<p><i>Top row</i>: dependence on cortical feedback widths and with weights kept fixed: and . <i>Bottom row</i>: dependence on cortical feedback weights and with widths kept fixed: , and . All values are normalized with respect to the case where relay cells only receive feedforward excitation from retinal ganglion cells. The parameters in <i>W</i><sub>G</sub> and <i>K</i><sub>RG</sub> are kept fixed (see <a href="http://www.ploscompbiol.org/article/info:doi/10.1371/journal.pcbi.1006156#pcbi.1006156.t001" target="_blank">Table 1</a>).</p
AbstractSimple cells in cat striate cortex are selective for spatial frequency. It is widely believe...
<p>A FD-cell response of the DDI model. In this model variant both the inhibitory and excitatory sig...
Feedback from the visual cortex (Vl) to the Lateral Geniculate Nucleus (LGN) in macaque monkey incre...
<p><i>Upper left</i>: the two dimensional spatial structure of the impulse-response function. <i>Bot...
<p>Effect of cortical feedback on temporal frequency tuning of relay cells are shown for different v...
<p><i>Top row</i>: predicted area-response curves of relay cells for different arrangements of corti...
<p><i>Left panels</i>: temporal evolution of the relay-cell impulse-response function (ON region) fo...
<p><i>Left</i>: Autocorrelation function of stimulus and relay cell response for different circuit c...
Despite half-a-century of research since the seminal work of Hubel and Wiesel, the role of the dorsa...
<p><i>Top</i>: panels showing spatial receptive field at different times. Curves below panels are on...
Despite half-a-century of research since the seminal work of Hubel and Wiesel, the role of the dorsa...
Visually evoked signals in the retina pass through the dorsal geniculate nucleus (dLGN) on the way t...
<div><p>Visually evoked signals in the retina pass through the dorsal geniculate nucleus (dLGN) on t...
<p><i>Two leftmost panels</i>: temporal impulse-response function with mixed excitatory and inhibito...
Despite its prominent placement between the retina and primary visual cortex in the early visual pat...
AbstractSimple cells in cat striate cortex are selective for spatial frequency. It is widely believe...
<p>A FD-cell response of the DDI model. In this model variant both the inhibitory and excitatory sig...
Feedback from the visual cortex (Vl) to the Lateral Geniculate Nucleus (LGN) in macaque monkey incre...
<p><i>Upper left</i>: the two dimensional spatial structure of the impulse-response function. <i>Bot...
<p>Effect of cortical feedback on temporal frequency tuning of relay cells are shown for different v...
<p><i>Top row</i>: predicted area-response curves of relay cells for different arrangements of corti...
<p><i>Left panels</i>: temporal evolution of the relay-cell impulse-response function (ON region) fo...
<p><i>Left</i>: Autocorrelation function of stimulus and relay cell response for different circuit c...
Despite half-a-century of research since the seminal work of Hubel and Wiesel, the role of the dorsa...
<p><i>Top</i>: panels showing spatial receptive field at different times. Curves below panels are on...
Despite half-a-century of research since the seminal work of Hubel and Wiesel, the role of the dorsa...
Visually evoked signals in the retina pass through the dorsal geniculate nucleus (dLGN) on the way t...
<div><p>Visually evoked signals in the retina pass through the dorsal geniculate nucleus (dLGN) on t...
<p><i>Two leftmost panels</i>: temporal impulse-response function with mixed excitatory and inhibito...
Despite its prominent placement between the retina and primary visual cortex in the early visual pat...
AbstractSimple cells in cat striate cortex are selective for spatial frequency. It is widely believe...
<p>A FD-cell response of the DDI model. In this model variant both the inhibitory and excitatory sig...
Feedback from the visual cortex (Vl) to the Lateral Geniculate Nucleus (LGN) in macaque monkey incre...