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1. Full Text Atp13a2 expression in the periaqueductal gray is decreased in the Pink1 -/- rat model of Parkinson disease
by Kelm-Nelson, Cynthia A and Stevenson, Sharon A and Ciucci, Michelle R
Neuroscience letters, ISSN 0304-3940, 05/2016, Volume 621, pp. 75 - 82
Ultrasonic vocalization | Periaqueductal gray | Pink1 | Alpha synuclein | Rat | Gad1 | Parkinson disease | Atp13a2 | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Biomarkers - metabolism | Tyrosine 3-Monooxygenase - metabolism | Protein Kinases - genetics | Rats, Long-Evans | Rats | Glucosylceramidase - metabolism | Parkinson Disease - genetics | Gene Knockout Techniques | Receptors, Dopamine D2 - metabolism | Periaqueductal Gray - metabolism | Receptors, Dopamine D1 - metabolism | Proton-Translocating ATPases - metabolism | Animals | Glutamate Decarboxylase - metabolism | Parkinson Disease - metabolism | Receptors, GABA-A - metabolism | CASP8 and FADD-Like Apoptosis Regulating Protein - metabolism | alpha-Synuclein - metabolism | Apoptosis | Gene expression | Parkinson's disease | RNA | Genes | GABA | Glutamate decarboxylase | Glutamate | Index Medicus
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2. Full Text Progeny of Olig2-Expressing Progenitors in the Gray and White Matter of the Adult Mouse Cerebral Cortex
by Dimou, Leda and Simon, Christiane and Kirchhoff, Frank and Takebayashi, Hirohide and Gotz, Magdalena
The Journal of neuroscience, ISSN 0270-6474, 10/2008, Volume 28, Issue 41, pp. 10434 - 10442
Forebrain | NG2 | Myelination | Lineage analysis | Stab wound injury | Oligodendrocyte progenitors | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Periaqueductal Gray - cytology | Cell Proliferation | Mitosis | Neuroglia - pathology | Stem Cells - cytology | Stem Cells - metabolism | Cerebral Cortex - cytology | Oligodendroglia - ultrastructure | Wounds, Stab - pathology | Neuroglia - cytology | Basic Helix-Loop-Helix Transcription Factors - metabolism | Cell Differentiation | Oligodendroglia - cytology | Genes, Reporter | Gene Expression | Basic Helix-Loop-Helix Transcription Factors - genetics | Animals, Genetically Modified | Mice, Inbred C57BL | Proteoglycans - metabolism | Antigens - metabolism | Oligodendrocyte Transcription Factor 2 | Nerve Tissue Proteins - genetics | Integrases | Nerve Tissue Proteins - metabolism | Animals | Tamoxifen - pharmacology | Neuroglia - metabolism | Mice | Myelin Sheath - ultrastructure | Index Medicus | stab wound injury | lineage analysis | myelination | forebrain | oligodendrocyte progenitors
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3. Full Text Stress induces analgesia via orexin 1 receptor-initiated endocannabinoid/CB1 signaling in the mouse periaqueductal gray
by Lee, Hsin-Jung and Chang, Lu-Yang and Ho, Yu-Cheng and Teng, Shu-Fang and Hwang, Ling-Ling and Mackie, Ken and Chiou, Lih-Chu
Neuropharmacology, ISSN 0028-3908, 06/2016, Volume 105, pp. 577 - 586
Periaqueductal gray | Pain | OX1 and OX2 receptors | Cannabinoid | Orexin | Stress-induced analgesia | Pharmacology & Pharmacy | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Benzoxazoles - pharmacology | Neurons - pathology | Pain Perception - physiology | Periaqueductal Gray - drug effects | Analgesics, Opioid - pharmacology | Male | Nociceptive Pain - drug therapy | Nociceptive Pain - metabolism | Isoquinolines - pharmacology | Pain Perception - drug effects | Receptor, Cannabinoid, CB1 - agonists | Stress, Psychological - metabolism | Urea - analogs & derivatives | Neurons - metabolism | Corticosterone - blood | Hypothalamus - drug effects | Neurons - drug effects | Orexin Receptors - metabolism | Stress, Psychological - drug therapy | Mice, Inbred C57BL | Nociceptive Pain - pathology | Proto-Oncogene Proteins c-fos - metabolism | Morpholines - pharmacology | Hypothalamus - pathology | Periaqueductal Gray - metabolism | Naphthalenes - pharmacology | Stress, Psychological - pathology | Receptor, Cannabinoid, CB1 - metabolism | Animals | Hypothalamus - metabolism | Signal Transduction - drug effects | Naloxone - pharmacology | Benzoxazines - pharmacology | Orexin Receptors - agonists | Pyridines - pharmacology | Receptor, Cannabinoid, CB1 - antagonists & inhibitors | Periaqueductal Gray - pathology | Urea - pharmacology | Physiological aspects | Medical colleges | Analgesia | Index Medicus
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4. Full Text Iron deposition in periaqueductal gray matter as a potential biomarker for chronic migraine
by Domínguez, Clara and López, Ana and Ramos-Cabrer, Pedro and Vieites-Prado, Alba and Pérez-Mato, Maria and Villalba, Carmen and Sobrino, Tomás and Rodriguez-Osorio, Xiana and Campos, Francisco and Castillo, José and Leira, Rogelio
Neurology, ISSN 0028-3878, 03/2019, Volume 92, Issue 10, pp. e1076 - e1085
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Biomarkers - metabolism | Red Nucleus - diagnostic imaging | Prospective Studies | Periaqueductal Gray - diagnostic imaging | Humans | Male | Iron - metabolism | Case-Control Studies | Globus Pallidus - diagnostic imaging | Periaqueductal Gray - metabolism | Migraine Disorders - metabolism | Magnetic Resonance Imaging | Red Nucleus - metabolism | Globus Pallidus - metabolism | Image Processing, Computer-Assisted | Sensitivity and Specificity | Adult | Female | Migraine Disorders - diagnostic imaging | Chronic Disease | Index Medicus | Abridged Index Medicus
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5. Full Text Periaqueductal gray glutamatergic transmission governs chronic stress-induced depression
by Ho, Yu-Cheng and Lin, Tzer-Bin and Hsieh, Ming-Chun and Lai, Cheng-Yuan and Chou, Dylan and Chau, Yat-Pang and Chen, Gin-Den and Peng, Hsien-Yu
Neuropsychopharmacology (New York, N.Y.), ISSN 0893-133X, 2018, Volume 43, Issue 2, pp. 302 - 312
Pharmacology & Pharmacy | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Depression - physiopathology | Receptors, Glucocorticoid - antagonists & inhibitors | Synaptic Transmission - physiology | gamma-Aminobutyric Acid - metabolism | Periaqueductal Gray - drug effects | Male | Receptors, Glucocorticoid - agonists | Depression - etiology | Depression - metabolism | Depression - chemically induced | Stress, Psychological - metabolism | Behavior, Animal - drug effects | Synaptic Transmission - drug effects | Anhedonia - physiology | Receptors, AMPA - metabolism | Disease Models, Animal | Rats | Behavior, Animal - physiology | Rats, Sprague-Dawley | Periaqueductal Gray - metabolism | Periaqueductal Gray - physiopathology | Patch-Clamp Techniques | Animals | Glutamic Acid - metabolism | Stress, Psychological - complications | Receptors, AMPA - antagonists & inhibitors | Stresses | Sucrose | Mental disorders | Glucocorticoids | Glutamic acid receptors (ionotropic) | Pathogenesis | Periaqueductal gray area | Pharmacology | Mental depression | α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors | Cell surface | Stress | Behavioral despair | Western blotting | Footshock | Receptors | Reduction | Endocytosis | Acids | Synaptic transmission | α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid | Hedonic response | Glutamatergic transmission | Sugars | Index Medicus | Original
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6. Full Text Periaqueductal gray afferents synapse onto dopamine and GABA neurons in the rat ventral tegmental area
by Omelchenko, Natalia and Sesack, Susan R
Journal of neuroscience research, ISSN 0360-4012, 04/2010, Volume 88, Issue 5, pp. 981 - 991
reward | tract‐tracing | ultrastructure | opiates | periaqueductal gray | Opiates | Tract-tracing | Periaqueductal gray | Reward | Ultrastructure | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Tyrosine 3-Monooxygenase - metabolism | Synaptic Transmission - physiology | Periaqueductal Gray - ultrastructure | gamma-Aminobutyric Acid - metabolism | Neuroanatomical Tract-Tracing Techniques | Secretory Vesicles - metabolism | Opioid-Related Disorders - metabolism | Male | Presynaptic Terminals - ultrastructure | Microscopy, Immunoelectron | Excitatory Postsynaptic Potentials - physiology | Neural Inhibition - physiology | Synapses - metabolism | Limbic System - physiology | Ventral Tegmental Area - ultrastructure | Dopamine - metabolism | Secretory Vesicles - ultrastructure | Inhibitory Postsynaptic Potentials - physiology | Rats | Neuropeptides - metabolism | Synapses - ultrastructure | Rats, Sprague-Dawley | Periaqueductal Gray - metabolism | Animals | Motivation - physiology | Ventral Tegmental Area - metabolism | Brain Mapping | Neural Pathways - metabolism | Presynaptic Terminals - metabolism | Glutamic Acid - metabolism | Neural Pathways - ultrastructure | Opioid-Related Disorders - physiopathology | Index Medicus | tract-tracing
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7. Full Text Periaqueductal gray neuronal activities underlie different aspects of defensive behaviors
by Deng, Hanfei and Xiao, Xiong and Wang, Zuoren
The Journal of neuroscience, ISSN 0270-6474, 07/2016, Volume 36, Issue 29, pp. 7580 - 7588
Electrophysiology | Innate behavior | Periaqueductal gray | Optogenetics | Defensive behavior | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Membrane Potentials - genetics | Periaqueductal Gray - cytology | Transduction, Genetic | Tinea | Mice, Inbred C57BL | Rats, Long-Evans | Gene Expression Regulation | Rats | Male | Membrane Potentials - physiology | Rhodopsin - metabolism | Carrier Proteins - genetics | Fear | Patch-Clamp Techniques | Animals | Carrier Proteins - metabolism | Rhodopsin - genetics | Conditioning (Psychology) | Neurons - physiology | Defense Mechanisms | Luminescent Proteins - genetics | Mice | Luminescent Proteins - metabolism | Index Medicus | defensive behavior | electrophysiology | periaqueductal gray | innate behavior | optogenetics
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8. Full Text Regulation of REM and Non-REM Sleep by Periaqueductal GABAergic Neurons
by Weber, Franz and Hoang Do, Johnny Phong and Chung, Shinjae and Beier, Kevin T and Bikov, Mike and Saffari Doost, Mohammad and Dan, Yang
Nature communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 354 - 13
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Calcium - metabolism | Sleep, REM - physiology | Pons - physiology | GABAergic Neurons - physiology | Electroencephalography | Polysomnography | Brain - physiology | Neural Pathways - physiology | Periaqueductal Gray - metabolism | Brain - metabolism | Animals | Ultradian Rhythm - physiology | Neural Pathways - metabolism | Periaqueductal Gray - physiology | Electromyography | Mice | Pons - metabolism | GABAergic Neurons - metabolism | Sleep - physiology | Neuroimaging | Brain | Pons | Calcium | Mesencephalon | Neurons | Periaqueductal gray area | Calcium imaging | Firing rate | Sleep (REM) | Rapid eye movement state | Eye movements | γ-Aminobutyric acid | Sleep | Consolidation | Sleep (NREM) | Gating | Index Medicus
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9. Full Text Activation of orexin 1 receptors in the periaqueductal gray of male rats leads to antinociception via retrograde endocannabinoid (2-arachidonoylglycerol)-induced disinhibition
by Ho, Yu-Cheng and Lee, Hsin-Jung and Tung, Li-Wei and Liao, Yan-Yu and Fu, Szu-Ying and Teng, Shu-Fang and Liao, Hsin-Tzu and Mackie, Ken and Chiou, Lih-Chu
The Journal of neuroscience, ISSN 0270-6474, 10/2011, Volume 31, Issue 41, pp. 14600 - 14610
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Cannabinoid Receptor Modulators - pharmacology | Benzoxazoles - pharmacology | Electric Stimulation | Neural Pathways - drug effects | Rats, Wistar | Receptors, G-Protein-Coupled - metabolism | gamma-Aminobutyric Acid - metabolism | Periaqueductal Gray - drug effects | Male | Receptors, Neuropeptide - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | Pain - metabolism | Neural Pathways - physiology | Lactones - pharmacology | Neural Inhibition - physiology | Biphenyl Compounds - pharmacology | Piperidines - pharmacology | Pain - drug therapy | Estrenes - pharmacology | Pyrrolidinones - pharmacology | Urea - analogs & derivatives | Endocannabinoids | Disease Models, Animal | Pyrazoles - pharmacology | Animals, Newborn | Orexins | Enzyme Inhibitors - pharmacology | Receptors, Neuropeptide - antagonists & inhibitors | Morpholines - pharmacology | Rats | Neuropeptides - metabolism | Pain Measurement - drug effects | Orexin Receptors | Pain - pathology | Arachidonic Acids - pharmacology | Naphthalenes - pharmacology | Calcium Channel Blockers | Glycerides - pharmacology | Patch-Clamp Techniques | Animals | Analysis of Variance | Benzoxazines - pharmacology | Receptors, G-Protein-Coupled - antagonists & inhibitors | Periaqueductal Gray - physiology | In Vitro Techniques | Neural Inhibition - drug effects | Inhibitory Postsynaptic Potentials - drug effects | Urea - pharmacology | Index Medicus
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