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Neural Mechanisms of Extinction Learning and Retrieval

https://doi.org/10.1038/sj.npp.1301555
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Psychobiologic Mechanisms of Posttraumatic Stress Disorder
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Cognitive Enhancers as Adjuncts to Psychotherapy
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Differential innervation of parvalbumin-immunoreactive interneurons of the basolateral amygdaloid complex by cortical and intrinsic inputs
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Projections of the ventral subiculum to the amygdala, septum, and hypothalamus: A PHAL anterograde tract‐tracing study in the rat
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The role of NMDA glutamate receptors, PKA, MAPK, and CAMKII in the hippocampus in extinction of conditioned fear
inferredcites →https://doi.org/10.1002/hipo.20144openalex-snapshot
Ventral hippocampal muscimol disrupts context‐specific fear memory retrieval after extinction in rats
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Post‐translational synaptic protein modification as substrate for long‐lasting, remote memory: An initial test
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Combining pharmacotherapy with cognitive behavioral therapy: Traditional and new approaches
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Chronic stress alters dendritic morphology in rat medial prefrontal cortex
inferredcites →https://doi.org/10.1002/syn.10279openalex-snapshot
Differential projections of the infralimbic and prelimbic cortex in the rat
inferredcites →https://doi.org/10.1002/syn.20291openalex-snapshot
Prefrontal infusion of PD098059 immediately after fear extinction training blocks extinction-associated prefrontal synaptic plasticity and decreases prefrontal ERK2 phosphorylation
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Responding for brain stimulation reward in the bed nucleus of the stria terminalis in alcohol‐preferring rats following alcohol and amphetamine pretreatments
inferredcites →https://doi.org/10.1002/syn.20448openalex-snapshot
Time course of extracellular catecholamine and glutamate levels in the rat medial prefrontal cortex during and after extinction of conditioned fear
inferredcites →https://doi.org/10.1007/bf00235901openalex-snapshot
Effect of selective hippocampal lesions in the rat on acquisition, performance, and extinction of bar pressing on a fixed ratio schedule
inferredcites →https://doi.org/10.1007/s00213-004-2121-2openalex-snapshot
Disruption of CB1 receptor signaling impairs extinction of spatial memory in mice
inferredcites →https://doi.org/10.1007/s00213-006-0514-0openalex-snapshot
The cannabinoid receptor agonist WIN 55,212-2 facilitates the extinction of contextual fear memory and spatial memory in rats
inferredcites →https://doi.org/10.1007/s002130050745openalex-snapshot
Evidence that GABA transmission mediates context-specific extinction of learned fear
inferredcites →https://doi.org/10.1007/s10571-005-4009-zopenalex-snapshot
Retrieval and the Extinction of Memory
inferredcites →https://doi.org/10.1016/0013-4694(74)90087-xopenalex-snapshot
Lateral amygdala unit activity: II. Habituating and non-habituating neurons
inferredcites →https://doi.org/10.1016/0014-4886(63)90094-3openalex-snapshot
Conditioning and extinction of a food-rewarded response after selective ablations of frontal cortex in rhesus monkeys
inferredcites →https://doi.org/10.1016/0031-9384(70)90271-4openalex-snapshot
The effect of hippocampal lesions on extinction and “hypothesis” behavior in rats
inferredcites →https://doi.org/10.1016/0031-9384(72)90333-2openalex-snapshot
Effects of septal driving of the hippocampal theta rhythm on resistance to extinction
inferredcites →https://doi.org/10.1016/0304-3940(93)90241-copenalex-snapshot
Extinction of emotional learning: Contribution of medial prefrontal cortex
inferredcites →https://doi.org/10.1016/0306-4522(93)90050-popenalex-snapshot
The intercalated cell masses project to the central and medial nuclei of the amygdala in cats
inferredcites →https://doi.org/10.1016/0306-4522(95)00417-3openalex-snapshot
Projections of the medial and lateral prefrontal cortices to the amygdala: a Phaseolus vulgaris leucoagglutinin study in the rat
inferredcites →https://doi.org/10.1016/0896-6273(95)90092-6openalex-snapshot
Fear conditioning enhances short-latency auditory responses of lateral amygdala neurons: Parallel recordings in the freely behaving rat
inferredcites →https://doi.org/10.1016/j.bbr.2003.09.021openalex-snapshot
Ventral medial prefrontal cortex and emotional perseveration: the memory for prior extinction training
inferredcites →https://doi.org/10.1016/j.bbr.2004.05.016openalex-snapshot
Pre- or post-training administration of the NMDA receptor blocker MK-801 impairs object recognition memory in rats
inferredcites →https://doi.org/10.1016/j.bbr.2005.08.016openalex-snapshot
Temporary inactivation of the medial and basolateral amygdala differentially affects TMT-induced fear behavior in rats
inferredcites →https://doi.org/10.1016/j.bbr.2006.05.012openalex-snapshot
d-Cycloserine facilitates extinction of a cocaine-induced conditioned place preference
inferredcites →https://doi.org/10.1016/j.bbrc.2007.01.125openalex-snapshot
Blockade of amygdala metabotropic glutamate receptor subtype 1 impairs fear extinction
inferredcites →https://doi.org/10.1016/j.biopsych.2005.01.023openalex-snapshot
d-cycloserine facilitates extinction of learned fear: Effects on reacquisition and generalized extinction
inferredcites →https://doi.org/10.1016/j.biopsych.2005.10.012openalex-snapshot
Brain Mechanisms of Fear Extinction: Historical Perspectives on the Contribution of Prefrontal Cortex
inferredcites →https://doi.org/10.1016/j.biopsych.2005.11.005openalex-snapshot
Imaging Genetics: Perspectives from Studies of Genetically Driven Variation in Serotonin Function and Corticolimbic Affective Processing
inferredcites →https://doi.org/10.1016/j.biopsych.2005.12.015openalex-snapshot
Contextual and Temporal Modulation of Extinction: Behavioral and Biological Mechanisms
inferredcites →https://doi.org/10.1016/j.biopsych.2006.03.010openalex-snapshot
Prefrontal Mechanisms in Extinction of Conditioned Fear
inferredcites →https://doi.org/10.1016/j.biopsych.2006.03.084openalex-snapshot
Effects of D-Cycloserine on Extinction: Translation From Preclinical to Clinical Work
inferredcites →https://doi.org/10.1016/j.biopsych.2006.06.004openalex-snapshot
Neurocircuitry Models of Posttraumatic Stress Disorder and Extinction: Human Neuroimaging Research—Past, Present, and Future
inferredcites →https://doi.org/10.1016/j.biopsych.2006.06.022openalex-snapshot
The Promise of Extinction Research for the Prevention and Treatment of Anxiety Disorders
inferredcites →https://doi.org/10.1016/j.biopsych.2006.10.011openalex-snapshot
Recall of Fear Extinction in Humans Activates the Ventromedial Prefrontal Cortex and Hippocampus in Concert
inferredcites →https://doi.org/10.1016/j.biopsych.2007.04.032openalex-snapshot
A Role for the Human Dorsal Anterior Cingulate Cortex in Fear Expression
inferredcites →https://doi.org/10.1016/j.biopsycho.2006.01.006openalex-snapshot
Extending animal models of fear conditioning to humans
inferredcites →https://doi.org/10.1016/j.biopsycho.2006.01.008openalex-snapshot
Fear extinction in rats: Implications for human brain imaging and anxiety disorders
inferredcites →https://doi.org/10.1016/j.brat.2004.03.013openalex-snapshot
Reinstatement of fear responses in human aversive conditioning
inferredcites →https://doi.org/10.1016/j.brat.2006.07.005openalex-snapshot
A randomized controlled trial of the effect of d-cycloserine on extinction and fear conditioning in humans
inferredcites →https://doi.org/10.1016/j.conb.2005.10.005openalex-snapshot
Fear extinction in rodents: basic insight to clinical promise
inferredcites →https://doi.org/10.1016/j.conb.2006.07.004openalex-snapshot
Prefrontal involvement in the regulation of emotion: convergence of rat and human studies
inferredcites →https://doi.org/10.1016/j.jpsychires.2006.05.006openalex-snapshot
A randomized controlled trial of the effect of d-cycloserine on exposure therapy for spider fear
inferredcites →https://doi.org/10.1016/j.jpsychires.2007.05.006openalex-snapshot
Effect of post-retrieval propranolol on psychophysiologic responding during subsequent script-driven traumatic imagery in post-traumatic stress disorder
inferredcites →https://doi.org/10.1016/j.neulet.2003.07.012openalex-snapshot
Effects of acetylcholine antagonist injection into the prefrontal cortex on the progress of lever-press extinction in rats
inferredcites →https://doi.org/10.1016/j.neuron.2004.08.042openalex-snapshot
Extinction Learning in Humans
inferredcites →https://doi.org/10.1016/j.neuron.2005.09.025openalex-snapshot
Contributions of the Amygdala to Emotion Processing: From Animal Models to Human Behavior
inferredcites →https://doi.org/10.1016/j.neuron.2005.10.029openalex-snapshot
A Specialized Subclass of Interneurons Mediates Dopaminergic Facilitation of Amygdala Function
inferredcites →https://doi.org/10.1016/j.neuron.2007.02.021openalex-snapshot
Consolidation of Fear Extinction Requires NMDA Receptor-Dependent Bursting in the Ventromedial Prefrontal Cortex
inferredcites →https://doi.org/10.1016/j.neuroscience.2004.01.006openalex-snapshot
Chronic behavioral stress induces apical dendritic reorganization in pyramidal neurons of the medial prefrontal cortex
inferredcites →https://doi.org/10.1016/j.neuroscience.2004.08.018openalex-snapshot
Disruption of reconsolidation but not consolidation of auditory fear conditioning by noradrenergic blockade in the amygdala
inferredcites →https://doi.org/10.1016/j.neuroscience.2005.01.020openalex-snapshot
Infralimbic cortex activation increases c-fos expression in intercalated neurons of the amygdala
inferredcites →https://doi.org/10.1016/j.neuroscience.2005.02.043openalex-snapshot
The lateral amygdala processes the value of conditioned and unconditioned aversive stimuli
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.07.025openalex-snapshot
On the participation of hippocampal p38 mitogen-activated protein kinase in extinction and reacquisition of inhibitory avoidance memory
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.08.003openalex-snapshot
Prolonged behavioral stress enhances synaptic connectivity in the basolateral amygdala
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.12.014openalex-snapshot
Network model of fear extinction and renewal functional pathways
inferredcites →https://doi.org/10.1016/j.neuroscience.2007.03.025openalex-snapshot
The role of different subregions of the basolateral amygdala in cue-induced reinstatement and extinction of food-seeking behavior
inferredcites →https://doi.org/10.1016/j.neuroscience.2007.03.042openalex-snapshot
Controllable versus uncontrollable stressors bi-directionally modulate conditioned but not innate fear
inferredcites →https://doi.org/10.1016/j.nlm.2005.01.001openalex-snapshot
Effects of multiple exposures to d-cycloserine on extinction of conditioned fear in rats
inferredcites →https://doi.org/10.1016/j.nlm.2005.10.001openalex-snapshot
The entorhinal cortex plays a role in extinction
inferredcites →https://doi.org/10.1016/j.nlm.2005.10.005openalex-snapshot
Chronic stress impairs recall of extinction of conditioned fear
inferredcites →https://doi.org/10.1016/j.nlm.2005.12.008openalex-snapshot
Enhancement of extinction memory consolidation: The role of the noradrenergic and GABAergic systems within the basolateral amygdala
inferredcites →https://doi.org/10.1016/j.nlm.2006.08.003openalex-snapshot
Hippocampal Mek/Erk signaling mediates extinction of contextual freezing behavior
inferredcites →https://doi.org/10.1016/j.nlm.2006.08.009openalex-snapshot
Methylene blue facilitates the extinction of fear in an animal model of susceptibility to learned helplessness
inferredcites →https://doi.org/10.1016/j.nlm.2006.11.007openalex-snapshot
Amygdala upregulation of NCAM polysialylation induced by auditory fear conditioning is not required for memory formation, but plays a role in fear extinction
inferredcites →https://doi.org/10.1016/j.nlm.2006.12.010openalex-snapshot
Effects of d-cycloserine on extinction of learned fear to an olfactory cue
inferredcites →https://doi.org/10.1016/j.nlm.2007.03.004openalex-snapshot
A developmental dissociation in reinstatement of an extinguished fear response in rats
inferredcites →https://doi.org/10.1016/j.pbb.2005.03.005openalex-snapshot
Extinction and reacquisition of a fear-motivated memory require activity of the Src family of tyrosine kinases in the CA1 region of the hippocampus
inferredcites →https://doi.org/10.1016/j.pneurobio.2006.08.003openalex-snapshot
PSA-NCAM in mammalian structural plasticity and neurogenesis
inferredcites →https://doi.org/10.1016/j.tics.2006.02.011openalex-snapshot
Genetics of emotional regulation: the role of the serotonin transporter in neural function
inferredcites →https://doi.org/10.1016/j.tins.2004.11.001openalex-snapshot
Mechanisms of memory stabilization: are consolidation and reconsolidation similar or distinct processes?
inferredcites →https://doi.org/10.1016/j.tins.2004.11.006openalex-snapshot
Post-translational protein modification as the substrate for long-lasting memory
inferredcites →https://doi.org/10.1016/s0006-3223(99)00144-4openalex-snapshot
Psychophysiologic assessment of aversive conditioning in posttraumatic stress disorder
inferredcites →https://doi.org/10.1016/s0006-8993(00)03013-4openalex-snapshot
Efferent projections of infralimbic and prelimbic areas of the medial prefrontal cortex in the Japanese monkey, Macaca fuscata
inferredcites →https://doi.org/10.1016/s0149-7634(99)00016-0openalex-snapshot
The neuroanatomical and neurochemical basis of conditioned fear
inferredcites →https://doi.org/10.1016/s0166-2236(02)02231-2openalex-snapshot
An emerging molecular and cellular framework for memory processing by the hippocampus
inferredcites →https://doi.org/10.1016/s0166-2236(98)01240-5openalex-snapshot
Intrinsic circuitry of the amygdaloid complex: common principles of organization in rats and cats
inferredcites →https://doi.org/10.1016/s0166-4328(98)00119-3openalex-snapshot
Effects of excitotoxic lesions of the basolateral amygdala on conditional discrimination learning with primary and conditioned reinforcement
inferredcites →https://doi.org/10.1016/s0306-4522(02)00446-3openalex-snapshot
Pathways for emotion: interactions of prefrontal and anterior temporal pathways in the amygdala of the rhesus monkey
inferredcites →https://doi.org/10.1016/s0306-4522(02)00455-4openalex-snapshot
Bidirectional synaptic plasticity in intercalated amygdala neurons and the extinction of conditioned fear responses
inferredcites →https://doi.org/10.1016/s0306-4522(96)00478-2openalex-snapshot
Projections of the lateral entorhinal cortex to the amygdala: a Phaseolus vulgaris leucoagglutinin study in the rat
inferredcites →https://doi.org/10.1016/s0896-6273(00)80375-xopenalex-snapshot
Fear Conditioning Enhances Different Temporal Components of Tone-Evoked Spike Trains in Auditory Cortex and Lateral Amygdala
inferredcites →https://doi.org/10.1016/s0896-6273(00)80475-4openalex-snapshot
Human Amygdala Activation during Conditioned Fear Acquisition and Extinction: a Mixed-Trial fMRI Study
inferredcites →https://doi.org/10.1016/s0896-6273(03)00352-0openalex-snapshot
Protein Synthesis Subserves Reconsolidation or Extinction Depending on Reminder Duration
inferredcites →https://doi.org/10.1016/s0896-6273(03)00728-1openalex-snapshot
Auditory-Evoked Spike Firing in the Lateral Amygdala and Pavlovian Fear Conditioning
inferredcites →https://doi.org/10.1016/s0959-4388(00)00078-7openalex-snapshot
Classical fear conditioning in functional neuroimaging
inferredcites →https://doi.org/10.1016/s0959-4388(02)00305-7openalex-snapshot
Molecular bases of long-term memories: a question of persistence
inferredcites →https://doi.org/10.1016/s1074-7427(03)00003-0openalex-snapshot
Memory extinction requires gene expression in rat hippocampus
inferredcites →https://doi.org/10.1017/s0033291703001612openalex-snapshot
Estimating post-traumatic stress disorder in the community: lifetime perspective and the impact of typical traumatic events
inferredcites →https://doi.org/10.1017/s1092852900020915openalex-snapshot
Recalling Safety: Cooperative Functions of the Ventromedial Prefrontal Cortex and the Hippocampus in Extinction
inferredcites →https://doi.org/10.1037//0021-843x.109.2.290openalex-snapshot
De novo conditioning in trauma-exposed individuals with and without posttraumatic stress disorder.
inferredcites →https://doi.org/10.1037//0033-2909.114.1.80openalex-snapshot
Context, time, and memory retrieval in the interference paradigms of Pavlovian learning.
inferredcites →https://doi.org/10.1037//0097-7403.5.4.368openalex-snapshot
Role of conditioned contextual stimuli in reinstatement of extinguished fear.
inferredcites →https://doi.org/10.1037//0735-7044.109.5.828openalex-snapshot
The role of the rat hippocampal system in several effects of context in extinction.
inferredcites →https://doi.org/10.1037//0735-7044.110.3.618openalex-snapshot
The NMDA antagonist MK-801 blocks the extinction of Pavlovian fear conditioning.
inferredcites →https://doi.org/10.1037//0735-7044.111.4.683openalex-snapshot
Functional inactivation of the lateral and basal nuclei of the amygdala by muscimol infusion prevents fear conditioning to an explicit conditioned stimulus and to contextual stimuli.
inferredcites →https://doi.org/10.1037//0735-7044.111.4.712openalex-snapshot
Normal conditioning inhibition and extinction of freezing and fear-potentiated startle following electrolytic lesions of medial prefrontal cortex in rats.
inferredcites →https://doi.org/10.1037//0735-7044.114.2.227openalex-snapshot
The effects of neurotoxic hippocampal lesions on two effects of context after fear extinction.
inferredcites →https://doi.org/10.1037//0735-7044.114.6.1058openalex-snapshot
Cortical involvement in acquisition and extinction of trace eyeblink conditioning.
inferredcites →https://doi.org/10.1037/0003-066x.61.8.741openalex-snapshot
Neural systems involved in fear and anxiety measured with fear-potentiated startle.
inferredcites →https://doi.org/10.1037/0097-7403.1.1.88openalex-snapshot
Reinstatement of fear to an extinguished conditioned stimulus.
inferredcites →https://doi.org/10.1037/0735-7044.109.4.681openalex-snapshot
Differential contribution of dorsal and ventral medial prefrontal cortex to the acquisition and extinction of conditioned fear in rats.
inferredcites →https://doi.org/10.1037/0735-7044.111.4.712openalex-snapshot
Normal conditioned inhibition and extinction of freezing and fear-potentiated startle following electrolytic lesions of medial prefrontal cortex in rats.
inferredcites →https://doi.org/10.1037/0735-7044.117.2.341openalex-snapshot
Effects of D-cycloserine on extinction of conditioned freezing.
inferredcites →https://doi.org/10.1037/0735-7044.117.6.1292openalex-snapshot
Opioid Receptors Regulate the Extinction of Pavlovian Fear Conditioning.
inferredcites →https://doi.org/10.1037/0735-7044.118.1.111openalex-snapshot
Blocking, Unblocking, and Overexpectation of Fear: A Role for Opioid Receptors in the Regulation of Pavlovian Association Formation.
inferredcites →https://doi.org/10.1037/0735-7044.118.2.389openalex-snapshot
Electrical Stimulation of Medial Prefrontal Cortex Reduces Conditioned Fear in a Temporally Specific Manner.
inferredcites →https://doi.org/10.1037/0735-7044.119.4.1023openalex-snapshot
The midbrain periaqueductal gray and fear extinction: Opioid receptor subtype and roles of cyclic AMP, protein kinase A, and mitogen-activated protein kinase.
inferredcites →https://doi.org/10.1037/0735-7044.119.6.1496openalex-snapshot
Single neurons in the medial prefrontal cortex of the rat exhibit tonic and phasic coding during trace fear conditioning.
inferredcites →https://doi.org/10.1037/0735-7044.119.6.1672openalex-snapshot
Facilitation of fear extinction by midbrain periaqueductal gray infusions of rb101(s), an inhibitor of enkephalin-degrading enzymes.
inferredcites →https://doi.org/10.1037/0735-7044.120.5.1159openalex-snapshot
D-cycloserine facilitates extinction but does not eliminate renewal of the conditioned emotional response.
inferredcites →https://doi.org/10.1037/0735-7044.121.1.131openalex-snapshot
A developmental dissociation of context and GABA effects on extinguished fear in rats.
inferredcites →https://doi.org/10.1037/0735-7044.121.3.501openalex-snapshot
The effect of yohimbine on the extinction of conditioned fear: A role for context.
inferredcites →https://doi.org/10.1037/h0026470openalex-snapshot
Hippocampus and internal inhibition.
inferredcites →https://doi.org/10.1037/h0077311openalex-snapshot
Effects of selective forebrain noradrenaline loss on behavioral inhibition in the rat.
inferredcites →https://doi.org/10.1037/h0088009openalex-snapshot
Behavioral changes associated with ablation of the amygdaloid complex in monkeys.
inferredcites →https://doi.org/10.1038/35021052openalex-snapshot
Fear memories require protein synthesis in the amygdala for reconsolidation after retrieval
inferredcites →https://doi.org/10.1038/89512openalex-snapshot
Two different lateral amygdala cell populations contribute to the initiation and storage of memory
inferredcites →https://doi.org/10.1038/nature00839openalex-snapshot
The endogenous cannabinoid system controls extinction of aversive memories
inferredcites →https://doi.org/10.1038/nature01138openalex-snapshot
Neurons in medial prefrontal cortex signal memory for fear extinction
inferredcites →https://doi.org/10.1038/nn1314openalex-snapshot
Human orbitofrontal cortex mediates extinction learning while accessing conditioned representations of value
inferredcites →https://doi.org/10.1038/nn1366openalex-snapshot
Amygdala-prefrontal coupling depends on a genetic variation of the serotonin transporter
inferredcites →https://doi.org/10.1038/nn1431openalex-snapshot
αCaMKII autophosphorylation contributes to rapid learning but is not necessary for memory
inferredcites →https://doi.org/10.1038/nn1463openalex-snapshot
5-HTTLPR polymorphism impacts human cingulate-amygdala interactions: a genetic susceptibility mechanism for depression
inferredcites →https://doi.org/10.1038/nn1718openalex-snapshot
Amygdala BDNF signaling is required for consolidation but not encoding of extinction
inferredcites →https://doi.org/10.1038/nn1943openalex-snapshot
A hippocampal Cdk5 pathway regulates extinction of contextual fear
inferredcites →https://doi.org/10.1038/nn958openalex-snapshot
Smaller hippocampal volume predicts pathologic vulnerability to psychological trauma
inferredcites →https://doi.org/10.1038/nrn1535openalex-snapshot
Neuronal signalling of fear memory
inferredcites →https://doi.org/10.1038/nrn2090openalex-snapshot
Molecular mechanisms of memory reconsolidation
inferredcites →https://doi.org/10.1038/sj.mp.4001939openalex-snapshot
Mechanisms of fear extinction
inferredcites →https://doi.org/10.1038/sj.mp.4001957openalex-snapshot
Hippocampus-specific deletion of BDNF in adult mice impairs spatial memory and extinction of aversive memories
inferredcites →https://doi.org/10.1038/sj.npp.1300066openalex-snapshot
Prefrontocortical Dopamine Loss in Rats Delays Long-Term Extinction of Contextual Conditioned Fear, and Reduces Social Interaction Without Affecting Short-Term Social Interaction Memory
inferredcites →https://doi.org/10.1038/sj.npp.1300655openalex-snapshot
Enhancing Cannabinoid Neurotransmission Augments the Extinction of Conditioned Fear
inferredcites →https://doi.org/10.1038/sj.npp.1300899openalex-snapshot
Systemic and Intra-Amygdala Administration of Glucocorticoid Agonist and Antagonist Modulate Extinction of Conditioned Fear
inferredcites →https://doi.org/10.1038/sj.npp.1301215openalex-snapshot
Glutamate NMDA Receptors within the Amygdala Participate in the Modulatory Effect of Glucocorticoids on Extinction of Conditioned Fear in Rats
inferredcites →https://doi.org/10.1038/sj.npp.1301224openalex-snapshot
Inhibition of Fatty-Acid Amide Hydrolase Accelerates Acquisition and Extinction Rates in a Spatial Memory Task
inferredcites →https://doi.org/10.1038/sj.npp.1301316openalex-snapshot
Acquisition of Fear Extinction Requires Activation of NR2B-Containing NMDA Receptors in the Lateral Amygdala
inferredcites →https://doi.org/10.1073/pnas.0502441102openalex-snapshot
Thickness of ventromedial prefrontal cortex in humans is correlated with extinction memory
inferredcites →https://doi.org/10.1073/pnas.0504011102openalex-snapshot
Stress duration modulates the spatiotemporal patterns of spine formation in the basolateral amygdala
inferredcites →https://doi.org/10.1073/pnas.0509184103openalex-snapshot
Glucocorticoids reduce phobic fear in humans
inferredcites →https://doi.org/10.1073/pnas.211433298openalex-snapshot
Retrieval of memory for fear-motivated training initiates extinction requiring protein synthesis in the rat hippocampus
inferredcites →https://doi.org/10.1080/02724990344000097openalex-snapshot
Experimental extinction in Pavlovian conditioning: Behavioural and neuroscience perspectives
inferredcites →https://doi.org/10.1093/cercor/bhi048openalex-snapshot
Mild, Short-term Stress Alters Dendritic Morphology in Rat Medial Prefrontal Cortex
inferredcites →https://doi.org/10.1093/cercor/bhi104openalex-snapshot
Repeated Stress Induces Dendritic Spine Loss in the Rat Medial Prefrontal Cortex
inferredcites →https://doi.org/10.1093/oso/9780198505013.003.0006openalex-snapshot
The role of the amygdala in conditioned and unconditioned fear and anxiety
inferredcites →https://doi.org/10.1093/oxfordjournals.bmb.a071789openalex-snapshot
DISTRIBUTION AND PHYSIOLOGICAL SIGNIFICANCE OF OPIOID RECEPTORS IN THE BRAIN
inferredcites →https://doi.org/10.1097/01.wnr.0000186599.66243.50openalex-snapshot
Orbitofrontal thickness, retention of fear extinction, and extraversion
inferredcites →https://doi.org/10.1097/01.wnr.0000201509.53750.bcopenalex-snapshot
A role for the prefrontal cortex in recall of recent and remote memories
inferredcites →https://doi.org/10.1097/01.wnr.0000220142.29413.6fopenalex-snapshot
Prefrontal dopamine D4 receptors are involved in encoding fear extinction
inferredcites →https://doi.org/10.1101/lm.119806openalex-snapshot
Different mechanisms of fear extinction dependent on length of time since fear acquisition
inferredcites →https://doi.org/10.1101/lm.191706openalex-snapshot
Extinction of conditioned taste aversion depends on functional protein synthesis but not on NMDA receptor activation in the ventromedial prefrontal cortex
inferredcites →https://doi.org/10.1101/lm.204806openalex-snapshot
Hippocampal train stimulation modulates recallof fear extinction independently of prefrontalcortex synaptic plasticity and lesions
inferredcites →https://doi.org/10.1101/lm.304606openalex-snapshot
Amnesia or retrieval deficit? Implications of a molecular approach to the question of reconsolidation
inferredcites →https://doi.org/10.1101/lm.306106openalex-snapshot
Microstimulation reveals opposing influences of prelimbic and infralimbic cortex on the expression of conditioned fear
inferredcites →https://doi.org/10.1101/lm.38101openalex-snapshot
Damage to the Lateral and Central, but Not Other, Amygdaloid Nuclei Prevents the Acquisition of Auditory Fear Conditioning
inferredcites →https://doi.org/10.1101/lm.477007openalex-snapshot
Hippocampal regulation of context-dependent neuronal activity in the lateral amygdala
inferredcites →https://doi.org/10.1101/lm.500907openalex-snapshot
Histone modifications around individual BDNF gene promoters in prefrontal cortex are associated with extinction of conditioned fear
inferredcites →https://doi.org/10.1101/lm.53303openalex-snapshot
Activation of the Cannabinoid Receptor Type 1 Decreases Glutamatergic and GABAergic Synaptic Transmission in the Lateral Amygdala of the Mouse
inferredcites →https://doi.org/10.1101/lm.54706openalex-snapshot
Differential involvement of the central amygdala in appetitive versus aversive learning
inferredcites →https://doi.org/10.1101/lm.60406openalex-snapshot
Electrolytic lesions of the medial prefrontal cortex do not interfere with long-term memory of extinction of conditioned fear
inferredcites →https://doi.org/10.1101/lm.625407openalex-snapshot
Reorganization of learning-associated prefrontal synaptic plasticity between the recall of recent and remote fear extinction memory
inferredcites →https://doi.org/10.1101/lm.7.2.97openalex-snapshot
Differential Fear Conditioning Induces Reciprocal Changes in the Sensory Responses of Lateral Amygdala Neurons to the CS+ and CS−
inferredcites →https://doi.org/10.1101/lm.71504openalex-snapshot
Adrenergic Transmission Facilitates Extinction of Conditional Fear in Mice
inferredcites →https://doi.org/10.1101/lm.77704openalex-snapshot
Postextinction Infusion of a Mitogen-Activated Protein Kinase Inhibitor Into the Medial Prefrontal Cortex Impairs Memory of the Extinction of Conditioned Fear
inferredcites →https://doi.org/10.1101/lm.77904openalex-snapshot
CB1 Cannabinoid Receptors Modulate Kinase and Phosphatase Activity During Extinction of Conditioned Fear in Mice
inferredcites →https://doi.org/10.1101/lm.78304openalex-snapshot
Like Extinction, Latent Inhibition of Conditioned Fear in Mice Is Blocked by Systemic Inhibition of L-Type Voltage-Gated Calcium Channels
inferredcites →https://doi.org/10.1101/lm.78604openalex-snapshot
Delayed Recall of Fear Extinction in Rats With Lesions of Ventral Medial Prefrontal Cortex
inferredcites →https://doi.org/10.1101/lm.78704openalex-snapshot
Factors Regulating the Effects of Hippocampal Inactivation on Renewal of Conditional Fear After Extinction
inferredcites →https://doi.org/10.1101/lm.79504openalex-snapshot
Emotional Perseveration: An Update on Prefrontal-Amygdala Interactions in Fear Extinction
inferredcites →https://doi.org/10.1101/lm.79704openalex-snapshot
Lesions of Rat Infralimbic Cortex Enhance Recovery and Reinstatement of an Appetitive Pavlovian Response
inferredcites →https://doi.org/10.1101/lm.82404openalex-snapshot
Extinction Memory Improvement by the Metabolic Enhancer Methylene Blue
inferredcites →https://doi.org/10.1101/lm.86104openalex-snapshot
Nonassociative learning processes determine expression and extinction of conditioned fear in mice
inferredcites →https://doi.org/10.1101/lm.91705openalex-snapshot
Electrolytic lesions of the dorsal hippocampus disrupt renewal of conditional fear after extinction
inferredcites →https://doi.org/10.1101/lm.96605openalex-snapshot
Systemic blockade of D2-like dopamine receptors facilitates extinction of conditioned fear in mice
inferredcites →https://doi.org/10.1101/sqb.1996.061.01.027openalex-snapshot
inferredcites →https://doi.org/10.1111/j.1460-9568.2004.03542.xopenalex-snapshot
Resistance to extinction is associated with impaired immediate early gene induction in medial prefrontal cortex and amygdala
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04272.xopenalex-snapshot
NMDA‐receptor blockade by CPP impairs post‐training consolidation of a rapidly acquired spatial representation in rat hippocampus
inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04434.xopenalex-snapshot
Opposing effects of amygdala and orbital prefrontal cortex lesions on the extinction of instrumental responding in macaque monkeys
inferredcites →https://doi.org/10.1111/j.1460-9568.2006.04603.xopenalex-snapshot
Enhancement of conditioned fear extinction by infusion of the GABAA agonist muscimol into the rat prefrontal cortex and amygdala
inferredcites →https://doi.org/10.1111/j.1460-9568.2006.04893.xopenalex-snapshot
Extinction of auditory fear conditioning requires MAPK/ERK activation in the basolateral amygdala
inferredcites →https://doi.org/10.1111/j.1460-9568.2006.04907.xopenalex-snapshot
Extinction is not a sufficient condition to prevent fear memories from undergoing reconsolidation in the basolateral amygdala
inferredcites →https://doi.org/10.1111/j.1460-9568.2006.05014.xopenalex-snapshot
Inactivation of the ventromedial prefrontal cortex reduces expression of conditioned fear and impairs subsequent recall of extinction
inferredcites →https://doi.org/10.1111/j.1460-9568.2007.05486.xopenalex-snapshot
Lesions of rat infralimbic cortex enhance renewal of extinguished appetitive Pavlovian responding
inferredcites →https://doi.org/10.1111/j.1527-3458.2006.00208.xopenalex-snapshot
Augmentation Treatment of Psychotherapy for Anxiety Disorders with D‐Cycloserine
inferredcites →https://doi.org/10.1111/j.1749-6632.2001.tb05830.xopenalex-snapshot
Plasticity of the Hippocampus: Adaptation to Chronic Stress and Allostatic Load
inferredcites →https://doi.org/10.1113/jphysiol.2004.063792openalex-snapshot
Extrasynaptic NR2B and NR2D subunits of NMDA receptors shape ‘superslow’ afterburst EPSC in rat hippocampus
inferredcites →https://doi.org/10.1124/mi.6.6.7openalex-snapshot
Animal Models and Brain Circuits in Drug Addiction
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.287.5451.248openalex-snapshot
Memory--a Century of Consolidation
inferredcites →https://doi.org/10.1126/science.290.5494.1170openalex-snapshot
NMDA Receptor-Dependent Synaptic Reinforcement as a Crucial Process for Memory Consolidation
inferredcites →https://doi.org/10.1146/annurev.ne.11.030188.001553openalex-snapshot
Behavioral Studies Of Pavlovian Conditioning
inferredcites →https://doi.org/10.1146/annurev.neuro.23.1.155openalex-snapshot
Emotion Circuits in the Brain
inferredcites →https://doi.org/10.1152/jn.00153.2004openalex-snapshot
New Vistas on Amygdala Networks in Conditioned Fear
inferredcites →https://doi.org/10.1152/jn.1972.35.2.202openalex-snapshot
Learning centers of rat brain mapped by measuring latencies of conditioned unit responses.
showing the first 200 of 248

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4099079openalex-extracted
Basal Amygdala Inputs to the Medial Prefrontal Cortex Mediate Fear Memory Strengthening
inferred← citeshttps://doi.org/10.2139/ssrn.4121839openalex-extracted
A Critical Role for Touch Neurons in a Skin-Brain Pathway for Stress Resilience
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inferred← citeshttps://doi.org/10.1001/jamapsychiatry.2013.1openalex-snapshot
Neuronal Network Plasticity and Recovery From Depression
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Effect of a Brief Memory Updating Intervention on Smoking Behavior
inferred← citeshttps://doi.org/10.1002/0471142301.ns0823s47openalex-snapshot
Fear Extinction in Rodents
inferred← citeshttps://doi.org/10.1002/9780470015902.a0024010openalex-snapshot
Impulsivity and Anxiety
inferred← citeshttps://doi.org/10.1002/9780470478509.neubb002039openalex-snapshot
Neural Basis of Fear Conditioning
inferred← citeshttps://doi.org/10.1002/9781118083222.ch10openalex-snapshot
Chronic Stress Effects on Corticolimbic Morphology
inferred← citeshttps://doi.org/10.1002/9781118083222.ch11openalex-snapshot
Effects of Chronic Stress on Memory and Neuroplasticity: Animal Studies
inferred← citeshttps://doi.org/10.1002/9781118083222.ch21openalex-snapshot
Stress and Glucocorticoid Effects on Memory
inferred← citeshttps://doi.org/10.1002/9781118315088.ch5openalex-snapshot
Neurobiology of Paediatric Anxiety
inferred← citeshttps://doi.org/10.1002/9781118381953.ch10openalex-snapshot
Systems neuroscience
inferred← citeshttps://doi.org/10.1002/9781118468135.ch6openalex-snapshot
Pavlovian Fear Conditioning
inferred← citeshttps://doi.org/10.1002/9781118650813.ch2openalex-snapshot
The Determining Conditions for Pavlovian Learning
inferred← citeshttps://doi.org/10.1002/9781118775349.ch45openalex-snapshot
Specific Phobias: Assessment and Treatment
inferred← citeshttps://doi.org/10.1002/9781119159193.ch4openalex-snapshot
Computational Models of Post‐traumatic Stress Disorder ( PTSD )
inferred← citeshttps://doi.org/10.1002/9781119170174.epcn102openalex-snapshot
The Cognitive Neuroscience of Fear Learning
inferred← citeshttps://doi.org/10.1002/9781119170174.epcn415openalex-snapshot
Explicit and Implicit Emotion Regulation
inferred← citeshttps://doi.org/10.1002/9781119375487.ch6openalex-snapshot
Neuroscience‐Informed Counseling Theory
inferred← citeshttps://doi.org/10.1002/9781119945901.ch7openalex-snapshot
Cortisol
inferred← citeshttps://doi.org/10.1002/9781394258963.refsopenalex-snapshot
References
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Hippocampal circuits underlie improvements in self‐reported anxiety following mindfulness training
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A Brief Guide to Studying Fear in Developing Rodents: Important Considerations and Common Pitfalls
inferred← citeshttps://doi.org/10.1002/cpz1.1040openalex-snapshot
Minimizing Variability in Developmental Fear Studies in Mice: Toward Improved Replicability in the Field
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Integrating research on development and fear learning: a vision for clinical neuroscience?
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Development of anxiety: the role of threat appraisal and fear learning
inferred← citeshttps://doi.org/10.1002/da.22219openalex-snapshot
GLUCOCORTICOIDS ENHANCE IN VIVO EXPOSURE-BASED THERAPY OF SPIDER PHOBIA
inferred← citeshttps://doi.org/10.1002/da.22449openalex-snapshot
TAKING THE PULSE OF PROLONGED EXPOSURE THERAPY: PHYSIOLOGICAL REACTIVITY TO TRAUMA IMAGERY AS AN OBJECTIVE MEASURE OF TREATMENT RESPONSE
inferred← citeshttps://doi.org/10.1002/da.22470openalex-snapshot
Amygdala-Cortical Connectivity: Associations with Anxiety, Development, and Threat
inferred← citeshttps://doi.org/10.1002/da.22583openalex-snapshot
Brain activation during fear extinction predicts exposure success
inferred← citeshttps://doi.org/10.1002/da.22678openalex-snapshot
COMT val158met polymorphism links to altered fear conditioning and extinction are modulated by PTSD and childhood trauma
inferred← citeshttps://doi.org/10.1002/da.23187openalex-snapshot
Altered fronto‐amygdalar functional connectivity predicts response to cognitive behavioral therapy in pediatric obsessive‐compulsive disorder
inferred← citeshttps://doi.org/10.1002/dev.20429openalex-snapshot
Animal models of early life stress: Implications for understanding resilience
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Animal models of early life stress: Implications for understanding resilience
inferred← citeshttps://doi.org/10.1002/dev.20531openalex-snapshot
Human amygdala development in the absence of species‐expected caregiving
inferred← citeshttps://doi.org/10.1002/dev.21437openalex-snapshot
Early weaning impairs fear extinction and decreases brain‐derived neurotrophic factor expression in the prefrontal cortex of adult male C57BL/6 mice
inferred← citeshttps://doi.org/10.1002/dev.22189openalex-snapshot
Return of fear following extinction in youth: An event‐related potential study
inferred← citeshttps://doi.org/10.1002/dev.70103openalex-snapshot
Racial Discrimination and Fear‐Based Symptoms: Links to Avoidance Behavior and Hippocampal Activity in Black Youth
inferred← citeshttps://doi.org/10.1002/dta.1377openalex-snapshot
Mitigation of post‐traumatic stress symptoms by Cannabis resin: A review of the clinical and neurobiological evidence
inferred← citeshttps://doi.org/10.1002/erv.1090openalex-snapshot
Eating in eating disorders
inferred← citeshttps://doi.org/10.1002/hbm.20769openalex-snapshot
Time‐varied characteristics of acupuncture effects in fMRI studies
inferred← citeshttps://doi.org/10.1002/hbm.20791openalex-snapshot
Contingency learning in human fear conditioning involves the ventral striatum
inferred← citeshttps://doi.org/10.1002/hbm.21120openalex-snapshot
Amygdala and hippocampus volumetry and diffusivity in relation to dreaming
inferred← citeshttps://doi.org/10.1002/hbm.22639openalex-snapshot
Neural substrates of approach‐avoidance conflict decision‐making
inferred← citeshttps://doi.org/10.1002/hbm.22837openalex-snapshot
Neural circuitry underlying effects of context on human pain-related fear extinction in a renewal paradigm
inferred← citeshttps://doi.org/10.1002/hbm.24915openalex-snapshot
Amygdala and nucleus accumbens involvement in appetitive extinction
inferred← citeshttps://doi.org/10.1002/hipo.20534openalex-snapshot
A behavioral analysis of the impact of voluntary physical activity on hippocampus‐dependent contextual conditioning
inferred← citeshttps://doi.org/10.1002/hipo.22669openalex-snapshot
Environmental enrichment and physical exercise revert behavioral and electrophysiological impairments caused by reduced adult neurogenesis
inferred← citeshttps://doi.org/10.1002/hipo.22738openalex-snapshot
Brain structural connectivity and context‐dependent extinction memory
inferred← citeshttps://doi.org/10.1002/hipo.22826openalex-snapshot
Involvement of the dorsal hippocampus in expression and extinction of cocaine‐induced conditioned place preference
inferred← citeshttps://doi.org/10.1002/hipo.23187openalex-snapshot
A computational model of systems memory consolidation and reconsolidation
inferred← citeshttps://doi.org/10.1002/hipo.23601openalex-snapshot
Distinct engrams control fear and extinction memory
inferred← citeshttps://doi.org/10.1002/jnr.22252openalex-snapshot
Fear learning and extinction are linked to neuronal plasticity through Rin1 signaling
inferred← citeshttps://doi.org/10.1002/jnr.23591openalex-snapshot
Positive effects of the traditional C hinese medicine MLC 901 in cognitive tasks
inferred← citeshttps://doi.org/10.1002/jnr.24860openalex-snapshot
A common genetic variant in fatty acid amide hydrolase is linked to alterations in fear extinction neural circuitry in a racially diverse, nonclinical sample of adults
inferred← citeshttps://doi.org/10.1002/jnr.25012openalex-snapshot
The role of cannabinoids in shaping lifespan neurodevelopment
inferred← citeshttps://doi.org/10.1002/jnr.25017openalex-snapshot
Hallucinogenic drugs and their potential for treating fear‐related disorders: Through the lens of fear extinction
inferred← citeshttps://doi.org/10.1002/jts.21813openalex-snapshot
Mild Traumatic Brain Injury and Treatment Response in Prolonged Exposure for PTSD
inferred← citeshttps://doi.org/10.1002/syn.20657openalex-snapshot
Alteration of synaptic transmission in the hippocampal‐mPFC pathway during extinction trials of context‐dependent fear memory in juvenile rat stress models
inferred← citeshttps://doi.org/10.1002/syn.20944openalex-snapshot
D‐cycloserine facilitates extinction of cocaine self‐administration in c57 mice
inferred← citeshttps://doi.org/10.1002/syn.21690openalex-snapshot
Excitatory synapses on dendritic shafts of the caudal basal amygdala exhibit elevated levels of GABAAreceptor α4 subunits following the induction of activity-based anorexia
inferred← citeshttps://doi.org/10.1002/syn.21847openalex-snapshot
Conditional self-discrimination enhances dendritic spine number and dendritic length at prefrontal cortex and hippocampal neurons of rats
inferred← citeshttps://doi.org/10.1002/wcs.1353openalex-snapshot
Threat processing: models and mechanisms
inferred← citeshttps://doi.org/10.1002/wcs.1390openalex-snapshot
Social anxiety disorder: a critical overview of neurocognitive research
inferred← citeshttps://doi.org/10.1007/7854_2009_7openalex-snapshot
Neuroanatomy of Anxiety
inferred← citeshttps://doi.org/10.1007/7854_2010_107openalex-snapshot
Advances in Animal Models of Drug Addiction
inferred← citeshttps://doi.org/10.1007/7854_2011_193openalex-snapshot
Stress-Induced Deficits in Cognition and Emotionality: A Role for Glutamate
inferred← citeshttps://doi.org/10.1007/7854_2017_1openalex-snapshot
Integrating NIMH Research Domain Criteria (RDoC) into PTSD Research
inferred← citeshttps://doi.org/10.1007/7854_2017_31openalex-snapshot
Sleep Disruption, Safety Learning, and Fear Extinction in Humans: Implications for Posttraumatic Stress Disorder
inferred← citeshttps://doi.org/10.1007/7854_2017_34openalex-snapshot
Subanesthetic Dose Ketamine in Posttraumatic Stress Disorder: A Role for Reconsolidation During Trauma-Focused Psychotherapy?
inferred← citeshttps://doi.org/10.1007/7854_2022_405openalex-snapshot
VR for Studying the Neuroscience of Emotional Responses
inferred← citeshttps://doi.org/10.1007/7854_2023_439openalex-snapshot
Is Fear Extinction Impairment Central to Psychopathology?
inferred← citeshttps://doi.org/10.1007/7854_2024_494openalex-snapshot
Exercise and Fear and Safety Learning
inferred← citeshttps://doi.org/10.1007/7854_2024_543openalex-snapshot
Sex Differences in Neural Circuits Underlying Fear Processing
inferred← citeshttps://doi.org/10.1007/978-1-0716-3218-5_11openalex-snapshot
Animal Models of PTSD: The Role of Fear Conditioning
inferred← citeshttps://doi.org/10.1007/978-1-0716-3218-5_3openalex-snapshot
Using Virtual Reality to Study Fear and Extinction in Children and Adolescents
inferred← citeshttps://doi.org/10.1007/978-1-0716-3465-3_7openalex-snapshot
Influence of Vagus Nerve Stimulation on Mood and Associated Disorders
inferred← citeshttps://doi.org/10.1007/978-1-4419-1428-6_1902openalex-snapshot
Neural Mechanisms of Extinction Learning and Retrieval
inferred← citeshttps://doi.org/10.1007/978-1-4419-1428-6_306openalex-snapshot
Extinction Learning
inferred← citeshttps://doi.org/10.1007/978-1-4419-1428-6_782openalex-snapshot
Learning Not to Fear
inferred← citeshttps://doi.org/10.1007/978-1-4614-3846-5_8openalex-snapshot
Fear Conditioning and Extinction
inferred← citeshttps://doi.org/10.1007/978-1-4614-6599-7_1openalex-snapshot
Fear Models in Animals and Humans
inferred← citeshttps://doi.org/10.1007/978-1-4939-2294-9_6openalex-snapshot
Cannabinoid Control of Fear Responses
inferred← citeshttps://doi.org/10.1007/978-1-4939-3777-6_11openalex-snapshot
Potentiation of the Startle Reflex as a Behavioral Measure of Anxiety
inferred← citeshttps://doi.org/10.1007/978-1-60327-329-9_4openalex-snapshot
Counteracting Molecular Pathways Regulating the Reduction of Fear: Implications for the Treatment of Anxiety Diseases
inferred← citeshttps://doi.org/10.1007/978-1-61779-313-4_11openalex-snapshot
Fear Conditioning and Extinction as a Model of PTSD in Mice
inferred← citeshttps://doi.org/10.1007/978-3-030-30687-8_2openalex-snapshot
Neurocircuitry of Anxiety Disorders
inferred← citeshttps://doi.org/10.1007/978-3-030-36319-2_13openalex-snapshot
Memory Modification as Treatment for PTSD: Neuroscientific Reality and Ethical Concerns
inferred← citeshttps://doi.org/10.1007/978-3-031-98921-6_9openalex-snapshot
Modulation of Memory Consolidation, Retrieval, and Extinction by Brain Histamine
inferred← citeshttps://doi.org/10.1007/978-3-032-06260-4_1openalex-snapshot
Foundations of Veterinary Psychiatry
inferred← citeshttps://doi.org/10.1007/978-3-032-12239-1_6openalex-snapshot
Cannabinoid Control of Fear Responses
inferred← citeshttps://doi.org/10.1007/978-3-032-26123-6_29openalex-snapshot
From Pheromones to Policies: Reinforcement Learning for Engineered Biological Swarms
inferred← citeshttps://doi.org/10.1007/978-3-319-02753-1_3openalex-snapshot
Effects of Virtual Training on Emotional Response
inferred← citeshttps://doi.org/10.1007/978-3-319-08613-2_61-1openalex-snapshot
Valproic Acid in the Treatment of Post traumatic Stress Disorder
inferred← citeshttps://doi.org/10.1007/978-3-319-40308-3_14openalex-snapshot
Modulation of Memory Consolidation, Retrieval and Extinction by Brain Histamine
inferred← citeshttps://doi.org/10.1007/978-3-319-42925-0_9openalex-snapshot
Emerging Data for Ketamine in Obsessive-Compulsive, Stress-Related, and Substance Use Disorders
inferred← citeshttps://doi.org/10.1007/978-3-319-45066-7_17openalex-snapshot
Stress and Memory Consolidation
inferred← citeshttps://doi.org/10.1007/978-3-319-47829-6_1090-1openalex-snapshot
Stress
inferred← citeshttps://doi.org/10.1007/978-3-319-53126-7_17openalex-snapshot
Stress and the Dynamic Fear Memory: Synaptic–Cellular Bases and Their Implication for Psychiatry Disorders
inferred← citeshttps://doi.org/10.1007/978-3-319-55065-7_1090openalex-snapshot
Stress
inferred← citeshttps://doi.org/10.1007/978-3-319-94593-4_2openalex-snapshot
Neural Circuits Mediating Fear Learning and Extinction
inferred← citeshttps://doi.org/10.1007/978-3-540-29678-2_12openalex-snapshot
Absence Epilepsy
inferred← citeshttps://doi.org/10.1007/978-3-540-29678-2_2743openalex-snapshot
Learning and Extinction
inferred← citeshttps://doi.org/10.1007/978-3-540-88955-7openalex-snapshot
Behavioral Neurobiology of the Endocannabinoid System
inferred← citeshttps://doi.org/10.1007/978-3-540-88955-7_8openalex-snapshot
Roles of the Endocannabinoid System in Learning and Memory
inferred← citeshttps://doi.org/10.1007/978-3-642-27772-6_161-2openalex-snapshot
Pavlovian Fear Conditioning
inferred← citeshttps://doi.org/10.1007/978-3-7091-0932-8_10openalex-snapshot
Synaptic Protein Degradation in Memory Reorganization
inferred← citeshttps://doi.org/10.1007/978-4-431-54541-5_2openalex-snapshot
Brain–Peripheral Organ Communication
inferred← citeshttps://doi.org/10.1007/978-88-470-5322-9_2openalex-snapshot
Neurobiology of Addiction
inferred← citeshttps://doi.org/10.1007/978-981-15-2902-3_5openalex-snapshot
Synaptic Modulation in the Effect of Ketamine
inferred← citeshttps://doi.org/10.1007/978-981-19-9331-2_11openalex-snapshot
Comparative Analysis of Machine Learning Algorithms for Author Age and Gender Identification
inferred← citeshttps://doi.org/10.1007/978-981-32-9705-0_26openalex-snapshot
The Role of Hormonal and Reproductive Status in the Treatment of Anxiety Disorders in Women
inferred← citeshttps://doi.org/10.1007/s00018-013-1316-2openalex-snapshot
Generating new neurons to circumvent your fears: the role of IGF signaling
inferred← citeshttps://doi.org/10.1007/s00213-008-1280-yopenalex-snapshot
The facilitative effects of d-cycloserine on extinction of a cocaine-induced conditioned place preference can be long lasting and resistant to reinstatement
inferred← citeshttps://doi.org/10.1007/s00213-009-1491-xopenalex-snapshot
The effects of yohimbine and amphetamine on fear expression and extinction in rats
inferred← citeshttps://doi.org/10.1007/s00213-010-2026-1openalex-snapshot
Reduction of fear-potentiated startle by benzodiazepines in C57BL/6J mice
inferred← citeshttps://doi.org/10.1007/s00213-011-2592-xopenalex-snapshot
A randomized, placebo-controlled laboratory study of the effects of d-cycloserine on craving in cocaine-dependent individuals
inferred← citeshttps://doi.org/10.1007/s00213-012-2710-4openalex-snapshot
Facilitation of extinction of operant behaviour in C57Bl/6 mice by chlordiazepoxide and d-cycloserine
inferred← citeshttps://doi.org/10.1007/s00213-013-3414-0openalex-snapshot
Opposing roles of prelimbic and infralimbic dopamine in conditioned cue and place preference
inferred← citeshttps://doi.org/10.1007/s00213-014-3607-1openalex-snapshot
Bidirectional effects of inhibiting or potentiating NMDA receptors on extinction after cocaine self-administration in rats
inferred← citeshttps://doi.org/10.1007/s00213-014-3665-4openalex-snapshot
The neurokinin-1 receptor antagonist aprepitant in co-morbid alcohol dependence and posttraumatic stress disorder: a human experimental study
inferred← citeshttps://doi.org/10.1007/s00213-014-3812-yopenalex-snapshot
Medial prefrontal cannabinoid CB1 receptors modulate consolidation and extinction of cocaine-associated memory in mice
inferred← citeshttps://doi.org/10.1007/s00213-016-4280-3openalex-snapshot
Effects of dorsal hippocampal orexin-2 receptor antagonism on the acquisition, expression, and extinction of morphine-induced place preference in rats
inferred← citeshttps://doi.org/10.1007/s00213-016-4388-5openalex-snapshot
N-acetylcysteine amide (AD4) reduces cocaine-induced reinstatement
inferred← citeshttps://doi.org/10.1007/s00213-017-4672-zopenalex-snapshot
Naloxone effects on extinction of ethanol- and cocaine-induced conditioned place preference in mice
inferred← citeshttps://doi.org/10.1007/s00213-018-4956-yopenalex-snapshot
Reproductive experience alters the involvement of N-methyl-D-aspartate receptors in fear extinction, but not fear conditioning, in female Sprague Dawley rats
inferred← citeshttps://doi.org/10.1007/s00213-018-4994-5openalex-snapshot
Vagus nerve stimulation as a tool for enhancing extinction in exposure-based therapies
inferred← citeshttps://doi.org/10.1007/s00213-018-5023-4openalex-snapshot
Preclinical studies of stress, extinction, and prefrontal cortex: intriguing leads and pressing questions
inferred← citeshttps://doi.org/10.1007/s00213-018-5024-3openalex-snapshot
Common neurocircuitry mediating drug and fear relapse in preclinical models
inferred← citeshttps://doi.org/10.1007/s00213-018-5030-5openalex-snapshot
Acute and long-lasting effects of oxytocin in cortico-limbic circuits: consequences for fear recall and extinction
inferred← citeshttps://doi.org/10.1007/s00213-018-5033-2openalex-snapshot
Neural circuits for a top-down control of fear and extinction
inferred← citeshttps://doi.org/10.1007/s00213-018-5080-8openalex-snapshot
Single stimulation of Y2 receptors in BNSTav facilitates extinction and dampens reinstatement of fear
inferred← citeshttps://doi.org/10.1007/s00213-018-5084-4openalex-snapshot
Neuroepigenetic mechanisms underlying fear extinction: emerging concepts
inferred← citeshttps://doi.org/10.1007/s00213-018-5098-yopenalex-snapshot
The emerging neuroscience of appetitive and drug cue extinction in humans
inferred← citeshttps://doi.org/10.1007/s00213-018-5109-zopenalex-snapshot
Hippocampal network oscillations at the interplay between innate anxiety and learned fear
inferred← citeshttps://doi.org/10.1007/s00213-018-5116-0openalex-snapshot
Glucocorticoid-induced enhancement of extinction—from animal models to clinical trials
inferred← citeshttps://doi.org/10.1007/s00213-018-5127-xopenalex-snapshot
Tempering aversive/traumatic memories with cannabinoids: a review of evidence from animal and human studies
inferred← citeshttps://doi.org/10.1007/s00213-019-05195-2openalex-snapshot
Individual variability in the recall of fear extinction is associated with phosphorylation of mitogen-activated protein kinase in the infralimbic cortex
inferred← citeshttps://doi.org/10.1007/s00213-020-05622-9openalex-snapshot
The infralimbic cortex and mGlu5 mediate the effects of chronic intermittent ethanol exposure on fear learning and memory
inferred← citeshttps://doi.org/10.1007/s00213-021-05935-3openalex-snapshot
Optogenetic manipulation of the prelimbic cortex during fear memory reconsolidation alters fear extinction in a preclinical model of comorbid PTSD/AUD
inferred← citeshttps://doi.org/10.1007/s00213-022-06254-xopenalex-snapshot
Learning processes in relapse to alcohol use: lessons from animal models
inferred← citeshttps://doi.org/10.1007/s00213-023-06523-3openalex-snapshot
Pharmacological diacylglycerol lipase inhibition impairs contextual fear extinction in mice
inferred← citeshttps://doi.org/10.1007/s00381-015-2807-2openalex-snapshot
Antioxidative enzymes in irradiated rat brain—indicators of different regional radiosensitivity
inferred← citeshttps://doi.org/10.1007/s00406-017-0805-yopenalex-snapshot
Striatal reward sensitivity predicts therapy-related neural changes in alcohol addiction
inferred← citeshttps://doi.org/10.1007/s00406-019-01056-3openalex-snapshot
Is glutamate associated with fear extinction and cognitive behavior therapy outcome in OCD? A pilot study
inferred← citeshttps://doi.org/10.1007/s00429-014-0727-7openalex-snapshot
Corticolimbic catecholamines in stress: a computational model of the appraisal of controllability
inferred← citeshttps://doi.org/10.1007/s00429-014-0796-7openalex-snapshot
Decision making in avoidance–reward conflict: a paradigm for non-human primates and humans
inferred← citeshttps://doi.org/10.1007/s00429-015-1013-zopenalex-snapshot
Brain morphology correlates of interindividual differences in conditioned fear acquisition and extinction learning
inferred← citeshttps://doi.org/10.1007/s00429-018-1720-3openalex-snapshot
Reduced resting-state functional connectivity of the basolateral amygdala to the medial prefrontal cortex in preweaning rats exposed to chronic early-life stress
inferred← citeshttps://doi.org/10.1007/s00429-022-02545-3openalex-snapshot
Analysis of lateral orbitofrontal cortex activation on acquisition of fear extinction and neuronal activities in fear circuit
inferred← citeshttps://doi.org/10.1007/s00702-009-0243-8openalex-snapshot
Neurotransmitters and prefrontal cortex–limbic system interactions: implications for plasticity and psychiatric disorders
inferred← citeshttps://doi.org/10.1007/s00702-010-0502-8openalex-snapshot
Aversive memory in sepsis survivor rats
inferred← citeshttps://doi.org/10.1007/s00702-024-02754-6openalex-snapshot
More than fear? Brain activation patterns of dental phobic patients before and after an exposure-based treatment
inferred← citeshttps://doi.org/10.1007/s10539-022-09834-5openalex-snapshot
Remembering emotions
inferred← citeshttps://doi.org/10.1007/s10545-018-0168-1openalex-snapshot
The role of suboptimal mitochondrial function in vulnerability to post‐traumatic stress disorder
inferred← citeshttps://doi.org/10.1007/s10571-016-0371-2openalex-snapshot
Involvement of AMPA/Kainate Glutamate Receptor in the Extinction and Reinstatement of Morphine-Induced Conditioned Place Preference: A Behavioral and Molecular Study
inferred← citeshttps://doi.org/10.1007/s10571-017-0464-6openalex-snapshot
Enhanced Histone Acetylation in the Infralimbic Prefrontal Cortex is Associated with Fear Extinction
inferred← citeshttps://doi.org/10.1007/s10942-014-0196-1openalex-snapshot
Rectifying Misconceptions: A Comprehensive Response to “Some Concerns About the Psychological Implications of Mindfulness: A Critical Analysis”
inferred← citeshttps://doi.org/10.1007/s11011-015-9727-4openalex-snapshot
Molecular mechanisms of D-cycloserine in facilitating fear extinction: insights from RNAseq
inferred← citeshttps://doi.org/10.1007/s11055-016-0367-xopenalex-snapshot
Extinction and Reconsolidation of Memory
inferred← citeshttps://doi.org/10.1007/s11055-021-01115-0openalex-snapshot
Spike Activity and Genome Instability in Neurons of the Amygdaloid Complex in Rats of Selected Strains with Contrasting Nervous System Arousability in Normal Conditions and Stress
inferred← citeshttps://doi.org/10.1007/s11064-013-1230-xopenalex-snapshot
Contextual Fear Conditioning in Maternal Separated Rats: The Amygdala as a Site for Alterations
inferred← citeshttps://doi.org/10.1007/s11571-010-9109-xopenalex-snapshot
Computational models of reinforcement learning: the role of dopamine as a reward signal
inferred← citeshttps://doi.org/10.1007/s11682-019-00229-xopenalex-snapshot
Resting-state causal connectivity of the bed nucleus of the stria terminalis in panic disorder
inferred← citeshttps://doi.org/10.1007/s11920-018-0887-xopenalex-snapshot
Stress Response Modulation Underlying the Psychobiology of Resilience
inferred← citeshttps://doi.org/10.1007/s12035-016-9817-2openalex-snapshot
Prolonged Induction of miR-212/132 and REST Expression in Rat Striatum Following Cocaine Self-Administration
inferred← citeshttps://doi.org/10.1007/s12035-018-0869-3openalex-snapshot
Cotinine: A Therapy for Memory Extinction in Post-traumatic Stress Disorder
inferred← citeshttps://doi.org/10.1007/s12035-018-1407-zopenalex-snapshot
Optogenetic Long-Term Depression Induction in the PVT-CeL Circuitry Mediates Decreased Fear Memory
inferred← citeshttps://doi.org/10.1007/s12035-023-03314-xopenalex-snapshot
Selective Disruption of Perineuronal Nets in Mice Lacking Crtl1 is Sufficient to Make Fear Memories Susceptible to Erasure
inferred← citeshttps://doi.org/10.1007/s12035-026-05868-yopenalex-snapshot
SirT2 Inhibition is Associated with Improvements in Depression-like Behavior and Memory Impairment in Olfactory Bulbectomized Mice
inferred← citeshttps://doi.org/10.1007/s12264-020-00603-6openalex-snapshot
Projections from Infralimbic Cortex to Paraventricular Thalamus Mediate Fear Extinction Retrieval
inferred← citeshttps://doi.org/10.1007/s12264-024-01294-zopenalex-snapshot
Memory Reconsolidation Updating in Substance Addiction: Applications, Mechanisms, and Future Prospects for Clinical Therapeutics
inferred← citeshttps://doi.org/10.1007/s12264-025-01367-7openalex-snapshot
How Fear Memory is Updated: From Reconsolidation to Extinction?
inferred← citeshttps://doi.org/10.1007/s12311-015-0670-zopenalex-snapshot
Cerebellar Contribution to Context Processing in Extinction Learning and Recall
inferred← citeshttps://doi.org/10.1007/s13311-022-01339-zopenalex-snapshot
BDNF Augmentation Using Riluzole Reverses Doxorubicin-Induced Decline in Cognitive Function and Neurogenesis
inferred← citeshttps://doi.org/10.1007/s40429-020-00333-9openalex-snapshot
Instrumental and Pavlovian Mechanisms in Alcohol Use Disorder
inferred← citeshttps://doi.org/10.1007/s40473-014-0015-0openalex-snapshot
Looking Beyond Fear and Extinction Learning: Considering Novel Treatment Targets for Anxiety
inferred← citeshttps://doi.org/10.1007/s40501-015-0035-8openalex-snapshot
Treatments for Post-traumatic Stress Disorder: Pharmaceutical and Electrophysiologic Considerations
inferred← citeshttps://doi.org/10.1007/s40501-022-00279-xopenalex-snapshot
Neuromodulation as an Augmenting Strategy for Behavioral Therapies for Anxiety and PTSD: a Narrative Review
inferred← citeshttps://doi.org/10.1007/s40708-014-0004-9openalex-snapshot
Towards virtual training of emotion regulation
inferred← citeshttps://doi.org/10.1007/s41105-019-00248-7openalex-snapshot
Bright light exposure augments cognitive behavioral therapy for panic and posttraumatic stress disorders: a pilot randomized control trial
inferred← citeshttps://doi.org/10.1007/s43076-023-00352-1openalex-snapshot
Yoga, Explicit, and Implicit Emotion Regulation: Long-Term and Current Yoga Practice Predicted More Attentional Focusing and Less Emotional Bias in a Go/No-Go Task
inferred← citeshttps://doi.org/10.1007/springerreference_226314openalex-snapshot
Exemplar Learning and Schematization in Language Development
inferred← citeshttps://doi.org/10.1016/b978-0-08-045396-5.00136-6openalex-snapshot
Fear Conditioning
inferred← citeshttps://doi.org/10.1016/b978-0-08-097086-8.55002-8openalex-snapshot
Anxiety and Fear Conditioning, Neural Basis of
inferred← citeshttps://doi.org/10.1016/b978-0-08-097086-8.55023-5openalex-snapshot
Fear-Potentiated Startle
inferred← citeshttps://doi.org/10.1016/b978-0-12-381431-9.00005-xopenalex-snapshot
The Effect of Context on Choice and Value
inferred← citeshttps://doi.org/10.1016/b978-0-12-385870-2.00048-2openalex-snapshot
Learning and Memory
inferred← citeshttps://doi.org/10.1016/b978-0-12-397045-9.00024-0openalex-snapshot
Exposure Therapy
inferred← citeshttps://doi.org/10.1016/b978-0-12-405941-2.00001-8openalex-snapshot
Frameworks of Alcohol Addiction
inferred← citeshttps://doi.org/10.1016/b978-0-12-415804-7.00028-9openalex-snapshot
Neuronal Network Plasticity and Network Interactions are Critically Dependent on Conditional Multireceptive (CMR) Brain Regions
inferred← citeshttps://doi.org/10.1016/b978-0-12-417041-4.00011-4openalex-snapshot
The role of endocannabinoid function in posttraumatic stress disorder
inferred← citeshttps://doi.org/10.1016/b978-0-12-417042-1.00010-3openalex-snapshot
Pharmacological Treatment of Cognitive Dysfunction in Neuropsychiatric Disorders
inferred← citeshttps://doi.org/10.1016/b978-0-12-417188-6.09997-7openalex-snapshot
Foreword: Interrelationships between Sleep and Affect
inferred← citeshttps://doi.org/10.1016/b978-0-12-802114-9.00003-2openalex-snapshot
Sex Differences in Anxiety Disorders: Gonadal Hormone Interactions with Pathophysiology, Neurobiology, and Treatment
inferred← citeshttps://doi.org/10.1016/b978-0-12-802175-0.00031-0openalex-snapshot
Stress Effects on Learning and Memory in Humans
inferred← citeshttps://doi.org/10.1016/b978-0-12-802574-1.00016-8openalex-snapshot
Nicotine and Posttraumatic Stress Disorder
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.21090-0openalex-snapshot
Emotional Learning: Animals ☆
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.21123-1openalex-snapshot
Allocating, Tagging, and Linking Memories
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