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Titlebook: Development and Regeneration of the Nervous System; S. Nona,J. Cronly-Dillon,M. Ferguson Book 1992 S. Nona, J. Cronly-Dillon, M. Ferguson,

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楼主: 夸大
发表于 2025-3-23 10:37:06 | 显示全部楼层
You, Your “Two Hats” and Growth Managementf any, signs of regional differentiation specific to the optic nerve, and may originate from the brain during development (Small ., 1987). Thus the astrocytes form the principal tissue framework and mechanical reinforcement of the optic nerve.
发表于 2025-3-23 17:08:58 | 显示全部楼层
https://doi.org/10.1007/978-981-16-2486-5re-target recognition, after altering the spatial relationships of eye and tectum (Sperry, 1943; Attardi and Sperry, 1963; Sperry, 1963). More recently, much work on neuronal pathfinding and map formation has been performed on one amphibian species, ..
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Development of fibre order in the amphibian visual system,re-target recognition, after altering the spatial relationships of eye and tectum (Sperry, 1943; Attardi and Sperry, 1963; Sperry, 1963). More recently, much work on neuronal pathfinding and map formation has been performed on one amphibian species, ..
发表于 2025-3-24 09:23:18 | 显示全部楼层
The cytoskeleton and the mechanism of synaptic plasticity,Numerous studies have demonstrated that interventions in the developing and mature nervous system can induce rearrangements of the synaptic patterns by the sprouting of new synapses and/or retraction of existing ones. In addition, existing synapses may also change such parameters as volume, shape, length of synaptic apposition, etc.
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Regeneration of axons in the optic nerve of the adult Browman-Wyse (BW) mutant rat,as been found that CNS fibres will regenerate into a peripheral nerve implanted into the brain (Richardson ., 1980). Accordingly, research has now focused on possible environmental factors within the CNS which might inhibit growth after injury. There are currently two areas of research which explore
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Polymeric matrices with functional groups for promoting tissue repair and axonal regeneration in thng them, the formation of a glial-connective scar tissue has received a great deal of interest and has been traditionally viewed as ‘mechanical obstacle’ to axonal elongation (Windle, 1956). However, this hypothesis has been questioned since several lines of experimental evidence have suggested that
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