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More mysterious yet, there are 10 times as many feedback connections -- from the neocortex to lower levels of the brain -- as there are feed-forward or bottom-up connections.
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The recent comprehensive connectivity map of the afferent and efferent neurons of the Drosophila MB revealed many potential feedback connections outside the MB (Aso et al., 2014a).
By integrating the targets of all WT TFs profiled with those of other cardiac TFs previously published, we found that Elk1/4 were embedded in the developmental cardiac GRN with many cross and feedback connections, suggesting that ELK1/4 play a significant role in normal and disease cardiac GRN logic.
The dual feedback model, a simplified version of the Drosophila PER-TIM feedback model [ 12], was found to be the most robust and entrainable among many feedback models with various connection logics [ 13].
Furthermore, the introduction of asymmetry to connectivity (with feedback connections weaker than feedforward connections) enhanced the diversity of timescales.
There is no feedback connections.
There exist forward connections as well as feedback connections.
This numerical result for nonvanishing feedback connections complements the analytical result for vanishing feedback delay above.
Fig. 1 Propagating stationary wave front of Eq. (1) for delayed feedback with spatial feedback connections taken from kernel class (C) without intra-area connections.
In contrast, cortico-cortical feedback connections may exhibit fiber bundles with fixed length yielding a constant feedback delay.
In addition to feedback connections, there are self-recurrent connections in all nodes of the context and hidden layers.
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