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<title>From the editors</title>
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<description>How the nervous system coordinates motor behaviours and how different neurological diseases affect this process are long-standing areas of neuroscience research. However, modern approaches continue to provide new insights into these fundamental questions, as illustrated by two articles in this month's issueOn page 507</description>
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<p>
<b>From the editors</b>
</p>
<p>Nature Reviews Neuroscience 10, 467 (2009). <a href="http://dx.doi.org/10.1038/nrn2677">doi:10.1038/nrn2677</a>
</p>
<p>How the nervous system coordinates motor behaviours and how different neurological diseases affect this process are long-standing areas of neuroscience research. However, modern approaches continue to provide new insights into these fundamental questions, as illustrated by two articles in this month's issueOn page 507</p>
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<dc:title>From the editors</dc:title>
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<dc:source>Nature Reviews Neuroscience 10, 467 (2009)</dc:source>
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<title>Cerebellum: An olive branch to two theories</title>
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<description>The cerebellum is thought to regulate motor learning, coordination and timing, but how its complex circuitry achieves these functions has been a continuous topic of investigation. Now, Mathy et al. show that climbing fibres can fire bursts of action potentials that both encode subthreshold </description>
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<p>
<b>Cerebellum: An olive branch to two theories</b>
</p>
<p>Nature Reviews Neuroscience 10, 468 (2009). <a href="http://dx.doi.org/10.1038/nrn2674">doi:10.1038/nrn2674</a>
</p>
<p>Author: Leonie Welberg</p>
<p>The cerebellum is thought to regulate motor learning, coordination and timing, but how its complex circuitry achieves these functions has been a continuous topic of investigation. Now, Mathy et al. show that climbing fibres can fire bursts of action potentials that both encode subthreshold </p>
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<dc:title>Cerebellum: An olive branch to two theories</dc:title>
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<dc:identifier>doi:10.1038/nrn2674</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 468 (2009)</dc:source>
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<title>MicroRNA: MicroRNAs have receptor subunits in a bind</title>
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<description>The number of glutamate receptors (GluRs) in the postsynaptic membrane is crucial to the efficacy of synaptic transmission, but the mechanisms that control receptor synthesis and localization are not well understood. Karr et al. have now shown that microRNAs regulate the expression levels of </description>
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<p>
<b>MicroRNA: MicroRNAs have receptor subunits in a bind</b>
</p>
<p>Nature Reviews Neuroscience 10, 469 (2009). <a href="http://dx.doi.org/10.1038/nrn2671">doi:10.1038/nrn2671</a>
</p>
<p>Author: Eleanor Beal</p>
<p>The number of glutamate receptors (GluRs) in the postsynaptic membrane is crucial to the efficacy of synaptic transmission, but the mechanisms that control receptor synthesis and localization are not well understood. Karr et al. have now shown that microRNAs regulate the expression levels of </p>
]]></content:encoded>
<dc:title>MicroRNA: MicroRNAs have receptor subunits in a bind</dc:title>
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<dc:identifier>doi:10.1038/nrn2671</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 469 (2009)</dc:source>
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<title>Development: Terminal differentiation</title>
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<description>The identity of a neuron is determined by the so-called terminal differentiation genes (TDGs), which are activated by specific transcription factors. It is largely unknown how the TDGs are selected during developmental processes. Bertrand and Hobert now show how specific cues are integrated into the </description>
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<p>
<b>Development: Terminal differentiation</b>
</p>
<p>Nature Reviews Neuroscience 10, 469 (2009). <a href="http://dx.doi.org/10.1038/nrn2678">doi:10.1038/nrn2678</a>
</p>
<p>Author: Claudia Wiedemann</p>
<p>The identity of a neuron is determined by the so-called terminal differentiation genes (TDGs), which are activated by specific transcription factors. It is largely unknown how the TDGs are selected during developmental processes. Bertrand and Hobert now show how specific cues are integrated into the </p>
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<dc:title>Development: Terminal differentiation</dc:title>
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<title>In Brief</title>
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<description>Neuronal circuits</description>
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<p>
<b>In Brief</b>
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<p>Nature Reviews Neuroscience 10, 470 (2009). <a href="http://dx.doi.org/10.1038/nrn2679">doi:10.1038/nrn2679</a>
</p>
<p>Neuronal circuits</p>
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<dc:title>In Brief</dc:title>
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<title>Synaptic plasticity: The advantages of youth</title>
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<description>The introduction of newborn granule cells to the circuitry of the olfactory bulb (OB) has been proposed to have a role in olfactory learning and memory. However, the nature of this contribution was unclear. In Nature Neuroscience, Lledo and colleagues report that newborn granule </description>
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<p>
<b>Synaptic plasticity: The advantages of youth</b>
</p>
<p>Nature Reviews Neuroscience 10, 470 (2009). <a href="http://dx.doi.org/10.1038/nrn2664">doi:10.1038/nrn2664</a>
</p>
<p>Author: Katherine Whalley</p>
<p>The introduction of newborn granule cells to the circuitry of the olfactory bulb (OB) has been proposed to have a role in olfactory learning and memory. However, the nature of this contribution was unclear. In Nature Neuroscience, Lledo and colleagues report that newborn granule </p>
]]></content:encoded>
<dc:title>Synaptic plasticity: The advantages of youth</dc:title>
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<dc:source>Nature Reviews Neuroscience 10, 470 (2009)</dc:source>
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<title>Sleep: What goes up, must come down</title>
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<description>The exact functions of sleep are unknown, but it is widely accepted that sleep is important for learning and memory. Two recent studies published in Science found that synaptic connections and synaptic protein markers that respectively increase their numbers and expression levels during wakefulness </description>
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<p>
<b>Sleep: What goes up, must come down</b>
</p>
<p>Nature Reviews Neuroscience 10, 470 (2009). <a href="http://dx.doi.org/10.1038/nrn2676">doi:10.1038/nrn2676</a>
</p>
<p>Author: Claudia Wiedemann</p>
<p>The exact functions of sleep are unknown, but it is widely accepted that sleep is important for learning and memory. Two recent studies published in Science found that synaptic connections and synaptic protein markers that respectively increase their numbers and expression levels during wakefulness </p>
]]></content:encoded>
<dc:title>Sleep: What goes up, must come down</dc:title>
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<dc:source>Nature Reviews Neuroscience 10, 470 (2009)</dc:source>
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<title>Learning and memory: HDAC2 is the one</title>
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<description>Inhibitors of histone deacetylase (HDAC) enzymes have been shown to improve learning and memory; however, multiple forms of HDAC exist, and the development of more effective HDAC inhibitors would benefit from knowing the specific HDAC(s) that are involved in the regulation of synaptic plasticity. Tsai </description>
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<p>
<b>Learning and memory: HDAC2 is the one</b>
</p>
<p>Nature Reviews Neuroscience 10, 471 (2009). <a href="http://dx.doi.org/10.1038/nrn2660">doi:10.1038/nrn2660</a>
</p>
<p>Author: Leonie Welberg</p>
<p>Inhibitors of histone deacetylase (HDAC) enzymes have been shown to improve learning and memory; however, multiple forms of HDAC exist, and the development of more effective HDAC inhibitors would benefit from knowing the specific HDAC(s) that are involved in the regulation of synaptic plasticity. Tsai </p>
]]></content:encoded>
<dc:title>Learning and memory: HDAC2 is the one</dc:title>
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<dc:source>Nature Reviews Neuroscience 10, 471 (2009)</dc:source>
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<title>Spine formation: Signalling growth</title>
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<description>Dysfunction of &#947;-secretase has been linked to early-onset Alzheimer's disease; however, the underlying molecular mechanisms are unknown. Inoue et al. have now shown that &#947;-secretase is localized to synaptic membranes, where it cleaves ephrin receptor A4 (EPHA4) on synaptic activation and triggers the </description>
<content:encoded><![CDATA[

<p>
<b>Spine formation: Signalling growth</b>
</p>
<p>Nature Reviews Neuroscience 10, 472 (2009). <a href="http://dx.doi.org/10.1038/nrn2673">doi:10.1038/nrn2673</a>
</p>
<p>Author: Claudia Wiedemann</p>
<p>Dysfunction of &#947;-secretase has been linked to early-onset Alzheimer's disease; however, the underlying molecular mechanisms are unknown. Inoue et al. have now shown that &#947;-secretase is localized to synaptic membranes, where it cleaves ephrin receptor A4 (EPHA4) on synaptic activation and triggers the </p>
]]></content:encoded>
<dc:title>Spine formation: Signalling growth</dc:title>
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<dc:identifier>doi:10.1038/nrn2673</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 472 (2009)</dc:source>
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<title>Neuronal metabolism: A question of balance</title>
<link>http://dx.doi.org/10.1038/nrn2669</link>
<description>The rate of glycolysis, the cell's energy-generating metabolic process, is lower in neurons than in astrocytes; however, why this is so is unknown. Herrero-Mendez et al. have now shown that, by actively downregulating glycolysis, neurons shift their metabolic balance towards pathways responsible for maintaining </description>
<content:encoded><![CDATA[

<p>
<b>Neuronal metabolism: A question of balance</b>
</p>
<p>Nature Reviews Neuroscience 10, 472 (2009). <a href="http://dx.doi.org/10.1038/nrn2669">doi:10.1038/nrn2669</a>
</p>
<p>Author: Katherine Whalley</p>
<p>The rate of glycolysis, the cell's energy-generating metabolic process, is lower in neurons than in astrocytes; however, why this is so is unknown. Herrero-Mendez et al. have now shown that, by actively downregulating glycolysis, neurons shift their metabolic balance towards pathways responsible for maintaining </p>
]]></content:encoded>
<dc:title>Neuronal metabolism: A question of balance</dc:title>
<dc:creator>Katherine Whalley</dc:creator>
<dc:identifier>doi:10.1038/nrn2669</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 472 (2009)</dc:source>
<dc:date>2009-06-10</dc:date>
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<title>Addiction: Let me count the genes</title>
<link>http://dx.doi.org/10.1038/nrn2675</link>
<description>Addictive drugs alter gene expression in the brain's reward system, notably in the nucleus accumbens (NAc). To investigate the underlying mechanisms, Renthal et al. carried out a genome-wide analysis of chronic cocaine-induced chromatin modifications and transcription-factor binding, revealing a role for sirtuins 1 and </description>
<content:encoded><![CDATA[

<p>
<b>Addiction: Let me count the genes</b>
</p>
<p>Nature Reviews Neuroscience 10, 472 (2009). <a href="http://dx.doi.org/10.1038/nrn2675">doi:10.1038/nrn2675</a>
</p>
<p>Author: Leonie Welberg</p>
<p>Addictive drugs alter gene expression in the brain's reward system, notably in the nucleus accumbens (NAc). To investigate the underlying mechanisms, Renthal et al. carried out a genome-wide analysis of chronic cocaine-induced chromatin modifications and transcription-factor binding, revealing a role for sirtuins 1 and </p>
]]></content:encoded>
<dc:title>Addiction: Let me count the genes</dc:title>
<dc:creator>Leonie Welberg</dc:creator>
<dc:identifier>doi:10.1038/nrn2675</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 472 (2009)</dc:source>
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<title>In Brief</title>
<link>http://dx.doi.org/10.1038/nrn2680</link>
<description>Reward</description>
<content:encoded><![CDATA[

<p>
<b>In Brief</b>
</p>
<p>Nature Reviews Neuroscience 10, 473 (2009). <a href="http://dx.doi.org/10.1038/nrn2680">doi:10.1038/nrn2680</a>
</p>
<p>Reward</p>
]]></content:encoded>
<dc:title>In Brief</dc:title>
<dc:identifier>doi:10.1038/nrn2680</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 473 (2009)</dc:source>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
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<title>New sites of action for GIRK and SK channels</title>
<link>http://dx.doi.org/10.1038/nrn2668</link>
<description>It was recently discovered that two different types of voltage-insensitive K+ channels, G protein-coupled inwardly rectifying K+ (GIRK) and small-conductance Ca2+-activated K+ (SK) channels, are located on dendritic branches, spines and shafts in the postsynaptic densities of </description>
<content:encoded><![CDATA[

<p>
<b>New sites of action for GIRK and SK channels</b>
</p>
<p>Nature Reviews Neuroscience 10, 475 (2009). <a href="http://dx.doi.org/10.1038/nrn2668">doi:10.1038/nrn2668</a>
</p>
<p>Authors: Rafael Luj&#225;n, James Maylie &amp; John P. Adelman</p>
<p>It was recently discovered that two different types of voltage-insensitive K+ channels, G protein-coupled inwardly rectifying K+ (GIRK) and small-conductance Ca2+-activated K+ (SK) channels, are located on dendritic branches, spines and shafts in the postsynaptic densities of </p>
]]></content:encoded>
<dc:title>New sites of action for GIRK and SK channels</dc:title>
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<dc:creator>James Maylie</dc:creator>
<dc:creator>John P. Adelman</dc:creator>
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<dc:source>Nature Reviews Neuroscience 10, 475 (2009)</dc:source>
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<title>Mitochondrial membrane permeabilization in neuronal injury</title>
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<description>Acute neurological conditions such as cerebrovascular diseases and trauma are associated with irreversible loss of neurons and glial cells. Severe or prolonged injury results in uncontrollable cell death within the core of lesions. Conversely, cells that are less severely damaged succumb in a relatively slow </description>
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<p>
<b>Mitochondrial membrane permeabilization in neuronal injury</b>
</p>
<p>Nature Reviews Neuroscience 10, 481 (2009). <a href="http://dx.doi.org/10.1038/nrn2665">doi:10.1038/nrn2665</a>
</p>
<p>Authors: Lorenzo Galluzzi, Klas Blomgren &amp; Guido Kroemer</p>
<p>Acute neurological conditions such as cerebrovascular diseases and trauma are associated with irreversible loss of neurons and glial cells. Severe or prolonged injury results in uncontrollable cell death within the core of lesions. Conversely, cells that are less severely damaged succumb in a relatively slow </p>
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<dc:title>Mitochondrial membrane permeabilization in neuronal injury</dc:title>
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<title>The diverse functional roles and regulation of neuronal gap junctions in the retina</title>
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<description>Electrical synaptic transmission through gap junctions underlies direct and rapid neuronal communication in the CNS. The diversity of functional roles that electrical synapses have is perhaps best exemplified in the vertebrate retina, in which gap junctions are formed by each of the five major neuron </description>
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<p>
<b>The diverse functional roles and regulation of neuronal gap junctions in the retina</b>
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<p>Nature Reviews Neuroscience 10, 495 (2009). <a href="http://dx.doi.org/10.1038/nrn2636">doi:10.1038/nrn2636</a>
</p>
<p>Authors: Stewart A. Bloomfield &amp; B&#233;la V&#246;lgyi</p>
<p>Electrical synaptic transmission through gap junctions underlies direct and rapid neuronal communication in the CNS. The diversity of functional roles that electrical synapses have is perhaps best exemplified in the vertebrate retina, in which gap junctions are formed by each of the five major neuron </p>
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<dc:title>The diverse functional roles and regulation of neuronal gap junctions in the retina</dc:title>
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<dc:identifier>doi:10.1038/nrn2636</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 495 (2009)</dc:source>
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<item rdf:about="http://dx.doi.org/10.1038/nrn2608">
<title>Circuits controlling vertebrate locomotion: moving in a new direction</title>
<link>http://dx.doi.org/10.1038/nrn2608</link>
<description>Neurobiologists have long sought to understand how circuits in the nervous system are organized to generate the precise neural outputs that underlie particular behaviours. The motor circuits in the spinal cord that control locomotion, commonly referred to as central pattern generator networks, provide an experimentally </description>
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<p>
<b>Circuits controlling vertebrate locomotion: moving in a new direction</b>
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<p>Nature Reviews Neuroscience 10, 507 (2009). <a href="http://dx.doi.org/10.1038/nrn2608">doi:10.1038/nrn2608</a>
</p>
<p>Author: Martyn Goulding</p>
<p>Neurobiologists have long sought to understand how circuits in the nervous system are organized to generate the precise neural outputs that underlie particular behaviours. The motor circuits in the spinal cord that control locomotion, commonly referred to as central pattern generator networks, provide an experimentally </p>
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<dc:title>Circuits controlling vertebrate locomotion: moving in a new direction</dc:title>
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<dc:source>Nature Reviews Neuroscience 10, 507 (2009)</dc:source>
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<item rdf:about="http://dx.doi.org/10.1038/nrn2652">
<title>Tests to assess motor phenotype in mice: a user's guide</title>
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<description>The characterization of mouse models of human disease is essential for understanding the underlying pathophysiology and developing new therapeutics. Many diseases are often associated with more than one model, and so there is a need to determine which model most closely represents the disease state </description>
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<p>
<b>Tests to assess motor phenotype in mice: a user's guide</b>
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<p>Nature Reviews Neuroscience 10, 519 (2009). <a href="http://dx.doi.org/10.1038/nrn2652">doi:10.1038/nrn2652</a>
</p>
<p>Authors: Simon P. Brooks &amp; Stephen B. Dunnett</p>
<p>The characterization of mouse models of human disease is essential for understanding the underlying pathophysiology and developing new therapeutics. Many diseases are often associated with more than one model, and so there is a need to determine which model most closely represents the disease state </p>
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<dc:title>Tests to assess motor phenotype in mice: a user's guide</dc:title>
<dc:creator>Simon P. Brooks</dc:creator>
<dc:creator>Stephen B. Dunnett</dc:creator>
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<dc:source>Nature Reviews Neuroscience 10, 519 (2009)</dc:source>
<dc:date>2009-06-10</dc:date>
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<item rdf:about="http://dx.doi.org/10.1038/nrn2653">
<title>Principles of neural ensemble physiology underlying the operation of brain&#8211;machine interfaces</title>
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<description>Research on brain&#8211;machine interfaces has been ongoing for at least a decade. During this period, simultaneous recordings of the extracellular electrical activity of hundreds of individual neurons have been used for direct, real-time control of various artificial devices. Brain&#8211;machine interfaces have also added greatly to </description>
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<p>
<b>Principles of neural ensemble physiology underlying the operation of brain&#8211;machine interfaces</b>
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<p>Nature Reviews Neuroscience 10, 530 (2009). <a href="http://dx.doi.org/10.1038/nrn2653">doi:10.1038/nrn2653</a>
</p>
<p>Authors: Miguel A. L. Nicolelis &amp; Mikhail A. Lebedev</p>
<p>Research on brain&#8211;machine interfaces has been ongoing for at least a decade. During this period, simultaneous recordings of the extracellular electrical activity of hundreds of individual neurons have been used for direct, real-time control of various artificial devices. Brain&#8211;machine interfaces have also added greatly to </p>
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<dc:title>Principles of neural ensemble physiology underlying the operation of brain&#8211;machine interfaces</dc:title>
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<dc:creator>Mikhail A. Lebedev</dc:creator>
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<dc:source>Nature Reviews Neuroscience 10, 530 (2009)</dc:source>
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