Works matching Interneurons
Results: 5000
Activation of nicotinic acetylcholine receptors enhances a slow calcium-dependent potassium conductance and reduces the firing of stratum oriens interneurons.
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- European Journal of Neuroscience, 2009, v. 30, n. 6, p. 1011, doi. 10.1111/j.1460-9568.2009.06914.x
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Neurobiology of Disease A Transient Developmental Window of Fast-Spiking Interneuron Dysfunction in a Mouse Model of Dravet Syndrome.
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- Journal of Neuroscience, 2018, v. 38, n. 36, p. 7912, doi. 10.1523/JNEUROSCI.0193-18.2018
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Identification and Characterization of a Novel Spontaneously Active Bursty GABAergic Interneuron in the Mouse Striatum.
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- Journal of Neuroscience, 2018, v. 38, n. 25, p. 5688, doi. 10.1523/JNEUROSCI.3354-17.2018
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Inhibition by Somatostatin Interneurons in Olfactory Cortex.
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- Frontiers in Neural Circuits, 2016, p. 1, doi. 10.3389/fncir.2016.00062
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Acetylcholine release in mouse hippocampal CA1 preferentially activates inhibitory-selective interneurons via α4β2* nicotinic receptor activation.
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- Frontiers in Cellular Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fncel.2015.00115
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Parvalbumin and neuropeptide Y expressing hippocampal GABA-ergic inhibitory interneuron numbers decline in a model of Gulf War illness.
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- Frontiers in Cellular Neuroscience, 2015, v. 8/9, p. 1, doi. 10.3389/fncel.2014.00447
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DISC1 knockdown impairs the tangential migration of cortical interneurons by affecting the actin cytoskeleton.
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- Frontiers in Cellular Neuroscience, 2014, p. 1, doi. 10.3389/fncel.2014.00190
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Dissociation of somatostatin and parvalbumin interneurons circuit dysfunctions underlying hippocampal theta and gamma oscillations impaired by amyloid β oligomers in vivo.
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- Brain Structure & Function, 2020, v. 225, n. 3, p. 935, doi. 10.1007/s00429-020-02044-3
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Somatostatin receptors (SSTR1-5) on inhibitory interneurons in the barrel cortex.
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- Brain Structure & Function, 2020, v. 225, n. 1, p. 387, doi. 10.1007/s00429-019-02011-7
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Tsc1 Loss in VIP-Lineage Cortical Interneurons Results in More VIP+ Interneurons and Enhanced Excitability.
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- Cells (2073-4409), 2024, v. 13, n. 1, p. 52, doi. 10.3390/cells13010052
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Comprehensive characterization of oscillatory signatures in a model circuit with PV- and SOM-expressing interneurons.
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- Biological Cybernetics, 2021, v. 115, n. 5, p. 487, doi. 10.1007/s00422-021-00894-6
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Maternal exposure to 3,3'-iminodipropionitrile targets late-stage differentiation of hippocampal granule cell lineages to affect brain-derived neurotrophic factor signaling and interneuron subpopulations in rat offspring.
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- Journal of Applied Toxicology, 2015, v. 35, n. 8, p. 884, doi. 10.1002/jat.3086
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Coherent ongoing subthreshold state of a cortical neural network regulated by slow- and fast-spiking interneurons.
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- Network: Computation in Neural Systems, 2006, v. 17, n. 4, p. 351, doi. 10.1080/09548980601009650
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Loss of KCC2 in GABAergic Neurons Causes Seizures and an Imbalance of Cortical Interneurons.
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- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.826427
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Disruption of KCC2 in Parvalbumin-Positive Interneurons Is Associated With a Decreased Seizure Threshold and a Progressive Loss of Parvalbumin-Positive Interneurons.
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- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2021.807090
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Specific subtypes of cortical GABA interneurons contribute to the neurovascular coupling response to basal forebrain stimulation.
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- Journal of Cerebral Blood Flow & Metabolism, 2008, v. 28, n. 2, p. 221, doi. 10.1038/sj.jcbfm.9600558
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Optogenetic activation of parvalbumin and somatostatin interneurons selectively restores theta-nested gamma oscillations and oscillation-induced spike timing-dependent long-term potentiation impaired by amyloid β oligomers.
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- BMC Biology, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s12915-019-0732-7
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Ethanol Affects Striatal Interneurons Directly and Projection Neurons Through a Reduction in Cholinergic Tone.
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- Neuropsychopharmacology, 2011, v. 36, n. 5, p. 1033, doi. 10.1038/npp.2010.241
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Histological characterization of interneurons in Alzheimer's disease reveals a loss of somatostatin interneurons in the temporal cortex.
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- Neuropathology, 2020, v. 40, n. 4, p. 336, doi. 10.1111/neup.12649
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Application of Medial Ganglionic Eminence Cell Transplantation in Diseases Associated With Interneuron Disorders.
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- Frontiers in Cellular Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fncel.2022.939294
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Zygotic Vsx1 Plays a Key Role in Defining V2a Interneuron Sub-Lineage by Directly Repressing tal1 Transcription in Zebrafish.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 10, p. 3600, doi. 10.3390/ijms21103600
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HIV-1 Tat causes cognitive deficits and selective loss of parvalbumin, somatostatin, and neuronal nitric oxide synthase expressing hippocampal CA1 interneuron subpopulations.
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- Journal of NeuroVirology, 2016, v. 22, n. 6, p. 747, doi. 10.1007/s13365-016-0447-2
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GABAAR-mediated tonic inhibition differentially modulates intrinsic excitability of VIP- and SST- expressing interneurons in layers 2/3 of the somatosensory cortex.
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- Frontiers in Cellular Neuroscience, 2023, p. 1, doi. 10.3389/fncel.2023.1270219
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Synaptic integration of rhythmogenic neurons in the locomotor circuitry: the case of Hb9 interneurons.
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- Annals of the New York Academy of Sciences, 2010, v. 1198, n. 1, p. 72, doi. 10.1111/j.1749-6632.2010.05533.x
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Early sequential formation of functional GABA<sub>A</sub> and glutamatergic synapses on CA1 interneurons of the rat foetal hippocampus.
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- European Journal of Neuroscience, 2002, v. 16, n. 2, p. 197, doi. 10.1046/j.1460-9568.2002.02073.x
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Innervation of interneurons immunoreactive for VIP by intrinsically bursting pyramidal cells and fast-spiking interneurons in infragranular layers of juvenile rat neocortex.
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- European Journal of Neuroscience, 2002, v. 16, n. 1, p. 11, doi. 10.1046/j.1460-9568.2002.02048.x
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Arid3c identifies an uncharacterized subpopulation of V2 interneurons during embryonic spinal cord development.
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- Frontiers in Cellular Neuroscience, 2024, p. 1, doi. 10.3389/fncel.2024.1466056
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Synaptic polarity of the interneuron circuit controlling C. elegans locomotion.
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- Frontiers in Computational Neuroscience, 2013, p. 1, doi. 10.3389/fncom.2013.00128
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Parvalbumin Interneurons Determine Emotional Valence Through Modulating Accumbal Output Pathways.
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- Frontiers in Behavioral Neuroscience, 2019, p. N.PAG, doi. 10.3389/fnbeh.2019.00110
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Thalamocortical Projection Neuron and Interneuron Numbers in the Visual Thalamic Nuclei of the Adult C57BL/6 Mouse.
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- Frontiers in Neuroanatomy, 2018, p. 1, doi. 10.3389/fnana.2018.00027
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Targeting Spinal Interneurons for Respiratory Recovery After Spinal Cord Injury.
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- Cells (2073-4409), 2025, v. 14, n. 4, p. 288, doi. 10.3390/cells14040288
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Synaptic Vesicle Glycoprotein 2A Knockout in Parvalbumin and Somatostatin Interneurons Drives Seizures in the Postnatal Mouse Brain.
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- Journal of Neuroscience, 2025, v. 45, n. 8, p. 1, doi. 10.1523/JNEUROSCI.1169-24.2024
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Reduction in parvalbumin-positive interneurons and inhibitory input in the cortex of mice with experimental autoimmune encephalomyelitis.
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- Experimental Brain Research, 2014, v. 232, n. 7, p. 2439, doi. 10.1007/s00221-014-3944-7
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Endogenous Serotonin Excites Striatal Cholinergic Interneurons via the Activation of 5-HT 2C, 5-HT6, and 5-HT7 Serotonin Receptors: Implications for Extrapyramidal Side Effects of Serotonin Reuptake Inhibitors.
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- Neuropsychopharmacology, 2007, v. 32, n. 8, p. 1840, doi. 10.1038/sj.npp.1301294
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Alterations of Interneurons of the Gerbil Hippocampus after Transient Cerebral Ischemia: Effect of Pitavastatin.
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- Neuropsychopharmacology, 2005, v. 30, n. 11, p. 2014, doi. 10.1038/sj.npp.1300798
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Chronic Stress Decreases the Number of Parvalbumin-Immunoreactive Interneurons in the Hippocampus: Prevention by Treatment with a Substance P Receptor (NK<sub>1</sub>) Antagonist.
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- Neuropsychopharmacology, 2005, v. 30, n. 1, p. 67, doi. 10.1038/sj.npp.1300581
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TRPC3 channel mediates excitation of striatal cholinergic interneurons.
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- Neurological Sciences, 2014, v. 35, n. 11, p. 1757, doi. 10.1007/s10072-014-1827-0
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Decreased response of interneurons in the medial prefrontal cortex to 5-HT receptor activation in the rat 6-hydroxydopamine Parkinson model.
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- Neurological Sciences, 2014, v. 35, n. 8, p. 1181, doi. 10.1007/s10072-014-1669-9
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Nicotinic receptor activation induces NMDA receptor independent long‐term potentiation of glutamatergic signalling in hippocampal oriens interneurons.
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- Journal of Physiology, 2021, v. 599, n. 2, p. 667, doi. 10.1113/JP280397
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Feedforward inhibition ahead of ictal wavefronts is provided by both parvalbumin‐ and somatostatin‐expressing interneurons.
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- Journal of Physiology, 2019, v. 597, n. 8, p. 2297, doi. 10.1113/JP277749
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Dichotomous parvalbumin interneuron populations in dorsolateral and dorsomedial striatum.
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- Journal of Physiology, 2018, v. 596, n. 16, p. 3695, doi. 10.1113/JP275936
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Parvalbumin fast‐spiking interneurons are selectively altered by paediatric traumatic brain injury.
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- Journal of Physiology, 2018, v. 596, n. 7, p. 1277, doi. 10.1113/JP275393
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Acetylcholine-dependent upregulation of TASK-1 channels in thalamic interneurons by a smooth muscle-like signalling pathway.
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- Journal of Physiology, 2017, v. 595, n. 17, p. 5875, doi. 10.1113/JP274527
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T-type calcium channels contribute to NMDA receptor independent synaptic plasticity in hippocampal regular-spiking oriens-alveus interneurons.
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- Journal of Physiology, 2017, v. 595, n. 11, p. 3449, doi. 10.1113/JP273695
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Postnatal Migration of Cerebellar Interneurons.
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- Brain Sciences (2076-3425), 2017, v. 7, n. 6, p. 62, doi. 10.3390/brainsci7060062
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Somatostatin and Somatostatin-Containing Interneurons—From Plasticity to Pathology.
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- Biomolecules (2218-273X), 2022, v. 12, n. 2, p. 312, doi. 10.3390/biom12020312
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Morphological Abnormalities in Nitric-Oxide-Synthase-Positive Striatal Interneurons of Schizophrenic Patients.
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- Neuropsychobiology, 2005, v. 52, n. 3, p. 111, doi. 10.1159/000087555
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Functional subdivision of feline spinal interneurons in reflex pathways from group Ib and II muscle afferents; an update.
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- European Journal of Neuroscience, 2010, v. 32, n. 6, p. 881, doi. 10.1111/j.1460-9568.2010.07354.x
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Generation of interneuron diversity in the mouse cerebral cortex.
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- European Journal of Neuroscience, 2010, v. 31, n. 12, p. 2136, doi. 10.1111/j.1460-9568.2010.07267.x
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Phosphodiesterase type IV inhibition prevents sequestration of CREB binding protein, protects striatal parvalbumin interneurons and rescues motor deficits in the R6/2 mouse model of Huntington’s disease.
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- European Journal of Neuroscience, 2009, v. 29, n. 5, p. 902, doi. 10.1111/j.1460-9568.2009.06649.x
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