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Synaptic Plasticity from Visual Cortex to Hippocampus: Systems Integration in Spatial Information Processing.
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- Neuroscientist, 2008, v. 14, n. 6, p. 584, doi. 10.1177/1073858408315655
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Role of mGlu5 in Persistent Forms of Hippocampal Synaptic Plasticity and the Encoding of Spatial Experience.
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- Cells (2073-4409), 2022, v. 11, n. 21, p. 3352, doi. 10.3390/cells11213352
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Intracerebral inoculation of healthy non-transgenic rats with a single aliquot of oligomeric amyloid-β (1-42) profoundly and progressively alters brain function throughout life.
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- Frontiers in Aging Neuroscience, 2024, p. 1, doi. 10.3389/fnagi.2024.1397901
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Changes in hippocampal volume, synaptic plasticity and amylin sensitivity in an animal model of type 2 diabetes are associated with increased vulnerability to amyloid-beta in advancing age.
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- Frontiers in Aging Neuroscience, 2024, p. 1, doi. 10.3389/fnagi.2024.1373477
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GluN2A or GluN2B subunits of the NMDA receptor contribute to changes in neuronal excitability and impairments in LTP in the hippocampus of aging mice but do not mediate detrimental effects of oligomeric Aβ (1-42).
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- Frontiers in Aging Neuroscience, 2024, p. 1, doi. 10.3389/fnagi.2024.1377085
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Strain-dependent regulation of hippocampal long-term potentiation by dopamine D1/D5 receptors in mice.
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- Frontiers in Behavioral Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fnbeh.2022.1023361
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The Intriguing Contribution of Hippocampal Long-Term Depression to Spatial Learning and Long-Term Memory.
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- Frontiers in Behavioral Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fnbeh.2022.806356
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Bidirectional Regulation of Hippocampal Synaptic Plasticity and Modulation of Cumulative Spatial Memory by Dopamine D2-Like Receptors.
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- Frontiers in Behavioral Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnbeh.2021.803574
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The Perirhinal Cortex Engages in Area and Layer-Specific Encoding of Item Dimensions.
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- Frontiers in Behavioral Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnbeh.2021.744669
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Frequency Facilitation at Mossy Fiber-CA3 Synapses of Freely Behaving Rats Is Regulated by Adenosine A1 Receptors.
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- Journal of Neuroscience, 2008, v. 28, n. 18, p. 4836, doi. 10.1523/JNEUROSCI.3729-07.2008
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The Metabotropic Glutamate Receptor, mGluR5, is a Key Determinant of Good and Bad Spatial Learning Performance and Hippocampal Synaptic Plasticity.
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- Cerebral Cortex, 2005, v. 15, n. 11, p. 1703, doi. 10.1093/cercor/bhi047
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The Metabotropic Glutamate Receptor mGluR3 is Critically Required for Hippocampal Long-term Depression and Modulates Long-term Potentiation in the Dentate Gyrus of Freely Moving Rats.
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- Cerebral Cortex, 2005, v. 15, n. 9, p. 1414
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The 5-Hydroxytryptamine<sub>4</sub> Receptor Exhibits Frequency-dependent Properties in Synaptic Plasticity and Behavioural Metaplasticity in the Hippocampal CA1 Region In vivo.
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- Cerebral Cortex, 2005, v. 15, n. 7, p. 1037, doi. 10.1093/cercor/bhh204
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Regulation by Metabotropic Glutamate Receptor 5 of LTP in the Dentate Gyrus of Freely Moving Rats: Relevance for Learning and Memory Formation.
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- Cerebral Cortex, 2004, v. 14, n. 2, p. 189, doi. 10.1093/cercor/bhg118
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Regulation of Depotentiation and Long-term Potentiation in the Dentate Gyrus of Freely Moving Rats by Dopamine D2-like Receptors.
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- Cerebral Cortex, 2003, v. 13, n. 2, p. 123, doi. 10.1093/cercor/13.2.123
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Modulation by Serotonin 5-HT4 Receptors of Long-term Potentiation and Depotentiation in the Dentate Gyrus of Freely Moving Rats.
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- Cerebral Cortex, 2002, v. 12, n. 2, p. 150, doi. 10.1093/cercor/12.2.150
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Depotentiation in the Dentate Gyrus of Freely Moving Rats is Modulated by D1/D5 Dopamine Receptors.
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- Cerebral Cortex, 2000, v. 10, n. 6, p. 614, doi. 10.1093/cercor/10.6.614
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Long-term Depression in Freely Moving Rats is Dependent upon Strain Variation, Induction Protocol and Behavioral State.
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- Cerebral Cortex, 2000, v. 10, n. 5, p. 482, doi. 10.1093/cercor/10.5.482
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Genetic Depletion of BDNF Impairs Extinction Learning of a Spatial Appetitive Task in the Presence or Absence of the Acquisition Context.
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- Frontiers in Behavioral Neuroscience, 2021, v. 15, p. N.PAG, doi. 10.3389/fnbeh.2021.658686
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Involvement of the Postrhinal and Perirhinal Cortices in Microscale and Macroscale Visuospatial Information Encoding.
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- Frontiers in Behavioral Neuroscience, 2020, p. N.PAG, doi. 10.3389/fnbeh.2020.556645
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Functional Compartmentalization of the Contribution of Hippocampal Subfields to Context-Dependent Extinction Learning.
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- Frontiers in Behavioral Neuroscience, 2019, v. 13, p. 1, doi. 10.3389/fnbeh.2019.00256
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Blocking VEGF by Bevacizumab Compromises Electrophysiological and Morphological Properties of Hippocampal Neurons.
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- Frontiers in Cellular Neuroscience, 2019, p. N.PAG, doi. 10.3389/fncel.2019.00113
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Differentiation in the protein synthesis-dependency of persistent synaptic plasticity in mossy fiber and associational/commissural CA3 synapses in vivo.
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- Frontiers in Integrative Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fnint.2013.00010
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Differentiation in the protein synthesis-dependency of persistent synaptic plasticity in mossy fiber and associational/commissural CA3 synapses in vivo.
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- Frontiers in Integrative Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fnint.2013.00010
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Synaptic depression in the CA1 region of freely behaving mice is highly dependent on afferent stimulation parameters.
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- Frontiers in Integrative Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fnint.2013.00001
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Learning-facilitated long-term depression and long-term potentiation at mossy fiber—CA3 synapses requires activation of β-adrenergic receptors.
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- Frontiers in Integrative Neuroscience, 2012, p. 1, doi. 10.3389/fnint.2012.00023
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Learning shifts the preferred theta phase of gamma oscillations in CA1.
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- Hippocampus, 2022, v. 32, n. 9, p. 695, doi. 10.1002/hipo.23460
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Frequency–dependency of the involvement of dopamine D1/D5 and beta‐adrenergic receptors in hippocampal LTD triggered by locus coeruleus stimulation.
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- Hippocampus, 2022, v. 32, n. 6, p. 449, doi. 10.1002/hipo.23419
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Cover Image, Volume 31, Issue 9.
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- Hippocampus, 2021, v. 31, n. 9, p. C1, doi. 10.1002/hipo.23384
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Preferential frequency‐dependent induction of synaptic depression by the lateral perforant path and of synaptic potentiation by the medial perforant path inputs to the dentate gyrus.
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- Hippocampus, 2021, v. 31, n. 9, p. 957, doi. 10.1002/hipo.23338
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Hippocampal subfield‐specific Homer1a expression is triggered by learning‐facilitated long‐term potentiation and long‐term depression at medial perforant path synapses.
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- Hippocampus, 2021, v. 31, n. 8, p. 897, doi. 10.1002/hipo.23333
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Cover Image, Volume 28, Issue 5.
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- Hippocampus, 2018, v. 28, n. 5, p. C1, doi. 10.1002/hipo.22848
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Novel encoding and updating of positional, or directional, spatial cues are processed by distinct hippocampal subfields: Evidence for parallel information processing and the “what” stream.
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- Hippocampus, 2018, v. 28, n. 5, p. 315, doi. 10.1002/hipo.22833
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Less means more: The magnitude of synaptic plasticity along the hippocampal dorso‐ventral axis is inversely related to the expression levels of plasticity‐related neurotransmitter receptors.
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- Hippocampus, 2018, v. 28, n. 2, p. 136, doi. 10.1002/hipo.22816
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Cover Image, Volume 28, Issue 2.
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- Hippocampus, 2018, v. 28, n. 2, p. C1, doi. 10.1002/hipo.22772
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Intrinsic cellular and molecular properties of in vivo hippocampal synaptic plasticity are altered in the absence of key synaptic matrix molecules.
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- Hippocampus, 2017, v. 27, n. 8, p. 920, doi. 10.1002/hipo.22742
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The 5-hydroxytryptamine<sub>4</sub> receptor enables differentiation of informational content and encoding in the hippocampus.
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- Hippocampus, 2016, v. 26, n. 7, p. 875, doi. 10.1002/hipo.22569
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The requirement of BDNF for hippocampal synaptic plasticity is experience-dependent.
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- Hippocampus, 2016, v. 26, n. 6, p. 739, doi. 10.1002/hipo.22555
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Hippocampal long-term potentiation that is elicited by perforant path stimulation or that occurs in conjunction with spatial learning is tightly controlled by beta-adrenoreceptors and the locus coeruleus.
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- Hippocampus, 2015, v. 25, n. 11, p. 1285, doi. 10.1002/hipo.22436
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BDNF contributes to the facilitation of hippocampal synaptic plasticity and learning enabled by environmental enrichment.
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- Hippocampus, 2015, v. 25, n. 1, p. 1, doi. 10.1002/hipo.22342
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The metabotropic glutamate receptor, mGlu5, is required for extinction learning that occurs in the absence of a context change.
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- Hippocampus, 2015, v. 25, n. 2, p. 149, doi. 10.1002/hipo.22359
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Antagonism of D1/ D5 receptors prevents long-term depression ( LTD) and learning-facilitated LTD at the perforant path-dentate gyrus synapse in freely behaving rats.
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- Hippocampus, 2014, v. 24, n. 12, p. 1615, doi. 10.1002/hipo.22340
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Place field stability requires the metabotropic glutamate receptor, mGlu5.
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- Hippocampus, 2014, v. 24, n. 11, p. 1330, doi. 10.1002/hipo.22314
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Early age-dependent impairments of context-dependent extinction learning, object recognition, and object-place learning occur in rats.
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- Hippocampus, 2014, v. 24, n. 3, p. 270, doi. 10.1002/hipo.22220
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Hippocampal long-term depression in freely behaving mice requires the activation of beta-adrenergic receptors.
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- Hippocampus, 2013, v. 23, n. 12, p. 1299, doi. 10.1002/hipo.22168
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Spatial olfactory learning facilitates long-term depression in the hippocampus.
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- Hippocampus, 2013, v. 23, n. 10, p. 963, doi. 10.1002/hipo.22158
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Endogenous hippocampal LTD that is enabled by spatial object recognition requires activation of NMDA receptors and the metabotropic glutamate receptor, mGlu5.
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- Hippocampus, 2013, v. 23, n. 2, p. 129, doi. 10.1002/hipo.22072
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Frequency dependency of NMDA receptor-dependent synaptic plasticity in the hippocampal CA1 region of freely behaving mice.
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- Hippocampus, 2012, v. 22, n. 12, p. 2238, doi. 10.1002/hipo.22041
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A single application of MK801 causes symptoms of acute psychosis, deficits in spatial memory, and impairment of synaptic plasticity in rats.
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- Hippocampus, 2008, v. 18, n. 2, p. 125, doi. 10.1002/hipo.20367
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Modulation by group 1 metabotropic glutamate receptors of depotentiation in the dentate gyrus of freely moving rats.
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- Hippocampus, 2008, v. 18, n. 1, p. 48, doi. 10.1002/hipo.20366
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