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Long-Term Potentiation and Memory
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19960506)368:3<371::aid-cne4>3.0.co;2-2openalex-snapshot
Unilateral LTP triggers bilateral increases in hippocampal neurotrophin and trk receptor mRNA expression in behaving rats: Evidence for interhemispheric communication
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19990111)403:2<229::aid-cne7>3.0.co;2-popenalex-snapshot
Projections from the lateral, basal, and accessory basal nuclei of the amygdala to the hippocampal formation in rat
inferredcites →https://doi.org/10.1002/(sici)1097-4695(199910)41:1<83::aid-neu11>3.0.co;2-zopenalex-snapshot
Molecular basis for induction of ocular dominance plasticity
inferredcites →https://doi.org/10.1002/(sici)1097-4695(199910)41:1<92::aid-neu12>3.0.co;2-uopenalex-snapshot
Synaptic plasticity at thalamocortical synapses in developing rat somatosensory cortex: LTP, LTD, and silent synapses
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1997)7:1<95::aid-hipo10>3.0.co;2-dopenalex-snapshot
LTP and spatial learning?Where to next?
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1998)8:1<48::aid-hipo5>3.0.co;2-3openalex-snapshot
Analysis of the interaction between arachidonic acid and metabotropic glutamate receptor activation reveals that phospholipase C acts as a coincidence detector in the expression of long-term potentiation in the rat dentate gyrus
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1999)9:5<519::aid-hipo5>3.0.co;2-yopenalex-snapshot
Activation of tyrosine receptor kinase plays a role in expression of long-term potentiation in the rat dentate gyrus
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1999)9:5<542::aid-hipo8>3.0.co;2-nopenalex-snapshot
Exposing rats to a predator impairs spatial working memory in the radial arm water maze
inferredcites →https://doi.org/10.1002/(sici)1098-1063(1999)9:6<609::aid-hipo1>3.0.co;2-aopenalex-snapshot
Neonatal aspiration lesions of the hippocampal formation impair visual recognition memory when assessed by paired-comparison task but not by delayed nonmatching-to-sample task
inferredcites →https://doi.org/10.1002/(sici)1098-2396(200002)35:2<151::aid-syn8>3.0.co;2-popenalex-snapshot
Evidence for the involvement of TNF and NF-?B in hippocampal synaptic plasticity
inferredcites →https://doi.org/10.1002/1098-1063(2000)10:4<352::aid-hipo2>3.0.co;2-dopenalex-snapshot
Multiple trace theory of human memory: Computational, neuroimaging, and neuropsychological results
inferredcites →https://doi.org/10.1002/1098-1063(2000)10:4<420::aid-hipo8>3.0.co;2-5openalex-snapshot
Hippocampal-neocortical interaction: A hierarchy of associativity
inferredcites →https://doi.org/10.1002/1098-1063(2000)10:4<431::aid-hipo9>3.0.co;2-zopenalex-snapshot
Protein synthesis in entorhinal cortex and long-term potentiation in dentate gyrus
inferredcites →https://doi.org/10.1002/1098-1063(2000)10:4<438::aid-hipo10>3.0.co;2-3openalex-snapshot
Plasticity at hippocampal to prefrontal cortex synapses: Dual roles in working memory and consolidation
inferredcites →https://doi.org/10.1002/1098-1063(2000)10:4<447::aid-hipo11>3.0.co;2-2openalex-snapshot
Synaptic plasticity in the hippocampal area CA1-subiculum projection: Implications for theories of memory
inferredcites →https://doi.org/10.1002/1098-1063(2000)10:6<684::aid-hipo1006>3.0.co;2-hopenalex-snapshot
Long-term potentiation of single subicular neurons in mice
inferredcites →https://doi.org/10.1002/cne.1327openalex-snapshot
Conservation of neuronal number and size in the entorhinal cortex of behaviorally characterized aged rats
inferredcites →https://doi.org/10.1002/hipo.10016openalex-snapshot
Individual differences in spatial memory among aged rats are related to hippocampal PKCγ immunoreactivity
inferredcites →https://doi.org/10.1002/hipo.10036openalex-snapshot
Analysis of the presynaptic signaling mechanisms underlying the inhibition of LTP in rat dentate gyrus by the tyrosine kinase inhibitor, genistein
inferredcites →https://doi.org/10.1002/hipo.10100openalex-snapshot
Regulated transcription of the immediate‐early gene Zif268: Mechanisms and gene dosage‐dependent function in synaptic plasticity and memory formation
inferredcites →https://doi.org/10.1002/hipo.10147openalex-snapshot
Analysis of the presynaptic signalling mechanisms underlying the inhibition of LTP in rat dentate gyrus by the tyrosine kinase inhibitor, genistein
inferredcites →https://doi.org/10.1002/hipo.450010410openalex-snapshot
Organization of CA1 projections to the subiculum: A PHA‐L analysis in the rat
inferredcites →https://doi.org/10.1002/hipo.450020409openalex-snapshot
Inverted‐U relationship between the level of peripheral corticosterone and the magnitude of hippocampal primed burst potentiation
inferredcites →https://doi.org/10.1002/hipo.450030203openalex-snapshot
Spatial learning and the saturation of long‐term potentiation
inferredcites →https://doi.org/10.1002/hipo.450030205openalex-snapshot
Cumulative long‐term potentiation in the rat dentate gyrus correlates with, but does not modify, performance in the water maze
inferredcites →https://doi.org/10.1002/hipo.450030210openalex-snapshot
Effects of glucocorticoids on hippocampal long‐term potentiation
inferredcites →https://doi.org/10.1002/hipo.450030405openalex-snapshot
Structural synaptic correlate of long‐term potentiation: Formation of axospinous synapses with multiple, completely partitioned transmission zones
inferredcites →https://doi.org/10.1002/hipo.450040406openalex-snapshot
Maturation of long‐term potentiation in the hippocampal dentate gyrus of the freely moving rat
inferredcites →https://doi.org/10.1002/hipo.450050604openalex-snapshot
Topographically specific hippocampal projections target functionally distinct prefrontal areas in the rhesus monkey
inferredcites →https://doi.org/10.1002/jnr.490390108openalex-snapshot
Decreased synaptic density in aged brains and its prevention by rearing under enriched environment as revealed by synaptophysin contents
inferredcites →https://doi.org/10.1002/syn.890050208openalex-snapshot
Morphological correlates of long‐term potentiation imply the modification of existing synapses, not synaptogenesis, in the hippocampal dentate gyrus
inferredcites →https://doi.org/10.1002/syn.890150409openalex-snapshot
A drug that facilitates glutamatergic transmission reduces exploratory activity and improves performance in a learning‐dependent task
inferredcites →https://doi.org/10.1006/brbi.1995.1012openalex-snapshot
Spatial Learning Impairment in Mice Infected with Legionella pneumophila or Administered Exogenous Interleukin-1-β
inferredcites →https://doi.org/10.1006/brbi.1998.0524openalex-snapshot
Selective Effects of Peripheral Lipopolysaccharide Administration on Contextual and Auditory-Cue Fear Conditioning
inferredcites →https://doi.org/10.1006/exnr.1999.7109openalex-snapshot
Brain-Derived Neurotrophic Factor Improves Long-Term Potentiation and Cognitive Functions after Transient Forebrain Ischemia in the Rat
inferredcites →https://doi.org/10.1006/exnr.2000.7415openalex-snapshot
Long-Term Environmental Enrichment Leads to Regional Increases in Neurotrophin Levels in Rat Brain
inferredcites →https://doi.org/10.1006/exnr.2000.7492openalex-snapshot
BDNF Protects against Spatial Memory Deficits Following Neonatal Hypoxia-Ischemia
inferredcites →https://doi.org/10.1006/exnr.2002.7966openalex-snapshot
Chronic Brain Inflammation Results in Cell Loss in the Entorhinal Cortex and Impaired LTP in Perforant Path-Granule Cell Synapses
inferredcites →https://doi.org/10.1006/mcne.2000.0922openalex-snapshot
Reduced Perisomatic Inhibition, Increased Excitatory Transmission, and Impaired Long-Term Potentiation in Mice Deficient for the Extracellular Matrix Glycoprotein Tenascin-R
inferredcites →https://doi.org/10.1006/nlme.1995.0008openalex-snapshot
Inhibitory Avoidance Training Induces Rapid and Selective Changes in3[H]AMPA Receptor Binding in the Rat Hippocampal Formation
inferredcites →https://doi.org/10.1006/nlme.1996.0046openalex-snapshot
Reversible Changes in Hippocampal3H-AMPA Binding Following Inhibitory Avoidance Training in the Rat
inferredcites →https://doi.org/10.1006/nlme.1997.3799openalex-snapshot
Memory Formation: The Sequence of Biochemical Events in the Hippocampus and Its Connection to Activity in Other Brain Structures
inferredcites →https://doi.org/10.1006/nlme.1998.3875openalex-snapshot
Norepinephrine Infused into the Basolateral Amygdala Posttraining Enhances Retention in a Spatial Water Maze Task
inferredcites →https://doi.org/10.1006/nlme.1999.3913openalex-snapshot
Time-Dependent Impairment of Inhibitory Avoidance Retention in Rats by Posttraining Infusion of a Mitogen-Activated Protein Kinase Kinase Inhibitor into Cortical and Limbic Structures
inferredcites →https://doi.org/10.1006/nlme.2001.4007openalex-snapshot
Two Critical Periods for cAMP-Dependent Protein Kinase Activity during Long-Term Memory Consolidation in the Crab Chasmagnathus
inferredcites →https://doi.org/10.1006/scdb.1999.0302openalex-snapshot
MAP kinase-mediated signalling to nucleosomes and immediate-early gene induction
inferredcites →https://doi.org/10.1007/978-0-585-37970-8_8openalex-snapshot
Effects of Cytokines on Cerebral Neurotransmission
inferredcites →https://doi.org/10.1007/978-1-4615-2015-3_31openalex-snapshot
The cyclic AMP system and Drosophila learning
inferredcites →https://doi.org/10.1007/978-1-4684-7971-3_39openalex-snapshot
A Patch-Clamp Study of Excitatory Amino Acid Activated Channels
inferredcites →https://doi.org/10.1007/bf00229361openalex-snapshot
Memory for spatial locations, motor responses, and objects: triple dissociation among the hippocampus, caudate nucleus, and extrastriate visual cortex
inferredcites →https://doi.org/10.1007/bf00230532openalex-snapshot
Effects of cingulate cortical lesions on avoidance learning and training-induced unit activity in rabbits
inferredcites →https://doi.org/10.1007/bf00238949openalex-snapshot
Dissociation between components of spatial memory in rats after recovery from the effects of retrohippocampal lesions
inferredcites →https://doi.org/10.1007/bf00973653openalex-snapshot
Antioxidant enzymatic systems in neuronal and glial cell-enriched fractions of rat brain during aging
inferredcites →https://doi.org/10.1007/bf01076588openalex-snapshot
The cyclic AMP system andDrosophila learning
inferredcites →https://doi.org/10.1007/bf01261506openalex-snapshot
Long-lasting morphological changes in dendritic spines of dentate granular cells following stimulation of the entorhinal area
inferredcites →https://doi.org/10.1007/bf02543972openalex-snapshot
Effect of low intake of n−3 fatty acids during development on brain phospholipid fatty acid composition and exploratory behavior in rats
inferredcites →https://doi.org/10.1007/bf02935553openalex-snapshot
The role of immediate early genes in the stabilization of long-term potentiation
inferredcites →https://doi.org/10.1016/0006-8993(78)90655-8openalex-snapshot
Impaired synaptic potentiation processes in the hippocampus of aged, memory-deficient rats
inferredcites →https://doi.org/10.1016/0006-8993(84)91008-4openalex-snapshot
Transient and enduring morphological correlates of synaptic activity and efficacy change in the rat hippocampal slice
inferredcites →https://doi.org/10.1016/0006-8993(85)91596-3openalex-snapshot
Age-related reduced affinity in [3H]nitrendipine labeling of brain voltage-dependent calcium channels
inferredcites →https://doi.org/10.1016/0006-8993(86)90579-2openalex-snapshot
Patterned stimulation at the theta frequency is optimal for the induction of hippocampal long-term potentiation
inferredcites →https://doi.org/10.1016/0006-8993(86)91486-1openalex-snapshot
Aged rats need a preserved complement of perforated axospinous synapses per hippocampal neuron to maintain good spatial memory
inferredcites →https://doi.org/10.1016/0006-8993(87)91429-6openalex-snapshot
Redistribution of synaptic vesicles during long-term potentiation in the hippocampus
inferredcites →https://doi.org/10.1016/0006-8993(88)90171-0openalex-snapshot
Synaptic interface surface area increases with long-term potentiation in the hippocampal dentate gyrus
inferredcites →https://doi.org/10.1016/0006-8993(88)91358-3openalex-snapshot
Lonf-term potentiation in the dentate gyrus is preferentially induced at theta rhythm periodicity
inferredcites →https://doi.org/10.1016/0006-8993(89)90380-6openalex-snapshot
Influence of epidermal growth factor on long-term potentiation in the hippocampal slice
inferredcites →https://doi.org/10.1016/0006-8993(90)91426-hopenalex-snapshot
Presynaptic ultrastructural correlates of long-term potentiation in the CA1 subfield of the hippocampus
inferredcites →https://doi.org/10.1016/0006-8993(90)91654-yopenalex-snapshot
Spinules in axospinous synapses of the rat dentate gyrus: changes in density following long-term potentiation
inferredcites →https://doi.org/10.1016/0006-8993(90)91745-3openalex-snapshot
Decreased density, but not number, N-methyl-D-aspartate, glycine and phencyclidine binding sites in hippocampus of senescent rats
inferredcites →https://doi.org/10.1016/0006-8993(91)90020-vopenalex-snapshot
Classical conditioning selectively increases AMPA receptor binding in rabbit hippocampus
inferredcites →https://doi.org/10.1016/0006-8993(91)90589-nopenalex-snapshot
Epidermal growth factor enhances short-term potentiation and facilitates induction of long-term potentiation in rat hippocampal slices
inferredcites →https://doi.org/10.1016/0006-8993(91)91001-hopenalex-snapshot
Age-related decreases of the N-methyl-d-aspartate receptor complex in the rat cerebral cortex and hippocampus
inferredcites →https://doi.org/10.1016/0006-8993(91)91683-ropenalex-snapshot
Induction of long-term potentiation is associated with an increase in the number of axospinous synapses with segmented postsynaptic densities
inferredcites →https://doi.org/10.1016/0006-8993(92)90938-6openalex-snapshot
Correlation between the induction of an immediate early gene,zif/268, and long-term potentiation in the dentate gyrus
inferredcites →https://doi.org/10.1016/0006-8993(92)90954-8openalex-snapshot
Reduced density of NMDA receptors and increased sensitivity to dizocilpine-induced learning impairment in aged rats
inferredcites →https://doi.org/10.1016/0006-8993(93)90468-3openalex-snapshot
Interleukin-1β, but not interleukin-6, impairs spatial navigation learning
inferredcites →https://doi.org/10.1016/0006-8993(93)90959-qopenalex-snapshot
Interleukin 1β inhibits synaptic strength and long-term potentiation in the rat CA1 hippocampus
inferredcites →https://doi.org/10.1016/0006-8993(94)91367-6openalex-snapshot
Effects of adrenalectomy on spatial memory performance and dentate gyrus morphology
inferredcites →https://doi.org/10.1016/0006-8993(94)91377-3openalex-snapshot
Attenuated hippocampal long-term potentiation in basolateral amygdala-lesioned rats
inferredcites →https://doi.org/10.1016/0006-8993(94)91720-5openalex-snapshot
LTP in the dentate gyrus is associated with a persistent NMDA receptor-dependent enhancement of synaptosomal glutamate release
inferredcites →https://doi.org/10.1016/0006-8993(95)00271-qopenalex-snapshot
Impairment of long-term potentiation in rats fed with vitamin E-deficient diet
inferredcites →https://doi.org/10.1016/0006-8993(95)00440-2openalex-snapshot
Reduced hippocampal CA1 Ca2+-induced long-term potentiation is associated with age-dependent impairment of spatial learning
inferredcites →https://doi.org/10.1016/0006-8993(95)00930-oopenalex-snapshot
Intracerebroventricular interleukin-1 receptor antagonist blocks the enhancement of fear conditioning and interference with escape produced by inescapable shock
inferredcites →https://doi.org/10.1016/0014-2999(90)90099-ropenalex-snapshot
Interleukin-1β inhibits long-term potentiation in the CA3 region of mouse hippocampal slices
inferredcites →https://doi.org/10.1016/0014-2999(91)90529-yopenalex-snapshot
Trans-ACPD enhances long-term potentiation in the hippocampus
inferredcites →https://doi.org/10.1016/0014-2999(95)00579-xopenalex-snapshot
1S,3R-ACPD dose dependently induces a slow onset potentiation in the dentate gyrus in vivo
inferredcites →https://doi.org/10.1016/0014-2999(96)00463-3openalex-snapshot
The synergism between ACPD and arachidonic acid on glutamate release in hippocampus is age-dependent
inferredcites →https://doi.org/10.1016/0014-2999(96)00464-5openalex-snapshot
Ageing is associated with changes in glutamate release, protein tyrosine kinase and protein kinase II in rat hippocampus
inferredcites →https://doi.org/10.1016/0022-5193(78)90230-8openalex-snapshot
A membrane hypothesis of aging
inferredcites →https://doi.org/10.1016/0024-3205(96)00318-9openalex-snapshot
Aging-related increase in hippocampal calcium channels
inferredcites →https://doi.org/10.1016/0028-3908(93)90123-kopenalex-snapshot
Characterisation of LTP induced by the activation of glutamate metabotropic receptors in area CA1 of the hippocampus
inferredcites →https://doi.org/10.1016/0028-3908(94)90181-3openalex-snapshot
Activation of metabotropic glutamate receptors is necessary for long-term potentiation in the dentate gyrus and for spatial learning
inferredcites →https://doi.org/10.1016/0028-3908(95)00107-hopenalex-snapshot
Long-term potentiation in mice lacking synapsins
inferredcites →https://doi.org/10.1016/0028-3908(95)00110-ropenalex-snapshot
Metabotropic glutamate receptor agonist trans-azetidine-2,4-dicarboxylic acid facilitates maintenance of LTP in the dentate gyrus in vivo
inferredcites →https://doi.org/10.1016/0028-3908(95)00115-mopenalex-snapshot
Evidence against a role for metabotropic glutamate receptors in mossy fiber LTP: the use of mutant mice and pharmacological antagonists
inferredcites →https://doi.org/10.1016/0028-3908(96)84654-5openalex-snapshot
Physiological and behavioral studies of mice Lacking type 4 mGluRS
inferredcites →https://doi.org/10.1016/0028-3932(84)90057-5openalex-snapshot
Preserved memory in retrograde amnesia: Sparing of a recently acquired skill
inferredcites →https://doi.org/10.1016/0028-3932(93)90031-topenalex-snapshot
Long-term potentiation of hippocampal afferents and efferents to prefrontal cortex: Implications for associative learning
inferredcites →https://doi.org/10.1016/0047-6374(92)90035-copenalex-snapshot
Age-related changes in antioxidant enzyme activities are region and organ, as well as sex, selective in the rat
inferredcites →https://doi.org/10.1016/0091-3057(80)90145-8openalex-snapshot
Two sensitive periods for the amnesic effect of anisomycin
inferredcites →https://doi.org/10.1016/0091-3057(93)90204-7openalex-snapshot
The potent free radical scavenger α-lipoic acid improves memory in aged mice: Putative relationship to NMDA receptor deficits
inferredcites →https://doi.org/10.1016/0092-8674(91)90149-sopenalex-snapshot
The trk tyrosine protein kinase mediates the mitogenic properties of nerve growth factor and neurotrophin-3
inferredcites →https://doi.org/10.1016/0092-8674(91)90419-yopenalex-snapshot
The trk proto-oncogene encodes a receptor for nerve growth factor
inferredcites →https://doi.org/10.1016/0092-8674(93)90613-uopenalex-snapshot
Modified hippocampal long-term potentiation in PKCγ-mutant mice
inferredcites →https://doi.org/10.1016/0092-8674(93)90614-vopenalex-snapshot
PKCγ mutant mice exhibit mild deficits in spatial and contextual learning
inferredcites →https://doi.org/10.1016/0092-8674(94)90108-2openalex-snapshot
Whisker-related neuronal patterns fail to develop in the trigeminal brainstem nuclei of NMDAR1 knockout mice
inferredcites →https://doi.org/10.1016/0092-8674(94)90204-6openalex-snapshot
Reduced hippocampal long-term potentiation and context-specific deficit in associative learning in mGluR1 mutant mice
inferredcites →https://doi.org/10.1016/0092-8674(94)90400-6openalex-snapshot
Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein
inferredcites →https://doi.org/10.1016/0092-8674(95)90009-8openalex-snapshot
CaMKII regulates the frequency-response function of hippocampal synapses for the production of both LTD and LTP
inferredcites →https://doi.org/10.1016/0092-8674(95)90010-1openalex-snapshot
Impairment of spatial but not contextual memory in CaMKII mutant mice with a selective loss of hippocampal ltp in the range of the θ frequency
inferredcites →https://doi.org/10.1016/0092-8674(95)90146-9openalex-snapshot
A genetic test of the effects of mutations in PKA on mossy fiber ltp and its relation to spatial and contextual learning
inferredcites →https://doi.org/10.1016/0092-8674(95)90401-8openalex-snapshot
Specificity of receptor tyrosine kinase signaling: Transient versus sustained extracellular signal-regulated kinase activation
inferredcites →https://doi.org/10.1016/0163-1047(92)90982-aopenalex-snapshot
Amnesia by post-training infusion of glutamate receptor antagonists into the amygdala, hippocampus, and entorhinal cortex
inferredcites →https://doi.org/10.1016/0165-3806(81)90092-4openalex-snapshot
Development of glutamate binding sites and their regulation by calcium in rat hippocampus
inferredcites →https://doi.org/10.1016/0166-2236(88)90061-6openalex-snapshot
Neural plasticity: A lifespan approachedited by Ted L. Petit and Gwen O. Ivy, Alan R. Liss, 1988. $59.50 (xii + 383 pages) ISBN 0 8451 2738 1
inferredcites →https://doi.org/10.1016/0166-2236(88)90143-9openalex-snapshot
Spatial learning and memory processes: the search for their neurobiological mechanisms in the rat
inferredcites →https://doi.org/10.1016/0166-2236(92)90051-9openalex-snapshot
Individual differences in the cognitive and neurobiological consequences of normal aging
inferredcites →https://doi.org/10.1016/0166-2236(93)90093-2openalex-snapshot
The TINS/TiPS Lecture the molecular biology of mammalian glutamate receptor channels
inferredcites →https://doi.org/10.1016/0166-2236(93)90122-3openalex-snapshot
Quantal analysis and synaptic anatomy — integrating two views of hippocampal plasticity
inferredcites →https://doi.org/10.1016/0166-2236(95)80003-kopenalex-snapshot
LTP — a structural model to explain the inconsistencies
inferredcites →https://doi.org/10.1016/0166-4328(86)90011-2openalex-snapshot
The effects of hippocampal lesions upon spatial and non-spatial tests of working memory
inferredcites →https://doi.org/10.1016/0166-4328(94)90032-9openalex-snapshot
Psychological stress repeatedly blocks hippocampal primed burst potentiation in behaving rats
inferredcites →https://doi.org/10.1016/0168-0102(94)90063-9openalex-snapshot
Working memory and prefrontal cortex
inferredcites →https://doi.org/10.1016/0169-328x(87)90044-1openalex-snapshot
Decreased level of nerve growth factor (NGF) and its messenger RNA in the aged rat brain
inferredcites →https://doi.org/10.1016/0169-328x(91)90136-lopenalex-snapshot
Kainic acid-induced seizures stimulate increased expression of nerve growth factor mRNA in rat hippocampus
inferredcites →https://doi.org/10.1016/0169-328x(93)90012-eopenalex-snapshot
Differential expression of immediate early genes after hippocampal long-term potentiation in awake rats
inferredcites →https://doi.org/10.1016/0169-328x(94)00187-jopenalex-snapshot
Krox20 may play a key role in the stabilization of long-term potentiation
inferredcites →https://doi.org/10.1016/0169-328x(94)90219-4openalex-snapshot
Neurotrophic factor mRNA expression in dentate gyrus is increased following in vivo stimulation of the angular bundle
inferredcites →https://doi.org/10.1016/0169-328x(95)00026-oopenalex-snapshot
Analysis of the decremental nature of LTP in the dentate gyrus
inferredcites →https://doi.org/10.1016/0169-328x(95)00206-8openalex-snapshot
Protein F1/GAP-43 and PKC gene expression patterns in hippocampus are altered 1–2 h after LTP
inferredcites →https://doi.org/10.1016/0197-0186(95)00097-6openalex-snapshot
CaM KINASE II IN LONG-TERM POTENTIATION
inferredcites →https://doi.org/10.1016/0197-4580(91)90032-fopenalex-snapshot
Quantitation of synaptic density in the septal nuclei of young and aged Fischer 344 rats
inferredcites →https://doi.org/10.1016/0197-4580(91)90072-ropenalex-snapshot
Hippocampal NGF levels are not reduced in the aged Fischer 344 rat
inferredcites →https://doi.org/10.1016/0197-4580(93)90001-ropenalex-snapshot
Age-related changes in excitatory amino acid receptors in two mouse strains
inferredcites →https://doi.org/10.1016/0197-4580(93)90007-xopenalex-snapshot
Similar effects of aging and corticosterone treatment on mouse hippocampal function
inferredcites →https://doi.org/10.1016/0197-4580(93)90009-zopenalex-snapshot
Age-related alterations in potentiation in the CA1 region in F344 rats
inferredcites →https://doi.org/10.1016/0197-4580(93)90030-fopenalex-snapshot
Acetyl-l-carnitine: Behavioral, electrophysiological, and neurochemical effects
inferredcites →https://doi.org/10.1016/0197-4580(93)90087-ropenalex-snapshot
BDNF and trkB mRNA expression in the hippocampal formation of aging rats
inferredcites →https://doi.org/10.1016/0197-4580(94)90101-5openalex-snapshot
Evolving aspects of the glucocorticoid hypothesis of brain aging: Hormonal modulation of neuronal calcium homeostasis
inferredcites →https://doi.org/10.1016/0301-0082(79)90005-4openalex-snapshot
A review of the hippocampal place cells
inferredcites →https://doi.org/10.1016/0304-3940(86)90487-8openalex-snapshot
Induction of hippocampal long-term potentiation using physiologically patterned stimulation
inferredcites →https://doi.org/10.1016/0304-3940(90)90069-lopenalex-snapshot
Long-term potentiation in the prefrontal cortex following stimulation of the hippocampal CA1/subicular region
inferredcites →https://doi.org/10.1016/0304-3940(93)90420-popenalex-snapshot
Brain-derived neurotrophic factor expression after long-term potentiation
inferredcites →https://doi.org/10.1016/0304-3940(94)90618-1openalex-snapshot
Age and strain differences in rat place learning and hippocampal dentate gyrus frequency-potentiation
inferredcites →https://doi.org/10.1016/0304-3940(95)11643-bopenalex-snapshot
Amygdala N-methyl-d-aspartate receptors participate in the induction of long-term potentiation in the dentate gyrus in vivo
inferredcites →https://doi.org/10.1016/0304-3940(95)12247-8openalex-snapshot
p53 involves cytosine arabinoside-induced apoptosis in cultured cerebellar granule neurons
inferredcites →https://doi.org/10.1016/0304-3940(95)12252-4openalex-snapshot
Interleukin-1β (IL-1β) and tumour necrosis factor (TNF) inhibit long-term potentiation in the rat dentate gyrus in vitro
inferredcites →https://doi.org/10.1016/0306-4522(87)90019-4openalex-snapshot
Long-term potentiation in the dentate gyrus: induction and increased glutamate release are blocked by d(−)aminophosphonovalerate
inferredcites →https://doi.org/10.1016/0306-4522(87)90192-8openalex-snapshot
Characterization of an N-methyl-d-aspartate receptor component of synaptic transmission in rat hippocampal slices
inferredcites →https://doi.org/10.1016/0306-4522(89)90001-8openalex-snapshot
Maintenance of long-term potentiation in rat dentate gyrus requires protein synthesis but not messenger RNA synthesis immediately post-tetanization
inferredcites →https://doi.org/10.1016/0306-4522(91)90060-2openalex-snapshot
Free radicals accelerate the decay of long-term potentiation in field CA1 of guinea-pig hippocampus
inferredcites →https://doi.org/10.1016/0306-4522(92)90242-topenalex-snapshot
Enhancement of extracellular protein concentrations during long-term potentiation in the rat hippocampal slice
inferredcites →https://doi.org/10.1016/0306-4522(94)90197-xopenalex-snapshot
Increase in synaptic vesicle proteins accompanies long-term potentiation in the dentate gyrus
inferredcites →https://doi.org/10.1016/0306-4522(95)00579-xopenalex-snapshot
The synergism between metabotropic glutamate receptor activation and arachidonic acid on glutamate release is occluded by induction of long-term potentiation in the dentate gyrus
inferredcites →https://doi.org/10.1016/0361-9230(84)90005-4openalex-snapshot
Anisomycin blocks the late phase of long-term potentiation in the dentate gyrus of freely moving rats
inferredcites →https://doi.org/10.1016/0361-9230(94)90089-2openalex-snapshot
Selective reduction of hippocampal dentate frequency potentiation in aged rats with impaired place learning
inferredcites →https://doi.org/10.1016/0376-8716(92)90037-dopenalex-snapshot
Effects of an oil enriched in gamma linolenic acid on locomotor activity and behaviour in the Morris Maze, following in utero ethanol exposure in rats
inferredcites →https://doi.org/10.1016/0531-5565(93)90042-copenalex-snapshot
A cluster analysis study of acetyl-l-carnitine effect on NMDA receptors in aging
inferredcites →https://doi.org/10.1016/0891-5849(94)00106-topenalex-snapshot
Brain synaptosomal aging: Free radicals and membrane fluidity
inferredcites →https://doi.org/10.1016/0896-6273(90)90118-yopenalex-snapshot
Differential expression of immediate early genes in the hippocampus and spinal cord
inferredcites →https://doi.org/10.1016/0896-6273(92)90248-copenalex-snapshot
Mechanisms underlying induction of homosynaptic long-term depression in area CA1 of the hippocampus
inferredcites →https://doi.org/10.1016/0896-6273(92)90304-vopenalex-snapshot
A regulatory subunit of the cAMP-dependent protein kinase down-regulated in aplysia sensory neurons during long-term sensitization
inferredcites →https://doi.org/10.1016/0896-6273(95)90046-2openalex-snapshot
Evidence for silent synapses: Implications for the expression of LTP
inferredcites →https://doi.org/10.1016/0896-6273(95)90076-4openalex-snapshot
Relative abundance of subunit mRNAs determines gating and Ca2+ permeability of AMPA receptors in principal neurons and interneurons in rat CNS
inferredcites →https://doi.org/10.1016/0896-6273(95)90299-6openalex-snapshot
Arc, a growth factor and activity-regulated gene, encodes a novel cytoskeleton-associated protein that is enriched in neuronal dendrites
inferredcites →https://doi.org/10.1016/0955-2235(92)90028-gopenalex-snapshot
Ciliary neurotrophic factor and its receptor complex
inferredcites →https://doi.org/10.1016/0959-4388(95)80023-9openalex-snapshot
Retrograde amnesia and memory consolidation: a neurobiological perspective
inferredcites →https://doi.org/10.1016/0960-0760(95)00069-copenalex-snapshot
Long-term control of neuronal excitability by corticosteroid hormones
inferredcites →https://doi.org/10.1016/s0006-3223(99)00123-7openalex-snapshot
Memory and socioemotional behavior in monkeys after hippocampal damage incurred in infancy or in adulthood
inferredcites →https://doi.org/10.1016/s0006-8993(01)02855-4openalex-snapshot
Correlation between hippocampal BDNF mRNA expression and memory performance in senescent rats
inferredcites →https://doi.org/10.1016/s0006-8993(02)03556-4openalex-snapshot
Nefiracetam induces a long-lasting facilitation of hippocampal postsynaptic responses in mice lacking the NMDA receptor ϵ1 subunit
inferredcites →https://doi.org/10.1016/s0006-8993(96)00776-7openalex-snapshot
Role of adrenal steroid mineralocorticoid and glucocorticoid receptors in long-term potentiation in the CA1 field of hippocampal slices
inferredcites →https://doi.org/10.1016/s0006-8993(96)01298-xopenalex-snapshot
Inhibitory avoidance learning alters the amygdala calcium/calmodulin-dependent protein kinase II activity in rats
inferredcites →https://doi.org/10.1016/s0006-8993(96)01448-5openalex-snapshot
Severe learning deficits in apolipoprotein E-knockout mice in a water maze task
inferredcites →https://doi.org/10.1016/s0006-8993(97)01215-8openalex-snapshot
Chronic neuroinflammation in rats reproduces components of the neurobiology of Alzheimer's disease
inferredcites →https://doi.org/10.1016/s0006-8993(98)00993-7openalex-snapshot
Expression of BDNF and trkB as a function of age and cognitive performance
inferredcites →https://doi.org/10.1016/s0006-8993(99)01592-9openalex-snapshot
Deprivation of endogenous brain-derived neurotrophic factor results in impairment of spatial learning and memory in adult rats
inferredcites →https://doi.org/10.1016/s0006-8993(99)02445-2openalex-snapshot
Human immunodeficiency virus-1 coat protein gp120 impairs contextual fear conditioning: a potential role in AIDS related learning and memory impairments
inferredcites →https://doi.org/10.1016/s0014-2999(97)85402-7openalex-snapshot
Class I mGlu receptor antagonist 1-aminoindan-1,5-dicarboxylic acid blocks contextual but not cue conditioning in rats
inferredcites →https://doi.org/10.1016/s0021-9258(18)53037-4openalex-snapshot
Long-term potentiation is associated with an increased activity of Ca2+/calmodulin-dependent protein kinase II.
inferredcites →https://doi.org/10.1016/s0028-3908(00)00037-xopenalex-snapshot
Fear conditioning-induced time- and subregion-specific increase in expression of mGlu5 receptor protein in rat hippocampus
inferredcites →https://doi.org/10.1016/s0028-3908(01)00122-8openalex-snapshot
Differential effects of enrichment on learning and memory function in NR2B transgenic mice
inferredcites →https://doi.org/10.1016/s0028-3908(01)00136-8openalex-snapshot
Effect of transgenic overexpression of NR2B on NMDA receptor function and synaptic plasticity in visual cortex
inferredcites →https://doi.org/10.1016/s0028-3908(01)00202-7openalex-snapshot
Decrease in calbindin content significantly alters LTP but not NMDA receptor and calcium channel properties
inferredcites →https://doi.org/10.1016/s0028-3908(02)00297-6openalex-snapshot
Galanin regulates spatial memory but not visual recognition memory or synaptic plasticity in perirhinal cortex
inferredcites →https://doi.org/10.1016/s0028-3908(96)00101-3openalex-snapshot
Effects of the metabotropic glutamate receptor antagonist MCPG on spatial and context-specific learning
inferredcites →https://doi.org/10.1016/s0028-3908(97)00073-7openalex-snapshot
Changes in protein synthesis and synthesis of the synaptic vesicle protein, synaptophysin, in entorhinal cortex following induction of long-term potentiation in dentate gyrus: an age-related study in the rat
inferredcites →https://doi.org/10.1016/s0028-3908(97)00129-9openalex-snapshot
(R,S)-α-methyl-4-carboxyphenylglycine (MCPG) fails to block long-term potentiation under urethane anaesthesia in vivo
inferredcites →https://doi.org/10.1016/s0028-3908(98)00039-2openalex-snapshot
Long-term potentiation in vivo in layers II/III of rat barrel cortex
inferredcites →https://doi.org/10.1016/s0028-3908(98)00048-3openalex-snapshot
Evidence that nerve growth factor plays a role in long-term potentiation in the rat dentate gyrus
inferredcites →https://doi.org/10.1016/s0028-3908(98)00058-6openalex-snapshot
Involvement of calcium/calmodulin-dependent protein kinases in the setting of a molecular switch involved in hippocampal LTP
inferredcites →https://doi.org/10.1016/s0028-3908(99)00169-0openalex-snapshot
Long-term potentiation in dentate gyrus of the rat is inhibited by the phosphoinositide 3–kinase inhibitor, wortmannin
inferredcites →https://doi.org/10.1016/s0028-3908(99)00203-8openalex-snapshot
Lack of expression of long-term potentiation in the dentate gyrus but not in the CA1 region of the hippocampus of μ-opioid receptor-deficient mice
inferredcites →https://doi.org/10.1016/s0031-9384(01)00471-1openalex-snapshot
Performance more than working memory disrupted by acute systemic inflammation in rats in appetitive tasks
inferredcites →https://doi.org/10.1016/s0031-9384(01)00516-9openalex-snapshot
Gene targeting reveals a role for the glutamate receptors mGluR5 and GluR2 in learning and memory
inferredcites →https://doi.org/10.1016/s0031-9384(01)00543-1openalex-snapshot
Environmental enrichment: Effects on spatial memory and hippocampal CREB immunoreactivity
inferredcites →https://doi.org/10.1016/s0079-6123(08)62118-4openalex-snapshot
Chapter 34 Synaptic modulation by neurotrophic factors
inferredcites →https://doi.org/10.1016/s0079-6603(08)60815-6openalex-snapshot
Early Growth Response Protein 1 (Egr-1): Prototype of a Zinc-finger Family of Transcription Factors
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Analysis of gene expression changes associated with long‐lasting synaptic enhancement in hippocampal slice cultures after repetitive exposures to glutamate
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High expression of disease‐related Cln6 in the cerebral cortex, purkinje cells, dentate gyrus, and hippocampal ca1 neurons
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Sex differences in synaptic plasticity underlying learning
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Ketone bodies effectively compete with glucose for neuronal acetyl‐CoA generation in rat hippocampal slices
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Mineralocorticoid receptor activation restores medial perforant path LTP in diabetic rats
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Cognitive training increases dendritic arborization in the dorsal hippocampal CA1 and CA3 neurons of female and male Long–Evans rats
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α7 nicotinic acetylcholine receptors induce long‐term synaptic enhancement in the dorsal but not ventral hippocampus
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A Role for Calcium/Calmodulin-Dependent Protein Kinase II in Cardiac Disease and Arrhythmia
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Extracellular Recordings of Synaptic Plasticity and Network Oscillations in Hippocampal Slices
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BDNF Function in Long-Term Synaptic Plasticity in the Dentate Gyrus In Vivo: Methods for Local Drug Delivery and Biochemical Analysis of Translation
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Network, Cellular, and Molecular Mechanisms Underlying Long-Term Memory Formation
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On the Origin and Evolution of Affective Capacities in Lower Vertebrates
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The Impact of an Imbalance Between Proinflammatory and Anti-inflammatory Influences on Synaptic function in the Aged Brain
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Neuroactive Steroids: Effects on Cognitive Functions
inferred← citeshttps://doi.org/10.1007/978-1-4020-6854-6_9openalex-snapshot
Pregnane Steroids and Short-Term Neural Plasticity
inferred← citeshttps://doi.org/10.1007/978-1-4419-1452-1_13openalex-snapshot
Cognitive Algorithms and Systems of Episodic Memory, Semantic Memory, and Their Learnings
inferred← citeshttps://doi.org/10.1007/978-1-4614-0436-1_1openalex-snapshot
Brain Structures and Consciousness
inferred← citeshttps://doi.org/10.1007/978-1-4614-4729-0_6openalex-snapshot
Mood Disorders and Immunity
inferred← citeshttps://doi.org/10.1007/978-1-4614-4788-7_35openalex-snapshot
Dysregulation of Neurogenic Calcium Signaling and Autism
inferred← citeshttps://doi.org/10.1007/978-1-4614-5836-4_43openalex-snapshot
Amyloid-Beta, BDNF, and the Mechanism of Neurodegeneration in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/978-1-4939-1154-7_16openalex-snapshot
O-GlcNAcylation of Neuronal Proteins: Roles in Neuronal Functions and in Neurodegeneration
inferred← citeshttps://doi.org/10.1007/978-1-4939-1761-7_14openalex-snapshot
The Behavioral Tagging Hypothesis and Its Implications for Long-Term Memory Formation
inferred← citeshttps://doi.org/10.1007/978-1-4939-7584-6_11openalex-snapshot
The Application of In Vivo Extracellular Recording Technique to Study the Biological Effects of Nanoparticles in Brain
inferred← citeshttps://doi.org/10.1007/978-1-59745-055-3_10openalex-snapshot
Group I Metabotropic Glutamate Receptors (mGlu1 and mGlu5)
inferred← citeshttps://doi.org/10.1007/978-1-59745-055-3_5openalex-snapshot
Ionotropic Glutamate Receptors in Synaptic Plasticity
inferred← citeshttps://doi.org/10.1007/978-1-60327-342-8_1openalex-snapshot
Reactive Oxygen Species, Synaptic Plasticity, and Memory
inferred← citeshttps://doi.org/10.1007/978-1-60761-462-3_11openalex-snapshot
Propofol Amnesia – What is Going on in the Brain?
inferred← citeshttps://doi.org/10.1007/978-1-60761-941-3_24openalex-snapshot
5-HT2C Receptors in Learning
inferred← citeshttps://doi.org/10.1007/978-1-62703-517-0_10openalex-snapshot
Electrophysiological Methods for Investigating Inhibitory Synaptic Plasticity
inferred← citeshttps://doi.org/10.1007/978-1-908517-18-0_2openalex-snapshot
Glutamate-Mediated Neuroplasticity Deficits in Mood Disorders
inferred← citeshttps://doi.org/10.1007/978-3-030-22009-9_702openalex-snapshot
Short-Term/Long-Term Memory
inferred← citeshttps://doi.org/10.1007/978-3-030-67928-6_24-1openalex-snapshot
The Hippocampus and Addiction: Focus on Plasticity and Circuitry in the Hippocampus
inferred← citeshttps://doi.org/10.1007/978-3-030-92392-1_24openalex-snapshot
The Hippocampus and Addiction: Focus on Plasticity and Circuitry in the Hippocampus
inferred← citeshttps://doi.org/10.1007/978-3-031-12390-0_9openalex-snapshot
Brain O-GlcNAcylation: From Molecular Mechanisms to Clinical Phenotype
inferred← citeshttps://doi.org/10.1007/978-3-031-28206-5_15openalex-snapshot
How Technology Is Changing Creativity
inferred← citeshttps://doi.org/10.1007/978-3-031-40858-8_155-1openalex-snapshot
Integrated Model of Traumatic Brain Injury Multiple Morbidity
inferred← citeshttps://doi.org/10.1007/978-3-031-54864-2_19openalex-snapshot
The Behavioral Tagging Hypothesis: A Mechanistic Approach for the Storage of Lasting Memories
inferred← citeshttps://doi.org/10.1007/978-3-031-54864-2_22openalex-snapshot
Behavioral Tagging: Unveiling the Intricacies of Memory Consolidation
inferred← citeshttps://doi.org/10.1007/978-3-031-54896-3_6openalex-snapshot
Pupillometry and Declarative Long-Term Memory
inferred← citeshttps://doi.org/10.1007/978-3-031-59038-2_3openalex-snapshot
The Nervous System and the Affective Neural Systems
inferred← citeshttps://doi.org/10.1007/978-3-031-62983-9_2openalex-snapshot
Engrams: From Behavior to Brain-Wide Networks
inferred← citeshttps://doi.org/10.1007/978-3-031-68550-7_14openalex-snapshot
Molecular Intersection of Activity-Dependent Gene Expression and Behavior: The Transcriptomic Signature of Long-Term Memory
inferred← citeshttps://doi.org/10.1007/978-3-031-88907-3_5openalex-snapshot
Neurophysiology of the Human Hippocampus
inferred← citeshttps://doi.org/10.1007/978-3-032-07448-5_34openalex-snapshot
Spike Timing Dependent Plasticity Organizes Type Ia Muscle Afferents in a Synthetic Nervous System
inferred← citeshttps://doi.org/10.1007/978-3-032-38398-3_12openalex-snapshot
Representational Drift in Memory Under Incremental Learning with Local Synaptic Mechanisms
inferred← citeshttps://doi.org/10.1007/978-3-319-12913-6_3openalex-snapshot
Fluorescent Proteins for Neuronal Imaging
inferred← citeshttps://doi.org/10.1007/978-3-319-16522-6_3openalex-snapshot
Signaling Pathways Relevant to Cognition-Enhancing Drug Targets
inferred← citeshttps://doi.org/10.1007/978-3-319-17641-3_8openalex-snapshot
Voltage Imaging in the Study of Hippocampal Circuit Function and Plasticity
inferred← citeshttps://doi.org/10.1007/978-3-319-47609-4_3openalex-snapshot
The Memory Labyrinth: Systems, Processes, and Boundaries
inferred← citeshttps://doi.org/10.1007/978-3-319-58811-7_9openalex-snapshot
Role of PDE9 in Cognition
inferred← citeshttps://doi.org/10.1007/978-3-319-62817-2_5openalex-snapshot
Learning as a Functional State of the Brain: Studies in Wild-Type and Transgenic Animals
inferred← citeshttps://doi.org/10.1007/978-3-319-69892-2_702-1openalex-snapshot
Short-Term/Long-Term Memory
inferred← citeshttps://doi.org/10.1007/978-3-540-29678-2_2215openalex-snapshot
Hippocampus: Organization, Maturation, and Operation in Cognition and Pathological Conditions
inferred← citeshttps://doi.org/10.1007/978-3-540-29678-2_2829openalex-snapshot
Long-Term Potentiation (LTP)
inferred← citeshttps://doi.org/10.1007/978-3-540-29678-2_3408openalex-snapshot
Memory, Molecular Mechanisms
inferred← citeshttps://doi.org/10.1007/978-3-642-27772-6_345-2openalex-snapshot
Long-Term Potentiation and Memory
inferred← citeshttps://doi.org/10.1007/978-3-662-46943-9_4openalex-snapshot
CNS Adverse Effects: From Functional Observation Battery/Irwin Tests to Electrophysiology
inferred← citeshttps://doi.org/10.1007/978-3-7091-1292-2_3openalex-snapshot
Perirhinal and Postrhinal Functional Inputs to the Hippocampus
inferred← citeshttps://doi.org/10.1007/978-4-431-55516-2_12openalex-snapshot
Optogenetic Imaging of Protein Activity in the Synapse Using 2-Photon Fluorescence Lifetime Imaging Microscopy
inferred← citeshttps://doi.org/10.1007/978-4-431-55763-0_15openalex-snapshot
Knowledge of Signal Transduction Provides an Approach to Attacking Memory Decline
inferred← citeshttps://doi.org/10.1007/978-4-431-87704-2_18openalex-snapshot
Computational Models of Cerebellar Long-Term Memory
inferred← citeshttps://doi.org/10.1007/978-94-007-0831-0_3openalex-snapshot
Stress, Dissociation and Schizophrenia
inferred← citeshttps://doi.org/10.1007/978-94-007-2774-8_5openalex-snapshot
The Role of Aβ and Tau Oligomers in the Pathogenesis of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/978-94-007-5237-5_15openalex-snapshot
Potential Therapeutic Targets for Improving Memory Impairments and Dementia: Clues Obtained from Memory-Enhanced Mice
inferred← citeshttps://doi.org/10.1007/978-94-007-7107-9_5openalex-snapshot
Intracellular Message Chains
inferred← citeshttps://doi.org/10.1007/978-981-15-7486-3_10openalex-snapshot
Mathematical Modelling of Magnesium Block-Driven NMDA Receptor Response in CA1 Pyramidal Neuron for Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/978-981-15-8763-4_18openalex-snapshot
Optogenetic Imaging of Protein Activity Using Two-Photon Fluorescence Lifetime Imaging Microscopy
inferred← citeshttps://doi.org/10.1007/978-981-16-1354-8_27openalex-snapshot
Memristor-Based Neural Network Circuit of Associative Memory with Multimodal Synergy
inferred← citeshttps://doi.org/10.1007/978-981-19-7327-7_6openalex-snapshot
Iron-Calcium Crosstalk in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1007/978-981-97-6341-2_7openalex-snapshot
Role of Branched-Chain Amino Acids in Traumatic Brain Injury
inferred← citeshttps://doi.org/10.1007/bf03077111openalex-snapshot
Acute stress, cortisol en het geheugen: hoe hangen ze samen?
inferred← citeshttps://doi.org/10.1007/s00018-008-8216-xopenalex-snapshot
Molecular and cellular basis of small- and intermediate-conductance, calcium-activated potassium channel function in the brain
inferred← citeshttps://doi.org/10.1007/s00018-015-1992-1openalex-snapshot
MT5-MMP is a new pro-amyloidogenic proteinase that promotes amyloid pathology and cognitive decline in a transgenic mouse model of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s00018-017-2742-3openalex-snapshot
Furin promotes dendritic morphogenesis and learning and memory in transgenic mice
inferred← citeshttps://doi.org/10.1007/s00018-022-04666-8openalex-snapshot
Galactic cosmic radiation exposure causes multifaceted neurocognitive impairments
inferred← citeshttps://doi.org/10.1007/s00018-023-04999-yopenalex-snapshot
The guanine nucleotide exchange factor RapGEF2 is required for ERK-dependent immediate-early gene (Egr1) activation during fear memory formation
inferred← citeshttps://doi.org/10.1007/s00018-024-05382-1openalex-snapshot
Neuroprotection by ADAM10 inhibition requires TrkB signaling in the Huntington’s disease hippocampus
inferred← citeshttps://doi.org/10.1007/s00213-004-2074-5openalex-snapshot
Angiotensin II blocks memory consolidation through an AT2 receptor-dependent mechanism
inferred← citeshttps://doi.org/10.1007/s00213-007-0816-xopenalex-snapshot
NMDA receptor modulation by d-cycloserine promotes episodic-like memory in mice
inferred← citeshttps://doi.org/10.1007/s00213-007-0873-1openalex-snapshot
Cocaine self-administration improves performance in a highly demanding water maze task
inferred← citeshttps://doi.org/10.1007/s00213-014-3693-0openalex-snapshot
5-HT7 receptor activation: procognitive and antiamnesic effects
inferred← citeshttps://doi.org/10.1007/s00213-020-05528-6openalex-snapshot
Synergistic antidepressant-like effect of capsaicin and citalopram reduces the side effects of citalopram on anxiety and working memory in rats
inferred← citeshttps://doi.org/10.1007/s00216-010-3968-1openalex-snapshot
The potential of microelectrode arrays and microelectronics for biomedical research and diagnostics
inferred← citeshttps://doi.org/10.1007/s00221-015-4349-yopenalex-snapshot
Effect of forced exercise and exercise withdrawal on memory, serum and hippocampal corticosterone levels in rats
inferred← citeshttps://doi.org/10.1007/s00221-015-4383-9openalex-snapshot
Early attenuation of long-term potentiation in senescence-accelerated mouse prone 8
inferred← citeshttps://doi.org/10.1007/s00401-018-1847-6openalex-snapshot
Evidence for altered dendritic spine compartmentalization in Alzheimer’s disease and functional effects in a mouse model
inferred← citeshttps://doi.org/10.1007/s00411-024-01085-0openalex-snapshot
Administration of low dose intranasal ketamine exerts a neuroprotective effect on whole brain irradiation injury model in wistar rats
inferred← citeshttps://doi.org/10.1007/s00422-014-0628-0openalex-snapshot
Short-term plasticity as cause–effect hypothesis testing in distal reward learning
inferred← citeshttps://doi.org/10.1007/s00424-010-0828-yopenalex-snapshot
Channelopathies linked to plasma membrane phosphoinositides
inferred← citeshttps://doi.org/10.1007/s00424-015-1764-7openalex-snapshot
TRPM4-dependent post-synaptic depolarization is essential for the induction of NMDA receptor-dependent LTP in CA1 hippocampal neurons
inferred← citeshttps://doi.org/10.1007/s00424-015-1782-5openalex-snapshot
Physiological impact of CB1 receptor expression by hippocampal GABAergic interneurons
inferred← citeshttps://doi.org/10.1007/s00424-025-03123-2openalex-snapshot
Mitochondrial ATP synthase 8 single-nucleotide polymorphism affects oxidative stress and survival of mice
inferred← citeshttps://doi.org/10.1007/s00429-015-1103-yopenalex-snapshot
Neuropeptide S ameliorates olfactory spatial memory impairment induced by scopolamine and MK801 through activation of cognate receptor-expressing neurons in the subiculum complex
inferred← citeshttps://doi.org/10.1007/s00429-019-01898-6openalex-snapshot
Deficiency of the palmitoyl acyltransferase ZDHHC7 impacts brain and behavior of mice in a sex-specific manner
inferred← citeshttps://doi.org/10.1007/s00429-020-02159-7openalex-snapshot
Intravenous infusion of bone marrow mononuclear cells promotes functional recovery and improves impaired cognitive function via inhibition of Rho guanine nucleotide triphosphatases and inflammatory signals in a model of chronic epilepsy
inferred← citeshttps://doi.org/10.1007/s00429-021-02275-yopenalex-snapshot
Acute stress reveals different impacts in male and female Zdhhc7-deficient mice
inferred← citeshttps://doi.org/10.1007/s00441-018-2800-7openalex-snapshot
Dopaminergic innervation and modulation of hippocampal networks
inferred← citeshttps://doi.org/10.1007/s00500-023-08366-8openalex-snapshot
RETRACTED ARTICLE: Near-infrared and visible light face recognition: a comprehensive survey
inferred← citeshttps://doi.org/10.1007/s00542-020-05058-3openalex-snapshot
Computational modeling of NMDA receptor response in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s00702-013-1152-4openalex-snapshot
Glutamatergic autoencephalitides: an emerging field
inferred← citeshttps://doi.org/10.1007/s00702-016-1609-3openalex-snapshot
Impaired synaptic plasticity in RASopathies: a mini-review
inferred← citeshttps://doi.org/10.1007/s00726-012-1346-3openalex-snapshot
d-Amino acids in brain neurotransmission and synaptic plasticity
inferred← citeshttps://doi.org/10.1007/s10439-023-03366-zopenalex-snapshot
Modeling Long-Term Facilitation of Respiration During Interval Exercise in Humans
inferred← citeshttps://doi.org/10.1007/s10517-008-0297-xopenalex-snapshot
Noopept stimulates the expression of NGF and BDNF in rat hippocampus
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