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1. Full Text AAV-Mediated Anterograde Transsynaptic Tagging: Mapping Corticocollicular Input-Defined Neural Pathways for Defense Behaviors
by Zingg, Brian and Chou, Xiao-lin and Zhang, Zheng-gang and Zhang, Li I and Mesik, Lukas and Liang, Feixue and Tao, Huizhong Whit
Neuron, ISSN 0896-6273, 01/2017, Volume 93, Issue 1, pp. 33 - 47
To decipher neural circuits underlying brain functions, viral tracers are widely applied to map input and output connectivity of neuronal populations. Despite... 
transsynaptic/transneuronal tracer | Cre and Flp system | AAV serotypes | superior colliculus | corticofugal projection | intersectional strategy | defensive behavior | mapping neural circuits | flight and freezing | SUPERIOR COLLICULUS | ORGANIZATION | VIRUS | VISUAL-CORTEX | CORPUS-CALLOSUM | IN-VIVO | MOUSE | NEURONS | PROJECTIONS | VECTORS | NEUROSCIENCES | Synapses - physiology | Visual Cortex - cytology | Superior Colliculi - physiology | Behavior, Animal - physiology | Auditory Cortex - physiology | Dependovirus | Cerebral Cortex - cytology | Escape Reaction - physiology | Neural Pathways - physiology | Visual Cortex - physiology | Integrases | Animals | Neural Pathways - cytology | Neurons - physiology | Superior Colliculi - cytology | Freezing Reaction, Cataleptic - physiology | Auditory Cortex - cytology | Cerebral Cortex - physiology | Mice | DNA Nucleotidyltransferases | Medical colleges | Neural circuitry | Gene expression | Neurons | Neurophysiology | Tracers (Biology) | Brain | Data analysis | Rodents | Viruses | Behavior | Labeling
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2. Full Text MEF2 negatively regulates learning-induced structural plasticity and memory formation
by Cole, Christina J and Mercaldo, Valentina and Restivo, Leonardo and Yiu, Adelaide P and Sekeres, Melanie J and Han, Jin-Hee and Vetere, Gisella and Pekar, Tetyana and Ross, P Joel and Neve, Rachael L and Frankland, Paul W and Josselyn, Sheena A
Nature Neuroscience, ISSN 1097-6256, 09/2012, Volume 15, Issue 9, pp. 1255 - 1264
Memory formation is thought to be mediated by dendritic-spine growth and restructuring. Myocyte enhancer factor 2 (MEF2) restricts spine growth in vitro,... 
DENDRITIC SPINES | LONG-TERM-MEMORY | ANTERIOR CINGULATE CORTEX | AMPA RECEPTOR TRAFFICKING | SPATIAL MEMORY | MENTAL-RETARDATION PROTEIN | SYNAPTIC PLASTICITY | TRANSCRIPTION FACTOR | EXPRESSION | NEUROSCIENCES | MYOCYTE ENHANCER FACTOR-2 | Immunohistochemistry | Male | Luciferases - genetics | Neuronal Plasticity - physiology | Neurons - physiology | Female | MEF2 Transcription Factors | Maze Learning - physiology | Myogenic Regulatory Factors - genetics | Receptors, AMPA - physiology | Conditioning (Psychology) - physiology | Mice, Inbred C57BL | Simplexvirus - genetics | Amygdala - metabolism | Dendritic Spines - physiology | In Situ Hybridization, Fluorescence | Myogenic Regulatory Factors - physiology | Dependovirus | Hippocampus - cytology | Blotting, Western | Endocytosis - physiology | Fear | Learning - physiology | Animals | Mice | Genetic Vectors | Hippocampus - physiology | Amygdala - physiology | Memory - physiology | Neuroplasticity | Physiological aspects | Transcription factors | Research | Memory
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3. Full Text Acetylcholine encodes long-lasting presynaptic plasticity at glutamatergic synapses in the dorsal striatum after repeated amphetamine exposure
by Wang, Wengang and Darvas, Martin and Storey, Granville P and Bamford, Ian J and Gibbs, Effrey T and Palmiter, Richard D and Bamford, Nigel S
Journal of Neuroscience, ISSN 0270-6474, 2013, Volume 33, Issue 25, pp. 10405 - 10426
Locomotion and cue-dependent behaviors are modified through corticostriatal signaling whereby short-term increases in dopamine availability can provoke... 
DORSOLATERAL STRIATUM | DRUG-ADDICTION | IN-VIVO | CORTICOSTRIATAL TERMINALS | BEHAVIORAL SENSITIZATION | ELECTROPHYSIOLOGICAL PROPERTIES | DOPAMINE NEUROTRANSMISSION | NEOSTRIATAL CHOLINERGIC INTERNEURONS | NEUROSCIENCES | NUCLEUS-ACCUMBENS | PARKINSONS-DISEASE | Dependovirus - genetics | Interneurons - physiology | Motor Activity - physiology | Receptors, Presynaptic - physiology | Neuronal Plasticity - drug effects | Male | Neostriatum - physiology | Excitatory Postsynaptic Potentials - physiology | Neuronal Plasticity - physiology | Receptors, Presynaptic - drug effects | Choline O-Acetyltransferase - physiology | Neostriatum - drug effects | Excitatory Postsynaptic Potentials - genetics | Choline O-Acetyltransferase - genetics | Synapses - drug effects | Neostriatum - cytology | Maze Learning - physiology | Synapses - physiology | Mice, Inbred C57BL | Amphetamine - pharmacology | Glutamic Acid - physiology | Mice, Knockout | Animals | Receptors, Dopamine D1 - physiology | Adrenergic Uptake Inhibitors - pharmacology | Receptors, Dopamine D2 - physiology | Mice | Postural Balance - physiology | Electrophysiological Phenomena | Acetylcholine - physiology | Genetic Vectors | Locomotion - physiology
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4. Full Text A Broad Role for Melanopsin in Nonvisual Photoreception
by Gooley, Joshua J and Lu, Jun and Fischer, Dietmar and Saper, Clifford B
Journal of Neuroscience, ISSN 0270-6474, 08/2003, Volume 23, Issue 18, pp. 7093 - 7106
The rod and cone photoreceptors that mediate visual phototransduction in mammals are not required for light-induced circadian entrainment, negative masking of... 
Adeno-associated virus | Ventrolateral preoptic nucleus | Retina | Hypothalamus | Suprachiasmatic | Melanopsin | Sleep | Intergeniculate | Entrainment | Subparaventricular | Masking | Pupillary light reflex | Circadian | Ganglion cells | Pretectal | EFFERENT PROJECTIONS | pupillary light reflex | masking | entrainment | CIRCADIAN-RHYTHMS | RETINOHYPOTHALAMIC TRACT | adeno-associated virus | INTERGENICULATE LEAFLET | intergeniculate | ventrolateral preoptic nucleus | pretectal | NEUROSCIENCES | LATERAL GENICULATE-NUCLEUS | melanopsin | sleep | RETINAL GANGLION-CELLS | ADENOASSOCIATED VIRAL VECTORS | circadian | ganglion cells | retina | SUPRACHIASMATIC NUCLEUS | suprachiasmatic | subparaventricular | hypothalamus | Dependovirus - genetics | Green Fluorescent Proteins | Rod Opsins - physiology | Superior Colliculi - physiology | Male | Geniculate Bodies - physiology | Neural Pathways - physiology | Photoreceptor Cells, Vertebrate - physiology | Luminescent Proteins - biosynthesis | Suprachiasmatic Nucleus - physiology | Cerebral Ventricles - physiology | Cerebral Ventricles - anatomy & histology | Dependovirus - physiology | RNA, Messenger - biosynthesis | Retinal Ganglion Cells - cytology | Rod Opsins - genetics | Tectum Mesencephali - anatomy & histology | Tectum Mesencephali - physiology | Light Signal Transduction - physiology | Preoptic Area - physiology | Retinal Ganglion Cells - physiology | Rod Opsins - biosynthesis | Superior Colliculi - anatomy & histology | Geniculate Bodies - anatomy & histology | Rats | Photoreceptor Cells, Vertebrate - cytology | Suprachiasmatic Nucleus - anatomy & histology | Neural Pathways - anatomy & histology | Animals | Cholera Toxin | Luminescent Proteins - genetics | Preoptic Area - anatomy & histology | Cerebral Ventricles - cytology | Behavioral | Systems | Cognitive
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5. Full Text ALK5-dependent TGF-beta signaling is a major determinant of late-stage adult neurogenesis
by He, YB and Zhang, H and Yung, A and Villeda, SA and Jaeger, PA and Olayiwola, O and Fainberg, N and Wyss-Coray, T
NATURE NEUROSCIENCE, ISSN 1097-6256, 07/2014, Volume 17, Issue 7, pp. 943 - 952
The transforming growth factor-beta (TGF-beta) signaling pathway serves critical functions in CNS development, but, apart from its proposed neuroprotective... 
PROGENITOR CELLS | RAT HIPPOCAMPAL-NEURONS | GROWTH-FACTOR-BETA | PROTEIN | TRANSFORMING GROWTH-FACTOR-BETA-1 | MICE | MECHANISMS | NEURAL STEM-CELL | EXPRESSION | NEUROSCIENCES | BRAIN | Immunohistochemistry | Male | Receptors, Transforming Growth Factor beta - physiology | Luciferases - genetics | Microarray Analysis | Gene Expression - physiology | Neurons - physiology | Fear - psychology | Female | Hippocampus - growth & development | Animals, Newborn | Protein-Serine-Threonine Kinases - physiology | Mice, Inbred C57BL | Transforming Growth Factor beta - physiology | Dependovirus | Blotting, Western | Stereotaxic Techniques | Microscopy, Confocal | Animals | Conditioning (Psychology) | Dentate Gyrus - physiology | Neurogenesis - physiology | Doxycycline - pharmacology | Signal Transduction - physiology | Mice | Genetic Vectors | Hippocampus - physiology | Memory - physiology
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6. Full Text NRF2 promotes neuronal survival in neurodegeneration and acute nerve damage
by Xiong, Wenjun and Garfinkel, Alexandra E. MacColl and Li, Yiqing and Benowitz, Larry I and Cepko, Constance L
Journal of Clinical Investigation, ISSN 0021-9738, 04/2015, Volume 125, Issue 4, pp. 1433 - 1445
Oxidative stress contributes to the loss of neurons in many disease conditions as well as during normal aging; however, small-molecule agents that reduce... 
RETINAL DEGENERATION | MEDICINE, RESEARCH & EXPERIMENTAL | DIFFUSIBLE FACTOR | OXIDATIVE STRESS | OPTIC-NERVE | PLACEBO-CONTROLLED PHASE-3 | MOUSE MODEL | AXON REGENERATION | PARTIAL RECOVERY | RETINITIS-PIGMENTOSA | CONE CELL-DEATH | NF-E2-Related Factor 2 - physiology | Dependovirus - genetics | Genetic Therapy | Catalase - therapeutic use | NF-E2-Related Factor 2 - therapeutic use | Oxidative Stress - physiology | Genetic Vectors - therapeutic use | Mice, Mutant Strains | Superoxide Dismutase - physiology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Neurons - physiology | NF-E2-Related Factor 2 - genetics | Optic Nerve Injuries - therapy | Transcription Factors - therapeutic use | Retinal Ganglion Cells - physiology | Transcription Factors - physiology | Catalase - physiology | Mice, Inbred C57BL | Optic Nerve Injuries - physiopathology | Nerve Crush | Retinal Cone Photoreceptor Cells - physiology | Genetic Vectors - genetics | Superoxide Dismutase - therapeutic use | Animals | Retinitis Pigmentosa - therapy | Mice | Nerve Degeneration | Apoptosis | Oxidative stress | Transcription factors | Nervous system | Development and progression | Degeneration | Genetic aspects | Health aspects | Antioxidants | Proteins | Enzymes | Statistical analysis | Optic nerve | Disease | Genes | Lipids | Photoreceptors | Physiology | Genetics | Neuroscience | Ophthalmology | Therapeutics
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7. Full Text Locomotor Rhythm Generation Linked to the Output of Spinal Shox2 Excitatory Interneurons
by Dougherty, Kimberly J and Zagoraiou, Laskaro and Satoh, Daisuke and Rozani, Ismini and Doobar, Staceyann and Arber, Silvia and Jessell, Thomas M and Kiehn, Ole
Neuron, ISSN 0896-6273, 11/2013, Volume 80, Issue 4, pp. 920 - 933
Locomotion is controlled by spinal networks that generate rhythm and coordinate left-right and flexor-extensor patterning. Defined populations of spinal... 
V2-DERIVED INTERNEURONS | CIRCUITS | LEFT-RIGHT COORDINATION | CORD | NEURONAL NETWORKS | COMMISSURAL INTERNEURONS | CENTRAL PATTERN GENERATOR | V2A INTERNEURONS | NEONATAL MOUSE | SPECIFICATION | NEUROSCIENCES | Immunohistochemistry | Dependovirus - genetics | Interneurons - physiology | Motor Neurons - physiology | Gene Silencing | Glutamic Acid - physiology | Male | Axons - physiology | Excitatory Amino Acid Agonists - pharmacology | Optogenetics | Serotonin - pharmacology | Neural Pathways - physiology | N-Methylaspartate - pharmacology | Animals | In Situ Hybridization | Spinal Cord - physiology | Vesicular Glutamate Transport Protein 2 - physiology | Mice | Electrophysiological Phenomena | Spinal Cord - cytology | Homeodomain Proteins - physiology | Locomotion - physiology | Locomotion - drug effects | Neurosciences | Genetic engineering | Analysis | Cells | Proteins | Rhythm | Transcription factors | Behavior | Grants | Neurons | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Fysiologi | Neurovetenskaper
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8. Full Text Linear transformation of thalamocortical input by intracortical excitation
by Li, Ya-Tang and Ibrahim, Leena A and Liu, Bao-Hua and Zhang, Li I and Tao, Huizhong Whit
Nature Neuroscience, ISSN 1097-6256, 09/2013, Volume 16, Issue 9, pp. 1324 - 1330
Neurons in thalamorecipient layers of sensory cortices integrate thalamocortical and intracortical inputs. Although we know that their functional properties... 
PRIMARY VISUAL-CORTEX | RESPONSE PROPERTIES | ORIENTATION SELECTIVITY | PRIMARY AUDITORY-CORTEX | NEURONS | THALAMIC INPUT | GABA(B) RECEPTORS | NEUROSCIENCES | LATERAL GENICULATE-NUCLEUS | SIMPLE CELLS | RECEPTIVE-FIELDS | Visual Fields - physiology | Mice, Inbred C57BL | Channelrhodopsins | Linear Models | Male | Optogenetics | Orientation - physiology | Cerebral Cortex - cytology | Nerve Net - physiology | Dependovirus - physiology | Visual Pathways - physiology | Animals | Thalamus - physiology | Brain Mapping | Parvalbumins - genetics | Cerebral Cortex - physiology | Female | Luminescent Proteins - genetics | Mice | Photic Stimulation | Luminescent Proteins - metabolism | Excitation (Physiology) | Gene silencing | Genetic transformation | Research | Properties | Neurons
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9. Full Text Disruption of Dopamine Neuron Activity Pattern Regulation through Selective Expression of a Human KCNN3 Mutation
by Soden, Marta E and Jones, Graham L and Sanford, Christina A and Chung, Amanda S and Güler, Ali D and Chavkin, Charles and Luján, Rafael and Zweifel, Larry S
Neuron, ISSN 0896-6273, 11/2013, Volume 80, Issue 4, pp. 997 - 1009
The calcium-activated small conductance potassium channel SK3 plays an essential role in the regulation of dopamine neuron activity patterns. Here we... 
NMDA RECEPTORS | POTASSIUM CHANNELS | FIRING PATTERN | IN-VIVO | ANTIPSYCHOTIC-DRUGS | CAG-REPEAT LENGTH | SK CHANNELS | NEUROSCIENCES | SMALL-CONDUCTANCE | PREFRONTAL CORTEX | VENTRAL TEGMENTAL AREA | Immunohistochemistry | Motor Activity - physiology | Small-Conductance Calcium-Activated Potassium Channels - genetics | Calcium Signaling - physiology | Humans | Motor Activity - drug effects | Excitatory Postsynaptic Potentials - drug effects | Psychomotor Performance - physiology | Receptors, N-Methyl-D-Aspartate - genetics | Attention - physiology | Reflex, Startle - drug effects | Dopaminergic Neurons - drug effects | Dopaminergic Neurons - physiology | Reflex, Startle - physiology | Action Potentials - drug effects | Dopamine - metabolism | Receptors, N-Methyl-D-Aspartate - drug effects | Hallucinogens - pharmacology | Conditioning, Classical - drug effects | N-Methylaspartate - metabolism | Mice, Transgenic | Sensory Gating - physiology | Excitatory Amino Acid Agonists - pharmacology | Dependovirus | Conditioning, Classical - physiology | Receptors, N-Methyl-D-Aspartate - physiology | Action Potentials - physiology | Animals | Calcium Signaling - drug effects | Mice | Electrophysiological Phenomena | In Vitro Techniques | Phenols | Methyl aspartate | Genetic aspects | Dopamine | Neurons | Analysis | Cell culture | Substance abuse treatment | Mental disorders | Parkinsons disease | Schizophrenia | Proteins | Rodents | Addictive behaviors | Physiology | Mutation | Behavior | Localization | Drug dosages
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10. Full Text An excitatory paraventricular nucleus to AgRP neuron circuit that drives hunger
by Krashes, Michael J and Shah, Bhavik P and Madara, Joseph C and Olson, David P and Strochlic, David E and Garfield, Alastair S and Vong, Linh and Pei, Hongjuan and Watabe-Uchida, Mitsuko and Uchida, Naoshige and Liberles, Stephen D and Lowell, Bradford B
Nature, ISSN 0028-0836, 2014, Volume 507, Issue 7491, pp. 238 - 242
Hunger is a hard-wired motivational state essential for survival. Agouti-related peptide (AgRP)-expressing neurons in the arcuate nucleus (ARC) at the base of... 
POMC NEURONS | LEPTIN | ENERGY-EXPENDITURE | PROTEIN | FOOD-INTAKE | NPY | MULTIDISCIPLINARY SCIENCES | FEEDING-BEHAVIOR | RECEPTORS | CELL-TYPES | HYPOTHALAMUS | Dependovirus - genetics | Paraventricular Hypothalamic Nucleus - physiology | Neural Pathways - drug effects | Neuronal Plasticity - drug effects | Arcuate Nucleus of Hypothalamus - cytology | Male | Neural Pathways - physiology | Cell Tracking | Eating - physiology | Satiety Response - physiology | Hunger - drug effects | Paraventricular Hypothalamic Nucleus - cytology | Clozapine - pharmacology | Thyrotropin-Releasing Hormone - metabolism | Neuronal Plasticity - physiology | Female | Food Deprivation | Integrases - metabolism | Agouti-Related Protein - deficiency | Appetite - physiology | Neurons - metabolism | Neurons - drug effects | Neurons, Afferent - drug effects | Peptide Fragments - metabolism | Arcuate Nucleus of Hypothalamus - metabolism | Appetite - drug effects | Clozapine - analogs & derivatives | Agouti-Related Protein - metabolism | Eating - drug effects | Rabies virus - genetics | Animals | Pituitary Adenylate Cyclase-Activating Polypeptide - metabolism | Brain Mapping | Mice | Neurons, Afferent - metabolism | Peptide Fragments - deficiency | Hunger - physiology | Physiological aspects | Electrophysiology | Neuropeptides | Physiological research | Hunger | Research | Studies | Brain | Neurons | Experiments | Light | Food
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11. Full Text Pyramidal Neurons in Prefrontal Cortex Receive Subtype-Specific Forms of Excitation and Inhibition
by Lee, Anthony T and Gee, Steven M and Vogt, Daniel and Patel, Tosha and Rubenstein, John L and Sohal, Vikaas S
Neuron, ISSN 0896-6273, 01/2014, Volume 81, Issue 1, pp. 61 - 68
Layer 5 pyramidal neurons comprise at least two subtypes: thick-tufted, subcortically projecting type A neurons, with prominent h-current, and thin-tufted,... 
HETEROGENEITY | DENDRITES | SYNAPTIC INTEGRATION | RECEPTOR MODULATION | CELLS | NEOCORTEX | CONNECTIVITY | MICROCIRCUIT | SCHIZOPHRENIA | PATTERNS | NEUROSCIENCES | Electric Stimulation | Calcium - metabolism | Channelrhodopsins | Male | Green Fluorescent Proteins - genetics | Nerve Net - drug effects | Excitatory Postsynaptic Potentials - drug effects | Nerve Net - physiology | Neural Pathways - physiology | Dependovirus - physiology | Neural Inhibition - physiology | Neurotransmitter Agents - pharmacology | Pyramidal Cells - physiology | Female | Pyramidal Cells - drug effects | Action Potentials - drug effects | Green Fluorescent Proteins - metabolism | Transduction, Genetic | Synapses - physiology | Prefrontal Cortex - cytology | Action Potentials - physiology | Patch-Clamp Techniques | Animals | Synapses - classification | Mice | In Vitro Techniques | Neural Inhibition - drug effects | Neurons | Neurosciences | Neurophysiology | Studies | Brain | Medical research | Light
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12. Full Text Cardiac-Specific YAP Activation Improves Cardiac Function and Survival in an Experimental Murine MI Model
by Lin, Zhiqiang and von Gise, Alexander and Zhou, Pingzhu and Gu, Fei and Ma, Qing and Jiang, Jianming and Yau, Allan L and Buck, Jessica N and Gouin, Katryna A and van Gorp, Pim R.R and Zhou, Bin and Chen, Jinghai and Seidman, Jonathan G and Wang, Da-Zhi and Pu, William T
Circulation Research, ISSN 0009-7330, 07/2014, Volume 115, Issue 3, pp. 354 - 363
RATIONALE:Yes-associated protein (YAP), the terminal effector of the Hippo signaling pathway, is crucial for regulating embryonic cardiomyocyte proliferation.... 
heart failure | regeneration | myocardial infarction | survival | CELLS | RECOMBINATION | CARDIAC & CARDIOVASCULAR SYSTEMS | ADENOASSOCIATED VIRUS | CARDIOMYOCYTE PROLIFERATION | HIPPO PATHWAY | ORGAN SIZE | HYPERTROPHY | HEART REGENERATION | PERIPHERAL VASCULAR DISEASE | SIZE-CONTROL | HEMATOLOGY | TARGETED EXPRESSION | Dependovirus - genetics | Myocardial Infarction - genetics | Myocardial Infarction - mortality | Cell Proliferation | Humans | Myocardial Contraction - physiology | Transcriptome | Myosin Heavy Chains - genetics | Apoptosis - genetics | Cardiomegaly | Regeneration - genetics | Myocardial Infarction - physiopathology | Phosphoproteins - physiology | Cell Survival - physiology | Disease Models, Animal | Myocytes, Cardiac - cytology | Mice, Transgenic | Survival Rate | Phosphoproteins - genetics | Regeneration - physiology | Adaptor Proteins, Signal Transducing - physiology | Animals | Myocytes, Cardiac - physiology | Adaptor Proteins, Signal Transducing - genetics | Mice | Apoptosis - physiology | YAP | AAV9
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