(A) Only the sparser and more selective distribution of MF-MVN synaptic weights resulting from the interplay between bursts and post-complex spike pauses facilitates an efficient reshaping of the learnt patterns (B), allowing phase-reversal learning to be achieved (C).</p
Most Hebbian learning rules or BCM rules used to describe receptive field development exhibit a spon...
Spike-timing-dependent plasticity (STDP) modifies the weight (or strength) of synaptic connections b...
<p>Panel A shows two iSTDP profiles, where vestibular synaptic weight change ( of equation (2) in Me...
(A) VOR gain adaptation with (red curve) and without (green curve) Purkinje spike burst-pause dynami...
(A) VOR gain and phase adaptation with (purple curve) and without (green curve) CF-evoked Purkinje s...
We simulated 6 REMs stages (for a total of 18000 s of simulation) between day 1 and 2 of VOR phase-r...
<p><b>(A)</b> Evolution of synaptic weights in the network during plasticity. After each batch of le...
We studied the hypothesis that synaptic dynamics is controlled by three basic principles: (A) Synaps...
<p>(A) Evolution of synaptic weights in the neural circuit on inputs from the MNIST database. (B) Ev...
The existing models for vestibulo-ocular reflex (VOR) and optokinetic response (OKR) learning utiliz...
<p>Distribution of synaptic weights for three different connection types: feedforward (left), feedba...
<p>Distribution of synaptic weights for different connection types: feedforward (left), feedback (mi...
<p>Boxplots showing the characteristics of the dense collar (<i>blue</i>) and lip (<i>orange</i>) of...
Markram and Tsodyks, by showing that the elevated synaptic efficacy observed with single-pulse LTP m...
<p><b>A</b>: Distribution of firing rates of excitatory neurons. The magenta line shows a log-normal...
Most Hebbian learning rules or BCM rules used to describe receptive field development exhibit a spon...
Spike-timing-dependent plasticity (STDP) modifies the weight (or strength) of synaptic connections b...
<p>Panel A shows two iSTDP profiles, where vestibular synaptic weight change ( of equation (2) in Me...
(A) VOR gain adaptation with (red curve) and without (green curve) Purkinje spike burst-pause dynami...
(A) VOR gain and phase adaptation with (purple curve) and without (green curve) CF-evoked Purkinje s...
We simulated 6 REMs stages (for a total of 18000 s of simulation) between day 1 and 2 of VOR phase-r...
<p><b>(A)</b> Evolution of synaptic weights in the network during plasticity. After each batch of le...
We studied the hypothesis that synaptic dynamics is controlled by three basic principles: (A) Synaps...
<p>(A) Evolution of synaptic weights in the neural circuit on inputs from the MNIST database. (B) Ev...
The existing models for vestibulo-ocular reflex (VOR) and optokinetic response (OKR) learning utiliz...
<p>Distribution of synaptic weights for three different connection types: feedforward (left), feedba...
<p>Distribution of synaptic weights for different connection types: feedforward (left), feedback (mi...
<p>Boxplots showing the characteristics of the dense collar (<i>blue</i>) and lip (<i>orange</i>) of...
Markram and Tsodyks, by showing that the elevated synaptic efficacy observed with single-pulse LTP m...
<p><b>A</b>: Distribution of firing rates of excitatory neurons. The magenta line shows a log-normal...
Most Hebbian learning rules or BCM rules used to describe receptive field development exhibit a spon...
Spike-timing-dependent plasticity (STDP) modifies the weight (or strength) of synaptic connections b...
<p>Panel A shows two iSTDP profiles, where vestibular synaptic weight change ( of equation (2) in Me...