<?xml version="1.0" encoding="UTF-8"?>

<rdf:RDF
   xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
   xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#"
   xmlns="http://purl.org/rss/1.0/"
   xmlns:dc="http://purl.org/dc/elements/1.1/"
   xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/"
   xmlns:dcterms="http://purl.org/dc/terms/"

>
<channel rdf:about="http://www.citeulike.org/about">
<pubDate>Sun, 27 Jul 2008 08:09:46 BST</pubDate>


	<title>CiteULike: j-ito's library [103 articles]</title>
	<description>CiteULike: j-ito's library [103 articles]</description>


	<link>http://www.citeulike.org/user/j-ito</link>
	<dc:publisher>CiteULike.org</dc:publisher>
	<dc:language>en-gb</dc:language>
	<dc:rights>Copyright &#169; 2004-2008 citeulike.org</dc:rights>
	<items>
    <rdf:Seq>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/3044872"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2907924"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2989233"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2985580"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/1202645"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/1202644"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2985526"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2985497"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2902689"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2985464"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2958834"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/1206800"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2939329"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2939322"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2939314"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2939302"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2939295"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2937772"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2925631"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2906898"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2906892"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/488473"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2869965"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2878671"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2860795"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2833110"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2858648"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2856350"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/1888394"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2804535"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2804527"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/505262"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2687128"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2687096"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2666145"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2647614"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/658837"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2547178"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2625448"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2625395"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2625387"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2461067"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2517071"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2412034"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/1292898"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2445142"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2425814"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/1151910"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2086031"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/j-ito/article/2363430"/>

	</rdf:Seq>
	</items>
	</channel>


<item rdf:about="http://www.citeulike.org/user/j-ito/article/3044872">
    <title>Discharge Synchrony during the Transition of Behavioral Goal Representations Encoded by Discharge Rates of Prefrontal Neurons</title>
    <link>http://www.citeulike.org/user/j-ito/article/3044872</link>
    <description>&lt;i&gt;Cereb. Cortex (9 February 2008), bhm234.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;To investigate the temporal relationship between synchrony in the discharge of neuron pairs and modulation of the discharge rate, we recorded the neuronal activity of the lateral prefrontal cortex of monkeys performing a behavioral task that required them to plan an immediate goal of action to attain a final goal. Information about the final goal was retrieved via visual instruction signals, whereas information about the immediate goal was generated internally. The synchrony of neuron pair discharges was analyzed separately from changes in the firing rate of individual neurons during a preparatory period. We focused on neuron pairs that exhibited a representation of the final goal followed by a representation of the immediate goal at a later stage. We found that changes in synchrony and discharge rates appeared to be complementary at different phases of the behavioral task. Synchrony was maximized during a specific phase in the preparatory period corresponding to a transitional stage when the neuronal activity representing the final goal was replaced with that representing the immediate goal. We hypothesize that the transient increase in discharge synchrony is an indication of a process that facilitates dynamic changes in the prefrontal neural circuits in order to undergo profound state changes. 10.1093/cercor/bhm234</description>
    <dc:title>Discharge Synchrony during the Transition of Behavioral Goal Representations Encoded by Discharge Rates of Prefrontal Neurons</dc:title>

    <dc:creator>Kazuhiro Sakamoto</dc:creator>
    <dc:creator>Hajime Mushiake</dc:creator>
    <dc:creator>Naohiro Saito</dc:creator>
    <dc:creator>Kazuyuki Aihara</dc:creator>
    <dc:creator>Masafumi Yano</dc:creator>
    <dc:creator>Jun Tanji</dc:creator>
    <dc:identifier>doi:10.1093/cercor/bhm234</dc:identifier>
    <dc:source>Cereb. Cortex (9 February 2008), bhm234.</dc:source>
    <dc:date>2008-07-26T18:33:50-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Cereb. Cortex</prism:publicationName>
    <prism:startingPage>bhm234</prism:startingPage>
    <prism:category>no-tag</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2907924">
    <title>Brain Circuits for the Internal Monitoring of Movements</title>
    <link>http://www.citeulike.org/user/j-ito/article/2907924</link>
    <description>&lt;i&gt;Annual Review of Neuroscience, Vol. 31, No. 1. (2008), pp. 317-338.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Each movement we make activates our own sensory receptors, thus causing a problem for the brain: the spurious, movement-related sensations must be discriminated from the sensory inputs that really matter, those representing our environment. Here we consider circuits for solving this problem in the primate brain. Such circuits convey a copy of each motor command, known as a corollary discharge (CD), to brain regions that use sensory input. In the visual system, CD signals may help to produce a stable visual percept from the jumpy images resulting from our rapid eye movements. A candidate pathway for providing CD for vision ascends from the superior colliculus to the frontal cortex in the primate brain. This circuit conveys warning signals about impending eye movements that are used for planning subsequent movements and analyzing the visual world. Identifying this circuit has provided a model for studying CD in other primate sensory systems and may lead to a better understanding of motor and mental disorders.</description>
    <dc:title>Brain Circuits for the Internal Monitoring of Movements</dc:title>

    <dc:creator>Marc Sommer</dc:creator>
    <dc:creator>Robert Wurtz</dc:creator>
    <dc:identifier>doi:10.1146/annurev.neuro.31.060407.125627</dc:identifier>
    <dc:source>Annual Review of Neuroscience, Vol. 31, No. 1. (2008), pp. 317-338.</dc:source>
    <dc:date>2008-06-19T15:46:34-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Annual Review of Neuroscience</prism:publicationName>
    <prism:volume>31</prism:volume>
    <prism:number>1</prism:number>
    <prism:startingPage>317</prism:startingPage>
    <prism:endingPage>338</prism:endingPage>
    <prism:category>eye-movement</prism:category>
    <prism:category>review</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2989233">
    <title>Behavioral states, network states and sensory response variability.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2989233</link>
    <description>&lt;i&gt;Journal of neurophysiology (9 July 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;We review data demonstrating that single-neuron sensory responses change with the states of the neural networks (indexed in terms of spectral properties of LFPs) in which those neurons are embedded. We start with broad network changes-different levels of anesthesia and sleep-and then move to studies demonstrating that the sensory response plasticity associated with attention and experience can also be conceptualized as functions of network state changes. This leads naturally to the recent data that can be interpreted to suggest that even brief experience can change sensory responses via changes in network states, and that trial-to-trial variability in sensory responses is a non-random function of network fluctuations, as well. We suggest that the central nervous system may have evolved specifically to deal with stimulus variability, and that the coupling network states may be central to sensory processing.</description>
    <dc:title>Behavioral states, network states and sensory response variability.</dc:title>

    <dc:creator>Alfredo Fontanini</dc:creator>
    <dc:creator>Donald B Katz</dc:creator>
    <dc:identifier>doi:10.1152/jn.90592.2008</dc:identifier>
    <dc:source>Journal of neurophysiology (9 July 2008)</dc:source>
    <dc:date>2008-07-11T18:26:07-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Journal of neurophysiology</prism:publicationName>
    <prism:issn>0022-3077</prism:issn>
    <prism:category>lfp</prism:category>
    <prism:category>review</prism:category>
    <prism:category>sponta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2985580">
    <title>Oscillatory activity in sensorimotor cortex of awake monkeys: synchronization of local field potentials and relation to behavior</title>
    <link>http://www.citeulike.org/user/j-ito/article/2985580</link>
    <description>&lt;i&gt;J Neurophysiol, Vol. 76, No. 6. (1 December 1996), pp. 3949-3967.&lt;/i&gt;</description>
    <dc:title>Oscillatory activity in sensorimotor cortex of awake monkeys: synchronization of local field potentials and relation to behavior</dc:title>

    <dc:creator>VN Murthy</dc:creator>
    <dc:creator>EE Fetz</dc:creator>
    <dc:source>J Neurophysiol, Vol. 76, No. 6. (1 December 1996), pp. 3949-3967.</dc:source>
    <dc:date>2008-07-10T16:21:45-00:00</dc:date>
    <prism:publicationYear>1996</prism:publicationYear>
    <prism:publicationName>J Neurophysiol</prism:publicationName>
    <prism:volume>76</prism:volume>
    <prism:number>6</prism:number>
    <prism:startingPage>3949</prism:startingPage>
    <prism:endingPage>3967</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>oscillation</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/1202645">
    <title>Synchronization of neurons during local field potential oscillations in sensorimotor cortex of awake monkeys.</title>
    <link>http://www.citeulike.org/user/j-ito/article/1202645</link>
    <description>&lt;i&gt;J Neurophysiol, Vol. 76, No. 6. (December 1996), pp. 3968-3982.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;1. The neural activity associated with 20- to 40-Hz oscillations in sensorimotor cortex of awake monkeys was investigated by recording action potentials of single and multiple units. At a given site, activity of many units became synchronized with local field potential (LFP) oscillations. Cycle-triggered histograms (CTHs) of unit spikes aligned on cycles of LFP oscillations indicated that about two thirds of the recorded units (n = 268) were entrained with LFP oscillations. On average, units had the highest probability of spiking 2.7 ms before peak LFP negativity, corresponding to a -27.6 degrees phase shift relative to the negative peak of the LFP. 2. The average relative modulation amplitude (RMA), defined as the ratio of amplitude of oscillatory component of CTH and the baseline multiplied by 100, was 45 +/- 27% (mean +/- SD). The RMAs of single units did not differ significantly from those of multiple units. 3. Phase shifts and RMAs did not vary systematically with the cortical depth of recorded units. 4. Autocorrelation histograms (ACHs) of entrained units exhibited clear 20- to 40-Hz periodicity if they were compiled with spikes that occurred during oscillatory episodes in LFPs. ACHs of spikes outside oscillatory episodes usually did not show periodicity. Global ACHs of all spikes typically showed weak or no evidence of periodic activity. 5. Cross-correlation histograms (CCHs) between pairs of units complied with all spikes, whether they occurred during or outside LFP oscillations, seldom revealed significant features (19 of 134 pairs or 14%). However, CCHs compiled with spikes that occurred during oscillatory episodes (OS-CCHs) had significant features in 67 of 134 pairs recorded ipsilaterally; in these 67 cases, units at both sites showed modulation in CTHs. 6. The latencies of the OS-CCH peaks (taking the medial unit as reference) were normally distributed about a mean of -0.5 +/- 13 ms. Normalized peak height of CCHs (peak/baseline x 100) was, on average, 14.3 +/- 11.2%. Peak latency and normalized peak amplitude did not change significantly with horizontal separation of recorded precentral pairs up to 14 mm. 7. Units in the left and right hemispheres could become synchronized during oscillations. Significant features in OS-CCH were detected in 22 of 42 pairs of units recorded bilaterally. The average peak latency was 0.2 +/- 8.0 ms and the average normalized peak amplitude was 10 +/- 8%. These parameters did not differ significantly from those for ipsilateral OS-CCHs. 8. Oscillations tended to affect both the temporal structure and net rate of unit firing. For each unit, the firing rate was clamped to a narrow range of frequencies during oscillatory episodes. The coefficient of variation (SD/mean) of firing rates was significantly reduced during oscillatory episodes compared with prior rates (P &#60; 0.001, paired t-test). However, the overall mean firing rate of each unit during all oscillatory episodes did not differ from its average rate immediately before the episodes. Thus oscillatory episodes tended to clamp mean firing rates to the cells' average rates outside episodes. 9. The strength of synchronization between units during oscillatory episodes was unrelated to their involvement in the task. For pairs of precentral units recorded ipsilaterally, the probability of occurrence of significant features in the OS-CCH was slightly larger when both units of the pair were task related (33 of 56 pairs or 59%) than when only one unit was task related (20 of 39 pairs or 51%) or neither unit was task related (7 of 16 or 44%). However, these differences were not statistically significant. The magnitude of the correlation peak and the latency to peak were also not significantly different for the three cases. 10. These results suggest that units across wide regions can become transiently synchronized specifically during LFP oscillations, even if their spikes are uncorrelated during nonoscillatory periods.</description>
    <dc:title>Synchronization of neurons during local field potential oscillations in sensorimotor cortex of awake monkeys.</dc:title>

    <dc:creator>VN Murthy</dc:creator>
    <dc:creator>EE Fetz</dc:creator>
    <dc:source>J Neurophysiol, Vol. 76, No. 6. (December 1996), pp. 3968-3982.</dc:source>
    <dc:date>2007-04-02T09:28:46-00:00</dc:date>
    <prism:publicationYear>1996</prism:publicationYear>
    <prism:publicationName>J Neurophysiol</prism:publicationName>
    <prism:issn>0022-3077</prism:issn>
    <prism:volume>76</prism:volume>
    <prism:number>6</prism:number>
    <prism:startingPage>3968</prism:startingPage>
    <prism:endingPage>3982</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/1202644">
    <title>Coherent 25- to 35-Hz oscillations in the sensorimotor cortex of awake behaving monkeys.</title>
    <link>http://www.citeulike.org/user/j-ito/article/1202644</link>
    <description>&lt;i&gt;Proc Natl Acad Sci U S A, Vol. 89, No. 12. (15 June 1992), pp. 5670-5674.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Synchronous 25- to 35-Hz oscillations were observed in local field potentials and unit activity in sensorimotor cortex of awake rhesus monkeys. The oscillatory episodes occurred often when the monkeys retrieved raisins from a Klüver board or from unseen locations using somatosensory feedback; they occurred less often during performance of repetitive wrist flexion and extension movements. The amplitude, duration, and frequency of oscillations were not directly related to movement parameters in behaviors studied so far. The occurrence of the oscillations was not consistently related to bursts of activity in forearm muscles, but cycle-triggered averages of electromyograms revealed synchronous modulation in flexor and extensor muscles. The phase of the oscillations changed continuously from the surface to the deeper layers of the cortex, reversing their polarity completely at depths exceeding 800 microns. The oscillations could become synchronized over a distance of 14 mm mediolaterally in precentral cortex. Coherent oscillations could also occur at pre- and postcentral sites separated by an estimated tangential intracortical distance of 20 mm. Activity of single units was commonly seen to burst in synchrony with field potential oscillations. These findings suggest that such oscillations may facilitate interactions between cells during exploratory and manipulative movements, requiring attention to sensorimotor integration.</description>
    <dc:title>Coherent 25- to 35-Hz oscillations in the sensorimotor cortex of awake behaving monkeys.</dc:title>

    <dc:creator>VN Murthy</dc:creator>
    <dc:creator>EE Fetz</dc:creator>
    <dc:source>Proc Natl Acad Sci U S A, Vol. 89, No. 12. (15 June 1992), pp. 5670-5674.</dc:source>
    <dc:date>2007-04-02T09:27:58-00:00</dc:date>
    <prism:publicationYear>1992</prism:publicationYear>
    <prism:publicationName>Proc Natl Acad Sci U S A</prism:publicationName>
    <prism:issn>0027-8424</prism:issn>
    <prism:volume>89</prism:volume>
    <prism:number>12</prism:number>
    <prism:startingPage>5670</prism:startingPage>
    <prism:endingPage>5674</prism:endingPage>
    <prism:category>hippocampus</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2985526">
    <title>Reliability, synchrony and noise.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2985526</link>
    <description>&lt;i&gt;Trends in neurosciences (4 July 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The brain is noisy. Neurons receive tens of thousands of highly fluctuating inputs and generate spike trains that appear highly irregular. Much of this activity is spontaneous - uncoupled to overt stimuli or motor outputs - leading to questions about the functional impact of this noise. Although noise is most often thought of as disrupting patterned activity and interfering with the encoding of stimuli, recent theoretical and experimental work has shown that noise can play a constructive role - leading to increased reliability or regularity of neuronal firing in single neurons and across populations. These results raise fundamental questions about how noise can influence neural function and computation.</description>
    <dc:title>Reliability, synchrony and noise.</dc:title>

    <dc:creator>G Bard Ermentrout</dc:creator>
    <dc:creator>Roberto F Galán</dc:creator>
    <dc:creator>Nathaniel N Urban</dc:creator>
    <dc:identifier>doi:10.1016/j.tins.2008.06.002</dc:identifier>
    <dc:source>Trends in neurosciences (4 July 2008)</dc:source>
    <dc:date>2008-07-10T15:55:08-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Trends in neurosciences</prism:publicationName>
    <prism:issn>0166-2236</prism:issn>
    <prism:category>review</prism:category>
    <prism:category>sponta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2985497">
    <title>Determinants of spontaneous activity in networks of cultured hippocampus.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2985497</link>
    <description>&lt;i&gt;Brain research (19 June 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The brain generates extensive spontaneous network activity patterns, even in the absence of extrinsic afferents. While the cognitive correlates of these complex activities are being unraveled, the rules that govern the generation, synchronization and spread of different patterns of intrinsic network activity in the brain are still enigmatic. Using hippocampal neurons grown in dissociated cultures, we are able to study these rules. Network activity emerges at 3-7 days in-vitro (DIV) independent of either ongoing excitatory or inhibitory synaptic activity. Network activity matures over the following several weeks in culture, when it becomes sensitive to chronic drug treatment. The size of the network determines its properties, such that dense networks have higher rates of less synchronized activity than that of sparse networks, which are more synchronized but rhythm at lower rates. Large networks cannot be triggered to fire by activating a single neuron. Small networks, on the other hand, do not burst spontaneously, but can be made to discharge a network burst by stimulating a single neuron. Thus, the strength of connectivity is inversely correlated with spontaneous activity and synchronicity. In the absence of confirmed 'leader' neurons, synchronous bursting network activity appears to be triggered by at least several local subthreshold synaptic events. We conclude that networks of neurons in culture can produce spontaneous synchronized activity and serve as a viable model system for the analysis of the rules that govern network activity in the brain.</description>
    <dc:title>Determinants of spontaneous activity in networks of cultured hippocampus.</dc:title>

    <dc:creator>Eyal Cohen</dc:creator>
    <dc:creator>Miriam Ivenshitz</dc:creator>
    <dc:creator>Veronique Amor-Baroukh</dc:creator>
    <dc:creator>Varda Greenberger</dc:creator>
    <dc:creator>Menahem Segal</dc:creator>
    <dc:identifier>doi:10.1016/j.brainres.2008.06.022</dc:identifier>
    <dc:source>Brain research (19 June 2008)</dc:source>
    <dc:date>2008-07-10T15:42:23-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Brain research</prism:publicationName>
    <prism:issn>0006-8993</prism:issn>
    <prism:category>networks</prism:category>
    <prism:category>sponta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2902689">
    <title>A quantitative theory of immediate visual recognition.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2902689</link>
    <description>&lt;i&gt;Progress in brain research, Vol. 165 (2007), pp. 33-56.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Human and non-human primates excel at visual recognition tasks. The primate visual system exhibits a strong degree of selectivity while at the same time being robust to changes in the input image. We have developed a quantitative theory to account for the computations performed by the feedforward path in the ventral stream of the primate visual cortex. Here we review recent predictions by a model instantiating the theory about physiological observations in higher visual areas. We also show that the model can perform recognition tasks on datasets of complex natural images at a level comparable to psychophysical measurements on human observers during rapid categorization tasks. In sum, the evidence suggests that the theory may provide a framework to explain the first 100-150 ms of visual object recognition. The model also constitutes a vivid example of how computational models can interact with experimental observations in order to advance our understanding of a complex phenomenon. We conclude by suggesting a number of open questions, predictions, and specific experiments for visual physiology and psychophysics.</description>
    <dc:title>A quantitative theory of immediate visual recognition.</dc:title>

    <dc:creator>T Serre</dc:creator>
    <dc:creator>G Kreiman</dc:creator>
    <dc:creator>M Kouh</dc:creator>
    <dc:creator>C Cadieu</dc:creator>
    <dc:creator>U Knoblich</dc:creator>
    <dc:creator>T Poggio</dc:creator>
    <dc:identifier>doi:10.1016/S0079-6123(06)65004-8</dc:identifier>
    <dc:source>Progress in brain research, Vol. 165 (2007), pp. 33-56.</dc:source>
    <dc:date>2008-06-17T15:15:35-00:00</dc:date>
    <prism:publicationYear>2007</prism:publicationYear>
    <prism:publicationName>Progress in brain research</prism:publicationName>
    <prism:issn>0079-6123</prism:issn>
    <prism:volume>165</prism:volume>
    <prism:startingPage>33</prism:startingPage>
    <prism:endingPage>56</prism:endingPage>
    <prism:category>model</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2985464">
    <title>Transcranial magnetic stimulation over posterior parietal cortex disrupts transsaccadic memory of multiple objects.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2985464</link>
    <description>&lt;i&gt;The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 28, No. 27. (2 July 2008), pp. 6938-6949.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The posterior parietal cortex (PPC) plays a role in spatial updating of goals for eye and arm movements across saccades, but less is known about its role in updating perceptual memory. We reported previously that transsaccadic memory has a capacity for storing the orientations of three to four Gabor patches either within a single fixation (fixation task) or between separate fixations (saccade task). Here, we tested the role of the PPC in transsaccadic memory in eight subjects by simultaneously applying single-pulse transcranial magnetic stimulation (TMS) over the right and left PPC, over several control sites, and comparing these to behavioral controls with no TMS. In TMS trials, we randomly delivered pulses at one of three different time intervals around the time of the saccade, or at an equivalent time in the fixation task. Controls confirmed that subjects could normally retain at least three visual features. TMS over the left PPC and a control site had no significant effect on this performance. However, TMS over the right PPC disrupted memory performance in both tasks. This TMS-induced effect was most disruptive in the saccade task, in particular when stimulation coincided more closely with saccade timing. Here, the capacity to compare presaccadic and postsaccadic features was reduced to one object, as expected if the spatial aspect of memory was disrupted. This finding suggests that right PPC plays a role in the spatial processing involved in transsaccadic memory of visual features. We propose that this process uses saccade-related feedback signals similar to those observed in spatial updating.</description>
    <dc:title>Transcranial magnetic stimulation over posterior parietal cortex disrupts transsaccadic memory of multiple objects.</dc:title>

    <dc:creator>SL Prime</dc:creator>
    <dc:creator>M Vesia</dc:creator>
    <dc:creator>JD Crawford</dc:creator>
    <dc:identifier>doi:10.1523/JNEUROSCI.0542-08.2008</dc:identifier>
    <dc:source>The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 28, No. 27. (2 July 2008), pp. 6938-6949.</dc:source>
    <dc:date>2008-07-10T15:29:38-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>The Journal of neuroscience : the official journal of the Society for Neuroscience</prism:publicationName>
    <prism:issn>1529-2401</prism:issn>
    <prism:volume>28</prism:volume>
    <prism:number>27</prism:number>
    <prism:startingPage>6938</prism:startingPage>
    <prism:endingPage>6949</prism:endingPage>
    <prism:category>eye-movement</prism:category>
    <prism:category>human</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2958834">
    <title>Biased competition through variations in amplitude of γ -oscillations</title>
    <link>http://www.citeulike.org/user/j-ito/article/2958834</link>
    <description>&lt;i&gt;Journal of Computational Neuroscience, Vol. 25, No. 1. (2008), pp. 89-107.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Abstract&#160;&#160;Experiments in visual cortex have shown that the firing rate of a neuron in response to the simultaneous presentation of a preferred and non-preferred stimulus within the receptive field is intermediate between that for the two stimuli alone (stimulus competition). Attention directed to one of the stimuli drives the response towards the response induced by the attended stimulus alone (selective attention). This study shows that a simple feedforward model with fixed synaptic conductance values can reproduce these two phenomena using synchronization in the gamma-frequency range to increase the effective synaptic gain for the responses to the attended stimulus. The performance of the model is robust to changes in the parameter values. The model predicts that the phase locking between presynaptic input and output spikes increases with attention.</description>
    <dc:title>Biased competition through variations in amplitude of γ -oscillations</dc:title>

    <dc:creator>Magteld Zeitler</dc:creator>
    <dc:creator>Pascal Fries</dc:creator>
    <dc:creator>Stan Gielen</dc:creator>
    <dc:identifier>doi:10.1007/s10827-007-0066-2</dc:identifier>
    <dc:source>Journal of Computational Neuroscience, Vol. 25, No. 1. (2008), pp. 89-107.</dc:source>
    <dc:date>2008-07-03T11:41:36-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Journal of Computational Neuroscience</prism:publicationName>
    <prism:volume>25</prism:volume>
    <prism:number>1</prism:number>
    <prism:startingPage>89</prism:startingPage>
    <prism:endingPage>107</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>model</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/1206800">
    <title>Brain Oscillations Control Timing of Single-Neuron Activity in Humans</title>
    <link>http://www.citeulike.org/user/j-ito/article/1206800</link>
    <description>&lt;i&gt;J. Neurosci., Vol. 27, No. 14. (4 April 2007), pp. 3839-3844.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;A growing body of animal research suggests that neurons represent information not only in terms of their firing rates but also by varying the timing of spikes relative to neuronal oscillations. Although researchers have argued that this temporal coding is critical in human memory and perception, no supporting data from humans have been reported. This study provides the first analysis of the temporal relationship between brain oscillations and single-neuron activity in humans. Recording from 1924 neurons, we find that neuronal activity in various brain regions increases at specific phases of brain oscillations. Neurons in widespread brain regions were phase locked to oscillations in the theta- (4-8 Hz) and gamma- (30- 90 Hz) frequency bands. In hippocampus, phase locking was prevalent in the delta- (1-4 Hz) and gamma-frequency bands. Individual neurons were phase locked to various phases of theta and delta oscillations, but they only were active at the trough of gamma oscillations. These findings provide support for the temporal-coding hypothesis in humans. Specifically, they indicate that theta and delta oscillations facilitate phase coding and that gamma oscillations help to decode combinations of simultaneously active neurons. 10.1523/JNEUROSCI.4636-06.2007</description>
    <dc:title>Brain Oscillations Control Timing of Single-Neuron Activity in Humans</dc:title>

    <dc:creator>Joshua Jacobs</dc:creator>
    <dc:creator>Michael Kahana</dc:creator>
    <dc:creator>Arne Ekstrom</dc:creator>
    <dc:creator>Itzhak Fried</dc:creator>
    <dc:identifier>doi:10.1523/JNEUROSCI.4636</dc:identifier>
    <dc:source>J. Neurosci., Vol. 27, No. 14. (4 April 2007), pp. 3839-3844.</dc:source>
    <dc:date>2007-04-04T23:02:39-00:00</dc:date>
    <prism:publicationYear>2007</prism:publicationYear>
    <prism:publicationName>J. Neurosci.</prism:publicationName>
    <prism:volume>27</prism:volume>
    <prism:number>14</prism:number>
    <prism:startingPage>3839</prism:startingPage>
    <prism:endingPage>3844</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>hippocampus</prism:category>
    <prism:category>human</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>theta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2939329">
    <title>Oscillatory Activity and Phase-Amplitude Coupling in the Human Medial Frontal Cortex during Decision Making.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2939329</link>
    <description>&lt;i&gt;Journal of cognitive neuroscience (29 May 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Abstract Electroencephalogram oscillations recorded both within and over the medial frontal cortex have been linked to a range of cognitive functions, including positive and negative feedback processing. Medial frontal oscillatory characteristics during decision making remain largely unknown. Here, we examined oscillatory activity of the human medial frontal cortex recorded while subjects played a competitive decision-making game. Distinct patterns of power and cross-trial phase coherence in multiple frequency bands were observed during different decision-related processes (e.g., feedback anticipation vs. feedback processing). Decision and feedback processing were accompanied by a broadband increase in cross-trial phase coherence at around 220 msec, and dynamic fluctuations in power. Feedback anticipation was accompanied by a shift in the power spectrum from relatively lower (delta and theta) to higher (alpha and beta) power. Power and cross-trial phase coherence were greater following losses compared to wins in theta, alpha, and beta frequency bands, but were greater following wins compared to losses in the delta band. Finally, we found that oscillation power in alpha and beta frequency bands were synchronized with the phase of delta and theta oscillations (&#34;phase-amplitude coupling&#34;). This synchronization differed between losses and wins, suggesting that phase-amplitude coupling might reflect a mechanism of feedback valence coding in the medial frontal cortex. Our findings link medial frontal oscillations to decision making, with relations among activity in different frequency bands suggesting a phase-utilizing coding of feedback valence information.</description>
    <dc:title>Oscillatory Activity and Phase-Amplitude Coupling in the Human Medial Frontal Cortex during Decision Making.</dc:title>

    <dc:creator>Michael X Cohen</dc:creator>
    <dc:creator>Christian E Elger</dc:creator>
    <dc:creator>Juergen Fell</dc:creator>
    <dc:identifier>doi:10.1162/jocn.2008.21020</dc:identifier>
    <dc:source>Journal of cognitive neuroscience (29 May 2008)</dc:source>
    <dc:date>2008-06-28T16:32:15-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Journal of cognitive neuroscience</prism:publicationName>
    <prism:issn>0898-929X</prism:issn>
    <prism:category>eeg</prism:category>
    <prism:category>gamma</prism:category>
    <prism:category>human</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>theta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2939322">
    <title>Phase/amplitude reset and theta-gamma interaction in the human medial temporal lobe during a continuous word recognition memory task.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2939322</link>
    <description>&lt;i&gt;Hippocampus, Vol. 15, No. 7. (2005), pp. 890-900.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;We analyzed intracranial electroencephalographic (EEG) recordings from the medial temporal lobes of 12 epilepsy patients during a continuous word recognition paradigm, contrasting trials of correctly recognized repeated words (hits) and correctly identified new words (correct rejections). Using a wavelet-based analysis, we investigated how power changes and phase clustering in different frequency bands contribute to the averaged event-related potentials (ERPs). In addition, we analyzed the actual mean phases of the different oscillations. Our analyses yielded the following results: (1) power changes contributed significantly only to the late components of the ERPs (&#62;400 ms) (2) earlier ERP components were produced by a stimulus-related broad-band phase and amplitude reset of ongoing oscillatory activity about 190 ms after stimulus onset that involved not only the theta band, but also covered alpha and lower beta band frequencies (3) phase and amplitude reset occurred during an epoch of increased phase entrainment over time that lasted for about two oscillation periods for all involved frequencies and was more pronounced for correct rejections than for hits. The broad-band phase and amplitude reset was observed for both hits and correct rejections, and therefore, did not appear to support a specific cognitive function, but rather to act as a general facilitating factor for the processes involved in this memory task. Further analyses of synchronization between oscillations and power changes in different frequency bands revealed a task-dependent modulation of gamma activity by the entrained theta cycle, a mechanism potentially related to memory encoding and retrieval in the rhinal cortex and hippocampus, respectively.</description>
    <dc:title>Phase/amplitude reset and theta-gamma interaction in the human medial temporal lobe during a continuous word recognition memory task.</dc:title>

    <dc:creator>F Mormann</dc:creator>
    <dc:creator>J Fell</dc:creator>
    <dc:creator>N Axmacher</dc:creator>
    <dc:creator>B Weber</dc:creator>
    <dc:creator>K Lehnertz</dc:creator>
    <dc:creator>CE Elger</dc:creator>
    <dc:creator>G Fernández</dc:creator>
    <dc:identifier>doi:10.1002/hipo.20117</dc:identifier>
    <dc:source>Hippocampus, Vol. 15, No. 7. (2005), pp. 890-900.</dc:source>
    <dc:date>2008-06-28T16:27:50-00:00</dc:date>
    <prism:publicationYear>2005</prism:publicationYear>
    <prism:publicationName>Hippocampus</prism:publicationName>
    <prism:issn>1050-9631</prism:issn>
    <prism:volume>15</prism:volume>
    <prism:number>7</prism:number>
    <prism:startingPage>890</prism:startingPage>
    <prism:endingPage>900</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>human</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>theta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2939314">
    <title>Gamma amplitudes are coupled to theta phase in human EEG during visual perception.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2939314</link>
    <description>&lt;i&gt;International journal of psychophysiology : official journal of the International Organization of Psychophysiology, Vol. 64, No. 1. (April 2007), pp. 24-30.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Human subjects typically keep about seven items (plus or minus two) in short-term memory (STM). A theoretical neuronal model has been proposed to explain this phenomenon with physiological parameters of brain oscillations in the gamma and theta frequency range, i.e., roughly 30-80 and 4-8 Hz, respectively. In that model, STM capacity equals the number of gamma cycles (e.g., 25 ms for 40 Hz), which fit into one theta cycle (e.g., 166 ms for 6 Hz). The model is based on two assumptions: (1) theta activity should modulate gamma activity; and (2) the theta/gamma ratio should correlate with human STM capacity. The first assumption is supported by electrophysiological data showing that the amplitude of gamma oscillations is modulated by the phase of theta activity. However, so far, this has only been demonstrated for intracranial recordings. We analyzed human event-related EEG oscillations recorded in a memory experiment in which 13 subjects perceived known and unknown visual stimuli. The paradigm revealed event-related oscillations in the gamma range, which depended significantly on the phase of simultaneous theta activity. Our data are the first scalp-recorded human EEG recordings revealing a relationship between the gamma amplitude and the phase of theta oscillations, supporting the first assumption of the above-mentioned theory. Interestingly, the involved frequencies revealed a 7:1 ratio. However, this ratio does not necessarily determine human STM capacity. Since such a correlation was not explicitly tested in our paradigm, our data are not conclusive about the second assumption. Instead of theta phase modulating gamma amplitude, it is also conceivable that focal gamma activity needs to be downsampled to theta activity, before it can interact with more distant brain regions.</description>
    <dc:title>Gamma amplitudes are coupled to theta phase in human EEG during visual perception.</dc:title>

    <dc:creator>T Demiralp</dc:creator>
    <dc:creator>Z Bayraktaroglu</dc:creator>
    <dc:creator>D Lenz</dc:creator>
    <dc:creator>S Junge</dc:creator>
    <dc:creator>NA Busch</dc:creator>
    <dc:creator>B Maess</dc:creator>
    <dc:creator>M Ergen</dc:creator>
    <dc:creator>CS Herrmann</dc:creator>
    <dc:identifier>doi:10.1016/j.ijpsycho.2006.07.005</dc:identifier>
    <dc:source>International journal of psychophysiology : official journal of the International Organization of Psychophysiology, Vol. 64, No. 1. (April 2007), pp. 24-30.</dc:source>
    <dc:date>2008-06-28T16:18:27-00:00</dc:date>
    <prism:publicationYear>2007</prism:publicationYear>
    <prism:publicationName>International journal of psychophysiology : official journal of the International Organization of Psychophysiology</prism:publicationName>
    <prism:issn>0167-8760</prism:issn>
    <prism:volume>64</prism:volume>
    <prism:number>1</prism:number>
    <prism:startingPage>24</prism:startingPage>
    <prism:endingPage>30</prism:endingPage>
    <prism:category>eeg</prism:category>
    <prism:category>gamma</prism:category>
    <prism:category>human</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>theta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2939302">
    <title>Au naturel.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2939302</link>
    <description>&lt;i&gt;Neuron, Vol. 58, No. 4. (22 May 2008), pp. 467-469.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Although adaptation is a ubiquitous property of neurons in the early visual pathway, the functional consequences in the natural visual environment are unknown. In this issue of Neuron, Mante et al. show, through a comprehensive set of in vivo experiments in the visual thalamus, that the basic functional mechanisms of adaptation that have been well studied with artificial probes capture the neuronal response in the natural environment and are predictable from properties of the visual scene that may be represented by local neural ensembles.</description>
    <dc:title>Au naturel.</dc:title>

    <dc:creator>GB Stanley</dc:creator>
    <dc:identifier>doi:10.1016/j.neuron.2008.05.003</dc:identifier>
    <dc:source>Neuron, Vol. 58, No. 4. (22 May 2008), pp. 467-469.</dc:source>
    <dc:date>2008-06-28T16:11:07-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Neuron</prism:publicationName>
    <prism:issn>1097-4199</prism:issn>
    <prism:volume>58</prism:volume>
    <prism:number>4</prism:number>
    <prism:startingPage>467</prism:startingPage>
    <prism:endingPage>469</prism:endingPage>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2939295">
    <title>Postnatal Development of Onset Transient Responses in Macaque V1 and V2 Neurons.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2939295</link>
    <description>&lt;i&gt;Journal of neurophysiology (25 June 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Vision of newborn infants is limited by immaturities in their visual brain. In adult primates the transient onset discharges of visual cortical neurons are thought to be intimately involved with capturing the rapid succession of brief images in visual scenes. Here we sought to determine the responsiveness and quality of transient responses in individual neurons of the primary visual cortex (V1) and visual area 2 (V2) of infant monkeys. We show that the transient component of neuronal firing to 640 millisecond stationary gratings was as robust and as reliable as in adults only 2 weeks after birth while the sustained component was more sluggish in infants than in adults. Thus, the cortical circuitry supporting onset transient responses is functionally mature near birth, and our findings predict that neonates, known for their 'impoverished vision', are capable of initiating relatively mature fixating eye movements and of performing in detection of simple objects far better than traditionally thought.</description>
    <dc:title>Postnatal Development of Onset Transient Responses in Macaque V1 and V2 Neurons.</dc:title>

    <dc:creator>Bin Zhang</dc:creator>
    <dc:creator>Earl L Smith Iii</dc:creator>
    <dc:creator>Yuzo M Chino</dc:creator>
    <dc:identifier>doi:10.1152/jn.90446.2008</dc:identifier>
    <dc:source>Journal of neurophysiology (25 June 2008)</dc:source>
    <dc:date>2008-06-28T16:05:43-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Journal of neurophysiology</prism:publicationName>
    <prism:issn>0022-3077</prism:issn>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2937772">
    <title>Theta and Gamma Coordination of Hippocampal Networks during Waking and Rapid Eye Movement Sleep</title>
    <link>http://www.citeulike.org/user/j-ito/article/2937772</link>
    <description>&lt;i&gt;J. Neurosci., Vol. 28, No. 26. (25 June 2008), pp. 6731-6741.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Rapid eye movement (REM) sleep has been considered a paradoxical state because, despite the high behavioral threshold to arousing perturbations, gross physiological patterns in the forebrain resemble those of waking states. To understand how intrahippocampal networks interact during REM sleep, we used 96 site silicon probes to record from different hippocampal subregions and compared the patterns of activity during waking exploration and REM sleep. Dentate/CA3 theta and gamma synchrony was significantly higher during REM sleep compared with active waking. In contrast, gamma power in CA1 and CA3-CA1 gamma coherence showed significant decreases in REM sleep. Changes in unit firing rhythmicity and unit-field coherence specified the local generation of these patterns. Although these patterns of hippocampal network coordination characterized the more common tonic periods of REM sleep ([~]95% of total REM), we also detected large phasic bursts of local field potential power in the dentate molecular layer that were accompanied by transient increases in the firing of dentate and CA1 neurons. In contrast to tonic REM periods, phasic REM epochs were characterized by higher theta and gamma synchrony among the dentate, CA3, and CA1 regions. These data suggest enhanced dentate processing, but limited CA3-CA1 coordination during tonic REM sleep. In contrast, phasic bursts of activity during REM sleep may provide windows of opportunity to synchronize the hippocampal trisynaptic loop and increase output to cortical targets. We hypothesize that tonic REM sleep may support off-line mnemonic processing, whereas phasic bursts of activity during REM may promote memory consolidation. 10.1523/JNEUROSCI.1227-08.2008</description>
    <dc:title>Theta and Gamma Coordination of Hippocampal Networks during Waking and Rapid Eye Movement Sleep</dc:title>

    <dc:creator>Sean Montgomery</dc:creator>
    <dc:creator>Anton Sirota</dc:creator>
    <dc:creator>Gyorgy Buzsaki</dc:creator>
    <dc:identifier>doi:10.1523/JNEUROSCI.1227-08.2008</dc:identifier>
    <dc:source>J. Neurosci., Vol. 28, No. 26. (25 June 2008), pp. 6731-6741.</dc:source>
    <dc:date>2008-06-27T17:05:12-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>J. Neurosci.</prism:publicationName>
    <prism:volume>28</prism:volume>
    <prism:number>26</prism:number>
    <prism:startingPage>6731</prism:startingPage>
    <prism:endingPage>6741</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>hippocampus</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>theta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2925631">
    <title>SYNCHRONIZATION OF NEURONAL RESPONSES IN PRIMARY VISUAL CORTEX OF MONKEYS VIEWING NATURAL IMAGES.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2925631</link>
    <description>&lt;i&gt;Journal of neurophysiology (18 June 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;When inspecting visual scenes, primates perform on average four saccadic eye movements per second which implies that scene segmentation, feature binding and identification of image components is accomplished in less than 200ms. Thus, individual neurons can contribute only a small number of discharges for these complex computations, suggesting that information is encoded not only in the discharge rate but also in the timing of action potentials. While monkeys inspected natural scenes we registered with multi-electrodes from primary visual cortex, the discharges of simultaneously recorded neurons. Relating these signals to eye movements, revealed that discharge rates peaked around 90ms after fixation onset and then decreased to near baseline levels within 200ms. Unitary event analysis revealed that preceding this increase in firing, there was an episode of enhanced response synchronization during which discharges of spatially distributed cells coincided within 5ms windows significantly more often than predicted by the discharge rates. This episode started 30ms after fixation onset and ended by the time discharge rates had reached their maximum. When the animals scanned a blank screen a small change in firing rate but no excess synchronization was observed. The short latency of the stimulation related synchronization phenomena suggests a fast acting mechanism for the coordination of spike timing that may contribute to the basic operations of scene segmentation.</description>
    <dc:title>SYNCHRONIZATION OF NEURONAL RESPONSES IN PRIMARY VISUAL CORTEX OF MONKEYS VIEWING NATURAL IMAGES.</dc:title>

    <dc:creator>Pedro E Maldonado</dc:creator>
    <dc:creator>Cecilia M Babul</dc:creator>
    <dc:creator>Wolf Singer</dc:creator>
    <dc:creator>Eugenio Rodriguez</dc:creator>
    <dc:creator>Denise Berger</dc:creator>
    <dc:creator>Sonja Grun</dc:creator>
    <dc:identifier>doi:10.1152/jn.00076.2008</dc:identifier>
    <dc:source>Journal of neurophysiology (18 June 2008)</dc:source>
    <dc:date>2008-06-25T10:26:41-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Journal of neurophysiology</prism:publicationName>
    <prism:issn>0022-3077</prism:issn>
    <prism:category>eye-movement</prism:category>
    <prism:category>first-spike</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2906898">
    <title>Population imaging of ongoing neuronal activity in the visual cortex of awake rats.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2906898</link>
    <description>&lt;i&gt;Nature neuroscience (15 June 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;It is unclear how the complex spatiotemporal organization of ongoing cortical neuronal activity recorded in anesthetized animals relates to the awake animal. We therefore used two-photon population calcium imaging in awake and subsequently anesthetized rats to follow action potential firing in populations of neurons across brain states, and examined how single neurons contributed to population activity. Firing rates and spike bursting in awake rats were higher, and pair-wise correlations were lower, compared with anesthetized rats. Anesthesia modulated population-wide synchronization and the relationship between firing rate and correlation. Overall, brain activity during wakefulness cannot be inferred using anesthesia.</description>
    <dc:title>Population imaging of ongoing neuronal activity in the visual cortex of awake rats.</dc:title>

    <dc:creator>David S Greenberg</dc:creator>
    <dc:creator>Arthur R Houweling</dc:creator>
    <dc:creator>Jason N D Kerr</dc:creator>
    <dc:identifier>doi:10.1038/nn.2140</dc:identifier>
    <dc:source>Nature neuroscience (15 June 2008)</dc:source>
    <dc:date>2008-06-19T09:03:09-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Nature neuroscience</prism:publicationName>
    <prism:issn>1097-6256</prism:issn>
    <prism:category>sponta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2906892">
    <title>Refinement of the retinogeniculate pathway.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2906892</link>
    <description>&lt;i&gt;The Journal of physiology (12 June 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Much of our present understanding about the mechanisms contributing to the activity dependent refinement of sensory connections comes from experiments done in the retinogeniculate pathway. In recent years the mouse has emerged as a model system of study. This review outlines the major changes in connectivity that occur in this species and a potential mechanism that can account for such remodeling. During early postnatal life when spontaneous activity of retinal ganglion cells sweeps across the retina in waves, retinal projections from the two eyes to the dorsal lateral geniculate nucleus (LGN) segregate to form non-overlapping eye specific domains. There is a loss of binocular innervation, a pruning of excitatory inputs from a dozen or more to one or two, and the emergence of inhibitory circuitry. Many of these changes underlie the development of precise eye specific visual maps and receptive field structure of LGN neurons. Retinal activity plays a major role both in the induction and maintenance of this refinement. The activity dependent influx of Ca(2+) through L-type channels and associated activation of CREB signaling may underlie the pruning and stabilization of developing retinogeniculate connections.</description>
    <dc:title>Refinement of the retinogeniculate pathway.</dc:title>

    <dc:creator>William Guido</dc:creator>
    <dc:identifier>doi:10.1113/jphysiol.2008.157115</dc:identifier>
    <dc:source>The Journal of physiology (12 June 2008)</dc:source>
    <dc:date>2008-06-19T09:01:45-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>The Journal of physiology</prism:publicationName>
    <prism:issn>1469-7793</prism:issn>
    <prism:category>review</prism:category>
    <prism:category>sponta</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/488473">
    <title>Comparison of Hilbert transform and wavelet methods for the analysis of neuronal synchrony.</title>
    <link>http://www.citeulike.org/user/j-ito/article/488473</link>
    <description>&lt;i&gt;J Neurosci Methods, Vol. 111, No. 2. (30 October 2001), pp. 83-98.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The quantification of phase synchrony between neuronal signals is of crucial importance for the study of large-scale interactions in the brain. Two methods have been used to date in neuroscience, based on two distinct approaches which permit a direct estimation of the instantaneous phase of a signal [Phys. Rev. Lett. 81 (1998) 3291; Human Brain Mapping 8 (1999) 194]. The phase is either estimated by using the analytic concept of Hilbert transform or, alternatively, by convolution with a complex wavelet. In both methods the stability of the instantaneous phase over a window of time requires quantification by means of various statistical dependence parameters (standard deviation, Shannon entropy or mutual information). The purpose of this paper is to conduct a direct comparison between these two methods on three signal sets: (1) neural models; (2) intracranial signals from epileptic patients; and (3) scalp EEG recordings. Levels of synchrony that can be considered as reliable are estimated by using the technique of surrogate data. Our results demonstrate that the differences between the methods are minor, and we conclude that they are fundamentally equivalent for the study of neuroelectrical signals. This offers a common language and framework that can be used for future research in the area of synchronization.</description>
    <dc:title>Comparison of Hilbert transform and wavelet methods for the analysis of neuronal synchrony.</dc:title>

    <dc:creator>M Le Van Quyen</dc:creator>
    <dc:creator>J Foucher</dc:creator>
    <dc:creator>J Lachaux</dc:creator>
    <dc:creator>E Rodriguez</dc:creator>
    <dc:creator>A Lutz</dc:creator>
    <dc:creator>J Martinerie</dc:creator>
    <dc:creator>FJ Varela</dc:creator>
    <dc:source>J Neurosci Methods, Vol. 111, No. 2. (30 October 2001), pp. 83-98.</dc:source>
    <dc:date>2006-02-01T12:23:12-00:00</dc:date>
    <prism:publicationYear>2001</prism:publicationYear>
    <prism:publicationName>J Neurosci Methods</prism:publicationName>
    <prism:issn>0165-0270</prism:issn>
    <prism:volume>111</prism:volume>
    <prism:number>2</prism:number>
    <prism:startingPage>83</prism:startingPage>
    <prism:endingPage>98</prism:endingPage>
    <prism:category>method</prism:category>
    <prism:category>oscillation</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2869965">
    <title>Uncovering Interactions in the Frequency Domain</title>
    <link>http://www.citeulike.org/user/j-ito/article/2869965</link>
    <description>&lt;i&gt;PLoS Comput Biol, Vol. 4, No. 5. (30 May 2008), e1000087.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Oscillatory activity plays a critical role in regulating biological processes at levels ranging from subcellular, cellular, and network to the whole organism, and often involves a large number of interacting elements. We shed light on this issue by introducing a novel approach called partial Granger causality to reliably reveal interaction patterns in multivariate data with exogenous inputs and latent variables in the frequency domain. The method is extensively tested with toy models, and successfully applied to experimental datasets, including (1) gene microarray data of HeLa cell cycle; (2) in vivo multi-electrode array (MEA) local field potentials (LFPs) recorded from the inferotemporal cortex of a sheep; and (3) in vivo LFPs recorded from distributed sites in the right hemisphere of a macaque monkey.</description>
    <dc:title>Uncovering Interactions in the Frequency Domain</dc:title>

    <dc:creator>Shuixia Guo</dc:creator>
    <dc:creator>Jianhua Wu</dc:creator>
    <dc:creator>Mingzhou Ding</dc:creator>
    <dc:creator>Jianfeng Feng</dc:creator>
    <dc:identifier>doi:10.1371/journal.pcbi.1000087</dc:identifier>
    <dc:source>PLoS Comput Biol, Vol. 4, No. 5. (30 May 2008), e1000087.</dc:source>
    <dc:date>2008-06-06T15:48:35-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>PLoS Comput Biol</prism:publicationName>
    <prism:volume>4</prism:volume>
    <prism:number>5</prism:number>
    <prism:startingPage>e1000087</prism:startingPage>
    <prism:publisher>Public Library of Science</prism:publisher>
    <prism:category>lfp</prism:category>
    <prism:category>method</prism:category>
    <prism:category>oscillation</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2878671">
    <title>Neuronal mechanisms of visual stability</title>
    <link>http://www.citeulike.org/user/j-ito/article/2878671</link>
    <description>&lt;i&gt;Vision Research, Vol. In Press, Corrected Proof&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Human vision is stable and continuous in spite of the incessant interruptions produced by saccadic eye movements. These rapid eye movements serve vision by directing the high resolution fovea rapidly from one part of the visual scene to another. They should detract from vision because they generate two major problems: displacement of the retinal image with each saccade and blurring of the image during the saccade. This review considers the substantial advances in understanding the neuronal mechanisms underlying this visual stability derived primarily from neuronal recording and inactivation studies in the monkey, an excellent model for systems in the human brain. For the first problem, saccadic displacement, two neuronal candidates are salient. First are the neurons in frontal and parietal cortex with shifting receptive fields that provide anticipatory activity with each saccade and are driven by a corollary discharge. These could provide the mechanism for a retinotopic hypothesis of visual stability and possibly for a transsaccadic memory hypothesis, The second neuronal mechanism is provided by neurons whose visual response is modulated by eye position (gain field neurons) or are largely independent of eye position (real position neurons), and these neurons could provide the basis for a spatiotopic hypothesis. For the second problem, saccadic suppression, visual masking and corollary discharge are well established mechanisms, and possible neuronal correlates have been identified for each.</description>
    <dc:title>Neuronal mechanisms of visual stability</dc:title>

    <dc:creator>Robert Wurtz</dc:creator>
    <dc:identifier>doi:10.1016/j.visres.2008.03.021</dc:identifier>
    <dc:source>Vision Research, Vol. In Press, Corrected Proof</dc:source>
    <dc:date>2008-06-10T07:03:03-00:00</dc:date>
    <prism:publicationName>Vision Research</prism:publicationName>
    <prism:volume>In Press, Corrected Proof</prism:volume>
    <prism:category>eye-movement</prism:category>
    <prism:category>review</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2860795">
    <title>Spontaneous Structure Formation in a Network of Chaotic Units with Variable Connection Strengths</title>
    <link>http://www.citeulike.org/user/j-ito/article/2860795</link>
    <description>&lt;i&gt;Physical Review Letters, Vol. 88, No. 2. (27 December 2001), 028701.&lt;/i&gt;</description>
    <dc:title>Spontaneous Structure Formation in a Network of Chaotic Units with Variable Connection Strengths</dc:title>

    <dc:creator>Junji Ito</dc:creator>
    <dc:creator>Kunihiko Kaneko</dc:creator>
    <dc:identifier>doi:10.1103/PhysRevLett.88.028701</dc:identifier>
    <dc:source>Physical Review Letters, Vol. 88, No. 2. (27 December 2001), 028701.</dc:source>
    <dc:date>2008-06-04T11:02:24-00:00</dc:date>
    <prism:publicationYear>2001</prism:publicationYear>
    <prism:publicationName>Physical Review Letters</prism:publicationName>
    <prism:volume>88</prism:volume>
    <prism:number>2</prism:number>
    <prism:startingPage>028701</prism:startingPage>
    <prism:publisher>American Physical Society</prism:publisher>
    <prism:category>model</prism:category>
    <prism:category>networks</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2833110">
    <title>Functional Mechanisms Shaping Lateral Geniculate Responses to Artificial and Natural Stimuli</title>
    <link>http://www.citeulike.org/user/j-ito/article/2833110</link>
    <description>&lt;i&gt;Neuron, Vol. 58, No. 4. (22 May 2008), pp. 625-638.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Summary Functional models of the early visual system should predict responses not only to simple artificial stimuli but also to sequences of complex natural scenes. An ideal testbed for such models is the lateral geniculate nucleus (LGN). Mechanisms shaping LGN responses include the linear receptive field and two fast adaptation processes, sensitive to luminance and contrast. We propose a compact functional model for these mechanisms that operates on sequences of arbitrary images. With the same parameters that fit the firing rate responses to simple stimuli, it predicts the bulk of the firing rate responses to complex stimuli, including natural scenes. Further improvements could result by adding a spiking mechanism, possibly one capable of bursts, but not by adding mechanisms of slow adaptation. We conclude that up to the LGN the responses to natural scenes can be largely explained through insights gained with simple artificial stimuli.</description>
    <dc:title>Functional Mechanisms Shaping Lateral Geniculate Responses to Artificial and Natural Stimuli</dc:title>

    <dc:creator>Valerio Mante</dc:creator>
    <dc:creator>Vincent Bonin</dc:creator>
    <dc:creator>Matteo Carandini</dc:creator>
    <dc:identifier>doi:10.1016/j.neuron.2008.03.011</dc:identifier>
    <dc:source>Neuron, Vol. 58, No. 4. (22 May 2008), pp. 625-638.</dc:source>
    <dc:date>2008-05-26T08:21:46-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Neuron</prism:publicationName>
    <prism:volume>58</prism:volume>
    <prism:number>4</prism:number>
    <prism:startingPage>625</prism:startingPage>
    <prism:endingPage>638</prism:endingPage>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2858648">
    <title>Saccades to a Remembered Location Elicit Spatially Specific Activation in the Human Retinotopic Visual Cortex.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2858648</link>
    <description>&lt;i&gt;Journal of cognitive neuroscience (29 May 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Abstract The possible impact upon the human visual cortex from saccades to remembered target locations was investigated using functional magnetic resonance imaging (fMRI). A specific location in the upper-right or upper-left visual quadrant served as the saccadic target. After a delay of 2400 msec, an auditory signal indicated whether to execute a saccade to that location (go trial) or to cancel the saccade and remain centrally fixated (no-go). Group fMRI analysis revealed activation specific to the remembered target location for executed saccades, in the contralateral lingual gyrus. No-go trials produced similar, albeit significantly reduced, effects. Individual retinotopic mapping confirmed that on go trials, quadrant-specific activations arose in those parts of ventral V1, V2, and V3 that coded the target location for the saccade, whereas on no-go trials, only the corresponding parts of V2 and V3 were significantly activated. These results indicate that a spatial-motor saccadic task (i.e., making an eye movement to a remembered location) is sufficient to activate the retinotopic visual cortex spatially corresponding to the target location, and that this activation is also present (though reduced) when no saccade is executed. We discuss the implications of finding that saccades to remembered locations can affect the early visual cortex, not just those structures conventionally associated with eye movements, in relation to recent ideas about attention, spatial working memory, and the notion that recently activated representations can be &#34;refreshed&#34; when needed.</description>
    <dc:title>Saccades to a Remembered Location Elicit Spatially Specific Activation in the Human Retinotopic Visual Cortex.</dc:title>

    <dc:creator>Joy J Geng</dc:creator>
    <dc:creator>Christian C Ruff</dc:creator>
    <dc:creator>Jon Driver</dc:creator>
    <dc:identifier>doi:10.1162/jocn.2008.21025</dc:identifier>
    <dc:source>Journal of cognitive neuroscience (29 May 2008)</dc:source>
    <dc:date>2008-06-03T10:07:25-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Journal of cognitive neuroscience</prism:publicationName>
    <prism:issn>0898-929X</prism:issn>
    <prism:category>eye-movement</prism:category>
    <prism:category>fmri</prism:category>
    <prism:category>human</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2856350">
    <title>Low-Frequency Local Field Potentials and Spikes in Primary Visual Cortex Convey Independent Visual Information</title>
    <link>http://www.citeulike.org/user/j-ito/article/2856350</link>
    <description>&lt;i&gt;J. Neurosci., Vol. 28, No. 22. (28 May 2008), pp. 5696-5709.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Local field potentials (LFPs) reflect subthreshold integrative processes that complement spike train measures. However, little is yet known about the differences between how LFPs and spikes encode rich naturalistic sensory stimuli. We addressed this question by recording LFPs and spikes from the primary visual cortex of anesthetized macaques while presenting a color movie. We then determined how the power of LFPs and spikes at different frequencies represents the visual features in the movie. We found that the most informative LFP frequency ranges were 1-8 and 60-100 Hz. LFPs in the range of 12-40 Hz carried little information about the stimulus, and may primarily reflect neuromodulatory inputs. Spike power was informative only at frequencies &#60;12 Hz. We further quantified &#34;signal correlations&#34; (correlations in the trial-averaged power response to different stimuli) and &#34;noise correlations&#34; (trial-by-trial correlations in the fluctuations around the average) of LFPs and spikes recorded from the same electrode. We found positive signal correlation between high-gamma LFPs (60-100 Hz) and spikes, as well as strong positive signal correlation within high-gamma LFPs, suggesting that high-gamma LFPs and spikes are generated within the same network. LFPs &#60;24 Hz shared strong positive noise correlations, indicating that they are influenced by a common source, such as a diffuse neuromodulatory input. LFPs &#60;40 Hz showed very little signal and noise correlations with LFPs &#62;40 Hz and with spikes, suggesting that low-frequency LFPs reflect neural processes that in natural conditions are fully decoupled from those giving rise to spikes and to high-gamma LFPs. 10.1523/JNEUROSCI.0009-08.2008</description>
    <dc:title>Low-Frequency Local Field Potentials and Spikes in Primary Visual Cortex Convey Independent Visual Information</dc:title>

    <dc:creator>Andrei Belitski</dc:creator>
    <dc:creator>Arthur Gretton</dc:creator>
    <dc:creator>Cesare Magri</dc:creator>
    <dc:creator>Yusuke Murayama</dc:creator>
    <dc:creator>Marcelo Montemurro</dc:creator>
    <dc:creator>Nikos Logothetis</dc:creator>
    <dc:creator>Stefano Panzeri</dc:creator>
    <dc:identifier>doi:10.1523/JNEUROSCI.0009-08.2008</dc:identifier>
    <dc:source>J. Neurosci., Vol. 28, No. 22. (28 May 2008), pp. 5696-5709.</dc:source>
    <dc:date>2008-06-02T10:17:41-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>J. Neurosci.</prism:publicationName>
    <prism:volume>28</prism:volume>
    <prism:number>22</prism:number>
    <prism:startingPage>5696</prism:startingPage>
    <prism:endingPage>5709</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>theta</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/1888394">
    <title>Adaptive coevolutionary networks: a review</title>
    <link>http://www.citeulike.org/user/j-ito/article/1888394</link>
    <description>&lt;i&gt;Journal of The Royal Society Interface&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Adaptive networks appear in many biological applications. They combine topological evolution of the network with dynamics in the network nodes. Recently, the dynamics of adaptive networks has been investigated in a number of parallel studies from different fields, ranging from genomics to game theory. Here we review these recent developments and show that they can be viewed from a unique angle. We demonstrate that all these studies are characterized by common themes, most prominently: complex dynamics and robust topological self-organization based on simple local rules.</description>
    <dc:title>Adaptive coevolutionary networks: a review</dc:title>

    <dc:creator>Thilo Gross</dc:creator>
    <dc:creator>Bernd Blasius</dc:creator>
    <dc:identifier>doi:10.1098/rsif.2007.1229</dc:identifier>
    <dc:source>Journal of The Royal Society Interface</dc:source>
    <dc:date>2007-11-09T08:19:02-00:00</dc:date>
    <prism:publicationName>Journal of The Royal Society Interface</prism:publicationName>
    <prism:category>model</prism:category>
    <prism:category>networks</prism:category>
    <prism:category>review</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2804535">
    <title>Transient Induced Gamma-Band Response in EEG as a Manifestation of Miniature Saccades</title>
    <link>http://www.citeulike.org/user/j-ito/article/2804535</link>
    <description>&lt;i&gt;Neuron, Vol. 58, No. 3. (8 May 2008), pp. 429-441.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Summary The induced gamma-band EEG response (iGBR) recorded on the scalp is widely assumed to reflect synchronous neural oscillation associated with object representation, attention, memory, and consciousness. The most commonly reported EEG iGBR is a broadband transient increase in power at the gamma range ~200-300 ms following stimulus onset. A conspicuous feature of this iGBR is the trial-to-trial poststimulus latency variability, which has been insufficiently addressed. Here, we show, using single-trial analysis of concomitant EEG and eye tracking, that this iGBR is tightly time locked to the onset of involuntary miniature eye movements and reflects a saccadic &#34;spike potential.&#34; The time course of the iGBR is related to an increase in the rate of saccades following a period of poststimulus saccadic inhibition. Thus, whereas neuronal gamma-band oscillations were shown conclusively with other methods, the broadband transient iGBR recorded by scalp EEG reflects properties of miniature saccade dynamics rather than neuronal oscillations.</description>
    <dc:title>Transient Induced Gamma-Band Response in EEG as a Manifestation of Miniature Saccades</dc:title>

    <dc:creator>Shlomit Yuval-Greenberg</dc:creator>
    <dc:creator>Orr Tomer</dc:creator>
    <dc:creator>Alon Keren</dc:creator>
    <dc:creator>Israel Nelken</dc:creator>
    <dc:creator>Leon Deouell</dc:creator>
    <dc:identifier>doi:10.1016/j.neuron.2008.03.027</dc:identifier>
    <dc:source>Neuron, Vol. 58, No. 3. (8 May 2008), pp. 429-441.</dc:source>
    <dc:date>2008-05-16T06:19:08-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Neuron</prism:publicationName>
    <prism:volume>58</prism:volume>
    <prism:number>3</prism:number>
    <prism:startingPage>429</prism:startingPage>
    <prism:endingPage>441</prism:endingPage>
    <prism:category>eeg</prism:category>
    <prism:category>eye-movement</prism:category>
    <prism:category>gamma</prism:category>
    <prism:category>human</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2804527">
    <title>The Effects of Visual Stimulation and Selective Visual Attention on Rhythmic Neuronal Synchronization in Macaque Area V4</title>
    <link>http://www.citeulike.org/user/j-ito/article/2804527</link>
    <description>&lt;i&gt;J. Neurosci., Vol. 28, No. 18. (30 April 2008), pp. 4823-4835.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Selective attention lends relevant sensory input priority access to higher-level brain areas and ultimately to behavior. Recent studies have suggested that those neurons in visual areas that are activated by an attended stimulus engage in enhanced gamma-band (30-70 Hz) synchronization compared with neurons activated by a distracter. Such precise synchronization could enhance the postsynaptic impact of cells carrying behaviorally relevant information. Previous studies have used the local field potential (LFP) power spectrum or spike-LFP coherence (SFC) to indirectly estimate spike synchronization. Here, we directly demonstrate zero-phase gamma-band coherence among spike trains of V4 neurons. This synchronization was particularly evident during visual stimulation and enhanced by selective attention, thus confirming the pattern inferred from LFP power and SFC. We therefore investigated the time course of LFP gamma-band power and found rapid dynamics consistent with interactions of top-down spatial and feature attention with bottom-up saliency. In addition to the modulation of synchronization during visual stimulation, selective attention significantly changed the prestimulus pattern of synchronization. Attention inside the receptive field of the recorded neuronal population enhanced gamma-band synchronization and strongly reduced alpha-band (9-11 Hz) synchronization in the prestimulus period. These results lend further support for a functional role of rhythmic neuronal synchronization in attentional stimulus selection. 10.1523/JNEUROSCI.4499-07.2008</description>
    <dc:title>The Effects of Visual Stimulation and Selective Visual Attention on Rhythmic Neuronal Synchronization in Macaque Area V4</dc:title>

    <dc:creator>Pascal Fries</dc:creator>
    <dc:creator>Thilo Womelsdorf</dc:creator>
    <dc:creator>Robert Oostenveld</dc:creator>
    <dc:creator>Robert Desimone</dc:creator>
    <dc:identifier>doi:10.1523/JNEUROSCI.4499-07.2008</dc:identifier>
    <dc:source>J. Neurosci., Vol. 28, No. 18. (30 April 2008), pp. 4823-4835.</dc:source>
    <dc:date>2008-05-16T06:11:15-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>J. Neurosci.</prism:publicationName>
    <prism:volume>28</prism:volume>
    <prism:number>18</prism:number>
    <prism:startingPage>4823</prism:startingPage>
    <prism:endingPage>4835</prism:endingPage>
    <prism:category>alpha</prism:category>
    <prism:category>gamma</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/505262">
    <title>The theta/gamma discrete phase code occuring during the hippocampal phase precession may be a more general brain coding scheme.</title>
    <link>http://www.citeulike.org/user/j-ito/article/505262</link>
    <description>&lt;i&gt;Hippocampus, Vol. 15, No. 7. (2005), pp. 913-922.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;In the hippocampus, oscillations in the theta and gamma frequency range occur together and interact in several ways, indicating that they are part of a common functional system. It is argued that these oscillations form a coding scheme that is used in the hippocampus to organize the readout from long-term memory of the discrete sequence of upcoming places, as cued by current position. This readout of place cells has been analyzed in several ways. First, plots of the theta phase of spikes vs. position on a track show a systematic progression of phase as rats run through a place field. This is termed the phase precession. Second, two cells with nearby place fields have a systematic difference in phase, as indicated by a cross-correlation having a peak with a temporal offset that is a significant fraction of a theta cycle. Third, several different decoding algorithms demonstrate the information content of theta phase in predicting the animal's position. It appears that small phase differences corresponding to jitter within a gamma cycle do not carry information. This evidence, together with the finding that principle cells fire preferentially at a given gamma phase, supports the concept of theta/gamma coding: a given place is encoded by the spatial pattern of neurons that fire in a given gamma cycle (the exact timing within a gamma cycle being unimportant); sequential places are encoded in sequential gamma subcycles of the theta cycle (i.e., with different discrete theta phase). It appears that this general form of coding is not restricted to readout of information from long-term memory in the hippocampus because similar patterns of theta/gamma oscillations have been observed in multiple brain regions, including regions involved in working memory and sensory integration. It is suggested that dual oscillations serve a general function: the encoding of multiple units of information (items) in a way that preserves their serial order. The relationship of such coding to that proposed by Singer and von der Malsburg is discussed; in their scheme, theta is not considered. It is argued that what theta provides is the absolute phase reference needed for encoding order. Theta/gamma coding therefore bears some relationship to the concept of &#34;word&#34; in digital computers, with word length corresponding to the number of gamma cycles within a theta cycle, and discrete phase corresponding to the ordered &#34;place&#34; within a word.</description>
    <dc:title>The theta/gamma discrete phase code occuring during the hippocampal phase precession may be a more general brain coding scheme.</dc:title>

    <dc:creator>J Lisman</dc:creator>
    <dc:identifier>doi:10.1002/hipo.20121</dc:identifier>
    <dc:source>Hippocampus, Vol. 15, No. 7. (2005), pp. 913-922.</dc:source>
    <dc:date>2006-02-14T17:32:39-00:00</dc:date>
    <prism:publicationYear>2005</prism:publicationYear>
    <prism:publicationName>Hippocampus</prism:publicationName>
    <prism:issn>1050-9631</prism:issn>
    <prism:volume>15</prism:volume>
    <prism:number>7</prism:number>
    <prism:startingPage>913</prism:startingPage>
    <prism:endingPage>922</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>theta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2687128">
    <title>LFP power spectra in V1 cortex: the graded effect of stimulus contrast.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2687128</link>
    <description>&lt;i&gt;Journal of neurophysiology, Vol. 94, No. 1. (July 2005), pp. 479-490.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;We recorded local field potentials (LFPs) and single-unit activity simultaneously in the macaque primary visual cortex (V1) and studied their responses to drifting sinusoidal gratings that were chosen to be &#34;optimal&#34; for the single units. Over all stimulus conditions, the LFP spectra have much greater power in the low-frequency band (&#60; or = 10 Hz) than higher frequencies and can be described as &#34;1/f.&#34; Analysis of the total power limited to the low, gamma (25-90 Hz), or broad (8-240 Hz) frequency bands of the LFP as a function of stimulus contrast indicates that the LFP power gradually increases with stimulus strength across a wide band in a manner roughly comparable to the increase in the simultaneously recorded spike activity. However, the low-frequency band power remains approximately constant across all stimulus contrasts. More specifically the gamma-band LFP power increases differentially more with respect to baseline than either higher or lower bands as stimulus contrast increases. At the highest stimulus contrasts, we report as others have previously, that the power spectrum of the LFP typically contains an obvious peak in the gamma-frequency band. The gamma-band peak emerges from the overall broadband enhancement in LFP power at stimulus contrasts where most single units' responses have begun to saturate. The temporal/spectral structures of the LFP located in the gamma band-which become most evident at the highest contrasts-provide additional constraints on potential mechanisms underlying the stimulus response properties of spiking neurons in V1.</description>
    <dc:title>LFP power spectra in V1 cortex: the graded effect of stimulus contrast.</dc:title>

    <dc:creator>JA Henrie</dc:creator>
    <dc:creator>R Shapley</dc:creator>
    <dc:identifier>doi:10.1152/jn.00919.2004</dc:identifier>
    <dc:source>Journal of neurophysiology, Vol. 94, No. 1. (July 2005), pp. 479-490.</dc:source>
    <dc:date>2008-04-18T07:24:00-00:00</dc:date>
    <prism:publicationYear>2005</prism:publicationYear>
    <prism:publicationName>Journal of neurophysiology</prism:publicationName>
    <prism:issn>0022-3077</prism:issn>
    <prism:volume>94</prism:volume>
    <prism:number>1</prism:number>
    <prism:startingPage>479</prism:startingPage>
    <prism:endingPage>490</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2687096">
    <title>Inferring spike trains from local field potentials.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2687096</link>
    <description>&lt;i&gt;Journal of neurophysiology, Vol. 99, No. 3. (March 2008), pp. 1461-1476.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;We investigated whether it is possible to infer spike trains solely on the basis of the underlying local field potentials (LFPs). Using support vector machines and linear regression models, we found that in the primary visual cortex (V1) of monkeys, spikes can indeed be inferred from LFPs, at least with moderate success. Although there is a considerable degree of variation across electrodes, the low-frequency structure in spike trains (in the 100-ms range) can be inferred with reasonable accuracy, whereas exact spike positions are not reliably predicted. Two kinds of features of the LFP are exploited for prediction: the frequency power of bands in the high gamma-range (40-90 Hz) and information contained in low-frequency oscillations (&#60;10 Hz), where both phase and power modulations are informative. Information analysis revealed that both features code (mainly) independent aspects of the spike-to-LFP relationship, with the low-frequency LFP phase coding for temporally clustered spiking activity. Although both features and prediction quality are similar during seminatural movie stimuli and spontaneous activity, prediction performance during spontaneous activity degrades much more slowly with increasing electrode distance. The general trend of data obtained with anesthetized animals is qualitatively mirrored in that of a more limited data set recorded in V1 of non-anesthetized monkeys. In contrast to the cortical field potentials, thalamic LFPs (e.g., LFPs derived from recordings in the dorsal lateral geniculate nucleus) hold no useful information for predicting spiking activity.</description>
    <dc:title>Inferring spike trains from local field potentials.</dc:title>

    <dc:creator>MJ Rasch</dc:creator>
    <dc:creator>A Gretton</dc:creator>
    <dc:creator>Y Murayama</dc:creator>
    <dc:creator>W Maass</dc:creator>
    <dc:creator>NK Logothetis</dc:creator>
    <dc:identifier>doi:10.1152/jn.00919.2007</dc:identifier>
    <dc:source>Journal of neurophysiology, Vol. 99, No. 3. (March 2008), pp. 1461-1476.</dc:source>
    <dc:date>2008-04-18T07:16:03-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Journal of neurophysiology</prism:publicationName>
    <prism:issn>0022-3077</prism:issn>
    <prism:volume>99</prism:volume>
    <prism:number>3</prism:number>
    <prism:startingPage>1461</prism:startingPage>
    <prism:endingPage>1476</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>sponta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2666145">
    <title>Neuronal activity in the primary visual cortex of the cat freely viewing natural images.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2666145</link>
    <description>&lt;i&gt;Neuroscience, Vol. 144, No. 4. (23 February 2007), pp. 1536-1543.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Many studies have now demonstrated that neurons in the visual cortex of cats and monkeys change their activity when stimuli are presented beyond their classical receptive field, and that these responses are not readily apparent from their receptive field properties. However few studies have been conducted to investigate the discharge properties of neurons in the visual cortex of animals when they are allow to freely view natural images. We employ tetrodes, which enable simultaneous and separable recordings of small numbers of neighboring neurons, to record 102 single units from 59 sites from areas 17 and 18 of two alert cats. While the animals viewed either natural images or black screens, they made frequent saccadic eye movements and gaze fixations. Fixations onto an image's location increased neuronal firing peaking at 80-100 ms after the fixation onset, to then decrease steadily with time despite continuous fixation. Saccades trigger a fast decrease in firing rate for both images and darkness. When we examined the incidence of correlated firing, we observed significant synchrony during the initial phases of visual fixations when the animals viewed natural scenes. Such synchrony was absent during saccadic eye movements and during eye movements in darkness. Our data revealed that scanning of natural scenes is associated with a rapid succession of distinct fixation-related activation patterns that included transient rate changes and excess coincident firing. The transient nature of these synchronization phenomena suggests a fast acting mechanism, which is in good agreement with the evidence that basic operations of scene analysis must be accomplished within a few tens of milliseconds in primary visual cortex.</description>
    <dc:title>Neuronal activity in the primary visual cortex of the cat freely viewing natural images.</dc:title>

    <dc:creator>PE Maldonado</dc:creator>
    <dc:creator>CM Babul</dc:creator>
    <dc:identifier>doi:10.1016/j.neuroscience.2006.11.021</dc:identifier>
    <dc:source>Neuroscience, Vol. 144, No. 4. (23 February 2007), pp. 1536-1543.</dc:source>
    <dc:date>2008-04-14T08:53:08-00:00</dc:date>
    <prism:publicationYear>2007</prism:publicationYear>
    <prism:publicationName>Neuroscience</prism:publicationName>
    <prism:issn>0306-4522</prism:issn>
    <prism:volume>144</prism:volume>
    <prism:number>4</prism:number>
    <prism:startingPage>1536</prism:startingPage>
    <prism:endingPage>1543</prism:endingPage>
    <prism:category>eye-movement</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2647614">
    <title>Entrainment of neuronal oscillations as a mechanism of attentional selection.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2647614</link>
    <description>&lt;i&gt;Science (New York, N.Y.), Vol. 320, No. 5872. (4 April 2008), pp. 110-113.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Whereas gamma-band neuronal oscillations clearly appear integral to visual attention, the role of lower-frequency oscillations is still being debated. Mounting evidence indicates that a key functional property of these oscillations is the rhythmic shifting of excitability in local neuronal ensembles. Here, we show that when attended stimuli are in a rhythmic stream, delta-band oscillations in the primary visual cortex entrain to the rhythm of the stream, resulting in increased response gain for task-relevant events and decreased reaction times. Because of hierarchical cross-frequency coupling, delta phase also determines momentary power in higher-frequency activity. These instrumental functions of low-frequency oscillations support a conceptual framework that integrates numerous earlier findings.</description>
    <dc:title>Entrainment of neuronal oscillations as a mechanism of attentional selection.</dc:title>

    <dc:creator>P Lakatos</dc:creator>
    <dc:creator>G Karmos</dc:creator>
    <dc:creator>AD Mehta</dc:creator>
    <dc:creator>I Ulbert</dc:creator>
    <dc:creator>CE Schroeder</dc:creator>
    <dc:identifier>doi:10.1126/science.1154735</dc:identifier>
    <dc:source>Science (New York, N.Y.), Vol. 320, No. 5872. (4 April 2008), pp. 110-113.</dc:source>
    <dc:date>2008-04-10T01:01:54-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Science (New York, N.Y.)</prism:publicationName>
    <prism:issn>1095-9203</prism:issn>
    <prism:volume>320</prism:volume>
    <prism:number>5872</prism:number>
    <prism:startingPage>110</prism:startingPage>
    <prism:endingPage>113</prism:endingPage>
    <prism:category>gamma</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>theta</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/658837">
    <title>Seeing at a glance, smelling in a whiff: rapid forms of perceptual decision making</title>
    <link>http://www.citeulike.org/user/j-ito/article/658837</link>
    <description>&lt;i&gt;Nature Reviews Neuroscience, Vol. 7, No. 6., pp. 485-491.&lt;/i&gt;</description>
    <dc:title>Seeing at a glance, smelling in a whiff: rapid forms of perceptual decision making</dc:title>

    <dc:creator>Naoshige Uchida</dc:creator>
    <dc:creator>Adam Kepecs</dc:creator>
    <dc:creator>Zachary Mainen</dc:creator>
    <dc:identifier>doi:10.1038/nrn1933</dc:identifier>
    <dc:source>Nature Reviews Neuroscience, Vol. 7, No. 6., pp. 485-491.</dc:source>
    <dc:date>2006-05-20T11:27:51-00:00</dc:date>
    <prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
    <prism:issn>1471-003X</prism:issn>
    <prism:volume>7</prism:volume>
    <prism:number>6</prism:number>
    <prism:startingPage>485</prism:startingPage>
    <prism:endingPage>491</prism:endingPage>
    <prism:publisher>Nature Publishing Group</prism:publisher>
    <prism:category>oscillation</prism:category>
    <prism:category>review</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2547178">
    <title>The temporal resolution of neural codes: does response latency have a unique role?</title>
    <link>http://www.citeulike.org/user/j-ito/article/2547178</link>
    <description>&lt;i&gt;Philos Trans R Soc Lond B Biol Sci, Vol. 357, No. 1424. (29 August 2002), pp. 987-1001.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;This article reviews the nature of the neural code in non-human primate cortex and assesses the potential for neurons to carry two or more signals simultaneously. Neurophysiological recordings from visual and motor systems indicate that the evidence for a role for precisely timed spikes relative to other spike times (ca. 1-10 ms resolution) is inconclusive. This indicates that the visual system does not carry a signal that identifies whether the responses were elicited when the stimulus was attended or not. Simulations show that the absence of such a signal reduces, but does not eliminate, the increased discrimination between stimuli that are attended compared with when the stimuli are unattended. The increased accuracy asymptotes with increased gain control, indicating limited benefit from increasing attention. The absence of a signal identifying the attentional state under which stimuli were viewed can produce the greatest discrimination between attended and unattended stimuli. Furthermore, the greatest reduction in discrimination errors occurs for a limited range of gain control, again indicating that attention effects are limited. By contrast to precisely timed patterns of spikes where the timing is relative to other spikes, response latency provides a fine temporal resolution signal (ca. 10 ms resolution) that carries information that is unavailable from coarse temporal response measures. Changes in response latency and changes in response magnitude can give rise to different predictions for the patterns of reaction times. The predictions are verified, and it is shown that the standard method for distinguishing executive and slave processes is only valid if the representations of interest, as evidenced by the neural code, are known. Overall, the data indicate that the signalling evident in neural signals is restricted to the spike count and the precise times of spikes relative to stimulus onset (response latency). These coding issues have implications for our understanding of cognitive models of attention and the roles of executive and slave systems.</description>
    <dc:title>The temporal resolution of neural codes: does response latency have a unique role?</dc:title>

    <dc:creator>MW Oram</dc:creator>
    <dc:creator>D Xiao</dc:creator>
    <dc:creator>B Dritschel</dc:creator>
    <dc:creator>KR Payne</dc:creator>
    <dc:identifier>doi:10.1098/rstb.2002.1113</dc:identifier>
    <dc:source>Philos Trans R Soc Lond B Biol Sci, Vol. 357, No. 1424. (29 August 2002), pp. 987-1001.</dc:source>
    <dc:date>2008-03-17T16:43:31-00:00</dc:date>
    <prism:publicationYear>2002</prism:publicationYear>
    <prism:publicationName>Philos Trans R Soc Lond B Biol Sci</prism:publicationName>
    <prism:issn>0962-8436</prism:issn>
    <prism:volume>357</prism:volume>
    <prism:number>1424</prism:number>
    <prism:startingPage>987</prism:startingPage>
    <prism:endingPage>1001</prism:endingPage>
    <prism:category>first-spike</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2625448">
    <title>Signal timing across the macaque visual system.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2625448</link>
    <description>&lt;i&gt;Journal of neurophysiology, Vol. 79, No. 6. (June 1998), pp. 3272-3278.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The onset latencies of single-unit responses evoked by flashing visual stimuli were measured in the parvocellular (P) and magnocellular (M) layers of the dorsal lateral geniculate nucleus (LGNd) and in cortical visual areas V1, V2, V3, V4, middle temporal area (MT), medial superior temporal area (MST), and in the frontal eye field (FEF) in individual anesthetized monkeys. Identical procedures were carried out to assess latencies in each area, often in the same monkey, thereby permitting direct comparisons of timing across areas. This study presents the visual flash-evoked latencies for cells in areas where such data are common (V1 and V2), and are therefore a good standard, and also in areas where such data are sparse (LGNd M and P layers, MT, V4) or entirely lacking (V3, MST, and FEF in anesthetized preparation). Visual-evoked onset latencies were, on average, 17 ms shorter in the LGNd M layers than in the LGNd P layers. Visual responses occurred in V1 before any other cortical area. The next wave of activation occurred concurrently in areas V3, MT, MST, and FEF. Visual response latencies in areas V2 and V4 were progressively later and more broadly distributed. These differences in the time course of activation across the dorsal and ventral streams provide important temporal constraints on theories of visual processing.</description>
    <dc:title>Signal timing across the macaque visual system.</dc:title>

    <dc:creator>MT Schmolesky</dc:creator>
    <dc:creator>Y Wang</dc:creator>
    <dc:creator>DP Hanes</dc:creator>
    <dc:creator>KG Thompson</dc:creator>
    <dc:creator>S Leutgeb</dc:creator>
    <dc:creator>JD Schall</dc:creator>
    <dc:creator>AG Leventhal</dc:creator>
    <dc:source>Journal of neurophysiology, Vol. 79, No. 6. (June 1998), pp. 3272-3278.</dc:source>
    <dc:date>2008-04-03T08:33:28-00:00</dc:date>
    <prism:publicationYear>1998</prism:publicationYear>
    <prism:publicationName>Journal of neurophysiology</prism:publicationName>
    <prism:issn>0022-3077</prism:issn>
    <prism:volume>79</prism:volume>
    <prism:number>6</prism:number>
    <prism:startingPage>3272</prism:startingPage>
    <prism:endingPage>3278</prism:endingPage>
    <prism:category>first-spike</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2625395">
    <title>Instantaneous correlation of excitation and inhibition during ongoing and sensory-evoked activities.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2625395</link>
    <description>&lt;i&gt;Nature neuroscience (30 March 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Temporal and quantitative relations between excitatory and inhibitory inputs in the cortex are central to its activity, yet they remain poorly understood. In particular, a controversy exists regarding the extent of correlation between cortical excitation and inhibition. Using simultaneous intracellular recordings in pairs of nearby neurons in vivo, we found that excitatory and inhibitory inputs are continuously synchronized and correlated in strength during spontaneous and sensory-evoked activities in the rat somatosensory cortex.</description>
    <dc:title>Instantaneous correlation of excitation and inhibition during ongoing and sensory-evoked activities.</dc:title>

    <dc:creator>Michael Okun</dc:creator>
    <dc:creator>Ilan Lampl</dc:creator>
    <dc:identifier>doi:10.1038/nn.2105</dc:identifier>
    <dc:source>Nature neuroscience (30 March 2008)</dc:source>
    <dc:date>2008-04-03T08:10:22-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Nature neuroscience</prism:publicationName>
    <prism:issn>1097-6256</prism:issn>
    <prism:category>sponta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2625387">
    <title>Structure of spontaneous UP and DOWN transitions self-organizing in a cortical network model.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2625387</link>
    <description>&lt;i&gt;PLoS computational biology, Vol. 4, No. 3. (March 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Synaptic plasticity is considered to play a crucial role in the experience-dependent self-organization of local cortical networks. In the absence of sensory stimuli, cerebral cortex exhibits spontaneous membrane potential transitions between an UP and a DOWN state. To reveal how cortical networks develop spontaneous activity, or conversely, how spontaneous activity structures cortical networks, we analyze the self-organization of a recurrent network model of excitatory and inhibitory neurons, which is realistic enough to replicate UP-DOWN states, with spike-timing-dependent plasticity (STDP). The individual neurons in the self-organized network exhibit a variety of temporal patterns in the two-state transitions. In addition, the model develops a feed-forward network-like structure that produces a diverse repertoire of precise sequences of the UP state. Our model shows that the self-organized activity well resembles the spontaneous activity of cortical networks if STDP is accompanied by the pruning of weak synapses. These results suggest that the two-state membrane potential transitions play an active role in structuring local cortical circuits.</description>
    <dc:title>Structure of spontaneous UP and DOWN transitions self-organizing in a cortical network model.</dc:title>

    <dc:creator>S Kang</dc:creator>
    <dc:creator>K Kitano</dc:creator>
    <dc:creator>T Fukai</dc:creator>
    <dc:identifier>doi:10.1371/journal.pcbi.1000022</dc:identifier>
    <dc:source>PLoS computational biology, Vol. 4, No. 3. (March 2008)</dc:source>
    <dc:date>2008-04-03T08:06:25-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>PLoS computational biology</prism:publicationName>
    <prism:issn>1553-7358</prism:issn>
    <prism:volume>4</prism:volume>
    <prism:number>3</prism:number>
    <prism:category>model</prism:category>
    <prism:category>sponta</prism:category>
    <prism:category>stdp</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2461067">
    <title>Measurements of Simultaneously Recorded Spiking Activity and Local Field Potentials Suggest that Spatial Selection Emerges in the Frontal Eye Field.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2461067</link>
    <description>&lt;i&gt;Neuron, Vol. 57, No. 4. (28 February 2008), pp. 614-625.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The frontal eye field (FEF) participates in selecting the location of behaviorally relevant stimuli for guiding attention and eye movements. We simultaneously recorded local field potentials (LFPs) and spiking activity in the FEF of monkeys performing memory-guided saccade and covert visual search tasks. We compared visual latencies and the time course of spatially selective responses in LFPs and spiking activity. Consistent with the view that LFPs represent synaptic input, visual responses appeared first in the LFPs followed by visual responses in the spiking activity. However, spatially selective activity identifying the location of the target in the visual search array appeared in the spikes about 30 ms before it appeared in the LFPs. Because LFPs reflect dendritic input and spikes measure neuronal output in a local brain region, this temporal relationship suggests that spatial selection necessary for attention and eye movements is computed locally in FEF from spatially nonselective inputs.</description>
    <dc:title>Measurements of Simultaneously Recorded Spiking Activity and Local Field Potentials Suggest that Spatial Selection Emerges in the Frontal Eye Field.</dc:title>

    <dc:creator>IE Monosov</dc:creator>
    <dc:creator>JC Trageser</dc:creator>
    <dc:creator>KG Thompson</dc:creator>
    <dc:identifier>doi:10.1016/j.neuron.2007.12.030</dc:identifier>
    <dc:source>Neuron, Vol. 57, No. 4. (28 February 2008), pp. 614-625.</dc:source>
    <dc:date>2008-03-03T15:48:38-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Neuron</prism:publicationName>
    <prism:issn>0896-6273</prism:issn>
    <prism:volume>57</prism:volume>
    <prism:number>4</prism:number>
    <prism:startingPage>614</prism:startingPage>
    <prism:endingPage>625</prism:endingPage>
    <prism:category>lfp</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2517071">
    <title>Phase-of-Firing Coding of Natural Visual Stimuli in Primary Visual Cortex.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2517071</link>
    <description>&lt;i&gt;Curr Biol (5 March 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;We investigated the hypothesis that neurons encode rich naturalistic stimuli in terms of their spike times relative to the phase of ongoing network fluctuations rather than only in terms of their spike count. We recorded local field potentials (LFPs) and multiunit spikes from the primary visual cortex of anaesthetized macaques while binocularly presenting a color movie. We found that both the spike counts and the low-frequency LFP phase were reliably modulated by the movie and thus conveyed information about it. Moreover, movie periods eliciting higher firing rates also elicited a higher reliability of LFP phase across trials. To establish whether the LFP phase at which spikes were emitted conveyed visual information that could not be extracted by spike rates alone, we compared the Shannon information about the movie carried by spike counts to that carried by the phase of firing. We found that at low LFP frequencies, the phase of firing conveyed 54% additional information beyond that conveyed by spike counts. The extra information available in the phase of firing was crucial for the disambiguation between stimuli eliciting high spike rates of similar magnitude. Thus, phase coding may allow primary cortical neurons to represent several effective stimuli in an easily decodable format.</description>
    <dc:title>Phase-of-Firing Coding of Natural Visual Stimuli in Primary Visual Cortex.</dc:title>

    <dc:creator>Marcelo A Montemurro</dc:creator>
    <dc:creator>Malte J Rasch</dc:creator>
    <dc:creator>Yusuke Murayama</dc:creator>
    <dc:creator>Nikos K Logothetis</dc:creator>
    <dc:creator>Stefano Panzeri</dc:creator>
    <dc:identifier>doi:10.1016/j.cub.2008.02.023</dc:identifier>
    <dc:source>Curr Biol (5 March 2008)</dc:source>
    <dc:date>2008-03-12T00:24:39-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Curr Biol</prism:publicationName>
    <prism:issn>0960-9822</prism:issn>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>sponta</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2412034">
    <title>Rapid Neural Coding in the Retina with Relative Spike Latencies</title>
    <link>http://www.citeulike.org/user/j-ito/article/2412034</link>
    <description>&lt;i&gt;Science, Vol. 319, No. 5866. (22 February 2008), pp. 1108-1111.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Natural vision is a highly dynamic process. Frequent body, head, and eye movements constantly bring new images onto the retina for brief periods, challenging our understanding of the neural code for vision. We report that certain retinal ganglion cells encode the spatial structure of a briefly presented image in the relative timing of their first spikes. This code is found to be largely invariant to stimulus contrast and robust to noisy fluctuations in response latencies. Mechanistically, the observed response characteristics result from different kinetics in two retinal pathways (&#34;ON&#34; and &#34;OFF&#34;) that converge onto ganglion cells. This mechanism allows the retina to rapidly and reliably transmit new spatial information with the very first spikes emitted by a neural population. 10.1126/science.1149639</description>
    <dc:title>Rapid Neural Coding in the Retina with Relative Spike Latencies</dc:title>

    <dc:creator>Tim Gollisch</dc:creator>
    <dc:creator>Markus Meister</dc:creator>
    <dc:identifier>doi:10.1126/science.1149639</dc:identifier>
    <dc:source>Science, Vol. 319, No. 5866. (22 February 2008), pp. 1108-1111.</dc:source>
    <dc:date>2008-02-22T10:01:31-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Science</prism:publicationName>
    <prism:volume>319</prism:volume>
    <prism:number>5866</prism:number>
    <prism:startingPage>1108</prism:startingPage>
    <prism:endingPage>1111</prism:endingPage>
    <prism:category>first-spike</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/1292898">
    <title>Transient Cortical Excitation at the Onset of Visual Fixation.</title>
    <link>http://www.citeulike.org/user/j-ito/article/1292898</link>
    <description>&lt;i&gt;Cereb Cortex (10 May 2007)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Primates actively examine the visual world by rapidly shifting gaze (fixation) over the elements in a scene. Despite this fact, we typically study vision by presenting stimuli with gaze held constant. To better understand the dynamics of natural vision, we examined how the onset of visual fixation affects ongoing neuronal activity in the absence of visual stimulation. We used multiunit activity and current source density measurements to index neuronal firing patterns and underlying synaptic processes in macaque V1. Initial averaging of neural activity synchronized to the onset of fixation suggested that a brief period of cortical excitation follows each fixation. Subsequent single-trial analyses revealed that 1) neuronal oscillation phase transits from random to a highly organized state just after the fixation onset, 2) this phase concentration is accompanied by increased spectral power in several frequency bands, and 3) visual response amplitude is enhanced at the specific oscillatory phase associated with fixation. We hypothesize that nonvisual inputs are used by the brain to increase cortical excitability at fixation onset, thus &#34;priming&#34; the system for new visual inputs generated at fixation. Despite remaining mechanistic questions, it appears that analysis of fixation-related responses may be useful in studying natural vision.</description>
    <dc:title>Transient Cortical Excitation at the Onset of Visual Fixation.</dc:title>

    <dc:creator>Csaba Rajkai</dc:creator>
    <dc:creator>Peter Lakatos</dc:creator>
    <dc:creator>Chi-Ming Chen</dc:creator>
    <dc:creator>Zsuzsa Pincze</dc:creator>
    <dc:creator>Gyorgy Karmos</dc:creator>
    <dc:creator>Charles E Schroeder</dc:creator>
    <dc:source>Cereb Cortex (10 May 2007)</dc:source>
    <dc:date>2007-05-13T21:38:43-00:00</dc:date>
    <prism:publicationYear>2007</prism:publicationYear>
    <prism:publicationName>Cereb Cortex</prism:publicationName>
    <prism:issn>1047-3211</prism:issn>
    <prism:category>eye-movement</prism:category>
    <prism:category>gamma</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2445142">
    <title>Large-scale model of mammalian thalamocortical systems</title>
    <link>http://www.citeulike.org/user/j-ito/article/2445142</link>
    <description>&lt;i&gt;Proceedings of the National Academy of Sciences (21 February 2008), 0712231105.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The understanding of the structural and dynamic complexity of mammalian brains is greatly facilitated by computer simulations. We present here a detailed large-scale thalamocortical model based on experimental measures in several mammalian species. The model spans three anatomical scales. (i) It is based on global (white-matter) thalamocortical anatomy obtained by means of diffusion tensor imaging (DTI) of a human brain. (ii) It includes multiple thalamic nuclei and six-layered cortical microcircuitry based on in vitro labeling and three-dimensional reconstruction of single neurons of cat visual cortex. (iii) It has 22 basic types of neurons with appropriate laminar distribution of their branching dendritic trees. The model simulates one million multicompartmental spiking neurons calibrated to reproduce known types of responses recorded in vitro in rats. It has almost half a billion synapses with appropriate receptor kinetics, short-term plasticity, and long-term dendritic spike-timing-dependent synaptic plasticity (dendritic STDP). The model exhibits behavioral regimes of normal brain activity that were not explicitly built-in but emerged spontaneously as the result of interactions among anatomical and dynamic processes. We describe spontaneous activity, sensitivity to changes in individual neurons, emergence of waves and rhythms, and functional connectivity on different scales. 10.1073/pnas.0712231105</description>
    <dc:title>Large-scale model of mammalian thalamocortical systems</dc:title>

    <dc:creator>Eugene Izhikevich</dc:creator>
    <dc:creator>Gerald Edelman</dc:creator>
    <dc:identifier>doi:10.1073/pnas.0712231105</dc:identifier>
    <dc:source>Proceedings of the National Academy of Sciences (21 February 2008), 0712231105.</dc:source>
    <dc:date>2008-02-28T20:15:52-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Proceedings of the National Academy of Sciences</prism:publicationName>
    <prism:startingPage>0712231105</prism:startingPage>
    <prism:category>model</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2425814">
    <title>Prestimulus oscillatory activity in the alpha band predicts visual discrimination ability.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2425814</link>
    <description>&lt;i&gt;J Neurosci, Vol. 28, No. 8. (20 February 2008), pp. 1816-1823.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Although the resting and baseline states of the human electroencephalogram and magnetoencephalogram (MEG) are dominated by oscillations in the alpha band (approximately 10 Hz), the functional role of these oscillations remains unclear. In this study we used MEG to investigate how spontaneous oscillations in humans presented before visual stimuli modulate visual perception. Subjects had to report if there was a subtle difference in gray levels between two superimposed presented discs. We then compared the prestimulus brain activity for correctly (hits) versus incorrectly (misses) identified stimuli. We found that visual discrimination ability decreased with an increase in prestimulus alpha power. Given that reaction times did not vary systematically with prestimulus alpha power changes in vigilance are not likely to explain the change in discrimination ability. Source reconstruction using spatial filters allowed us to identify the brain areas accounting for this effect. The dominant sources modulating visual perception were localized around the parieto-occipital sulcus. We suggest that the parieto-occipital alpha power reflects functional inhibition imposed by higher level areas, which serves to modulate the gain of the visual stream.</description>
    <dc:title>Prestimulus oscillatory activity in the alpha band predicts visual discrimination ability.</dc:title>

    <dc:creator>H van Dijk</dc:creator>
    <dc:creator>JM Schoffelen</dc:creator>
    <dc:creator>R Oostenveld</dc:creator>
    <dc:creator>O Jensen</dc:creator>
    <dc:identifier>doi:10.1523/JNEUROSCI.1853-07.2008</dc:identifier>
    <dc:source>J Neurosci, Vol. 28, No. 8. (20 February 2008), pp. 1816-1823.</dc:source>
    <dc:date>2008-02-25T15:19:16-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>J Neurosci</prism:publicationName>
    <prism:issn>1529-2401</prism:issn>
    <prism:volume>28</prism:volume>
    <prism:number>8</prism:number>
    <prism:startingPage>1816</prism:startingPage>
    <prism:endingPage>1823</prism:endingPage>
    <prism:category>alpha</prism:category>
    <prism:category>eeg</prism:category>
    <prism:category>human</prism:category>
    <prism:category>oscillation</prism:category>
    <prism:category>sponta</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/1151910">
    <title>High gamma power is phase-locked to theta oscillations in human neocortex.</title>
    <link>http://www.citeulike.org/user/j-ito/article/1151910</link>
    <description>&lt;i&gt;Science, Vol. 313, No. 5793. (15 September 2006), pp. 1626-1628.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;We observed robust coupling between the high- and low-frequency bands of ongoing electrical activity in the human brain. In particular, the phase of the low-frequency theta (4 to 8 hertz) rhythm modulates power in the high gamma (80 to 150 hertz) band of the electrocorticogram, with stronger modulation occurring at higher theta amplitudes. Furthermore, different behavioral tasks evoke distinct patterns of theta/high gamma coupling across the cortex. The results indicate that transient coupling between low- and high-frequency brain rhythms coordinates activity in distributed cortical areas, providing a mechanism for effective communication during cognitive processing in humans.</description>
    <dc:title>High gamma power is phase-locked to theta oscillations in human neocortex.</dc:title>

    <dc:creator>RT Canolty</dc:creator>
    <dc:creator>E Edwards</dc:creator>
    <dc:creator>SS Dalal</dc:creator>
    <dc:creator>M Soltani</dc:creator>
    <dc:creator>SS Nagarajan</dc:creator>
    <dc:creator>HE Kirsch</dc:creator>
    <dc:creator>MS Berger</dc:creator>
    <dc:creator>NM Barbaro</dc:creator>
    <dc:creator>RT Knight</dc:creator>
    <dc:identifier>doi:10.1126/science.1128115</dc:identifier>
    <dc:source>Science, Vol. 313, No. 5793. (15 September 2006), pp. 1626-1628.</dc:source>
    <dc:date>2007-03-09T20:00:35-00:00</dc:date>
    <prism:publicationYear>2006</prism:publicationYear>
    <prism:publicationName>Science</prism:publicationName>
    <prism:issn>1095-9203</prism:issn>
    <prism:volume>313</prism:volume>
    <prism:number>5793</prism:number>
    <prism:startingPage>1626</prism:startingPage>
    <prism:endingPage>1628</prism:endingPage>
    <prism:category>eeg</prism:category>
    <prism:category>gamma</prism:category>
    <prism:category>human</prism:category>
    <prism:category>lfp</prism:category>
    <prism:category>oscillation</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2086031">
    <title>Different Processing Phases for Features, Figures, and Selective Attention in the Primary Visual Cortex.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2086031</link>
    <description>&lt;i&gt;Neuron, Vol. 56, No. 5. (6 December 2007), pp. 785-792.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Our visual system imposes structure onto images that usually contain a diversity of surfaces, contours, and colors. Psychological theories propose that there are multiple steps in this process that occur in hierarchically organized regions of the cortex: early visual areas register basic features, higher areas bind them into objects, and yet higher areas select the objects that are relevant for behavior. Here we test these theories by recording from the primary visual cortex (area V1) of monkeys. We demonstrate that the V1 neurons first register the features (at a latency of 48 ms), then segregate figures from the background (after 57 ms), and finally select relevant figures over irrelevant ones (after 137 ms). We conclude that the psychological processing stages map onto distinct time episodes that unfold in the visual cortex after the presentation of a new stimulus, so that area V1 may contribute to all these processing steps.</description>
    <dc:title>Different Processing Phases for Features, Figures, and Selective Attention in the Primary Visual Cortex.</dc:title>

    <dc:creator>Pieter R Roelfsema</dc:creator>
    <dc:creator>Michiel Tolboom</dc:creator>
    <dc:creator>Paul S Khayat</dc:creator>
    <dc:identifier>doi:10.1016/j.neuron.2007.10.006</dc:identifier>
    <dc:source>Neuron, Vol. 56, No. 5. (6 December 2007), pp. 785-792.</dc:source>
    <dc:date>2007-12-10T15:29:41-00:00</dc:date>
    <prism:publicationYear>2007</prism:publicationYear>
    <prism:publicationName>Neuron</prism:publicationName>
    <prism:issn>0896-6273</prism:issn>
    <prism:volume>56</prism:volume>
    <prism:number>5</prism:number>
    <prism:startingPage>785</prism:startingPage>
    <prism:endingPage>792</prism:endingPage>
    <prism:category>vision</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/j-ito/article/2363430">
    <title>Data Sharing for Computational Neuroscience.</title>
    <link>http://www.citeulike.org/user/j-ito/article/2363430</link>
    <description>&lt;i&gt;Neuroinformatics (8 February 2008)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Computational neuroscience is a subfield of neuroscience that develops models to integrate complex experimental data in order to understand brain function. To constrain and test computational models, researchers need access to a wide variety of experimental data. Much of those data are not readily accessible because neuroscientists fall into separate communities that study the brain at different levels and have not been motivated to provide data to researchers outside their community. To foster sharing of neuroscience data, a workshop was held in 2007, bringing together experimental and theoretical neuroscientists, computer scientists, legal experts and governmental observers. Computational neuroscience was recommended as an ideal field for focusing data sharing, and specific methods, strategies and policies were suggested for achieving it. A new funding area in the NSF/NIH Collaborative Research in Computational Neuroscience (CRCNS) program has been established to support data sharing, guided in part by the workshop recommendations. The new funding area is dedicated to the dissemination of high quality data sets with maximum scientific value for computational neuroscience. The first round of the CRCNS data sharing program supports the preparation of data sets which will be publicly available in 2008. These include electrophysiology and behavioral (eye movement) data described towards the end of this article.</description>
    <dc:title>Data Sharing for Computational Neuroscience.</dc:title>

    <dc:creator>Jeffrey Teeters</dc:creator>
    <dc:creator>Kenneth Harris</dc:creator>
    <dc:creator>K Millman</dc:creator>
    <dc:creator>Bruno Olshausen</dc:creator>
    <dc:creator>Friedrich Sommer</dc:creator>
    <dc:identifier>doi:10.1007/s12021-008-9009-y</dc:identifier>
    <dc:source>Neuroinformatics (8 February 2008)</dc:source>
    <dc:date>2008-02-11T17:49:42-00:00</dc:date>
    <prism:publicationYear>2008</prism:publicationYear>
    <prism:publicationName>Neuroinformatics</prism:publicationName>
    <prism:issn>1539-2791</prism:issn>
    <prism:category>eye-movement</prism:category>
</item>



</rdf:RDF>

