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Despite natural occurrences that occur across the Animal Kingdom and work in a growing number of systems, regeneration is still poorly understood.
Indeed, SlIPT4 is probably at the origin of a greater hormonal imbalance than SlIPT3, which may have impaired proper shoot and root systems regeneration.
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This suggests some capacity for nervous system regeneration.
In both cases, system regeneration is required to restore its availability.
Understanding central nervous system regeneration also entails designing the appropriate molecular, cellular, and behavioral assays.
In contrast, such aging is almost entirely induced by the periodic high-temperature events, such as those related to various system regeneration regimes.
Military weapon systems availability can be affected by system failures or by damage to the system, and in either case, system regeneration is needed.
We investigated the timing and sequence of events during nervous system regeneration in this organism.
New, practical models of central nervous system regeneration are required and should provide molecular tools and resources.
We provide here a biotechnological framework for studies of central nervous system regeneration in the tunicate Ciona.
Recent studies demonstrated that skin-derived precursor cells (SKPs) could promote central nervous system regeneration in spinal cord injury model or the neonatal peripheral neuron.
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