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| TABLE OF CONTENTS 
 
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| September 2015 Volume 18, Issue 9 | 
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  |  |  Focus 
  Editorial 
  News and Views 
  Overview 
  Q&A 
  Historical Commentary 
  Brief Communications 
  Articles 
  Resource 
  Technical Report 
 
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    	|   			    | An open access journal dedicated to highlighting the most important scientific advances in Parkinson's disease research, spanning the motor and non-motor disorders of Parkinson's disease. 
 Part of the Nature Partner Journals series, npj Parkinson's Disease is published in partnership with the Parkinson's Disease Foundation.
 
 Open for submissions: http://bit.ly/1uUh8YB
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    	        	  	                                                  | Focus |  Top | 
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                                                | Editorial |  Top | 
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  | ChR2 coming of age   p1191doi:10.1038/nn.4103
 10 years ago, channelrhodopsin-2 was expressed in neurons and shown to control their activity. In this issue, we consider how the field has developed since these early optogenetic experiments.
 
 
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  | News and Views |  Top | 
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  | Overview |  Top | 
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  | Optogenetics and the future of neuroscience   pp1200 - 1201Edward S Boyden
 doi:10.1038/nn.4094
 
 
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  | Q&A |  Top | 
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  | Optogenetics: 10 years after ChR2 in neurons—views from the community   pp1202 - 1212Antoine Adamantidis,  Silvia Arber,  Jaideep S Bains,  Ernst Bamberg,  Antonello Bonci et al.
 doi:10.1038/nn.4106
 On the anniversary of the Boyden et al. (2005) paper that introduced the use of channelrhodopsin in neurons, Nature Neuroscience asks selected members of the community to comment on the utility, impact and future of this important technique.
 
 
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  | Historical Commentary |  Top | 
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  | Optogenetics: 10 years of microbial opsins in neuroscience   pp1213 - 1225Karl Deisseroth
 doi:10.1038/nn.4091
 Over the past decade, modern optogenetics has emerged from the convergence of developments in microbial opsin engineering, genetic methods for targeting, and optical strategies for light delivery. In this Historical Commentary, Karl Deisseroth reflects on the optogenetic landscape, from the important steps but slow progress in the beginning to the acceleration in discovery seen in recent years.
 
 
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  | Brief Communications |  Top | 
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  | Modifiers of C9orf72 dipeptide repeat toxicity connect nucleocytoplasmic transport defects to FTD/ALS   pp1226 - 1229Ana Jovičić,  Jerome Mertens,  Steven Boeynaems,  Elke Bogaert,  Noori Chai et al.
 doi:10.1038/nn.4085
 C9orf72 mutations are the most common cause of amyotrophic lateral sclerosis and frontotemporal dementia. With unbiased screens in Saccharomyces cerevisiae, Jovicic et al. identified potent modifiers of toxicity of dipeptide repeat proteins produced by unconventional translation of the C9orf72 repeat expansions, pointing to nucleocytoplasmic transport impairments as potential disease mechanisms.
 
 
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  | Coding the direct/indirect pathways by D1 and D2 receptors is not valid for accumbens projections   pp1230 - 1232Yonatan M Kupchik,  Robyn M Brown,  Jasper A Heinsbroek,  Mary Kay Lobo,  Danielle J Schwartz et al.
 doi:10.1038/nn.4068
 It is widely assumed that D1 and D2 dopamine receptor-expressing striatal neurons code for discrete pathways in the basal ganglia. Combining optogenetics and electrophysiology, the authors show that this output architecture does not apply to nucleus accumbens neurons. Current thinking attributing D1/D2 selectivity to accumbens projections thus should be reconsidered.
 
 
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  | Instrumental learning of traits versus rewards: dissociable neural correlates and effects on choice   pp1233 - 1235Leor M Hackel,  Bradley B Doll and  David M Amodio
 doi:10.1038/nn.4080
 Humans learn about people and objects through positive and negative experiences, yet they can look beyond rewards to encode trait-level attributes such as generosity. The authors show that neural activity and choices reflect feedback-based learning about rewards and traits of people and slot machines and that trait learning strongly drives decisions about new social interactions.
 
 See also: News and Views by Hsu & Jenkins
 
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    	  	      | Articles |  Top | 
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  | EAG2 potassium channel with evolutionarily conserved function as a brain tumor target   pp1236 - 1246Xi Huang,  Ye He,  Adrian M Dubuc,  Rintaro Hashizume,  Wei Zhang et al.
 doi:10.1038/nn.4088
 This study shows conserved EAG2 potassium channel function in brain tumorigenesis and metastasis, cooperation of different potassium channels for mitotic volume regulation, and EAG2 enrichment at the trailing edge for local volume regulation and cell motility. The authors identified the FDA-approved drug thioridazine as an EAG2 blocker of potential therapeutic value.
 
 
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  | Cellular evidence for efference copy in Drosophila visuomotor processing   pp1247 - 1255Anmo J Kim,  Jamie K Fitzgerald and  Gaby Maimon
 doi:10.1038/nn.4083
 The authors show that fruit flies briefly silence visual processing during voluntary flight turns, which likely helps flies to ignore the image of the world sweeping over the retina during such turns.
 
 See also: News and Views by Krapp
 
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  | LSD1n is an H4K20 demethylase regulating memory formation via transcriptional elongation control   pp1256 - 1264Jianxun Wang,  Francesca Telese,  Yuliang Tan,  Wenbo Li,  Chunyu Jin et al.
 doi:10.1038/nn.4069
 The authors show that the neuron-specific LSD1 variant (LSD1n) promotes transcription initiation and elongation in response to neuronal activity. LSD1n is essential for spatial learning and long-term memory formation. LSD1n exhibits novel substrate specificity for histone H4 K20 methylation.
 
 Watch an audio-visual summary of the paper here
 
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  | GABAergic mechanisms regulated by miR-33 encode state-dependent fear   pp1265 - 1271Vladimir Jovasevic,  Kevin A Corcoran,  Katherine Leaderbrand,  Naoki Yamawaki,  Anita L Guedea et al.
 doi:10.1038/nn.4084
 Some stress-related memories are state-dependent: they cannot be retrieved unless the brain is in the same state as during initial encoding. The authors show that hippocampal extrasynaptic GABAA receptors, regulated by miR-33, support state-dependent contextual fear conditioning by altering the processing of context memories within the extended hippocampal circuit.
 
 See also: News and Views by Holmes & Chen
 
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  | Naturalistic stimulation drives opposing heterosynaptic plasticity at two inputs to songbird cortex   pp1272 - 1280W Hamish Mehaffey and  Allison J Doupe
 doi:10.1038/nn.4078
 This study examines how key inputs to a brain area vital for song production can interact cooperatively to change each other. The authors show that naturalistic stimulation patterns drive bidirectional in vitro plasticity in synaptic inputs to a song production area, and use this understanding to manipulate song plasticity in vivo.
 
 
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  | Determinants of different deep and superficial CA1 pyramidal cell dynamics during sharp-wave ripples   pp1281 - 1290Manuel Valero,  Elena Cid,  Robert G Averkin,  Juan Aguilar,  Alberto Sanchez-Aguilera et al.
 doi:10.1038/nn.4074
 Using a combination of electrophysiological and neurochemical techniques the authors report that deep and superficial CA1 pyramidal neurons behave differently during hippocampal sharp-wave ripples, with deep cells becoming hyperpolarized and superficial cells undergoing depolarization. The study also reveals some of the microcircuit mechanisms that underlie this spatiotemporal specialization, including the involvement of CA2 pyramidal cells and the role of perisomatic inhibition.
 
 
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  | Hippocampal circuit dysfunction in the Tc1 mouse model of Down syndrome   pp1291 - 1298Jonathan Witton,  Ragunathan Padmashri,  Larissa E Zinyuk,  Victor I Popov,  Igor Kraev et al.
 doi:10.1038/nn.4072
 The authors report that the ultrastructure and plasticity of excitatory synapses connecting dentate gyrus and CA3 of the hippocampus are severely compromised in a transchromosomic mouse model of Down syndrome. These alterations are accompanied by unstable information coding by CA3 and CA1 place cells, which may contribute to aspects of impaired cognition in the disease.
 
 
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  | Dynamic rewiring of neural circuits in the motor cortex in mouse models of Parkinson's disease   pp1299 - 1309Lili Guo,  Huan Xiong,  Jae-Ick Kim,  Yu-Wei Wu,  Rupa R Lalchandani et al.
 doi:10.1038/nn.4082
 Using in vivo imaging, the authors explore how dopamine loss in Parkinson/'s disease mouse models affects synaptic plasticity in motor cortex. They find that dopamine D1 and D2 receptor signaling distinctly regulates dendritic spine dynamics and that dopamine loss results in atypical synaptic adaptations. These mechanisms may contribute to impaired motor performance in Parkinson's disease.
 
 See also: News and Views by Calabresi & Di Filippo
 
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  | Learning to expect the unexpected: rapid updating in primate cerebellum during voluntary self-motion   pp1310 - 1317Jessica X Brooks,  Jerome Carriot and  Kathleen E Cullen
 doi:10.1038/nn.4077
 By recording from cerebellar output neurons during motor learning, the authors provide direct evidence for an elegant computation requiring the comparison of predicted and actual sensory feedback to signal unexpected sensation. Their results suggest that rapid updating of the cerebellum's internal model enables the brain to learn to expect unexpected sensory input.
 
 
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  | Oscillatory dynamics coordinating human frontal networks in support of goal maintenance   pp1318 - 1324Bradley Voytek,  Andrew S Kayser,  David Badre,  David Fegen,  Edward F Chang et al.
 doi:10.1038/nn.4071
 Humans have a capacity for hierarchical cognitive control—the ability to simultaneously control immediate actions while holding more abstract goals in mind. The authors show that neural oscillations establish dynamic communication networks within the frontal cortex and that these oscillations coordinate local neural activity with increasing cognitive control.
 
 
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    	  	      | Resource |  Top | 
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  | Identification of neurodegenerative factors using translatome-regulatory network analysis   pp1325 - 1333Lars Brichta,  William Shin,  Vernice Jackson-Lewis,  Javier Blesa,  Ee-Lynn Yap et al.
 doi:10.1038/nn.4070
 To elucidate novel molecular mechanisms underlying neurodegeneration in Parkinson's disease, the authors generated mice for cell type-specific profiling of dopaminergic neurons. Regulatory network analysis of translatome libraries from dopaminergic neurons under degenerative stress facilitated the identification of intrinsic upstream regulators that oppose degeneration. This strategy can be generalized to investigate degeneration of other classes of neurons.
 
 
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  | Technical Report |  Top | 
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  | Cell type-specific manipulation with GFP-dependent Cre recombinase   pp1334 - 1341Jonathan C Y Tang,  Stephanie Rudolph,  Onkar S Dhande,  Victoria E Abraira,  Seungwon Choi et al.
 doi:10.1038/nn.4081
 GFP reporter lines are useful for labeling specific cell types. Here, the authors developed a method to convert GFP expression directly into Cre recombinase activity. GFP-dependent Cre was delivered via electroporation or AAV to neural tissues in the mouse, and could be used for optogenetic control of specific cell types.
 
 
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