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The hypothalamus as a primary coordinator of memory updating
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Hyperphagia, Rage, and Dementia Accompanying a Ventromedial Hypothalamic Neoplasm
inferredcites →https://doi.org/10.1002/ana.21881openalex-snapshot
Reduced amygdala activity during aversive conditioning in human narcolepsy
inferredcites →https://doi.org/10.1006/nlme.2002.4080openalex-snapshot
Stress and Memory: Opposing Effects of Glucocorticoids on Memory Consolidation and Memory Retrieval,
inferredcites →https://doi.org/10.1007/7854_2016_45openalex-snapshot
Orexin/Hypocretin and Organizing Principles for a Diversity of Wake-Promoting Neurons in the Brain
inferredcites →https://doi.org/10.1007/bf00686763openalex-snapshot
Distribution of Alzheimer's neurofibrillary changes in the brain stem and hypothalamus of senile dementia
inferredcites →https://doi.org/10.1007/bf03001275openalex-snapshot
Species-specific defense reactions and avoidance learning
inferredcites →https://doi.org/10.1007/s00213-012-2736-7openalex-snapshot
The brain orexin system and almorexant in fear-conditioned startle reactions in the rat
inferredcites →https://doi.org/10.1007/s00429-013-0626-3openalex-snapshot
Orexins (hypocretins) contribute to fear and avoidance in rats exposed to a single episode of footshocks
inferredcites →https://doi.org/10.1016/0006-8993(76)91048-9openalex-snapshot
Hypothalamic neuronal responses associated with the sight of food
inferredcites →https://doi.org/10.1016/0014-4886(76)90089-3openalex-snapshot
Modulation during learning of the responses of neurons in the lateral hypothalamus to the sight of food
inferredcites →https://doi.org/10.1016/0014-4886(76)90189-8openalex-snapshot
Effects of hunger on the responses of neurons in the lateral hypothalamus to the sight and taste of food
inferredcites →https://doi.org/10.1016/0031-9384(80)90215-2openalex-snapshot
The effect of post-training lateral hypothalamic self-stimulation on aversive and appetitive classical conditioning
inferredcites →https://doi.org/10.1016/0031-9384(84)90064-7openalex-snapshot
Memory for feeding time: Possible dependence on coupled circadian oscillators
inferredcites →https://doi.org/10.1016/0166-4328(93)90091-4openalex-snapshot
Emotional memory systems in the brain
inferredcites →https://doi.org/10.1016/0304-3940(87)90325-9openalex-snapshot
Hypothalamic pathology in Alzheimer's disease
inferredcites →https://doi.org/10.1016/0361-9230(88)90100-1openalex-snapshot
Internal and external information processing by lateral hypothalamic glucose-sensitive and insensitive neurons during bar press feeding in the monkey
inferredcites →https://doi.org/10.1016/b978-0-444-59489-1.00009-4openalex-snapshot
Orexin, stress, and anxiety/panic states
inferredcites →https://doi.org/10.1016/j.autneu.2010.08.004openalex-snapshot
Orexin links emotional stress to autonomic functions
inferredcites →https://doi.org/10.1016/j.bbr.2008.03.042openalex-snapshot
Investigation of the hypothalamic defensive system in the mouse
inferredcites →https://doi.org/10.1016/j.bbr.2018.05.032openalex-snapshot
Orexin signaling during social defeat stress influences subsequent social interaction behaviour and recognition memory
inferredcites →https://doi.org/10.1016/j.brainres.2005.03.002openalex-snapshot
Orexin-A (hypocretin-1) is possibly involved in generation of anxiety-like behavior
inferredcites →https://doi.org/10.1016/j.brainres.2018.09.011openalex-snapshot
How orexin signals bias action: Hypothalamic and accumbal circuits
inferredcites →https://doi.org/10.1016/j.cell.2009.08.035openalex-snapshot
A Neural Circuit Mechanism Integrating Motivational State with Memory Expression in Drosophila
inferredcites →https://doi.org/10.1016/j.celrep.2014.03.055openalex-snapshot
Coreleased Orexin and Glutamate Evoke Nonredundant Spike Outputs and Computations in Histamine Neurons
inferredcites →https://doi.org/10.1016/j.cmet.2010.09.013openalex-snapshot
Glucose Stimulation of Hypothalamic MCH Neurons Involves KATP Channels, Is Modulated by UCP2, and Regulates Peripheral Glucose Homeostasis
inferredcites →https://doi.org/10.1016/j.conb.2008.08.003openalex-snapshot
Reinforcement learning: The Good, The Bad and The Ugly
inferredcites →https://doi.org/10.1016/j.conb.2014.07.006openalex-snapshot
Hypocretin (orexin) neuromodulation of stress and reward pathways
inferredcites →https://doi.org/10.1016/j.cub.2010.03.061openalex-snapshot
Sex Peptide Receptor and Neuronal TOR/S6K Signaling Modulate Nutrient Balancing in Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2011.03.032openalex-snapshot
Remembering Nutrient Quality of Sugar in Drosophila
inferredcites →https://doi.org/10.1016/j.cub.2011.03.058openalex-snapshot
Drosophila Evaluates and Learns the Nutritional Value of Sugars
inferredcites →https://doi.org/10.1016/j.cub.2017.06.024openalex-snapshot
Lateral Hypothalamic GABAergic Neurons Encode Reward Predictions that Are Relayed to the Ventral Tegmental Area to Regulate Learning
inferredcites →https://doi.org/10.1016/j.cub.2017.06.082openalex-snapshot
Energy Balance: Lateral Hypothalamus Hoards Food Memories
inferredcites →https://doi.org/10.1016/j.cub.2020.07.061openalex-snapshot
Ultra-sparse Connectivity within the Lateral Hypothalamus
inferredcites →https://doi.org/10.1016/j.jmp.2008.12.005openalex-snapshot
Reinforcement learning in the brain
inferredcites →https://doi.org/10.1016/j.neulet.2008.11.060openalex-snapshot
Cataplexy: An affair of pleasure or an unpleasant affair?
inferredcites →https://doi.org/10.1016/j.neuron.2005.04.035openalex-snapshot
Behavioral Correlates of Activity in Identified Hypocretin/Orexin Neurons
inferredcites →https://doi.org/10.1016/j.neuron.2011.08.027openalex-snapshot
Activation of Central Orexin/Hypocretin Neurons by Dietary Amino Acids
inferredcites →https://doi.org/10.1016/j.neuron.2013.02.018openalex-snapshot
Hypothalamic Survival Circuits: Blueprints for Purposive Behaviors
inferredcites →https://doi.org/10.1016/j.neuron.2016.04.035openalex-snapshot
Inhibitory Input from the Lateral Hypothalamus to the Ventral Tegmental Area Disinhibits Dopamine Neurons and Promotes Behavioral Activation
inferredcites →https://doi.org/10.1016/j.neuron.2018.11.005openalex-snapshot
A Neural Circuit Mechanism for Encoding Aversive Stimuli in the Mesolimbic Dopamine System
inferredcites →https://doi.org/10.1016/j.neuropharm.2018.10.024openalex-snapshot
Reactive and predictive homeostasis: Roles of orexin/hypocretin neurons
inferredcites →https://doi.org/10.1016/j.neuroscience.2004.05.012openalex-snapshot
Orexins/hypocretins cause sharp wave- and θ-related synaptic plasticity in the hippocampus via glutamatergic, gabaergic, noradrenergic, and cholinergic signaling
inferredcites →https://doi.org/10.1016/j.neuroscience.2009.04.074openalex-snapshot
Intracranial self-stimulation to the lateral hypothalamus, a memory improving treatment, results in hippocampal changes in gene expression
inferredcites →https://doi.org/10.1016/j.nlm.2016.10.005openalex-snapshot
Cellular activation of hypothalamic hypocretin/orexin neurons facilitates short-term spatial memory in mice
inferredcites →https://doi.org/10.1016/j.nlm.2017.10.014openalex-snapshot
Orexin/hypocretin treatment restores hippocampal-dependent memory in orexin-deficient mice
inferredcites →https://doi.org/10.1016/j.peptides.2003.09.006openalex-snapshot
Increased susceptibility to LTP generation and changes in NMDA-NR1 and -NR2B subunits mRNA expression in rat hippocampus after MCH administration
inferredcites →https://doi.org/10.1016/j.peptides.2009.06.024openalex-snapshot
A role for Melanin-Concentrating Hormone in learning and memory
inferredcites →https://doi.org/10.1016/j.phrs.2018.12.024openalex-snapshot
Activation of Agrp neurons modulates memory-related cognitive processes in mice
inferredcites →https://doi.org/10.1016/j.physbeh.2012.05.019openalex-snapshot
Orexin-A induces anxiety-like behavior through interactions with glutamatergic receptors in the bed nucleus of the stria terminalis of rats
inferredcites →https://doi.org/10.1016/j.physbeh.2013.03.023openalex-snapshot
Lateral hypothalamus as a sensor-regulator in respiratory and metabolic control
inferredcites →https://doi.org/10.1016/j.physbeh.2013.10.005openalex-snapshot
Optogenetic examination identifies a context-specific role for orexins/hypocretins in anxiety-related behavior
inferredcites →https://doi.org/10.1016/j.pneurobio.2020.101771openalex-snapshot
Role of spontaneous and sensory orexin network dynamics in rapid locomotion initiation
inferredcites →https://doi.org/10.1016/j.tem.2019.08.010openalex-snapshot
Hypothalamic Heuristics for Survival
inferredcites →https://doi.org/10.1016/j.tins.2015.06.005openalex-snapshot
Orexins and fear: implications for the treatment of anxiety disorders
inferredcites →https://doi.org/10.1016/j.yfrne.2016.11.002openalex-snapshot
Sleep & metabolism: The multitasking ability of lateral hypothalamic inhibitory circuitries
inferredcites →https://doi.org/10.1016/j.ygcen.2011.03.028openalex-snapshot
Anatomical organization of the melanin-concentrating hormone peptide family in the mammalian brain
inferredcites →https://doi.org/10.1016/s0091-6773(78)92441-0openalex-snapshot
Post-trial hippocampal and lateral hypothalamic electrical stimulation
inferredcites →https://doi.org/10.1016/s0092-8674(00)80949-6openalex-snapshot
Orexins and Orexin Receptors: A Family of Hypothalamic Neuropeptides and G Protein-Coupled Receptors that Regulate Feeding Behavior
inferredcites →https://doi.org/10.1016/s0149-7634(01)00009-4openalex-snapshot
Mouse defensive behaviors: pharmacological and behavioral assays for anxiety and panic
inferredcites →https://doi.org/10.1016/s0196-9781(01)00591-5openalex-snapshot
Melanin concentrating hormone increase hippocampal synaptic transmission in the rat
inferredcites →https://doi.org/10.1016/s0361-9230(97)00141-xopenalex-snapshot
Severe Reduction of Rat Defensive Behavior to a Predator by Discrete Hypothalamic Chemical Lesions
inferredcites →https://doi.org/10.1016/s0896-6273(02)01132-7openalex-snapshot
Hypocretin/Orexin Excites Hypocretin Neurons via a Local Glutamate Neuron—A Potential Mechanism for Orchestrating the Hypothalamic Arousal System
inferredcites →https://doi.org/10.1016/s0896-6273(03)00331-3openalex-snapshot
Hypothalamic Orexin Neurons Regulate Arousal According to Energy Balance in Mice
inferredcites →https://doi.org/10.1016/s0896-6273(04)00251-xopenalex-snapshot
Physiological Properties of Hypothalamic MCH Neurons Identified with Selective Expression of Reporter Gene after Recombinant Virus Infection
inferredcites →https://doi.org/10.1037/h0036976openalex-snapshot
Dissociation between learning and remembering in rats with lesions in the lateral hypothalamus.
inferredcites →https://doi.org/10.1038/222282a0openalex-snapshot
Glucose and Osmosensitive Neurones of the Rat Hypothalamus
inferredcites →https://doi.org/10.1038/79690openalex-snapshot
A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains
inferredcites →https://doi.org/10.1038/nature21066openalex-snapshot
Gamma oscillations organize top-down signalling to hypothalamus and enable food seeking
inferredcites →https://doi.org/10.1038/ncomms11395openalex-snapshot
Awake dynamics and brain-wide direct inputs of hypothalamic MCH and orexin networks
inferredcites →https://doi.org/10.1038/ncomms7266openalex-snapshot
Antagonistic interplay between hypocretin and leptin in the lateral hypothalamus regulates stress responses
inferredcites →https://doi.org/10.1038/ncomms7704openalex-snapshot
Metabolic learning and memory formation by the brain influence systemic metabolic homeostasis
inferredcites →https://doi.org/10.1038/nm.2075openalex-snapshot
A key role for orexin in panic anxiety
inferredcites →https://doi.org/10.1038/nm741openalex-snapshot
Antidepressant, anxiolytic and anorectic effects of a melanin-concentrating hormone-1 receptor antagonist
inferredcites →https://doi.org/10.1038/nn.3522openalex-snapshot
Optogenetic identification of a rapid eye movement sleep modulatory circuit in the hypothalamus
inferredcites →https://doi.org/10.1038/nn.3810openalex-snapshot
Motivational activation: a unifying hypothesis of orexin/hypocretin function
inferredcites →https://doi.org/10.1038/nn.4220openalex-snapshot
Lateral hypothalamic circuits for feeding and reward
inferredcites →https://doi.org/10.1038/nrn2092openalex-snapshot
The neural circuit of orexin (hypocretin): maintaining sleep and wakefulness
inferredcites →https://doi.org/10.1038/nrn2963openalex-snapshot
Making memories last: the synaptic tagging and capture hypothesis
inferredcites →https://doi.org/10.1038/nrn3677openalex-snapshot
Hippocampal synaptic plasticity, spatial memory and anxiety
inferredcites →https://doi.org/10.1038/nrn3837openalex-snapshot
The role of orexin in motivated behaviours
inferredcites →https://doi.org/10.1038/s41467-019-10484-7openalex-snapshot
Natural hypothalamic circuit dynamics underlying object memorization
inferredcites →https://doi.org/10.1038/s41582-019-0226-9openalex-snapshot
Narcolepsy — clinical spectrum, aetiopathophysiology, diagnosis and treatment
inferredcites →https://doi.org/10.1038/s41593-017-0023-yopenalex-snapshot
Accumbal D2 cells orchestrate innate risk-avoidance according to orexin signals
inferredcites →https://doi.org/10.1038/s41593-018-0198-xopenalex-snapshot
Parallel circuits from the bed nuclei of stria terminalis to the lateral hypothalamus drive opposing emotional states
inferredcites →https://doi.org/10.1038/srep29480openalex-snapshot
The integrative role of orexin/hypocretin neurons in nociceptive perception and analgesic regulation
inferredcites →https://doi.org/10.1046/j.1460-9568.2002.02404.xopenalex-snapshot
Lateral hypothalamic lesions impair flavour‐nutrient and flavour‐toxin trace learning in rats
inferredcites →https://doi.org/10.1073/pnas.0702676104openalex-snapshot
Control of hypothalamic orexin neurons by acid and CO 2
inferredcites →https://doi.org/10.1073/pnas.0802687105openalex-snapshot
Adaptive sugar sensors in hypothalamic feeding circuits
inferredcites →https://doi.org/10.1073/pnas.0900939106openalex-snapshot
Dissecting the brain's fear system reveals the hypothalamus is critical for responding in subordinate conspecific intruders
inferredcites →https://doi.org/10.1073/pnas.1320325110openalex-snapshot
Orexin/hypocretin system modulates amygdala-dependent threat learning through the locus coeruleus
inferredcites →https://doi.org/10.1073/pnas.1619700114openalex-snapshot
Orexin-driven GAD65 network of the lateral hypothalamus sets physical activity in mice
inferredcites →https://doi.org/10.1073/pnas.95.1.322openalex-snapshot
The hypocretins: Hypothalamus-specific peptides with neuroexcitatory activity
inferredcites →https://doi.org/10.1093/sleep/zsz296openalex-snapshot
A circuit perspective on narcolepsy
inferredcites →https://doi.org/10.1098/rstb.2012.0007openalex-snapshot
Match and mismatch: conservation physiology, nutritional ecology and the timescales of biological adaptation
inferredcites →https://doi.org/10.1111/bph.14476openalex-snapshot
Neuronal histamine and the memory of emotionally salient events
inferredcites →https://doi.org/10.1111/ejn.13207openalex-snapshot
Brain glucose feedback predicts food choice (Commentary on Wakabayashi et al.)
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Low‐voltage‐activated A‐current controls the firing dynamics of mouse hypothalamic orexin neurons
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Disrupting the melanin‐concentrating hormone receptor 1 in mice leads to cognitive deficits and alterations of NMDA receptor function
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Hypothalamic sites responding to predator threats – the role of the dorsal premammillary nucleus in unconditioned and conditioned antipredatory defensive behavior
inferredcites →https://doi.org/10.1111/j.1582-4934.2005.tb00380.xopenalex-snapshot
Metabolic state signalling through central hypocretin/orexin neurons
inferredcites →https://doi.org/10.1111/j.1748-1716.2008.01922.xopenalex-snapshot
Physiological functions of glucose‐inhibited neurones
inferredcites →https://doi.org/10.1111/j.1748-1716.2009.02021.xopenalex-snapshot
Orexins/hypocretins control bistability of hippocampal long‐term synaptic plasticity through co‐activation of multiple kinases
inferredcites →https://doi.org/10.1111/j.1753-4887.1981.tb06752.xopenalex-snapshot
Proceedings of the National Academy of Sciences of the United States of America
inferredcites →https://doi.org/10.1111/nure.12045openalex-snapshot
Ghrelin, neuropeptide Y, and other feeding-regulatory peptides active in the hippocampus: role in learning and memory
inferredcites →https://doi.org/10.1113/jphysiol.2011.217000openalex-snapshot
Orexin neurons as conditional glucosensors: paradoxical regulation of sugar sensing by intracellular fuels
inferredcites →https://doi.org/10.1113/jphysiol.2012.243493openalex-snapshot
Lateral hypothalamic GAD65 neurons are spontaneously firing and distinct from orexin‐ and melanin‐concentrating hormone neurons
inferredcites →https://doi.org/10.1126/science.1226018openalex-snapshot
To Favor Survival Under Food Shortage, the Brain Disables Costly Memory
inferredcites →https://doi.org/10.1126/science.aax9238openalex-snapshot
REM sleep–active MCH neurons are involved in forgetting hippocampus-dependent memories
inferredcites →https://doi.org/10.1146/annurev-physiol-021115-104948openalex-snapshot
Three Pillars for the Neural Control of Appetite
inferredcites →https://doi.org/10.1152/ajpregu.00527.2010openalex-snapshot
Multiple hypothalamic circuits sense and regulate glucose levels
inferredcites →https://doi.org/10.1152/jn.01052.2009openalex-snapshot
Major Impairments of Glutamatergic Transmission and Long-Term Synaptic Plasticity in the Hippocampus of Mice Lacking the Melanin-Concentrating Hormone Receptor-1
inferredcites →https://doi.org/10.1186/1471-2202-4-19openalex-snapshot
A role of melanin-concentrating hormone producing neurons in the central regulation of paradoxical sleep
inferredcites →https://doi.org/10.1186/1756-6606-1-19openalex-snapshot
Circadian and dark-pulse activation of orexin/hypocretin neurons
inferredcites →https://doi.org/10.1186/s12993-018-0151-xopenalex-snapshot
Narcolepsy and emotional experience: a review of the literature
inferredcites →https://doi.org/10.1212/wnl.56.11.1597openalex-snapshot
Hypothalamic amnesia with spontaneous confabulations: A clinicopathologic study
inferredcites →https://doi.org/10.1523/eneuro.0012-18.2018openalex-snapshot
Fast and Slow Oscillations Recruit Molecularly-Distinct Subnetworks of Lateral Hypothalamic NeuronsIn Situ
inferredcites →https://doi.org/10.1523/eneuro.0273-17.2018openalex-snapshot
Reduced Orexin System Function Contributes to Resilience to Repeated Social Stress
inferredcites →https://doi.org/10.1523/jneurosci.0305-19.2019openalex-snapshot
Dynamic Network Activation of Hypothalamic MCH Neurons in REM Sleep and Exploratory Behavior
inferredcites →https://doi.org/10.1523/jneurosci.0706-12.2012openalex-snapshot
Optogenetic Probing of Fast Glutamatergic Transmission from Hypocretin/Orexin to Histamine NeuronsIn Situ
inferredcites →https://doi.org/10.1523/jneurosci.1130-13.2013openalex-snapshot
Orexin Receptor-1 in the Locus Coeruleus Plays an Important Role in Cue-Dependent Fear Memory Consolidation
inferredcites →https://doi.org/10.1523/jneurosci.23-05-01557.2003openalex-snapshot
The Wake-Promoting Hypocretin–Orexin Neurons Are in an Intrinsic State of Membrane Depolarization
inferredcites →https://doi.org/10.1523/jneurosci.3388-13.2014openalex-snapshot
Acute Suppressive and Long-Term Phase Modulation Actions of Orexin on the Mammalian Circadian Clock
inferredcites →https://doi.org/10.1523/jneurosci.3459-04.2004openalex-snapshot
Interaction between the Corticotropin-Releasing Factor System and Hypocretins (Orexins): A Novel Circuit Mediating Stress Response
inferredcites →https://doi.org/10.1523/jneurosci.3903-15.2016openalex-snapshot
Orexin Neurons Respond Differentially to Auditory Cues Associated with Appetitive versus Aversive Outcomes
inferredcites →https://doi.org/10.1523/jneurosci.4925-04.2005openalex-snapshot
Physiological Changes in Glucose Differentially Modulate the Excitability of Hypothalamic Melanin-Concentrating Hormone and Orexin NeuronsIn Situ
inferredcites →https://doi.org/10.1523/jneurosci.5269-14.2015openalex-snapshot
Optogenetic Evidence for Inhibitory Signaling from Orexin to MCH Neurons via Local Microcircuits
inferredcites →https://doi.org/10.1677/joe.1.06964openalex-snapshot
The neuroendocrine system of invertebrates: a developmental and evolutionary perspective
inferredcites →https://doi.org/10.3389/fnbeh.2012.00081openalex-snapshot
Glutamate and GABA as rapid effectors of hypothalamic “peptidergic” neurons
inferredcites →https://doi.org/10.3389/fnins.2013.00012openalex-snapshot
The Dilemmas of the Gourmet Fly: The Molecular and Neuronal Mechanisms of Feeding and Nutrient Decision Making in Drosophila
inferredcites →https://doi.org/10.3389/fnsys.2014.00192openalex-snapshot
A unifying computational framework for stability and flexibility of arousal
inferredcites →https://doi.org/10.3389/fnsys.2018.00014openalex-snapshot
Lateral Hypothalamus as a Motivation-Cognition Interface in the Control of Feeding Behavior
inferredcites →https://doi.org/10.7554/elife.01462openalex-snapshot
Hypothalamic melanin concentrating hormone neurons communicate the nutrient value of sugar
inferredcites →https://doi.org/10.7554/elife.19920openalex-snapshot
Internal states drive nutrient homeostasis by modulating exploration-exploitation trade-off
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Alterations of learning and memory are accompanied by alterations in the expression of 5-HT receptors, glucocorticoid receptor and brain-derived neurotrophic factor in different brain regions of an animal model of depression generated by neonatally male treatment with clomipramine in male rats
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Transcriptomic analysis to identify genes associated with hypothalamus vulnerability in aging mice with cognitive decline
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Orexin A ameliorates high altitude induced memory retrieval impairment via BDNF/TrkB and PI3K/AKT/mTOR signaling pathways
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Hypothalamic pregnenolone mediates recognition memory in the context of metabolic disorders
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The basolateral amygdala and lateral hypothalamus bias learning towards motivationally significant events
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Taste perceptual circuit for the generation of autonomous responses in virtual creatures
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Hypothalamic involvement in multiple system atrophy: A structural MRI study
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Flavorants enhance nicotine vapor self-administration in diet-induced obese female mice
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2024.105924openalex-snapshot
Survival in a world of complex dangers
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2024.05.018openalex-snapshot
Hypothalamic MRI-derived microstructure is associated with neurocognitive aging in humans
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2023.120340openalex-snapshot
Sleep dysfunction mediates the relationship between hypothalamic-insula connectivity and anxiety-depression symptom severity bidirectionally in young adults
inferred← citeshttps://doi.org/10.1016/j.neuron.2024.02.019openalex-snapshot
TGR5-mediated lateral hypothalamus-dCA3-dorsolateral septum circuit regulates depressive-like behavior in male mice
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2025.110513openalex-snapshot
How may the hypothalamus control distinct types and stages of memory?
inferred← citeshttps://doi.org/10.1016/j.nlm.2022.107657openalex-snapshot
Targeting the lateral hypothalamus with short hairpin RNAs reduces habitual behaviour following extended instrumental training in rats
inferred← citeshttps://doi.org/10.1016/j.peptides.2023.171128openalex-snapshot
A role for MCH neuron firing in modulating hippocampal plasticity threshold
inferred← citeshttps://doi.org/10.1016/j.physbeh.2021.113415openalex-snapshot
Introduction to the special issue: Homeostatic vs. Hedonic feeding
inferred← citeshttps://doi.org/10.1016/j.tins.2022.04.006openalex-snapshot
Construction of complex memories via parallel distributed cortical–subcortical iterative integration
inferred← citeshttps://doi.org/10.1016/j.yfrne.2021.100926openalex-snapshot
On the role of sex steroids in biological functions by classical and non-classical pathways. An update
inferred← citeshttps://doi.org/10.1016/j.ynstr.2024.100654openalex-snapshot
Hyperexcitation of the glutamatergic neurons in lateral hypothalamus induced by chronic pain contributes to depression-like behavior and learning and memory impairment in male mice
inferred← citeshttps://doi.org/10.1021/acs.jproteome.2c00691openalex-snapshot
Exercise Alleviates Behavioral Disorders but Shapes Brain Metabolism of APP/PS1 Mice in a Region- and Exercise-Specific Manner
inferred← citeshttps://doi.org/10.1038/s41598-022-13361-4openalex-snapshot
Hypothalamic connectivities predict individual differences in ADT-elicited changes in working memory and quality of life in prostate cancer patients
inferred← citeshttps://doi.org/10.1038/s41598-023-47200-xopenalex-snapshot
Fractal complexity of daily physical activity and cognitive function in a midlife cohort
inferred← citeshttps://doi.org/10.1055/s-0041-1726088openalex-snapshot
Cognitive Deficits in Pediatric Craniopharyngioma: An Updated Review
inferred← citeshttps://doi.org/10.1080/09291016.2026.2635609openalex-snapshot
“Rewiring the hypothalamus: emerging neuroendocrine and neurotechnological approaches to obesity”
inferred← citeshttps://doi.org/10.1093/brain/awab345openalex-snapshot
Multimodal mechanisms of human socially reinforced learning across neurodegenerative diseases
inferred← citeshttps://doi.org/10.1093/function/zqad059openalex-snapshot
Hypothalamic MCH Neurons: From Feeding to Cognitive Control
inferred← citeshttps://doi.org/10.1093/ijnp/pyaf072openalex-snapshot
Neuropsychiatric- and cognitive post-acute sequelae of SARS-CoV-2 infection – evidence from K18-hACE C57BL/6 J mice
inferred← citeshttps://doi.org/10.1097/tld.0000000000000358openalex-snapshot
Applying Trauma- and Violence-Informed Care to Speech-Language Pathology Practice Across the Lifespan
inferred← citeshttps://doi.org/10.1101/2020.11.03.366849openalex-snapshot
Conjunctive spatial and idiothetic codes are topographically organized in the GABAergic cells of the lateral septum
inferred← citeshttps://doi.org/10.1101/2022.12.01.518339openalex-snapshot
A role for MCH neuron firing in hippocampal plasticity and learning
inferred← citeshttps://doi.org/10.1101/2023.05.08.539627openalex-snapshot
Asymmetric control of food intake by left and right vagal sensory neurons
inferred← citeshttps://doi.org/10.1101/2023.05.18.541308openalex-snapshot
Transient targeting of hypothalamic orexin neurons alleviates seizures in a mouse model of epilepsy
inferred← citeshttps://doi.org/10.1101/2023.07.19.549648openalex-snapshot
Exploratory rearing is governed by hypothalamic MCH cells according to the locus coeruleus
inferred← citeshttps://doi.org/10.1101/2024.12.06.24318618openalex-snapshot
Efficient multi-phenotype genome-wide analysis identifies genetic associations for unsupervised deep-learning-derived high-dimensional brain imaging phenotypes
inferred← citeshttps://doi.org/10.1111/ejn.16673openalex-snapshot
Critical Regions and Connections Form Pathways and Clusters in the Mouse Brain
inferred← citeshttps://doi.org/10.1111/head.14850openalex-snapshot
Preserved working memory performance along with subcortical modulation during peri‐ictal phases in spontaneous migraine attacks
inferred← citeshttps://doi.org/10.1111/jne.13259openalex-snapshot
Eat, seek, rest? An orexin/hypocretin perspective
inferred← citeshttps://doi.org/10.1210/endrev/bnab042openalex-snapshot
From Molecule to Behavior: Hypocretin/orexin Revisited From a Sex-dependent Perspective
inferred← citeshttps://doi.org/10.1212/wnl.0000000000209603openalex-snapshot
Association Between Hypothalamic Volume and Metabolism, Cognition, and Behavior in Patients With Amyotrophic Lateral Sclerosis
inferred← citeshttps://doi.org/10.1371/journal.pbio.3001383openalex-snapshot
Conjunctive spatial and self-motion codes are topographically organized in the GABAergic cells of the lateral septum
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002768openalex-snapshot
Slow-wave sleep drives sleep-dependent renormalization of synaptic AMPA receptor levels in the hypothalamus
inferred← citeshttps://doi.org/10.14336/ad.2021.0109openalex-snapshot
SARS-CoV-2 Emergency and Long-Term Cognitive Impairment in Older People
inferred← citeshttps://doi.org/10.1523/jneurosci.0015-24.2024openalex-snapshot
Exploratory Rearing Is Governed by Hypothalamic Melanin-Concentrating Hormone Neurons According to Locus Ceruleus
inferred← citeshttps://doi.org/10.1523/jneurosci.1806-24.2025openalex-snapshot
Hypothalamic Control of Learned Flight Induced by Threat Imminence
inferred← citeshttps://doi.org/10.20944/preprints202305.0394.v1openalex-snapshot
Stop Eating Brain: The Role of the Cerebellum in Satiation
inferred← citeshttps://doi.org/10.2174/9798898815523126010004openalex-snapshot
Introduction to Memory and Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.25170/cylinder.v10i1.5479openalex-snapshot
Rancang Bangun Alat Kompres Demam Digital Suhu Hangat
inferred← citeshttps://doi.org/10.31083/j.fbl2711318openalex-snapshot
Quo vadis PGRMC? Grand-Scale Biology in Human Health and Disease
inferred← citeshttps://doi.org/10.31234/osf.io/jkmpqopenalex-snapshot
Survival Decisions in a Multidimensional World
inferred← citeshttps://doi.org/10.3233/jad-230886openalex-snapshot
Communication Regarding the Myocardial Ischemia/Reperfusion and Cognitive Impairment: A Narrative Literature Review
inferred← citeshttps://doi.org/10.3233/jad-240028openalex-snapshot
Eye Tracking During Visual Paired-Comparison Tasks: A Systematic Review and Meta-Analysis of the Diagnostic Test Accuracy for Detecting Cognitive Decline
inferred← citeshttps://doi.org/10.3389/fnagi.2022.964336openalex-snapshot
Distribution and inter-regional relationship of amyloid-beta plaque deposition in a 5xFAD mouse model of Alzheimer’s disease
inferred← citeshttps://doi.org/10.3389/fnbeh.2022.852235openalex-snapshot
Response Flexibility: The Role of the Lateral Habenula
inferred← citeshttps://doi.org/10.3389/fnins.2021.639313openalex-snapshot
Orexin/Hypocretin and MCH Neurons: Cognitive and Motor Roles Beyond Arousal
inferred← citeshttps://doi.org/10.3389/fnins.2021.644313openalex-snapshot
Neuropeptides as Primary Mediators of Brain Circuit Connectivity
inferred← citeshttps://doi.org/10.3389/fnins.2022.947295openalex-snapshot
The role of hypothalamic endoplasmic reticulum stress in schizophrenia and antipsychotic-induced weight gain: A narrative review
inferred← citeshttps://doi.org/10.3389/fnins.2026.1791299openalex-snapshot
The impact of the Lab4 probiotic on neurodegenerative processes in a murine Alzheimer’s disease model
inferred← citeshttps://doi.org/10.3389/fnins.2026.1918594openalex-snapshot
Tracing melanin-concentrating hormone function: decades of memory research and emerging links to Alzheimer’s disease
inferred← citeshttps://doi.org/10.3390/biom12020263openalex-snapshot
Unlocking the Memory Component of Alzheimer’s Disease: Biological Processes and Pathways across Brain Regions
inferred← citeshttps://doi.org/10.3390/brainsci11020239openalex-snapshot
Androgen Affects the Inhibitory Avoidance Memory by Primarily Acting on Androgen Receptor in the Brain in Adolescent Male Rats
inferred← citeshttps://doi.org/10.3390/medicina60010077openalex-snapshot
Androgen Deprivation Therapy for Prostate Cancer: Focus on Cognitive Function and Mood
inferred← citeshttps://doi.org/10.3390/molecules26071978openalex-snapshot
Involvement of Neuropeptide Galanin Receptors 2 and 3 in Learning, Memory and Anxiety in Aging Mice
inferred← citeshttps://doi.org/10.37349/eds.2025.1008125openalex-snapshot
Role of brain cholecystokinin in neuronal homeostasis: rediscovering novel functions of an old neuropeptide
inferred← citeshttps://doi.org/10.64898/2026.06.26.734738openalex-snapshot
Melanin-concentrating hormone signaling regulates prefrontal updating of learned avoidance
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