Nature Neuroscience, ISSN 1097-6256, 11/2015, Volume 18, Issue 11, pp. 1606 - 1616
Selective serotonin reuptake inhibitors (SSRIs) are widely used antidepressants, but the mechanisms by which they influence behavior are only partially...
PATTERN SEPARATION | BEHAVIORAL ACTIONS | ANXIETY | NEUROTROPHIC FACTOR | ADULT HIPPOCAMPAL NEUROGENESIS | RAT HIPPOCAMPUS | ANIMAL-MODEL | MAJOR DEPRESSION | STRESS | NEUROSCIENCES | ENHANCED SYNAPTIC PLASTICITY | Fluoxetine - pharmacology | Animals | Dentate Gyrus - drug effects | Cytoplasmic Granules - drug effects | Mice, Transgenic | Antidepressive Agents, Second-Generation - pharmacology | Neurogenesis - drug effects | Neurons - drug effects | Receptor, Serotonin, 5-HT1A - metabolism | Care and treatment | Dentate gyrus | Receptors | Serotonin | Depression, Mental | Physiological aspects | Health aspects | Antidepressant | Fluoxetine | Depression | 5HT1AR | Dentate Gyrus | SSRI | Adult Neurogenesis | Adult Born Granule Cells | Granule Cells | Mature Granule Cells | Anxiety | Htr1a | HPA Axis | Hippocampus
PATTERN SEPARATION | BEHAVIORAL ACTIONS | ANXIETY | NEUROTROPHIC FACTOR | ADULT HIPPOCAMPAL NEUROGENESIS | RAT HIPPOCAMPUS | ANIMAL-MODEL | MAJOR DEPRESSION | STRESS | NEUROSCIENCES | ENHANCED SYNAPTIC PLASTICITY | Fluoxetine - pharmacology | Animals | Dentate Gyrus - drug effects | Cytoplasmic Granules - drug effects | Mice, Transgenic | Antidepressive Agents, Second-Generation - pharmacology | Neurogenesis - drug effects | Neurons - drug effects | Receptor, Serotonin, 5-HT1A - metabolism | Care and treatment | Dentate gyrus | Receptors | Serotonin | Depression, Mental | Physiological aspects | Health aspects | Antidepressant | Fluoxetine | Depression | 5HT1AR | Dentate Gyrus | SSRI | Adult Neurogenesis | Adult Born Granule Cells | Granule Cells | Mature Granule Cells | Anxiety | Htr1a | HPA Axis | Hippocampus
Journal Article
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Full Text
Rapid erasure of hippocampal memory following inhibition of dentate gyrus granule cells
Nature Communications, ISSN 2041-1723, 03/2016, Volume 7, Issue 1, p. 10923
The hippocampus is critical for the acquisition and retrieval of episodic and contextual memories. Lesions of the dentate gyrus, a principal input of the...
ENTORHINAL CORTEX | CONSOLIDATION | FEAR MEMORY | MOTOR-RESPONSES | CA3 | MULTIDISCIPLINARY SCIENCES | MICE | LONG-TERM POTENTIATION | CORTICAL INPUT | RECEPTORS | RETRIEVAL | Synaptic Transmission - physiology | Signal Transduction | Mice, Inbred C57BL | Receptors, Neuropeptide Y - metabolism | Male | Mice, Transgenic | Neurons - cytology | Dentate Gyrus - cytology | Animals | Conditioning (Psychology) | Models, Biological | Neuronal Plasticity | Adenosine - metabolism | Female | Entorhinal Cortex - physiology | Memory - physiology
ENTORHINAL CORTEX | CONSOLIDATION | FEAR MEMORY | MOTOR-RESPONSES | CA3 | MULTIDISCIPLINARY SCIENCES | MICE | LONG-TERM POTENTIATION | CORTICAL INPUT | RECEPTORS | RETRIEVAL | Synaptic Transmission - physiology | Signal Transduction | Mice, Inbred C57BL | Receptors, Neuropeptide Y - metabolism | Male | Mice, Transgenic | Neurons - cytology | Dentate Gyrus - cytology | Animals | Conditioning (Psychology) | Models, Biological | Neuronal Plasticity | Adenosine - metabolism | Female | Entorhinal Cortex - physiology | Memory - physiology
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 4, p. e10400
A leading candidate in the process of memory formation is hippocampal long-term potentiation (LTP), a persistent enhancement in synaptic strength evoked by the...
Potentiation | Protein kinase C | Synaptic strength | Long-term potentiation | Stimulation | Associative learning | Kinases | Learning | Electrodes | Eyelid conditioning | Proteins | Molecular modelling | Transgenic animals | Rodents | Kinematics | Long term memory | Inhibition | Conditioning | Hippocampus | Synapses | Strength
Potentiation | Protein kinase C | Synaptic strength | Long-term potentiation | Stimulation | Associative learning | Kinases | Learning | Electrodes | Eyelid conditioning | Proteins | Molecular modelling | Transgenic animals | Rodents | Kinematics | Long term memory | Inhibition | Conditioning | Hippocampus | Synapses | Strength
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 6, p. e11130
We have studied the motor abilities and associative learning capabilities of adult mice placed in different enriched environments. Three-month-old animals were...
ADULT NEUROGENESIS | MULTIDISCIPLINARY SCIENCES | SYNAPTIC-TRANSMISSION | NEURONS | CELL-PROLIFERATION | LONG-TERM POTENTIATION | CA3-CA1 SYNAPSE | DENTATE GYRUS | GRANULE CELLS | TRANSGENIC MICE | BEHAVING MICE | Learning | Psychomotor Performance | Rotarod Performance Test | Animals | Mice, Inbred C57BL | Evoked Potentials | Male | Mice | Hippocampus - cytology | Hippocampus - physiology | Neurogenesis | Associative learning | Analysis | Enrichment | Bioengineering | Neurosciences | Memory | Bromodeoxyuridine | Nervous system | Motor task performance | Cell growth | Transgenic animals | Rodents | Conditioning | Age | Antigens | Motor ability | Classical conditioning | Eyelid conditioning | Studies | Motor skill learning | Housing conditions | Alzheimers disease | Hippocampus | Rats as laboratory animals | Hippocampus (Brain) | Rates (Animals de laboratori) | Hipocamp (Cervell) | Neurobiologia | Neurobiology
ADULT NEUROGENESIS | MULTIDISCIPLINARY SCIENCES | SYNAPTIC-TRANSMISSION | NEURONS | CELL-PROLIFERATION | LONG-TERM POTENTIATION | CA3-CA1 SYNAPSE | DENTATE GYRUS | GRANULE CELLS | TRANSGENIC MICE | BEHAVING MICE | Learning | Psychomotor Performance | Rotarod Performance Test | Animals | Mice, Inbred C57BL | Evoked Potentials | Male | Mice | Hippocampus - cytology | Hippocampus - physiology | Neurogenesis | Associative learning | Analysis | Enrichment | Bioengineering | Neurosciences | Memory | Bromodeoxyuridine | Nervous system | Motor task performance | Cell growth | Transgenic animals | Rodents | Conditioning | Age | Antigens | Motor ability | Classical conditioning | Eyelid conditioning | Studies | Motor skill learning | Housing conditions | Alzheimers disease | Hippocampus | Rats as laboratory animals | Hippocampus (Brain) | Rates (Animals de laboratori) | Hipocamp (Cervell) | Neurobiologia | Neurobiology
Journal Article
PLoS ONE, ISSN 1932-6203, 2009, Volume 4, Issue 10, p. e7592
Background Prionopathies are characterized by spongiform brain degeneration, myoclonia, dementia, and periodic electroencephalographic (EEG) disturbances. The...
Potentiation | Bioengineering | Brain | Kainic acid receptors | γ-Aminobutyric acid A receptors | Memory | Genomics | Genes | Electrophysiology | Electroencephalography | Genomes | Biology | Glutamic acid receptors | Kinases | Neurogenesis | Proteins | Plasticity (functional) | Electrophysiological recording | Receptors | Ubiquitination | Histopathology | Pathways | Neurodegeneration | α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid | Rodents | Dementia disorders | Degeneration | Behavior | Prion protein | Alzheimer's disease | Bioinformatics | Death & dying | Neurodegenerative diseases | Neurons | EEG | Long-term potentiation | Paired-pulse facilitation | Excitability | Gene expression | Plasticity (synaptic) | DNA microarrays | Acids | Cell death | In vivo methods and tests | Mice | Hippocampus | Neurotransmission | Apoptosis
Potentiation | Bioengineering | Brain | Kainic acid receptors | γ-Aminobutyric acid A receptors | Memory | Genomics | Genes | Electrophysiology | Electroencephalography | Genomes | Biology | Glutamic acid receptors | Kinases | Neurogenesis | Proteins | Plasticity (functional) | Electrophysiological recording | Receptors | Ubiquitination | Histopathology | Pathways | Neurodegeneration | α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid | Rodents | Dementia disorders | Degeneration | Behavior | Prion protein | Alzheimer's disease | Bioinformatics | Death & dying | Neurodegenerative diseases | Neurons | EEG | Long-term potentiation | Paired-pulse facilitation | Excitability | Gene expression | Plasticity (synaptic) | DNA microarrays | Acids | Cell death | In vivo methods and tests | Mice | Hippocampus | Neurotransmission | Apoptosis
Journal Article
Cerebral Cortex, ISSN 1047-3211, 2012, Volume 22, Issue 3, pp. 550 - 566
We studied, in behaving mice, the contribution of CB1 receptors to the activity-dependent changes induced at the hippocampal CA3-CA1 synapse by associative...
CB1 | hippocampus | trace eyeblink conditioning | CB1 knockout mice | siRNA | mice | long-term potentiation | SELECTIVE ANTAGONIST | WATER-MAZE | BEHAVIORAL-CHANGES | NEUROSCIENCES | ADENOSINE A RECEPTORS | VIVO GENE DELIVERY | RADIAL MAZE | SPATIAL MEMORY | RAT HIPPOCAMPUS | CA3-CA1 SYNAPSE | Synaptic Transmission - physiology | CA1 Region, Hippocampal - physiology | Synaptic Transmission - genetics | CA3 Region, Hippocampal - physiology | Mice, Inbred C57BL | Male | Neural Pathways - physiology | Association Learning - physiology | Receptor, Cannabinoid, CB1 - physiology | Mice, Knockout | Neuronal Plasticity - genetics | Animals | Neuronal Plasticity - physiology | Receptor, Cannabinoid, CB1 - agonists | CA3 Region, Hippocampal - metabolism | Neural Pathways - metabolism | CA1 Region, Hippocampal - metabolism | Mice | Receptor, Cannabinoid, CB1 - deficiency
CB1 | hippocampus | trace eyeblink conditioning | CB1 knockout mice | siRNA | mice | long-term potentiation | SELECTIVE ANTAGONIST | WATER-MAZE | BEHAVIORAL-CHANGES | NEUROSCIENCES | ADENOSINE A RECEPTORS | VIVO GENE DELIVERY | RADIAL MAZE | SPATIAL MEMORY | RAT HIPPOCAMPUS | CA3-CA1 SYNAPSE | Synaptic Transmission - physiology | CA1 Region, Hippocampal - physiology | Synaptic Transmission - genetics | CA3 Region, Hippocampal - physiology | Mice, Inbred C57BL | Male | Neural Pathways - physiology | Association Learning - physiology | Receptor, Cannabinoid, CB1 - physiology | Mice, Knockout | Neuronal Plasticity - genetics | Animals | Neuronal Plasticity - physiology | Receptor, Cannabinoid, CB1 - agonists | CA3 Region, Hippocampal - metabolism | Neural Pathways - metabolism | CA1 Region, Hippocampal - metabolism | Mice | Receptor, Cannabinoid, CB1 - deficiency
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 11/2007, Volume 27, Issue 45, pp. 12139 - 12146
Experimentally induced long-term potentiation (LTP) is a persistent increase in synaptic strength that decays across time. In contrast, changes in synaptic...
Electrophysiology | Associative learning | Mice | Long-term potentiation | Hippocampus | Synaptic plasticity | RABBIT FOLLOWING STIMULATION | hippocampus | LATE-PHASE | ELEMENT-BINDING PROTEIN | mice | NEUROSCIENCES | LASTING POTENTIATION | associative learning | electrophysiology | MEMORY | IN-VIVO | synaptic plasticity | PERFORANT PATH | DENTATE GYRUS | long-term potentiation | TRANSGENIC MICE | Conditioning, Eyelid - physiology | Excitatory Postsynaptic Potentials - physiology | Animals | Synapses - physiology | Mice, Inbred C57BL | Long-Term Potentiation - physiology | Male | Conditioning, Classical - physiology | Blinking - physiology
Electrophysiology | Associative learning | Mice | Long-term potentiation | Hippocampus | Synaptic plasticity | RABBIT FOLLOWING STIMULATION | hippocampus | LATE-PHASE | ELEMENT-BINDING PROTEIN | mice | NEUROSCIENCES | LASTING POTENTIATION | associative learning | electrophysiology | MEMORY | IN-VIVO | synaptic plasticity | PERFORANT PATH | DENTATE GYRUS | long-term potentiation | TRANSGENIC MICE | Conditioning, Eyelid - physiology | Excitatory Postsynaptic Potentials - physiology | Animals | Synapses - physiology | Mice, Inbred C57BL | Long-Term Potentiation - physiology | Male | Conditioning, Classical - physiology | Blinking - physiology
Journal Article
PLOS ONE, ISSN 1932-6203, 10/2009, Volume 4, Issue 10, p. e7592
Background: Prionopathies are characterized by spongiform brain degeneration, myoclonia, dementia, and periodic electroencephalographic (EEG) disturbances. The...
PROTEIN | SEIZURES | BEHAVIOR | MULTIDISCIPLINARY SCIENCES | NULL MICE | LTP | RAT HIPPOCAMPUS | KAINIC ACID | CA3-CA1 SYNAPSE | DEFICIENT MICE | KNOCKOUT MICE | Prions - genetics | Synaptic Transmission - genetics | Mice, Inbred C57BL | Gene Expression Regulation | Male | Mice, Transgenic | Receptors, Glutamate - biosynthesis | Electroencephalography - methods | Hippocampus - metabolism | Animals | Synapses - metabolism | Neuronal Plasticity | Long-Term Potentiation | Mice | Receptors, GABA-A - metabolism | Mutation | Degeneració del sistema nerviós | Neurobiologia | Prions | Neurobiology | Prionic proteins
PROTEIN | SEIZURES | BEHAVIOR | MULTIDISCIPLINARY SCIENCES | NULL MICE | LTP | RAT HIPPOCAMPUS | KAINIC ACID | CA3-CA1 SYNAPSE | DEFICIENT MICE | KNOCKOUT MICE | Prions - genetics | Synaptic Transmission - genetics | Mice, Inbred C57BL | Gene Expression Regulation | Male | Mice, Transgenic | Receptors, Glutamate - biosynthesis | Electroencephalography - methods | Hippocampus - metabolism | Animals | Synapses - metabolism | Neuronal Plasticity | Long-Term Potentiation | Mice | Receptors, GABA-A - metabolism | Mutation | Degeneració del sistema nerviós | Neurobiologia | Prions | Neurobiology | Prionic proteins
Journal Article
PLOS ONE, ISSN 1932-6203, 04/2010, Volume 5, Issue 4
A leading candidate in the process of memory formation is hippocampal long-term potentiation (LTP), a persistent enhancement in synaptic strength evoked by the...
MAINTENANCE | CONSOLIDATION | TRANSMISSION | KINASE-M-ZETA | LATE-PHASE | BIOLOGY | POSTSYNAPTIC AMPA RECEPTORS | LTP | LONG-TERM POTENTIATION | CA3-CA1 SYNAPSE | BEHAVING MICE
MAINTENANCE | CONSOLIDATION | TRANSMISSION | KINASE-M-ZETA | LATE-PHASE | BIOLOGY | POSTSYNAPTIC AMPA RECEPTORS | LTP | LONG-TERM POTENTIATION | CA3-CA1 SYNAPSE | BEHAVING MICE
Journal Article
Frontiers in Behavioral Neuroscience, ISSN 1662-5153, 05/2009, Volume 3, Issue MAY, p. 7
The hippocampal CA3-CA1 synapse is an excellent experimental model for studying the interactions between short-and long-term plastic changes taking place...
Mice | Presynaptic mechanisms | Long-term potentiation | Hippocampus | CA3-CA1 synapse | RABBIT FOLLOWING STIMULATION | HIPPOCAMPAL SLICES | hippocampus | presynaptic mechanisms | CONDITIONED EYELID RESPONSES | mice | SYNAPTIC PLASTICITY | NEUROSCIENCES | LASTING POTENTIATION | PYRAMIDAL NEURONS | PAIRED-PULSE FACILITATION | BEHAVIORAL SCIENCES | DEPENDENT SHIFT | long-term potentiation | Potentiation | Short term | Extinction | Paired-pulse facilitation | Associative learning | Collateral | Unconditioned stimulus | Experiments | Electrodes | Eyelid conditioning | Trigeminal nerve | Plasticity | Conditioned stimulus | Synaptic depression | Trends | Laboratory animals | CA3-CA1 | Long-Term Potentiation
Mice | Presynaptic mechanisms | Long-term potentiation | Hippocampus | CA3-CA1 synapse | RABBIT FOLLOWING STIMULATION | HIPPOCAMPAL SLICES | hippocampus | presynaptic mechanisms | CONDITIONED EYELID RESPONSES | mice | SYNAPTIC PLASTICITY | NEUROSCIENCES | LASTING POTENTIATION | PYRAMIDAL NEURONS | PAIRED-PULSE FACILITATION | BEHAVIORAL SCIENCES | DEPENDENT SHIFT | long-term potentiation | Potentiation | Short term | Extinction | Paired-pulse facilitation | Associative learning | Collateral | Unconditioned stimulus | Experiments | Electrodes | Eyelid conditioning | Trigeminal nerve | Plasticity | Conditioned stimulus | Synaptic depression | Trends | Laboratory animals | CA3-CA1 | Long-Term Potentiation
Journal Article
Neuropsychopharmacology, ISSN 0893-133X, 06/2009, Volume 34, Issue 7, pp. 1865 - 1874
Previous in vitro studies have characterized the electrophysiological and molecular signaling pathways of adenosine tonic modulation on long-lasting synaptic...
Journal Article
Neuropsychopharmacology, ISSN 0893-133X, 06/2009, Volume 34, Issue 7, pp. 1865 - 1874
Previous in vitro studies have characterized the electrophysiological and molecular signaling pathways of adenosine tonic modulation on long-lasting synaptic...
Mice | Adenosine A2A receptor | Classical conditioning | Long-term potentiation | Hippocampus | CA3-CA1 synapse | NERVOUS-SYSTEM | hippocampus | NMDA RECEPTORS | PSYCHIATRY | MEMORY STORAGE | mice | NEUROSCIENCES | classical conditioning | MOTOR-RESPONSES | ENDOGENOUS ADENOSINE | PHARMACOLOGY & PHARMACY | adenosine A(2A) receptor | DENTATE GYRUS | ANTAGONISTS | SCH 58261 | long-term potentiation | TRANSGENIC MICE | Male | Neurons - cytology | Receptor, Adenosine A2A - physiology | Nerve Net - drug effects | Adenosine A2 Receptor Antagonists | Excitatory Postsynaptic Potentials - drug effects | Nerve Net - physiology | Excitatory Postsynaptic Potentials - physiology | Neuroprotective Agents - pharmacology | Long-Term Potentiation - drug effects | Wakefulness | Neurons - physiology | Long-Term Potentiation - physiology | Neurons - drug effects | Electric Stimulation - methods | Synapses - drug effects | Blinking - drug effects | Conditioning, Classical - drug effects | Synapses - physiology | Mice, Inbred C57BL | Biophysics | Pyrimidines - pharmacology | Hippocampus - cytology | Conditioning, Classical - physiology | Association Learning - physiology | Association Learning - drug effects | Blinking - physiology | Triazoles - pharmacology | Animals
Mice | Adenosine A2A receptor | Classical conditioning | Long-term potentiation | Hippocampus | CA3-CA1 synapse | NERVOUS-SYSTEM | hippocampus | NMDA RECEPTORS | PSYCHIATRY | MEMORY STORAGE | mice | NEUROSCIENCES | classical conditioning | MOTOR-RESPONSES | ENDOGENOUS ADENOSINE | PHARMACOLOGY & PHARMACY | adenosine A(2A) receptor | DENTATE GYRUS | ANTAGONISTS | SCH 58261 | long-term potentiation | TRANSGENIC MICE | Male | Neurons - cytology | Receptor, Adenosine A2A - physiology | Nerve Net - drug effects | Adenosine A2 Receptor Antagonists | Excitatory Postsynaptic Potentials - drug effects | Nerve Net - physiology | Excitatory Postsynaptic Potentials - physiology | Neuroprotective Agents - pharmacology | Long-Term Potentiation - drug effects | Wakefulness | Neurons - physiology | Long-Term Potentiation - physiology | Neurons - drug effects | Electric Stimulation - methods | Synapses - drug effects | Blinking - drug effects | Conditioning, Classical - drug effects | Synapses - physiology | Mice, Inbred C57BL | Biophysics | Pyrimidines - pharmacology | Hippocampus - cytology | Conditioning, Classical - physiology | Association Learning - physiology | Association Learning - drug effects | Blinking - physiology | Triazoles - pharmacology | Animals
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2009, Volume 4, Issue 12
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2010, Volume 5, Issue 4
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 11/2007, Volume 27, Issue 45, pp. 12139 - 12146
Experimentally induced long-term potentiation (LTP) is a persistent increase in synaptic strength that decays across time. In contrast, changes in synaptic...
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2009, Volume 4, Issue 10, p. e7592
Prionopathies are characterized by spongiform brain degeneration, myoclonia, dementia, and periodic electroencephalographic (EEG) disturbances. The hallmark of...
Animal experimentation | Brain | Cell death | Prions | Analysis | Genetic research | Mice | Electroencephalography | Glutamate | Gene expression | Dementia
Animal experimentation | Brain | Cell death | Prions | Analysis | Genetic research | Mice | Electroencephalography | Glutamate | Gene expression | Dementia
Journal Article
PloS one, 04/2010, Volume 5, Issue 4, p. e10400
A leading candidate in the process of memory formation is hippocampal long-term potentiation (LTP), a persistent enhancement in synaptic strength evoked by the...
Animals | Excitatory Postsynaptic Potentials | Memory | Long-Term Potentiation | CA1 Region, Hippocampal | CA3 Region, Hippocampal | Conditioning, Eyelid | Mice | Protein Kinase C - antagonists & inhibitors | Hippocampus - physiology | Association Learning
Animals | Excitatory Postsynaptic Potentials | Memory | Long-Term Potentiation | CA1 Region, Hippocampal | CA3 Region, Hippocampal | Conditioning, Eyelid | Mice | Protein Kinase C - antagonists & inhibitors | Hippocampus - physiology | Association Learning
Journal Article
Translational Neuroscience, ISSN 2081-3856, 6/2013, Volume 4, Issue 2, pp. 134 - 143
During the past few years, there have been many important contributions to the better understanding of the different types of memory and the putative neural...
Learning and memory | Neurology | Neurosciences | Medicine & Public Health | Synaptic strength | Long-term potentiation | Neurobiology | Neurosurgery | HIPPOCAMPAL CA3-CA1 SYNAPSE | ALZHEIMERS-DISEASE | ACQUISITION | INVOLVEMENT | RECEPTOR | LTP | NEUROSCIENCES | CONSCIOUS MICE | MODULATION | BEHAVING MICE
Learning and memory | Neurology | Neurosciences | Medicine & Public Health | Synaptic strength | Long-term potentiation | Neurobiology | Neurosurgery | HIPPOCAMPAL CA3-CA1 SYNAPSE | ALZHEIMERS-DISEASE | ACQUISITION | INVOLVEMENT | RECEPTOR | LTP | NEUROSCIENCES | CONSCIOUS MICE | MODULATION | BEHAVING MICE
Journal Article
PLoS ONE, 01/2009, Volume 4, Issue 12
Journal Article
02/2017, ISBN 1118540719, 24
Long‐term potentiation (LTP) is usually evoked by high‐frequency stimulation (HFS) of selected afferent pathways, resulting in a long‐lasting enhancement of...
cortical functions | high‐frequency stimulation | associative learning | hippocampus | long‐term potentiation | plastic neural mechanism | Experience‐Dependent Plasticity | memory storage
cortical functions | high‐frequency stimulation | associative learning | hippocampus | long‐term potentiation | plastic neural mechanism | Experience‐Dependent Plasticity | memory storage
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