Titlebook: Axon Growth and Regeneration; Methods and Protocol Andrew J. Murray Book 2014 Springer Science+Business Media New York 2014 Axon growth.Axo

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Stroke and Hypotensive Syndromes,ry of novel neuro-stimulatory agents that promote regeneration is hampered by a gap between high content analysis platforms using neuronal cells and time-consuming preclinical animal models. In this regard, tissue explant cultures, which are easily manageable and more closely resemble the in vivo si

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Hypothalamic Control of Lactations of biological tissues are incorporated into liposomes, added to growth cones in culture and changes in morphology are then assessed. Alternatively purified or recombinant molecules in aqueous solution may be added directly to the cultures. In both cases after a defined period of time (up to 1 h),

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Akira Arimura,Andrew V. Schallythe CNS under ex vivo conditions..In this chapter, we describe in detail the reconstruction of the mesocortical and nigrostriatal dopaminergic projection system culturing tissue slices from the ventral tegmental area/substantia nigra (VTA/SN) with the prefrontal cortex (PFC) or the striatum (STR). T

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Fatih Tanriverdi,Fahrettin Kelestimurtained from a variety of sources, then cultured within collagen hydrogels to explore cellular responses and interactions in response to substances under test or under conditions that mimic physiological or pathological environments. Cell populations are labelled then either mixed within gels or arra

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https://doi.org/10.1007/978-1-4684-2598-7n severed, injured nerves must be able to regenerate and reconnect to the structures they previously controlled within 12–18 months before sensation and motion are permanently lost. Nerve sprouts from the proximal stump will spontaneously migrate toward the distal stump in the event of a nerve trans

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Hypothalamus and Endocrine Functionsr not, when there is a partial or a complete transection. The majority of acute human SCI is not followed by complete transection, but there is a combination of contusion, compression, and possibly partial transection. The method described here is a compressive mouse model that presents a combinatio

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Current Topics in Molecular Endocrinologyos. Here we report a rapid and efficient approach to transfect adult mouse dorsal root ganglion neurons in vivo with precise spatiotemporal control via electroporation. This approach will allow both gain- and loss-of-function experiments in vivo to study the function of adult sensory neurons, such a