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Rapid Erasure of Long-Term Memory Associations in the Cortex by an Inhibitor of PKMζ
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hipo.20171openalex-snapshot
Protein kinase Mζ enhances excitatory synaptic transmission by increasing the number of active postsynaptic AMPA receptors
inferredcites →https://doi.org/10.1016/0163-1047(93)91145-dopenalex-snapshot
Taste memory: The role of protein synthesis in gustatory cortex
inferredcites →https://doi.org/10.1016/0166-4328(80)90023-6openalex-snapshot
Post-ingestion interference with brain function prevents attenuation of neophobia in rats
inferredcites →https://doi.org/10.1016/0166-4328(94)90097-3openalex-snapshot
Neural substrates for conditioned taste aversion in the rat
inferredcites →https://doi.org/10.1016/j.conb.2007.02.006openalex-snapshot
The neuroscience of remote memory
inferredcites →https://doi.org/10.1016/j.neuron.2004.09.003openalex-snapshot
Rites of Passage of the Engram
inferredcites →https://doi.org/10.1016/s0021-9258(18)60537-xopenalex-snapshot
A quantitative Model for the Kinetics of cAMP-dependent Protein Kinase (Type II) activity
inferredcites →https://doi.org/10.1037/0735-7044.117.6.1416openalex-snapshot
Novel Tastes Elevate c-fos Expression in the Central Amygdala and Insular Cortex: Implication for Taste Aversion Learning.
inferredcites →https://doi.org/10.1037/0735-7044.120.6.1257openalex-snapshot
Effects of lesions of the bed nucleus of the stria terminalis, lateral hypothalamus, or insular cortex on conditioned taste aversion and conditioned odor aversion.
inferredcites →https://doi.org/10.1038/312101a0openalex-snapshot
Neurobiology: Memory and molecular turnover
inferredcites →https://doi.org/10.1038/nn1628openalex-snapshot
Bidirectional behavioral plasticity of memory reconsolidation depends on amygdalar protein kinase A
inferredcites →https://doi.org/10.1038/nn829openalex-snapshot
Protein kinase Mζ is necessary and sufficient for LTP maintenance
inferredcites →https://doi.org/10.1038/nrn1344openalex-snapshot
Molecular mechanisms of taste-recognition memory
inferredcites →https://doi.org/10.1093/chemse/6.2.143openalex-snapshot
Qualitative discrimination of sweet stimuli: behavioural study on rats
inferredcites →https://doi.org/10.1093/oso/9780198502678.001.0001openalex-snapshot
Memory From A to Z
inferredcites →https://doi.org/10.1101/lm.32305openalex-snapshot
Hippocampal inactivation enhances taste learning
inferredcites →https://doi.org/10.1111/j.1460-9568.2006.05009.xopenalex-snapshot
Different signal transduction cascades are activated simultaneously in the rat insular cortex and hippocampus following novel taste learning
inferredcites →https://doi.org/10.1111/j.2044-8279.1933.tb02913.xopenalex-snapshot
REMEMBERING: A STUDY IN EXPERIMENTAL AND SOCIAL PSYCHOLOGY
inferredcites →https://doi.org/10.1126/science.1058165openalex-snapshot
Memory Extinction, Learning Anew, and Learning the New: Dissociations in the Molecular Machinery of Learning in Cortex
inferredcites →https://doi.org/10.1126/science.1086881openalex-snapshot
Stability of Retrieved Memory: Inverse Correlation with Trace Dominance
inferredcites →https://doi.org/10.1126/science.1128657openalex-snapshot
Storage of Spatial Information by the Maintenance Mechanism of LTP
inferredcites →https://doi.org/10.1126/science.1135935openalex-snapshot
Schemas and Memory Consolidation
inferredcites →https://doi.org/10.1146/annurev.psych.55.090902.142050openalex-snapshot
The Neurobiology of Consolidations, Or, How Stable is the Engram?
inferredcites →https://doi.org/10.1152/jn.00198.2004openalex-snapshot
Neural Signature of Taste Familiarity in the Gustatory Cortex of the Freely Behaving Rat
inferredcites →https://doi.org/10.1371/journal.pbio.0030107openalex-snapshot
The Stability of a Stochastic CaMKII Switch: Dependence on the Number of Enzyme Molecules and Protein Turnover
inferredcites →https://doi.org/10.1523/jneurosci.17-13-05129.1997openalex-snapshot
NMDA Receptor and the Tyrosine Phosphorylation of Its 2B Subunit in Taste Learning in the Rat Insular Cortex
inferredcites →https://doi.org/10.1523/jneurosci.18-23-10037.1998openalex-snapshot
Specific and Differential Activation of Mitogen-Activated Protein Kinase Cascades by Unfamiliar Taste in the Insular Cortex of the Behaving Rat
inferredcites →https://doi.org/10.1523/jneurosci.20-23-08954.2000openalex-snapshot
The Effect of Lesions of the Insular Cortex on Instrumental Conditioning: Evidence for a Role in Incentive Memory
inferredcites →https://doi.org/10.5860/choice.41-0062openalex-snapshot
Memory from A to Z: keywords, concepts, and beyond
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Persistent Increases of PKMM in Sensorimotor Cortex Maintain Procedural long-Term Memory Storage
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Hypermethylation of Prkcz Regulated by E6/Dnmt1 Inhibits Invasion and Emt Via Cdc42 in Hpv-Related Head and Neck Squamous Cell Carcinoma
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Spinal protein kinase M ζ contributes to the maintenance of peripheral inflammation‐primed persistent nociceptive sensitization after plantar incision
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inferred← citeshttps://doi.org/10.1007/s00359-013-0862-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10072-012-1241-4openalex-snapshot
Dietary cholesterol alters memory and synaptic structural plasticity in young rat brain
inferred← citeshttps://doi.org/10.1007/s10517-015-2813-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10517-015-2920-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11055-016-0234-9openalex-snapshot
The Effects of Protein Kinase Inhibitor Mzeta on Retention and Reconsolidation of Long-Term Memory in Conditioned Food Aversion in Snails
inferred← citeshttps://doi.org/10.1007/s11055-018-0624-2openalex-snapshot
Molecular Mechanism of Memory Modification
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NMDA Receptor Dependent Long-term Potentiation in Chronic Pain
inferred← citeshttps://doi.org/10.1007/s12031-011-9671-7openalex-snapshot
Inactivation of PKMζ in the NAc Shell Abolished Cocaine-Conditioned Reward
inferred← citeshttps://doi.org/10.1007/s12035-018-1144-3openalex-snapshot
Sustained CaMKII Delta Gene Expression Is Specifically Required for Long-Lasting Memories in Mice
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Synaptic Plasticity
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Biophysically plausible models of synaptic plasticity
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PKMζ, LTP Maintenance, and Long-Term Memory Storage
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2014.04.002openalex-snapshot
Up-regulation of PKMζ expression in the anterior cingulate cortex following experimental tooth movement in rats
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‘Tagging’ along memories in aging: Synaptic tagging and capture mechanisms in the aged hippocampus
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inferred← citeshttps://doi.org/10.1016/j.brainresbull.2013.12.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.brainresbull.2023.02.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.celrep.2015.05.034openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.conb.2015.06.008openalex-snapshot
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Hippocampal Activation of Rac1 Regulates the Forgetting of Object Recognition Memory
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inferred← citeshttps://doi.org/10.1016/j.heliyon.2017.e00338openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.isci.2018.07.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neuint.2016.07.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neulet.2009.02.037openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neulet.2014.03.038openalex-snapshot
Upregulation of glutamatergic transmission in anterior cingulate cortex in the diabetic rats with neuropathic pain
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2009.11.001openalex-snapshot
Early detection of age-related memory deficits in individual mice
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.03.001openalex-snapshot
Behavioral Phenotyping Strategies for Mutant Mice
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.08.027openalex-snapshot
Inducible and Selective Erasure of Memories in the Mouse Brain via Chemical-Genetic Manipulation
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.10.055openalex-snapshot
Translational Control of Long-Lasting Synaptic Plasticity and Memory
inferred← citeshttps://doi.org/10.1016/j.neuron.2017.05.039openalex-snapshot
The Biology of Forgetting—A Perspective
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2008.07.027openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neuropharm.2016.07.015openalex-snapshot
Forgetting of what was once learned: Exploring the role of postsynaptic ionotropic glutamate receptors on memory formation, maintenance, and decay
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2007.10.016openalex-snapshot
A role for protein kinase A and protein kinase Mζ in muscarinic acetylcholine receptor–initiated persistent synaptic enhancement in rat hippocampus in vivo
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2008.08.042openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neuroscience.2011.11.057openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neuroscience.2016.08.014openalex-snapshot
Contribution of synaptic plasticity in the insular cortex to chronic pain
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2017.12.030openalex-snapshot
Peripheral Synthesis of an Atypical Protein Kinase C Mediates the Enhancement of Excitability and the Development of Mechanical Hyperalgesia Produced by Nerve Growth Factor
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2018.09.011openalex-snapshot
aPKC-Mediated Persistent Increase in AMPA/NMDA Ratio in the VTA Participates in the Neuroadaptive Signal Necessary to Induce NAc Synaptic Plasticity After Cocaine Administration
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PKM-ζ Expression Is Important in Consolidation of Memory in Prelimbic Cortex Formed by the Process of Behavioral Tagging
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2021.12.028openalex-snapshot
PKMζ Maintains Remote Contextual Fear Memory by Inhibiting GluA2-Dependent AMPA Receptor Endocytosis in the Prelimbic Cortex
inferred← citeshttps://doi.org/10.1016/j.nlm.2007.10.012openalex-snapshot
The substrate for long-lasting memory: If not protein synthesis, then what?
inferred← citeshttps://doi.org/10.1016/j.nlm.2010.12.008openalex-snapshot
Cognitive neuroepigenetics: A role for epigenetic mechanisms in learning and memory
inferred← citeshttps://doi.org/10.1016/j.nlm.2010.12.010openalex-snapshot
Long-term aversive taste memory requires insular and amygdala protein degradation
inferred← citeshttps://doi.org/10.1016/j.nlm.2012.05.003openalex-snapshot
Intra-amygdala infusion of the protein kinase Mzeta inhibitor ZIP disrupts foreground context fear memory
inferred← citeshttps://doi.org/10.1016/j.nlm.2013.03.009openalex-snapshot
The ubiquitin–proteasome system as a critical regulator of synaptic plasticity and long-term memory formation
inferred← citeshttps://doi.org/10.1016/j.nlm.2013.06.008openalex-snapshot
Cellular, molecular, and epigenetic mechanisms in non-associative conditioning: Implications for pain and memory
inferred← citeshttps://doi.org/10.1016/j.nlm.2013.09.016openalex-snapshot
Psychological and neural mechanisms of experimental extinction: A selective review
inferred← citeshttps://doi.org/10.1016/j.nlm.2014.02.011openalex-snapshot
Protein kinase C mediates memory consolidation of taste avoidance conditioning in Lymnaea stagnalis
inferred← citeshttps://doi.org/10.1016/j.nlm.2016.06.010openalex-snapshot
The role of nuclear PKMζ in memory maintenance
inferred← citeshttps://doi.org/10.1016/j.nlm.2016.07.008openalex-snapshot
Persistent increased PKMζ in long-term and remote spatial memory
inferred← citeshttps://doi.org/10.1016/j.nlm.2016.07.028openalex-snapshot
The memory gene KIBRA is a bidirectional regulator of synaptic and structural plasticity in the adult brain
inferred← citeshttps://doi.org/10.1016/j.nlm.2016.11.003openalex-snapshot
Consolidation of spatial memory in the rat: Findings using zeta-inhibitory peptide
inferred← citeshttps://doi.org/10.1016/j.npep.2015.09.004openalex-snapshot
Angiotensin IV possibly acts through PKMzeta in the hippocampus to regulate cognitive memory in rats
inferred← citeshttps://doi.org/10.1016/j.pain.2012.03.006openalex-snapshot
Contribution of PKMζ-dependent and independent amplification to components of experimental neuropathic pain
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2008.10.001openalex-snapshot
Epigenetic principles and mechanisms underlying nervous system functions in health and disease
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2010.07.001openalex-snapshot
Astrocytes and human cognition: Modeling information integration and modulation of neuronal activity
inferred← citeshttps://doi.org/10.1016/j.tins.2013.03.004openalex-snapshot
How to erase memory traces of pain and fear
inferred← citeshttps://doi.org/10.1016/j.ydbio.2022.05.007openalex-snapshot
Polarity proteins: Shaping dendritic spines and memory
inferred← citeshttps://doi.org/10.1016/j.yfrne.2013.07.008openalex-snapshot
Storing maternal memories: Hypothesizing an interaction of experience and estrogen on sensory cortical plasticity to learn infant cues
inferred← citeshttps://doi.org/10.1016/j.ynpai.2020.100049openalex-snapshot
Sex differences in the role of atypical PKC within the basolateral nucleus of the amygdala in a mouse hyperalgesic priming model
inferred← citeshttps://doi.org/10.1016/s0079-6123(07)00002-7openalex-snapshot
Chapter 2 PKMζ, LTP maintenance, and the dynamic molecular biology of memory storage
inferred← citeshttps://doi.org/10.1016/s0079-6123(07)00017-9openalex-snapshot
Chapter 17 New tricks for an old slug: The critical role of postsynaptic mechanisms in learning and memory in Aplysia
inferred← citeshttps://doi.org/10.1017/s0140525x08003403openalex-snapshot
Taste learning in rodents: Compounds and individual taste cues recognition
inferred← citeshttps://doi.org/10.1017/s1745855209006449openalex-snapshot
The Implications of Memory Research and ‘Memory Erasers’: A Conversation with Yadin Dudai
inferred← citeshttps://doi.org/10.1037/a0012993openalex-snapshot
What does it take to demonstrate memory erasure? Theoretical comment on Norrholm et al. (2008).
inferred← citeshttps://doi.org/10.1037/a0014260openalex-snapshot
Peripheral delivery of a ROCK inhibitor improves learning and working memory.
inferred← citeshttps://doi.org/10.1037/a0016343openalex-snapshot
Protein kinase Mzeta maintains fear memory in the amygdala but not in the hippocampus.
inferred← citeshttps://doi.org/10.1037/bne0000140openalex-snapshot
Intracerebellar infusion of the protein kinase M zeta (PKMζ) inhibitor zeta-inhibitory peptide (ZIP) disrupts eyeblink classical conditioning.
inferred← citeshttps://doi.org/10.1038/mp.2017.219openalex-snapshot
Protein kinase Mζ in medial prefrontal cortex mediates depressive-like behavior and antidepressant response
inferred← citeshttps://doi.org/10.1038/nature11802openalex-snapshot
PKM-ζ is not required for hippocampal synaptic plasticity, learning and memory
inferred← citeshttps://doi.org/10.1038/nature11803openalex-snapshot
Prkcz null mice show normal learning and memory
inferred← citeshttps://doi.org/10.1038/ncomms8897openalex-snapshot
Rescue of long-term memory after reconsolidation blockade
inferred← citeshttps://doi.org/10.1038/nn.2531openalex-snapshot
PKMζ maintains memories by regulating GluR2-dependent AMPA receptor trafficking
inferred← citeshttps://doi.org/10.1038/nn.2745openalex-snapshot
Temporary disruption of fear-potentiated startle following PKMζ inhibition in the amygdala
inferred← citeshttps://doi.org/10.1038/nn.3920openalex-snapshot
Visual recognition memory, manifested as long-term habituation, requires synaptic plasticity in V1
inferred← citeshttps://doi.org/10.1038/npp.2009.80openalex-snapshot
Cognitive Flexibility is Associated with KIBRA Variant and Modulated by Recent Tobacco Use
inferred← citeshttps://doi.org/10.1038/npp.2011.63openalex-snapshot
PKMζ Maintains Drug Reward and Aversion Memory in the Basolateral Amygdala and Extinction Memory in the Infralimbic Cortex
inferred← citeshttps://doi.org/10.1038/npp.2012.243openalex-snapshot
A Critical Role for Protein Degradation in the Nucleus Accumbens Core in Cocaine Reward Memory
inferred← citeshttps://doi.org/10.1038/npp.2013.20openalex-snapshot
Memory of Conditioned Taste Aversion Is Erased by Inhibition of PI3K in the Insular Cortex
inferred← citeshttps://doi.org/10.1038/npp.2015.56openalex-snapshot
Overexpression of Protein Kinase Mζ in the Prelimbic Cortex Enhances the Formation of Long-Term Fear Memory
inferred← citeshttps://doi.org/10.1038/nrn.2015.18openalex-snapshot
The right time to learn: mechanisms and optimization of spaced learning
inferred← citeshttps://doi.org/10.1038/nrn2807openalex-snapshot
Modelling the molecular mechanisms of synaptic plasticity using systems biology approaches
inferred← citeshttps://doi.org/10.1038/nrn2949openalex-snapshot
How does PKMζ maintain long-term memory?
inferred← citeshttps://doi.org/10.1038/s41380-024-02521-9openalex-snapshot
Active forgetting and neuropsychiatric diseases
inferred← citeshttps://doi.org/10.1038/s41386-018-0170-1openalex-snapshot
PKMζ in the nucleus accumbens acts to dampen cocaine seeking
inferred← citeshttps://doi.org/10.1038/s41467-020-17484-yopenalex-snapshot
Zeta Inhibitory Peptide attenuates learning and memory by inducing NO-mediated downregulation of AMPA receptors
inferred← citeshttps://doi.org/10.1038/s41467-023-39652-6openalex-snapshot
Blood transcriptomic signatures associated with molecular changes in the brain and clinical outcomes in Parkinson’s disease
inferred← citeshttps://doi.org/10.1038/s41539-019-0048-yopenalex-snapshot
Is plasticity of synapses the mechanism of long-term memory storage?
inferred← citeshttps://doi.org/10.1038/s41583-024-00817-xopenalex-snapshot
Remapping revisited: how the hippocampus represents different spaces
inferred← citeshttps://doi.org/10.1038/s41586-019-0931-yopenalex-snapshot
Neural circuits underlying a psychotherapeutic regimen for fear disorders
inferred← citeshttps://doi.org/10.1038/s41598-019-40823-zopenalex-snapshot
Histone acetylation determines transcription of atypical protein kinases in rat neurons
inferred← citeshttps://doi.org/10.1038/s41598-020-60046-xopenalex-snapshot
Role of prelimbic cortex PKC and PKMζ in fear memory reconsolidation and persistence following reactivation
inferred← citeshttps://doi.org/10.1038/s41598-020-75130-5openalex-snapshot
GSK-3β activation is required for ZIP-induced disruption of learned fear
inferred← citeshttps://doi.org/10.1042/bj20130220openalex-snapshot
Protein kinase C pharmacology: refining the toolbox
inferred← citeshttps://doi.org/10.1042/ns20190019openalex-snapshot
aPKC in neuronal differentiation, maturation and function
inferred← citeshttps://doi.org/10.1073/pnas.0806064106openalex-snapshot
Fos and Jun potentiate individual release sites and mobilize the reserve synaptic-vesicle pool at the Drosophila larval motor synapse
inferred← citeshttps://doi.org/10.1073/pnas.1004433107openalex-snapshot
Drosophila Orb2 targets genes involved in neuronal growth, synapse formation, and protein turnover
inferred← citeshttps://doi.org/10.1073/pnas.1109680108openalex-snapshot
Mechanism for long-term memory formation when synaptic strengthening is impaired
inferred← citeshttps://doi.org/10.1073/pnas.1710819114openalex-snapshot
Noradrenergic activation of the basolateral amygdala maintains hippocampus-dependent accuracy of remote memory
inferred← citeshttps://doi.org/10.1074/jbc.m112.357244openalex-snapshot
Cellular Pharmacology of Protein Kinase Mζ (PKMζ) Contrasts with Its in Vitro Profile
inferred← citeshttps://doi.org/10.1074/jbc.m115.676221openalex-snapshot
Zeta Inhibitory Peptide Disrupts Electrostatic Interactions That Maintain Atypical Protein Kinase C in Its Active Conformation on the Scaffold p62
inferred← citeshttps://doi.org/10.1093/cercor/bhr323openalex-snapshot
Overexpression of PKMζ Alters Morphology and Function of Dendritic Spines in Cultured Cortical Neurons
inferred← citeshttps://doi.org/10.1093/sleep/zsz028openalex-snapshot
Cortical zeta-inhibitory peptide injection reduces local sleep need
inferred← citeshttps://doi.org/10.1097/01.nt.0000357409.96435.26openalex-snapshot
New Data on Memory Molecule Could Benefit Phantom Limb Pain and Other Disorders
inferred← citeshttps://doi.org/10.1097/aln.0b013e31818344daopenalex-snapshot
We Care, Therefore We Are: Anesthesia-related Morbidity and Mortality
inferred← citeshttps://doi.org/10.1098/rstb.2008.0320openalex-snapshot
Predicting not to predict too much: how the cellular machinery of memory anticipates the uncertain future
inferred← citeshttps://doi.org/10.1098/rstb.2013.0140openalex-snapshot
Cellular and subcellular localization of PKMζ
inferred← citeshttps://doi.org/10.1098/rstb.2013.0284openalex-snapshot
How the mechanisms of long-term synaptic potentiation and depression serve experience-dependent plasticity in primary visual cortex
inferred← citeshttps://doi.org/10.1101/2020.02.05.935759openalex-snapshot
Transcriptome analysis of hippocampal subfields identifies gene expression profiles associated with long-term active place avoidance memory
inferred← citeshttps://doi.org/10.1101/825810openalex-snapshot
Distinct roles for motor cortical and thalamic inputs to striatum during motor learning and execution
inferred← citeshttps://doi.org/10.1101/lm.025148.111openalex-snapshot
Inhibiting PKMζ reveals dorsal lateral and dorsal medial striatum store the different memories needed to support adaptive behavior
inferred← citeshttps://doi.org/10.1101/lm.036806.114openalex-snapshot
Frontal neurons modulate memory retrieval across widely varying temporal scales
inferred← citeshttps://doi.org/10.1101/lm.038844.115openalex-snapshot
Atypical PKCs in memory maintenance: the roles of feedback and redundancy
inferred← citeshttps://doi.org/10.1101/lm.042044.116openalex-snapshot
Computational model of a positive BDNF feedback loop in hippocampal neurons following inhibitory avoidance training
inferred← citeshttps://doi.org/10.1101/lm.044362.116openalex-snapshot
Primary auditory cortex regulates threat memory specificity
inferred← citeshttps://doi.org/10.1101/lm.049395.119openalex-snapshot
How can memories last for days, years, or a lifetime? Proposed mechanisms for maintaining synaptic potentiation and memory
inferred← citeshttps://doi.org/10.1101/lm.1139508openalex-snapshot
PKMζ inactivation induces spatial familiarity
inferred← citeshttps://doi.org/10.1101/lm.1183309openalex-snapshot
Boundary conditions for the maintenance of memory by PKMζ in neocortex
inferred← citeshttps://doi.org/10.1101/lm.2026311openalex-snapshot
PKA and PKC are required for long-term but not short-term in vivo operant memory in Aplysia
inferred← citeshttps://doi.org/10.1101/lm.2253311openalex-snapshot
Intra-amygdala ZIP injections impair the memory of learned active avoidance responses and attenuate conditioned taste-aversion acquisition in rats
inferred← citeshttps://doi.org/10.1111/acer.12211openalex-snapshot
Deletion ofPrkczIncreases Intermittent Ethanol Consumption in Mice
inferred← citeshttps://doi.org/10.1111/apha.12921openalex-snapshot
Discovering long‐term potentiation ( LTP ) – recollections and reflections on what came after
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