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<title>Nature Reviews Neuroscience</title>
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<title>A new perspective on the role of the orbitofrontal cortex in adaptive behaviour</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/YDbabVkoaTA/nrn2753</link>
<description>The orbitofrontal cortex (OFC) is crucial for changing established behaviour in the face of unexpected outcomes. This function has been attributed to the role of the OFC in response inhibition or to the idea that the OFC is a rapidly flexible associative-learning area. However, recent </description>
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<p>
<b>A new perspective on the role of the orbitofrontal cortex in adaptive behaviour</b>
</p>
<p>Nature Reviews Neuroscience 10, 885 (2009). <a href="http://dx.doi.org/10.1038/nrn2753">doi:10.1038/nrn2753</a>
</p>
<p>Authors: Geoffrey Schoenbaum, Matthew R. Roesch, Thomas A. Stalnaker &amp; Yuji K. Takahashi</p>
<p>The orbitofrontal cortex (OFC) is crucial for changing established behaviour in the face of unexpected outcomes. This function has been attributed to the role of the OFC in response inhibition or to the idea that the OFC is a rapidly flexible associative-learning area. However, recent </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/YDbabVkoaTA" height="1" width="1"/>]]></content:encoded>
<dc:title>A new perspective on the role of the orbitofrontal cortex in adaptive behaviour</dc:title>
<dc:creator>Geoffrey Schoenbaum</dc:creator>
<dc:creator>Matthew R. Roesch</dc:creator>
<dc:creator>Thomas A. Stalnaker</dc:creator>
<dc:creator>Yuji K. Takahashi</dc:creator>
<dc:identifier>doi:10.1038/nrn2753</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 885 (2009)</dc:source>
<dc:date>2009-11-11</dc:date>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
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<prism:doi>10.1038/nrn2753</prism:doi>
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<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Perspectives</prism:section>
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<title>Understanding microRNAs in neurodegeneration</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/CvsCI8Erf5E/nrn2726</link>
<description>Interest in the functions of microRNAs (miRNAs) in the nervous system has recently expanded to include their roles in neurodegeneration. Investigations have begun to reveal the influence of miRNAs on both neuronal survival and the accumulation of toxic proteins that are associated with neurodegeneration, and </description>
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<p>
<b>Understanding microRNAs in neurodegeneration</b>
</p>
<p>Nature Reviews Neuroscience 10, 837 (2009). <a href="http://dx.doi.org/10.1038/nrn2726">doi:10.1038/nrn2726</a>
</p>
<p>Authors: Stephen M. Eacker, Ted M. Dawson &amp; Valina L. Dawson</p>
<p>Interest in the functions of microRNAs (miRNAs) in the nervous system has recently expanded to include their roles in neurodegeneration. Investigations have begun to reveal the influence of miRNAs on both neuronal survival and the accumulation of toxic proteins that are associated with neurodegeneration, and </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/CvsCI8Erf5E" height="1" width="1"/>]]></content:encoded>
<dc:title>Understanding microRNAs in neurodegeneration</dc:title>
<dc:creator>Stephen M. Eacker</dc:creator>
<dc:creator>Ted M. Dawson</dc:creator>
<dc:creator>Valina L. Dawson</dc:creator>
<dc:identifier>doi:10.1038/nrn2726</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 837 (2009)</dc:source>
<dc:date>2009-11-11</dc:date>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:publicationDate>2009-11-11</prism:publicationDate>
<prism:doi>10.1038/nrn2726</prism:doi>
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<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Progress</prism:section>
<prism:startingPage>837</prism:startingPage>
<prism:endingPage>841</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrn2741">
<title>Plasticity and stability of visual field maps in adult primary visual cortex</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/Y4OgsFcKFwI/nrn2741</link>
<description>It is important to understand the balance between cortical plasticity and stability in various systems and across spatial scales in the adult brain. Here we review studies of adult plasticity in primary visual cortex (V1), which has a key role in distributing visual information. There </description>
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<p>
<b>Plasticity and stability of visual field maps in adult primary visual cortex</b>
</p>
<p>Nature Reviews Neuroscience 10, 873 (2009). <a href="http://dx.doi.org/10.1038/nrn2741">doi:10.1038/nrn2741</a>
</p>
<p>Authors: Brian A. Wandell &amp; Stelios M. Smirnakis</p>
<p>It is important to understand the balance between cortical plasticity and stability in various systems and across spatial scales in the adult brain. Here we review studies of adult plasticity in primary visual cortex (V1), which has a key role in distributing visual information. There </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/Y4OgsFcKFwI" height="1" width="1"/>]]></content:encoded>
<dc:title>Plasticity and stability of visual field maps in adult primary visual cortex</dc:title>
<dc:creator>Brian A. Wandell</dc:creator>
<dc:creator>Stelios M. Smirnakis</dc:creator>
<dc:identifier>doi:10.1038/nrn2741</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 873 (2009)</dc:source>
<dc:date>2009-11-11</dc:date>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:publicationDate>2009-11-11</prism:publicationDate>
<prism:doi>10.1038/nrn2741</prism:doi>
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<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>873</prism:startingPage>
<prism:endingPage>884</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrn2760">
<title>Neurodegenerative disease: APP: what's on the inside matters</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/XXaWqc-KsiU/nrn2760</link>
<description>Cleavage of the amyloid precursor protein (APP) at the cell surface produces extracellular amyloid-β peptides (Aβ) and the APP intracellular domain, AICD. The predominant hypotheses in the Alzheimer's disease (AD) field have traditionally focused on a causative role for Aβ; however, a new </description>
<content:encoded><![CDATA[

<p>
<b>Neurodegenerative disease: APP: what's on the inside matters</b>
</p>
<p>Nature Reviews Neuroscience 10, 836 (2009). <a href="http://dx.doi.org/10.1038/nrn2760">doi:10.1038/nrn2760</a>
</p>
<p>Author: Katherine Whalley</p>
<p>Cleavage of the amyloid precursor protein (APP) at the cell surface produces extracellular amyloid-&#946; peptides (A&#946;) and the APP intracellular domain, AICD. The predominant hypotheses in the Alzheimer's disease (AD) field have traditionally focused on a causative role for A&#946;; however, a new </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/XXaWqc-KsiU" height="1" width="1"/>]]></content:encoded>
<dc:title>Neurodegenerative disease: APP: what's on the inside matters</dc:title>
<dc:creator>Katherine Whalley</dc:creator>
<dc:identifier>doi:10.1038/nrn2760</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 836 (2009)</dc:source>
<dc:date>2009-11-11</dc:date>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:publicationDate>2009-11-11</prism:publicationDate>
<prism:doi>10.1038/nrn2760</prism:doi>
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<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>836</prism:startingPage>
<prism:endingPage>836</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrn2764">
<title>Learning and memory: Dopamine drives the circuit</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/6gv8_cnwxUs/nrn2764</link>
<description>Flies rely on their sense of smell to navigate their environment. Mushroom body neurons have a key role in olfactory memory, but little is known about the circuits that provide these cells with relevant information. Two studies now identify distinct dopaminergic projections to specific mushroom </description>
<content:encoded><![CDATA[

<p>
<b>Learning and memory: Dopamine drives the circuit</b>
</p>
<p>Nature Reviews Neuroscience 10, 832 (2009). <a href="http://dx.doi.org/10.1038/nrn2764">doi:10.1038/nrn2764</a>
</p>
<p>Author: Leonie Welberg</p>
<p>Flies rely on their sense of smell to navigate their environment. Mushroom body neurons have a key role in olfactory memory, but little is known about the circuits that provide these cells with relevant information. Two studies now identify distinct dopaminergic projections to specific mushroom </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/6gv8_cnwxUs" height="1" width="1"/>]]></content:encoded>
<dc:title>Learning and memory: Dopamine drives the circuit</dc:title>
<dc:creator>Leonie Welberg</dc:creator>
<dc:identifier>doi:10.1038/nrn2764</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 832 (2009)</dc:source>
<dc:date>2009-11-11</dc:date>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
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<prism:volume>10</prism:volume>
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<prism:startingPage>832</prism:startingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrn2765">
<title>Neuroimmunology: Crawling into the brain</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/gbj82rr8_Ng/nrn2765</link>
<description>A study involving real-time imaging of effector T cells provides new insight into how autoreactive T cells interact with cerebral structures and access the central nervous system (CNS) to cause autoimmune disease.Flügel and colleagues induced experimental autoimmune encephalomyelitis in rats with intravenous injection of </description>
<content:encoded><![CDATA[

<p>
<b>Neuroimmunology: Crawling into the brain</b>
</p>
<p>Nature Reviews Neuroscience 10, 834 (2009). <a href="http://dx.doi.org/10.1038/nrn2765">doi:10.1038/nrn2765</a>
</p>
<p>Author: Lucy Bird</p>
<p>A study involving real-time imaging of effector T cells provides new insight into how autoreactive T cells interact with cerebral structures and access the central nervous system (CNS) to cause autoimmune disease.Fl&#252;gel and colleagues induced experimental autoimmune encephalomyelitis in rats with intravenous injection of </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/gbj82rr8_Ng" height="1" width="1"/>]]></content:encoded>
<dc:title>Neuroimmunology: Crawling into the brain</dc:title>
<dc:creator>Lucy Bird</dc:creator>
<dc:identifier>doi:10.1038/nrn2765</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 834 (2009)</dc:source>
<dc:date>2009-11-11</dc:date>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:publicationDate>2009-11-11</prism:publicationDate>
<prism:doi>10.1038/nrn2765</prism:doi>
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<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>834</prism:startingPage>
<prism:endingPage>835</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrn2765</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrn2763">
<title>microRNAs at the synapse</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/gDcLmszWQNE/nrn2763</link>
<description>MicroRNAs (miRNAs) are emerging as key modulators of post-transcriptional gene regulation in a plethora of tissues, including the nervous system. Recent evidence points to a widespread role for neural miRNAs at various stages of synaptic development, including dendritogenesis, synapse formation and synapse maturation. Furthermore, studies </description>
<content:encoded><![CDATA[

<p>
<b>microRNAs at the synapse</b>
</p>
<p>Nature Reviews Neuroscience 10, 842 (2009). <a href="http://dx.doi.org/10.1038/nrn2763">doi:10.1038/nrn2763</a>
</p>
<p>Author: Gerhard Schratt</p>
<p>MicroRNAs (miRNAs) are emerging as key modulators of post-transcriptional gene regulation in a plethora of tissues, including the nervous system. Recent evidence points to a widespread role for neural miRNAs at various stages of synaptic development, including dendritogenesis, synapse formation and synapse maturation. Furthermore, studies </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/gDcLmszWQNE" height="1" width="1"/>]]></content:encoded>
<dc:title>microRNAs at the synapse</dc:title>
<dc:creator>Gerhard Schratt</dc:creator>
<dc:identifier>doi:10.1038/nrn2763</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 842 (2009)</dc:source>
<dc:date>2009-11-04</dc:date>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:publicationDate>2009-11-04</prism:publicationDate>
<prism:doi>10.1038/nrn2763</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrn2763</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>842</prism:startingPage>
<prism:endingPage>849</prism:endingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrn2735">
<title>Plasticity during stroke recovery: from synapse to behaviour</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/ExLfEvMhZ_Y/nrn2735</link>
<description>Reductions in blood flow to the brain of sufficient duration and extent lead to stroke, which results in damage to neuronal networks and the impairment of sensation, movement or cognition. Evidence from animal models suggests that a time-limited window of neuroplasticity opens following a stroke, </description>
<content:encoded><![CDATA[

<p>
<b>Plasticity during stroke recovery: from synapse to behaviour</b>
</p>
<p>Nature Reviews Neuroscience 10, 861 (2009). <a href="http://dx.doi.org/10.1038/nrn2735">doi:10.1038/nrn2735</a>
</p>
<p>Authors: Timothy H. Murphy &amp; Dale Corbett</p>
<p>Reductions in blood flow to the brain of sufficient duration and extent lead to stroke, which results in damage to neuronal networks and the impairment of sensation, movement or cognition. Evidence from animal models suggests that a time-limited window of neuroplasticity opens following a stroke, </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/ExLfEvMhZ_Y" height="1" width="1"/>]]></content:encoded>
<dc:title>Plasticity during stroke recovery: from synapse to behaviour</dc:title>
<dc:creator>Timothy H. Murphy</dc:creator>
<dc:creator>Dale Corbett</dc:creator>
<dc:identifier>doi:10.1038/nrn2735</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 861 (2009)</dc:source>
<dc:date>2009-11-04</dc:date>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:publicationDate>2009-11-04</prism:publicationDate>
<prism:doi>10.1038/nrn2735</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrn2735</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>861</prism:startingPage>
<prism:endingPage>872</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrn2735</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrn2738">
<title>TrkB signalling pathways in LTP and learning</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/7OSMx5DBYM0/nrn2738</link>
<description>Understanding the mechanisms that underlie learning is one of the most fascinating and central aims of neurobiological research. Hippocampal long-term potentiation (LTP) is widely regarded as a prime candidate for the cellular mechanism of learning. The receptor tyrosine kinase TrkB (also known as NTRK2), known </description>
<content:encoded><![CDATA[

<p>
<b>TrkB signalling pathways in LTP and learning</b>
</p>
<p>Nature Reviews Neuroscience 10, 850 (2009). <a href="http://dx.doi.org/10.1038/nrn2738">doi:10.1038/nrn2738</a>
</p>
<p>Author: Liliana Minichiello</p>
<p>Understanding the mechanisms that underlie learning is one of the most fascinating and central aims of neurobiological research. Hippocampal long-term potentiation (LTP) is widely regarded as a prime candidate for the cellular mechanism of learning. The receptor tyrosine kinase TrkB (also known as NTRK2), known </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/7OSMx5DBYM0" height="1" width="1"/>]]></content:encoded>
<dc:title>TrkB signalling pathways in LTP and learning</dc:title>
<dc:creator>Liliana Minichiello</dc:creator>
<dc:identifier>doi:10.1038/nrn2738</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 850 (2009)</dc:source>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:doi>10.1038/nrn2738</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrn2738</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
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<prism:startingPage>850</prism:startingPage>
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<item rdf:about="http://dx.doi.org/10.1038/nrn2766">
<title>Neural coding: Oscillations help to decode spike patterns</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/k3riHkuvtw0/nrn2766</link>
<description>In sensory processing, a neuron's firing rate and the timing of the spikes relative to the stimulus onset together encode information. In reality, however, stimuli are often ongoing, raising the question of what else could provide a reference point for spike timing. Previous studies suggested </description>
<content:encoded><![CDATA[

<p>
<b>Neural coding: Oscillations help to decode spike patterns</b>
</p>
<p>Nature Reviews Neuroscience 10, 834 (2009). <a href="http://dx.doi.org/10.1038/nrn2766">doi:10.1038/nrn2766</a>
</p>
<p>Author: Monica Hoyos Flight</p>
<p>In sensory processing, a neuron's firing rate and the timing of the spikes relative to the stimulus onset together encode information. In reality, however, stimuli are often ongoing, raising the question of what else could provide a reference point for spike timing. Previous studies suggested </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/k3riHkuvtw0" height="1" width="1"/>]]></content:encoded>
<dc:title>Neural coding: Oscillations help to decode spike patterns</dc:title>
<dc:creator>Monica Hoyos Flight</dc:creator>
<dc:identifier>doi:10.1038/nrn2766</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 834 (2009)</dc:source>
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<prism:doi>10.1038/nrn2766</prism:doi>
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<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>834</prism:startingPage>
<prism:endingPage>835</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrn2766</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrn2767">
<title>Neurogenesis: A mother–daughter relationship</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/BG9ppPSdgq8/nrn2767</link>
<description>Radial glia in the ventricular zone (VZ) of the developing cortex divide asymmetrically, producing a self-renewing radial glial cell that remains in the VZ and a cell that differentiates into a neuron or an intermediate progenitor. How these differing fates are determined was unknown; however, </description>
<content:encoded><![CDATA[

<p>
<b>Neurogenesis: A mother&#8211;daughter relationship</b>
</p>
<p>Nature Reviews Neuroscience 10, 833 (2009). <a href="http://dx.doi.org/10.1038/nrn2767">doi:10.1038/nrn2767</a>
</p>
<p>Author: Katherine Whalley</p>
<p>Radial glia in the ventricular zone (VZ) of the developing cortex divide asymmetrically, producing a self-renewing radial glial cell that remains in the VZ and a cell that differentiates into a neuron or an intermediate progenitor. How these differing fates are determined was unknown; however, </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/BG9ppPSdgq8" height="1" width="1"/>]]></content:encoded>
<dc:title>Neurogenesis: A mother–daughter relationship</dc:title>
<dc:creator>Katherine Whalley</dc:creator>
<dc:identifier>doi:10.1038/nrn2767</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 833 (2009)</dc:source>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:doi>10.1038/nrn2767</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrn2767</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>833</prism:startingPage>
<prism:endingPage>833</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrn2767</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrn2768">
<title>Epigenetics: Stressed for life</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/0wubFdhEq8k/nrn2768</link>
<description>Early-life stress (ELS) has long-lasting effects on the brain, and the epigenetic mechanisms underlying them are beginning to be unravelled. Murgatroyd et al. now show that methyl-CpG-binding protein 2 (MeCP2)-mediated regulation of arginine vasopressin (Avp) gene expression in parvocellular hypothalamus </description>
<content:encoded><![CDATA[

<p>
<b>Epigenetics: Stressed for life</b>
</p>
<p>Nature Reviews Neuroscience 10, 836 (2009). <a href="http://dx.doi.org/10.1038/nrn2768">doi:10.1038/nrn2768</a>
</p>
<p>Author: Leonie Welberg</p>
<p>Early-life stress (ELS) has long-lasting effects on the brain, and the epigenetic mechanisms underlying them are beginning to be unravelled. Murgatroyd et al. now show that methyl-CpG-binding protein 2 (MeCP2)-mediated regulation of arginine vasopressin (Avp) gene expression in parvocellular hypothalamus </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/0wubFdhEq8k" height="1" width="1"/>]]></content:encoded>
<dc:title>Epigenetics: Stressed for life</dc:title>
<dc:creator>Leonie Welberg</dc:creator>
<dc:identifier>doi:10.1038/nrn2768</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 836 (2009)</dc:source>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:doi>10.1038/nrn2768</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrn2768</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>836</prism:startingPage>
<prism:endingPage>836</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrn2768</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrn2769">
<title>Development: Initiation of a new connection</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/uMpxREjm5Ac/nrn2769</link>
<description>The molecular mechanisms that regulate synapse formation are not well understood. Eroglu et al. show that thrombospondin (TSP) binding to the neuronal α2δ-1 receptor initiates the formation of new synapses in vitro and in vivo and that the anti-epileptic and analgesic drug </description>
<content:encoded><![CDATA[

<p>
<b>Development: Initiation of a new connection</b>
</p>
<p>Nature Reviews Neuroscience 10, 833 (2009). <a href="http://dx.doi.org/10.1038/nrn2769">doi:10.1038/nrn2769</a>
</p>
<p>Author: Claudia Wiedemann</p>
<p>The molecular mechanisms that regulate synapse formation are not well understood. Eroglu et al. show that thrombospondin (TSP) binding to the neuronal &#945;2&#948;-1 receptor initiates the formation of new synapses in vitro and in vivo and that the anti-epileptic and analgesic drug </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/uMpxREjm5Ac" height="1" width="1"/>]]></content:encoded>
<dc:title>Development: Initiation of a new connection</dc:title>
<dc:creator>Claudia Wiedemann</dc:creator>
<dc:identifier>doi:10.1038/nrn2769</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 833 (2009)</dc:source>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:doi>10.1038/nrn2769</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrn2769</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>833</prism:startingPage>
<prism:endingPage>833</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrn2769</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrn2770">
<title>In Brief</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/3POQQbGHDXQ/nrn2770</link>
<description>Pain</description>
<content:encoded><![CDATA[

<p>
<b>In Brief</b>
</p>
<p>Nature Reviews Neuroscience 10, 834 (2009). <a href="http://dx.doi.org/10.1038/nrn2770">doi:10.1038/nrn2770</a>
</p>
<p>Pain</p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/3POQQbGHDXQ" height="1" width="1"/>]]></content:encoded>
<dc:title>In Brief</dc:title>
<dc:identifier>doi:10.1038/nrn2770</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 834 (2009)</dc:source>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:doi>10.1038/nrn2770</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrn2770</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>834</prism:startingPage>
<prism:endingPage>834</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrn2770</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrn2771">
<title>In Brief</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/6EocD6edpA4/nrn2771</link>
<description>Place cells</description>
<content:encoded><![CDATA[

<p>
<b>In Brief</b>
</p>
<p>Nature Reviews Neuroscience 10, 835 (2009). <a href="http://dx.doi.org/10.1038/nrn2771">doi:10.1038/nrn2771</a>
</p>
<p>Place cells</p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/6EocD6edpA4" height="1" width="1"/>]]></content:encoded>
<dc:title>In Brief</dc:title>
<dc:identifier>doi:10.1038/nrn2771</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 835 (2009)</dc:source>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:doi>10.1038/nrn2771</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrn2771</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>835</prism:startingPage>
<prism:endingPage>835</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrn2771</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrn2772">
<title>From the editors</title>
<link>http://feeds.nature.com/~r/nrn/rss/current/~3/6minUfx7Epc/nrn2772</link>
<description>The fortieth annual Society for Neuroscience meeting this year welcomed over 30,000 delegates and was again a resounding success, with talks and posters pointing to important developments and approaches in neuroscience, several of which will feature in forthcoming issues of Nature Reviews Neuroscience.MicroRNAs </description>
<content:encoded><![CDATA[

<p>
<b>From the editors</b>
</p>
<p>Nature Reviews Neuroscience 10, 831 (2009). <a href="http://dx.doi.org/10.1038/nrn2772">doi:10.1038/nrn2772</a>
</p>
<p>The fortieth annual Society for Neuroscience meeting this year welcomed over 30,000 delegates and was again a resounding success, with talks and posters pointing to important developments and approaches in neuroscience, several of which will feature in forthcoming issues of Nature Reviews Neuroscience.MicroRNAs </p>
<img src="http://feeds.feedburner.com/~r/nrn/rss/current/~4/6minUfx7Epc" height="1" width="1"/>]]></content:encoded>
<dc:title>From the editors</dc:title>
<dc:identifier>doi:10.1038/nrn2772</dc:identifier>
<dc:source>Nature Reviews Neuroscience 10, 831 (2009)</dc:source>
<prism:publicationName>Nature Reviews Neuroscience</prism:publicationName>
<prism:doi>10.1038/nrn2772</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrn2772</prism:url>
<prism:volume>10</prism:volume>
<prism:number>12</prism:number>
<prism:section>From The Editors</prism:section>
<prism:startingPage>831</prism:startingPage>
<prism:endingPage>831</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrn2772</feedburner:origLink></item>
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