14220
dc.description.abstractIn recent years it has been noted that the adult brain has the 'self-repair capacity' to replace lost neurons in several regions of the central neural system (CNS), such as the olfactory bulb, hippocampus, adult human subependymal zone and the cortex. Neural stem cells (NSCs) within these neurogenic regions can proliferate and differentiate into neurons or glia, thus providing a tool of replacement cells to those lost during normal cell turnover and after brain injury. Neurogenesis involves the self-renewal and proliferation of NSCs, as well as its differentiation into neurons and glia which are tightly regulated by both intrinsic and extrinsic factors. Newborn neurons and glia then migrate to appropriate regions in the brain, and integrate into neuronal circuits (Heese et al., 2006).en_US
dc.format.extent19 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Science::Biological sciences::Human anatomy and physiology::Neurobiologyen_US
dc.titleCharacterizing the signaling pathways of nerve growth factor in neuronal stem cells.en_US
dc.typeResearch Reporten_US
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.ispartofseries.reportRG 117/05en_US


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