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AgRP neurons: Regulators of feeding, energy expenditure, and behavior

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/bbrc.1999.0675openalex-snapshot
Changes in Hypothalamic Agouti-Related Protein (AGRP), but not α-MSH or Pro-Opiomelanocortin Concentrations in Dietary-Obese and Food-Restricted Rats
inferredcites →https://doi.org/10.1007/s11055-010-9253-0openalex-snapshot
Regulation of Food Consumption during Pregnancy and Lactation in Mice
inferredcites →https://doi.org/10.1016/0031-9384(79)90306-8openalex-snapshot
GABA and hypothalamic feeding systems. I. Topographic analysis of the effects of microinjections of muscimol
inferredcites →https://doi.org/10.1016/0031-9384(81)90366-8openalex-snapshot
Hypothalamic paraventricular nucleus lesions produce overeating and obesity in the rat
inferredcites →https://doi.org/10.1016/0031-9384(84)90176-8openalex-snapshot
Nociceptive thresholds following food restriction and return to free-feeding
inferredcites →https://doi.org/10.1016/0196-9781(84)90165-7openalex-snapshot
Neuropeptide Y: A potent inducer of consummatory behavior in rats
inferredcites →https://doi.org/10.1016/0303-7207(94)90113-9openalex-snapshot
The human melanocyte stimulating hormone receptor has evolved to become “super-sensitive” to melanocortin peptides
inferredcites →https://doi.org/10.1016/0306-4522(85)90260-xopenalex-snapshot
The anatomy of neuropeptide-y-containing neurons in rat brain
inferredcites →https://doi.org/10.1016/0306-4522(90)90181-3openalex-snapshot
Effect of corticotropin releasing hormone and neuropeptide Y on electrophysiological activity of sympathetic nerves to interscapular brown adipose tissue
inferredcites →https://doi.org/10.1016/0361-9230(85)90100-5openalex-snapshot
Feeding and drinking elicited by central injection of neuropeptide Y: Evidence for a hypothalamic site(s) of action
inferredcites →https://doi.org/10.1016/j.cell.2005.08.035openalex-snapshot
Divergence of Melanocortin Pathways in the Control of Food Intake and Energy Expenditure
inferredcites →https://doi.org/10.1016/j.cell.2009.04.022openalex-snapshot
Loss of GABAergic Signaling by AgRP Neurons to the Parabrachial Nucleus Leads to Starvation
inferredcites →https://doi.org/10.1016/j.cell.2013.11.002openalex-snapshot
Parallel, Redundant Circuit Organization for Homeostatic Control of Feeding Behavior
inferredcites →https://doi.org/10.1016/j.cell.2014.05.017openalex-snapshot
Natural Neural Projection Dynamics Underlying Social Behavior
inferredcites →https://doi.org/10.1016/j.cell.2014.09.010openalex-snapshot
O-GlcNAc Transferase Enables AgRP Neurons to Suppress Browning of White Fat
inferredcites →https://doi.org/10.1016/j.cell.2014.12.026openalex-snapshot
Visualizing Hypothalamic Network Dynamics for Appetitive and Consummatory Behaviors
inferredcites →https://doi.org/10.1016/j.cell.2015.01.033openalex-snapshot
Sensory Detection of Food Rapidly Modulates Arcuate Feeding Circuits
inferredcites →https://doi.org/10.1016/j.cell.2015.02.024openalex-snapshot
Hypothalamic Agrp Neurons Drive Stereotypic Behaviors beyond Feeding
inferredcites →https://doi.org/10.1016/j.cell.2016.02.044openalex-snapshot
AgRP Neurons Control Systemic Insulin Sensitivity via Myostatin Expression in Brown Adipose Tissue
inferredcites →https://doi.org/10.1016/j.cell.2016.05.011openalex-snapshot
Sensory Neurons that Detect Stretch and Nutrients in the Digestive System
inferredcites →https://doi.org/10.1016/j.cell.2018.02.057openalex-snapshot
A Neural Circuit for the Suppression of Pain by a Competing Need State
inferredcites →https://doi.org/10.1016/j.cell.2019.04.026openalex-snapshot
Functional Ontogeny of Hypothalamic Agrp Neurons in Neonatal Mouse Behaviors
inferredcites →https://doi.org/10.1016/j.cell.2019.10.031openalex-snapshot
Genetic Identification of Vagal Sensory Neurons That Control Feeding
inferredcites →https://doi.org/10.1016/j.celrep.2017.11.036openalex-snapshot
Nutritive, Post-ingestive Signals Are the Primary Regulators of AgRP Neuron Activity
inferredcites →https://doi.org/10.1016/j.cmet.2006.07.002openalex-snapshot
The circadian rhythm of glucocorticoids is regulated by a gating mechanism residing in the adrenal cortical clock
inferredcites →https://doi.org/10.1016/j.cmet.2007.02.004openalex-snapshot
Diet-Induced Obesity Causes Severe but Reversible Leptin Resistance in Arcuate Melanocortin Neurons
inferredcites →https://doi.org/10.1016/j.cmet.2007.05.004openalex-snapshot
Insulin Action in AgRP-Expressing Neurons Is Required for Suppression of Hepatic Glucose Production
inferredcites →https://doi.org/10.1016/j.cmet.2013.09.009openalex-snapshot
Rapid versus Delayed Stimulation of Feeding by the Endogenously Released AgRP Neuron Mediators GABA, NPY, and AgRP
inferredcites →https://doi.org/10.1016/j.cmet.2016.04.006openalex-snapshot
Parabrachial CGRP Neurons Control Meal Termination
inferredcites →https://doi.org/10.1016/j.cmet.2018.10.016openalex-snapshot
Defined Paraventricular Hypothalamic Populations Exhibit Differential Responses to Food Contingent on Caloric State
inferredcites →https://doi.org/10.1016/j.cmet.2018.12.015openalex-snapshot
β Cell Dysfunction in Type 2 Diabetes: Drained of Energy?
inferredcites →https://doi.org/10.1016/j.cmet.2019.01.023openalex-snapshot
Transcriptional Basis for Rhythmic Control of Hunger and Metabolism within the AgRP Neuron
inferredcites →https://doi.org/10.1016/j.cmet.2020.12.018openalex-snapshot
Hypothalamic detection of macronutrients via multiple gut-brain pathways
inferredcites →https://doi.org/10.1016/j.conb.2020.08.009openalex-snapshot
Exploring internal state-coding across the rodent brain
inferredcites →https://doi.org/10.1016/j.cub.2016.11.019openalex-snapshot
Thirst
inferredcites →https://doi.org/10.1016/j.cub.2018.09.055openalex-snapshot
Hypothalamic Neurons that Regulate Feeding Can Influence Sleep/Wake States Based on Homeostatic Need
inferredcites →https://doi.org/10.1016/j.molmet.2014.07.002openalex-snapshot
Ablation of AgRP neurons impairs adaption to restricted feeding
inferredcites →https://doi.org/10.1016/j.neuron.2009.07.010openalex-snapshot
Linking Genetically Defined Neurons to Behavior through a Broadly Applicable Silencing Allele
inferredcites →https://doi.org/10.1016/j.neuron.2016.01.040openalex-snapshot
DREADDs for Neuroscientists
inferredcites →https://doi.org/10.1016/j.neuron.2016.08.032openalex-snapshot
Hunger-Driven Motivational State Competition
inferredcites →https://doi.org/10.1016/j.neuron.2016.10.021openalex-snapshot
Coding and Plasticity in the Mammalian Thermosensory System
inferredcites →https://doi.org/10.1016/j.neuron.2017.06.014openalex-snapshot
Toward a Wiring Diagram Understanding of Appetite Control
inferredcites →https://doi.org/10.1016/j.neuron.2017.09.043openalex-snapshot
Dynamics of Gut-Brain Communication Underlying Hunger
inferredcites →https://doi.org/10.1016/j.neuron.2019.02.028openalex-snapshot
The Paraventricular Hypothalamus Regulates Satiety and Prevents Obesity via Two Genetically Distinct Circuits
inferredcites →https://doi.org/10.1016/j.physbeh.2009.10.004openalex-snapshot
Acute exposure to a high-fat diet alters meal patterns and body composition
inferredcites →https://doi.org/10.1016/j.pneurobio.2015.03.002openalex-snapshot
Taste, olfactory, and food reward value processing in the brain
inferredcites →https://doi.org/10.1016/j.tem.2020.04.006openalex-snapshot
Integrating Hunger with Rival Motivations
inferredcites →https://doi.org/10.1016/j.tins.2018.03.007openalex-snapshot
The Parabrachial Nucleus: CGRP Neurons Function as a General Alarm
inferredcites →https://doi.org/10.1016/j.tins.2020.10.007openalex-snapshot
The Emerging Science of Interoception: Sensing, Integrating, Interpreting, and Regulating Signals within the Self
inferredcites →https://doi.org/10.1016/j.yfrne.2015.07.002openalex-snapshot
Developmental influences on circuits programming susceptibility to obesity
inferredcites →https://doi.org/10.1016/s0006-8993(00)02580-4openalex-snapshot
Leptin receptor, NPY, POMC mRNA expression in the diet-induced obese mouse brain
inferredcites →https://doi.org/10.1016/s0006-8993(97)00184-4openalex-snapshot
Heterogeneity in the neuropeptide Y-containing neurons of the rat arcuate nucleus: GABAergic and non-GABAergic subpopulations
inferredcites →https://doi.org/10.1016/s0006-8993(98)00837-3openalex-snapshot
Feeding effects of hypothalamic injection of melanocortin 4 receptor ligands
inferredcites →https://doi.org/10.1016/s0092-8674(00)81865-6openalex-snapshot
Targeted Disruption of the Melanocortin-4 Receptor Results in Obesity in Mice
inferredcites →https://doi.org/10.1016/s0092-8674(05)80067-4openalex-snapshot
Molecular characterization of the mouse agouti locus
inferredcites →https://doi.org/10.1016/s0896-6273(03)00063-1openalex-snapshot
The Distribution and Mechanism of Action of Ghrelin in the CNS Demonstrates a Novel Hypothalamic Circuit Regulating Energy Homeostasis
inferredcites →https://doi.org/10.1017/cbo9780511565595openalex-snapshot
Temperature Regulation in Laboratory Rodents
inferredcites →https://doi.org/10.1037/a0035942openalex-snapshot
Clarifying the roles of homeostasis and allostasis in physiological regulation.
inferredcites →https://doi.org/10.1038/014351d0openalex-snapshot
A Large Meteor
inferredcites →https://doi.org/10.1038/1082openalex-snapshot
Coexpression of Agrp and NPY in fasting-activated hypothalamic neurons
inferredcites →https://doi.org/10.1038/2146openalex-snapshot
Making the most of transgenic mice
inferredcites →https://doi.org/10.1038/2404openalex-snapshot
A frameshift mutation in MC4R associated with dominantly inherited human obesity
inferredcites →https://doi.org/10.1038/2407openalex-snapshot
A frameshift mutation in human MC4R is associated with a dominant form of obesity
inferredcites →https://doi.org/10.1038/35007534openalex-snapshot
Central nervous system control of food intake
inferredcites →https://doi.org/10.1038/35078085openalex-snapshot
Leptin activates anorexigenic POMC neurons through a neural network in the arcuate nucleus
inferredcites →https://doi.org/10.1038/37379openalex-snapshot
Leptin inhibits hypothalamic neurons by activation of ATP-sensitive potassium channels
inferredcites →https://doi.org/10.1038/381415a0openalex-snapshot
Sensitivity to leptin and susceptibility to seizures of mice lacking neuropeptide Y
inferredcites →https://doi.org/10.1038/382250a0openalex-snapshot
Role of leptin in the neuroendocrine response to fasting
inferredcites →https://doi.org/10.1038/385165a0openalex-snapshot
Role of melanocortinergic neurons in feeding and the agouti obesity syndrome
inferredcites →https://doi.org/10.1038/5070openalex-snapshot
Response of melanocortin–4 receptor–deficient mice to anorectic and orexigenic peptides
inferredcites →https://doi.org/10.1038/77660openalex-snapshot
Insulin activates ATP-sensitive K+ channels in hypothalamic neurons of lean, but not obese rats
inferredcites →https://doi.org/10.1038/emboj.2011.452openalex-snapshot
Ubiquitin‐mediated regulation of RhoGTPase signalling: IAPs and HACE1 enter the fray
inferredcites →https://doi.org/10.1038/emboj.2012.250openalex-snapshot
Hypothalamic AgRP‐neurons control peripheral substrate utilization and nutrient partitioning
inferredcites →https://doi.org/10.1038/nature10899openalex-snapshot
Deciphering a neuronal circuit that mediates appetite
inferredcites →https://doi.org/10.1038/nature11270openalex-snapshot
Deconstruction of a neural circuit for hunger
inferredcites →https://doi.org/10.1038/nature11846openalex-snapshot
Concurrent activation of striatal direct and indirect pathways during action initiation
inferredcites →https://doi.org/10.1038/nature12354openalex-snapshot
Ultrasensitive fluorescent proteins for imaging neuronal activity
inferredcites →https://doi.org/10.1038/nature12596openalex-snapshot
Genetic identification of a neural circuit that suppresses appetite
inferredcites →https://doi.org/10.1038/nature12956openalex-snapshot
An excitatory paraventricular nucleus to AgRP neuron circuit that drives hunger
inferredcites →https://doi.org/10.1038/nature14416openalex-snapshot
Neurons for hunger and thirst transmit a negative-valence teaching signal
inferredcites →https://doi.org/10.1038/nature24636openalex-snapshot
Fully integrated silicon probes for high-density recording of neural activity
inferredcites →https://doi.org/10.1038/ng1197-273openalex-snapshot
Overexpression of Agrt leads to obesity in transgenic mice
inferredcites →https://doi.org/10.1038/nmeth.1808openalex-snapshot
Principles for applying optogenetic tools derived from direct comparative analysis of microbial opsins
inferredcites →https://doi.org/10.1038/nn.2167openalex-snapshot
Synaptic release of GABA by AgRP neurons is required for normal regulation of energy balance
inferredcites →https://doi.org/10.1038/nn.2739openalex-snapshot
AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training
inferredcites →https://doi.org/10.1038/nn.4011openalex-snapshot
A neural basis for melanocortin-4 receptor–regulated appetite
inferredcites →https://doi.org/10.1038/nn.4220openalex-snapshot
Lateral hypothalamic circuits for feeding and reward
inferredcites →https://doi.org/10.1038/nn.4274openalex-snapshot
Agouti-related peptide neural circuits mediate adaptive behaviors in the starved state
inferredcites →https://doi.org/10.1038/nn.4392openalex-snapshot
Dynamic GABAergic afferent modulation of AgRP neurons
inferredcites →https://doi.org/10.1038/nn.4574openalex-snapshot
Cancer-induced anorexia and malaise are mediated by CGRP neurons in the parabrachial nucleus
inferredcites →https://doi.org/10.1038/nn1455openalex-snapshot
Anatomy and regulation of the central melanocortin system
inferredcites →https://doi.org/10.1038/nn1548openalex-snapshot
Agouti-related peptide–expressing neurons are mandatory for feeding
inferredcites →https://doi.org/10.1038/nrn.2016.125openalex-snapshot
Circuit modules linking internal states and social behaviour in flies and mice
inferredcites →https://doi.org/10.1038/nrn.2017.71openalex-snapshot
Neural circuits underlying thirst and fluid homeostasis
inferredcites →https://doi.org/10.1038/s41467-018-08239-xopenalex-snapshot
Regulation of substrate utilization and adiposity by Agrp neurons
inferredcites →https://doi.org/10.1038/s41467-019-12478-xopenalex-snapshot
Hypothalamic neuronal circuits regulating hunger-induced taste modification
inferredcites →https://doi.org/10.1038/s41467-020-14291-3openalex-snapshot
NPY mediates the rapid feeding and glucose metabolism regulatory functions of AgRP neurons
inferredcites →https://doi.org/10.1038/s41467-020-17171-yopenalex-snapshot
Meta-analysis of multidecadal biodiversity trends in Europe
inferredcites →https://doi.org/10.1038/s41467-020-17720-5openalex-snapshot
Transcriptomic analysis links diverse hypothalamic cell types to fibroblast growth factor 1-induced sustained diabetes remission
inferredcites →https://doi.org/10.1038/s41551-019-0373-8openalex-snapshot
Multimodal in vivo brain electrophysiology with integrated glass microelectrodes
inferredcites →https://doi.org/10.1038/s41586-018-0049-7openalex-snapshot
Genetic identification of leptin neural circuits in energy and glucose homeostases
inferredcites →https://doi.org/10.1038/s41586-021-03299-4openalex-snapshot
Hunger enhances food-odour attraction through a neuropeptide Y spotlight
inferredcites →https://doi.org/10.1038/s41593-020-0684-9openalex-snapshot
High-fat food biases hypothalamic and mesolimbic expression of consummatory drives
inferredcites →https://doi.org/10.1038/s42255-018-0029-0openalex-snapshot
Perineuronal net formation during the critical period for neuronal maturation in the hypothalamic arcuate nucleus
inferredcites →https://doi.org/10.1038/s42255-020-0229-2openalex-snapshot
Profound and redundant functions of arcuate neurons in obesity development
inferredcites →https://doi.org/10.1038/sj.ijo.0801610openalex-snapshot
Changes in energy metabolism in response to 48 h of overfeeding and fasting in Caucasians and Pima Indians
inferredcites →https://doi.org/10.1038/srep16810openalex-snapshot
Diet composition, not calorie intake, rapidly alters intrinsic excitability of hypothalamic AgRP/NPY neurons in mice
inferredcites →https://doi.org/10.1046/j.1365-2826.1997.00554.xopenalex-snapshot
Intracerebroventricular Neuropeptide Y Acutely Influences Glucose Metabolism and Insulin Sensitivity in the Rat
inferredcites →https://doi.org/10.1055/s-2002-38252openalex-snapshot
Effect of Acute Cold Exposure on the Expression of the Adiponectin, Resistin and Leptin Genes in Rat White and Brown Adipose Tissues
inferredcites →https://doi.org/10.1056/nejm199602013340503openalex-snapshot
Serum Immunoreactive-Leptin Concentrations in Normal-Weight and Obese Humans
inferredcites →https://doi.org/10.1073/pnas.1621065114openalex-snapshot
AgRP to Kiss1 neuron signaling links nutritional state and fertility
inferredcites →https://doi.org/10.1073/pnas.1817503116openalex-snapshot
Connectional architecture of a mouse hypothalamic circuit node controlling social behavior
inferredcites →https://doi.org/10.1073/pnas.2004941117openalex-snapshot
Chronic G q signaling in AgRP neurons does not cause obesity
inferredcites →https://doi.org/10.1073/pnas.82.11.3940openalex-snapshot
Neuropeptide Y injected in the paraventricular hypothalamus: a powerful stimulant of feeding behavior.
inferredcites →https://doi.org/10.1073/pnas.95.25.15043openalex-snapshot
The neuropeptide Y/agouti gene-related protein (AGRP) brain circuitry in normal, anorectic, and monosodium glutamate-treated mice
inferredcites →https://doi.org/10.1074/jbc.m109.039339openalex-snapshot
Pertussis Toxin-sensitive Signaling of Melanocortin-4 Receptors in Hypothalamic GT1-7 Cells Defines Agouti-related Protein as a Biased Agonist
inferredcites →https://doi.org/10.1096/fasebj.8.8.8181666openalex-snapshot
Obesity, diabetes, and neoplasia in yellow A vy /‐ mice: ectopic expression of the agouti gene
inferredcites →https://doi.org/10.1096/fj.04-3434fjeopenalex-snapshot
Postembryonic ablation of AgRP neurons in mice leads to a lean, hypophagic phenotype
inferredcites →https://doi.org/10.1101/gad.11.5.593openalex-snapshot
Hypothalamic expression of ART, a novel gene related to agouti, is up-regulated in obese and diabetic mutant mice.
inferredcites →https://doi.org/10.1101/gad.7.3.454openalex-snapshot
Cloning of the mouse agouti gene predicts a secreted protein ubiquitously expressed in mice carrying the lethal yellow mutation.
inferredcites →https://doi.org/10.1111/febs.15791openalex-snapshot
Hunger‐driven adaptive prioritization of behavior
inferredcites →https://doi.org/10.1111/j.1469-185x.1965.tb00794.xopenalex-snapshot
ADAPTATION OF MICE TO COLD
inferredcites →https://doi.org/10.1126/science.1115524openalex-snapshot
NPY/AgRP Neurons Are Essential for Feeding in Adult Mice but Can Be Ablated in Neonates
inferredcites →https://doi.org/10.1126/science.1241812openalex-snapshot
The Inhibitory Circuit Architecture of the Lateral Hypothalamus Orchestrates Feeding
inferredcites →https://doi.org/10.1126/science.1325670openalex-snapshot
The Cloning of a Family of Genes That Encode the Melanocortin Receptors
inferredcites →https://doi.org/10.1126/science.278.5335.135openalex-snapshot
Antagonism of Central Melanocortin Receptors in Vitro and in Vivo by Agouti-Related Protein
inferredcites →https://doi.org/10.1126/science.7624778openalex-snapshot
Recombinant Mouse OB Protein: Evidence for a Peripheral Signal Linking Adiposity and Central Neural Networks
inferredcites →https://doi.org/10.1128/mcb.22.14.5027-5035.2002openalex-snapshot
Neither Agouti-Related Protein nor Neuropeptide Y Is Critically Required for the Regulation of Energy Homeostasis in Mice
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/ajpendo.00230.2001openalex-snapshot
Effects of dietary fat types on body fatness, leptin, and ARC leptin receptor, NPY, and AgRP mRNA expression
inferredcites →https://doi.org/10.1152/ajplegacy.1952.172.1.162openalex-snapshot
Increase of Food Intake Induced by Electrical Stimulation of the Lateral Hypothalamus
inferredcites →https://doi.org/10.1152/ajpregu.00185.2009openalex-snapshot
Role of hypoleptinemia during cold adaptation in Brandt's voles (Lasiopodomys brandtii)
inferredcites →https://doi.org/10.1152/ajpregu.1998.274.1.r62openalex-snapshot
Hyperphagia in cold-exposed rats is accompanied by decreased plasma leptin but unchanged hypothalamic NPY
inferredcites →https://doi.org/10.1152/physrev.00015.2003openalex-snapshot
Brown Adipose Tissue: Function and Physiological Significance
inferredcites →https://doi.org/10.1172/jci118891openalex-snapshot
Identification of targets of leptin action in rat hypothalamus.
inferredcites →https://doi.org/10.1172/jci46229openalex-snapshot
Rapid, reversible activation of AgRP neurons drives feeding behavior in mice
inferredcites →https://doi.org/10.1210/en.142.3.1050openalex-snapshot
Immediate and Prolonged Patterns of Agouti-Related Peptide-(83-132)-Induced c-Fos Activation in Hypothalamic and Extrahypothalamic Sites
inferredcites →https://doi.org/10.1210/en.2014-1169openalex-snapshot
Role of Melanocortin Signaling in Neuroendocrine and Metabolic Actions of Leptin in Male Rats With Uncontrolled Diabetes
inferredcites →https://doi.org/10.1210/er.2017-00111openalex-snapshot
Obesity Pathogenesis: An Endocrine Society Scientific Statement
inferredcites →https://doi.org/10.1292/jvms.67.639openalex-snapshot
Changes in Orexin-A and Neuropeptide Y Expression in the Hypothalamus of Obese and Lean Zucker Diabetic Fatty Rats
inferredcites →https://doi.org/10.1371/journal.pbio.0030415openalex-snapshot
Effects of Hypothalamic Neurodegeneration on Energy Balance
inferredcites →https://doi.org/10.1523/eneuro.0207-17.2017openalex-snapshot
Aberrant Cortical Activity in Multiple GCaMP6-Expressing Transgenic Mouse Lines
inferredcites →https://doi.org/10.1523/jneurosci.0798-17.2017openalex-snapshot
AgRP Neurons Can Increase Food Intake during Conditions of Appetite Suppression and Inhibit Anorexigenic Parabrachial Neurons
inferredcites →https://doi.org/10.1523/jneurosci.0958-18.2018openalex-snapshot
AGRP Neurons Project to the Medial Preoptic Area and Modulate Maternal Nest-Building
inferredcites →https://doi.org/10.1523/jneurosci.4861-12.2014openalex-snapshot
Leptin Modulates the Intrinsic Excitability of AgRP/NPY Neurons in the Arcuate Nucleus of the Hypothalamus
inferredcites →https://doi.org/10.2337/diabetes.48.4.828openalex-snapshot
Leptin receptor mRNA identifies a subpopulation of neuropeptide Y neurons activated by fasting in rat hypothalamus.
inferredcites →https://doi.org/10.2337/diabetes.49.2.244openalex-snapshot
Effects of streptozotocin-induced diabetes and insulin treatment on the hypothalamic melanocortin system and muscle uncoupling protein 3 expression in rats.
inferredcites →https://doi.org/10.2337/diabetes.53.8.1949openalex-snapshot
PYY3–36 Reinforces Insulin Action on Glucose Disposal in Mice Fed a High-Fat Diet
inferredcites →https://doi.org/10.3389/fnana.2015.00040openalex-snapshot
Whole-brain mapping of the direct inputs and axonal projections of POMC and AgRP neurons
inferredcites →https://doi.org/10.3892/ijmm.12.3.379openalex-snapshot
Acute intracerebroventricular administration of either carboxyl-terminal or amino-terminal fragments of agouti-related peptide produces a long-term decrease in energy expenditure in rats
inferredcites →https://doi.org/10.7554/elife.07122openalex-snapshot
Arcuate hypothalamic AgRP and putative POMC neurons show opposite changes in spiking across multiple timescales
inferredcites →https://doi.org/10.7554/elife.18640openalex-snapshot
Hunger neurons drive feeding through a sustained, positive reinforcement signal
inferredcites →https://doi.org/10.7554/elife.44527openalex-snapshot
Need-based prioritization of behavior
inferredcites →https://doi.org/10.7554/elife.46348openalex-snapshot
Sustained NPY signaling enables AgRP neurons to drive feeding
inferredcites →https://doi.org/10.7554/elife.55909openalex-snapshot
Obesity causes selective and long-lasting desensitization of AgRP neurons to dietary fat
inferredcites →https://doi.org/10.7554/elife.58764openalex-snapshot
Cold-induced hyperphagia requires AgRP neuron activation in mice
inferredcites →https://doi.org/10.7554/elife.63671openalex-snapshot
Leptin receptor neurons in the dorsomedial hypothalamus regulate diurnal patterns of feeding, locomotion, and metabolism

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

inferred← citeshttps://doi.org/10.2139/ssrn.4777231openalex-extracted
Effects of Feed Supplemented with Enzyme-Hydrolyzed Black Soldier Fly (Bsf) on Growth Performance,Antioxidant Capacity, Hepatointestinal Morphology, Feeding and its Related Genes Expression of the Spotted Sea Bass (Lateolabrax Maculatus)
inferred← citeshttps://doi.org/10.2139/ssrn.4836207openalex-extracted
Effects of Feed Supplemented with Enzyme-Hydrolyzed Black Soldier Fly (Bsf) on Growth Performance,Antioxidant Capacity, Hepatointestinal Morphology, Feeding and its Related Genes Expression of Spotted Sea Bass (Lateolabrax Maculatus)
inferred← citeshttps://doi.org/10.1002/advs.202204487openalex-snapshot
Fasting: From Physiology to Pathology
inferred← citeshttps://doi.org/10.1002/bies.202400016openalex-snapshot
A unified theoretical framework underlying the regulation of motivated behavior
inferred← citeshttps://doi.org/10.1002/cne.25619openalex-snapshot
An atlas and database of neuropeptide gene expression in the adult zebrafish forebrain
inferred← citeshttps://doi.org/10.1002/oby.70202openalex-snapshot
G Protein‐Coupled Receptor 17 (Gpr17) Enhances Leptin and Insulin Sensitivity in Lean and Obese Mouse Models
inferred← citeshttps://doi.org/10.1007/978-3-031-40116-9_22openalex-snapshot
Brain Regulation of Feeding and Energy Homeostasis
inferred← citeshttps://doi.org/10.1007/978-3-032-10099-3_32openalex-snapshot
The Hungry Mind: Exploring Hypothalamic Dysfunction in Prader-Willi Syndrome
inferred← citeshttps://doi.org/10.1007/978-3-032-24097-2_5openalex-snapshot
Neurobiology of Obesity and Aging: Bridging the Gap Between Metabolic and Brain Health
inferred← citeshttps://doi.org/10.1007/978-3-319-12125-3_22-2openalex-snapshot
Brain Regulation of Feeding and Energy Homeostasis
inferred← citeshttps://doi.org/10.1007/s10142-026-01987-wopenalex-snapshot
Integrative exome sequencing and multi-omics analysis elucidates the regulatory role of rare variants in metabolic syndrome
inferred← citeshttps://doi.org/10.1007/s10989-024-10680-0openalex-snapshot
Spexin (Neuropeptide Q): Distribution, Functional Roles, and Emerging Therapeutic Perspectives
inferred← citeshttps://doi.org/10.1007/s11154-025-10007-4openalex-snapshot
LEAP2 as a therapeutic target in obesity and cardiometabolic disorders
inferred← citeshttps://doi.org/10.1007/s11154-026-10038-5openalex-snapshot
From diet to hypothalamic dysfunction: Neuroanatomical and hormonal integration of the microbiota-hypothalamus-adipose tissue axis
inferred← citeshttps://doi.org/10.1007/s12264-024-01335-7openalex-snapshot
Neuronal Regulation of Feeding and Energy Metabolism: A Focus on the Hypothalamus and Brainstem
inferred← citeshttps://doi.org/10.1007/s13105-026-01185-zopenalex-snapshot
Dietary bioactive compounds modulating satiety and appetite: mechanisms of action
inferred← citeshttps://doi.org/10.1016/b978-0-443-29068-8.00065-9openalex-snapshot
Food intake: Behavioral endocrinology
inferred← citeshttps://doi.org/10.1016/j.appet.2022.106146openalex-snapshot
Brain regulation of hunger and motivation: The case for integrating homeostatic and hedonic concepts and its implications for obesity and addiction
inferred← citeshttps://doi.org/10.1016/j.apsb.2026.06.035openalex-snapshot
Rationale of renewed efforts in developing MC4R modulators to treat metabolic disorders
inferred← citeshttps://doi.org/10.1016/j.cbpb.2025.111174openalex-snapshot
N-terminal domains and site-specific glycosylation regulate the secretion of avian melanocortin inverse agonists, agouti signaling protein (ASIP) and agouti-related protein (AGRP)
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112789openalex-snapshot
AgRP neurons are not indispensable for body weight maintenance in adult mice
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115659openalex-snapshot
The gut-brain axis mechanism of normal appetite induced by kynurenic acid
inferred← citeshttps://doi.org/10.1016/j.cmet.2024.01.003openalex-snapshot
Region-specific transcriptomic responses to obesity and diabetes in macaque hypothalamus
inferred← citeshttps://doi.org/10.1016/j.cub.2024.02.074openalex-snapshot
A brainstem to hypothalamic arcuate nucleus GABAergic circuit drives feeding
inferred← citeshttps://doi.org/10.1016/j.envres.2025.121151openalex-snapshot
Modulated regulation of the stress-feeding-growth neuroendocrine cascade in Chinese sea bass (Lateolabrax maculatus) under temperature and salinity changes
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112797openalex-snapshot
Angiotensin AT1R expressing cells within the ventral hypothalamus modulate integrative control of cardiometabolic functions
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110768openalex-snapshot
Leptin and G-protein coupled receptor (GPCR) signaling: Therapeutic potential in obesity
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133570openalex-snapshot
Inhalation of diesel exhaust particulate matter accelerates weight gain via regulation of hypothalamic appetite-related genes and gut microbiota metabolism
inferred← citeshttps://doi.org/10.1016/j.job.2026.100813openalex-snapshot
Cephalic phase response in systemic glucose metabolism: How taste triggers glucose homeostasis
inferred← citeshttps://doi.org/10.1016/j.joim.2024.03.001openalex-snapshot
Acupuncture for obesity and related diseases: Insight for regulating neural circuit
inferred← citeshttps://doi.org/10.1016/j.marenvres.2025.107315openalex-snapshot
Comparative survey on the central melanocortin system reveals specific neuroendocrine response in Chinese seabass (Lateolabrax maculatus) and humpback grouper (Cromileptes altivelis) under salinity changes
inferred← citeshttps://doi.org/10.1016/j.mce.2025.112554openalex-snapshot
5,7,3′,4′,5′-pentamethoxyflavone (PMF) exhibits anti-obesity and neuroprotective effects in an obese zebrafish model
inferred← citeshttps://doi.org/10.1016/j.metabol.2023.155677openalex-snapshot
Perinatal metabolic inflammation in the hypothalamus impairs the development of homeostatic feeding circuitry
inferred← citeshttps://doi.org/10.1016/j.metabol.2026.156595openalex-snapshot
An obligatory role for AgRP neurons in maintaining body temperature during time-restricted feeding
inferred← citeshttps://doi.org/10.1016/j.molmet.2021.101366openalex-snapshot
Refeeding activates neurons in the dorsomedial hypothalamus to inhibit food intake and promote positive valence
inferred← citeshttps://doi.org/10.1016/j.molmet.2023.101835openalex-snapshot
High-fat diet feeding disrupts the coupling of thermoregulation to energy homeostasis
inferred← citeshttps://doi.org/10.1016/j.molmet.2024.101886openalex-snapshot
Identification of AgRP cells in the murine hindbrain that drive feeding
inferred← citeshttps://doi.org/10.1016/j.molmet.2025.102258openalex-snapshot
Dax1 in AgRP neurons regulates thermogenesis via GR-HDAC3-mediated CRFR1 suppression
inferred← citeshttps://doi.org/10.1016/j.molmet.2025.102300openalex-snapshot
Sustained diabetes remission induced by FGF1 involves a shift in transcriptionally distinct AgRP neuron subpopulations
inferred← citeshttps://doi.org/10.1016/j.molmet.2026.102372openalex-snapshot
AgRP neuron activity predicts and tracks the glycemic response to oral glucose
inferred← citeshttps://doi.org/10.1016/j.neuron.2025.09.036openalex-snapshot
Reversal of diet-induced obesity by central insulin sensitizer FSTL1
inferred← citeshttps://doi.org/10.1016/j.neuron.2025.12.025openalex-snapshot
Granular motivational interaction and behavioral choice during feeding
inferred← citeshttps://doi.org/10.1016/j.neuron.2026.03.038openalex-snapshot
Mitochondrial fission factor regulates mitochondrial Ca2+ homeostasis and neuronal activity in AgRP neurons
inferred← citeshttps://doi.org/10.1016/j.neuron.2026.05.010openalex-snapshot
A hypothalamic circuit for anticipating future changes in energy balance
inferred← citeshttps://doi.org/10.1016/j.npep.2024.102461openalex-snapshot
Upregulation of Xbp1 in NPY/AgRP neurons reverses diet-induced obesity and ameliorates leptin and insulin resistance
inferred← citeshttps://doi.org/10.1016/j.obmed.2025.100588openalex-snapshot
Obesity-driven hunger: From pathophysiology to intervention
inferred← citeshttps://doi.org/10.1016/j.peptides.2025.171356openalex-snapshot
The intricate relationship between circadian rhythms and gastrointestinal peptides in obesity
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2024.102682openalex-snapshot
Opposing effects of nicotine on hypothalamic arcuate nucleus POMC and NPY neurons
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2023.110907openalex-snapshot
Are decreased cocaine- and amphetamine regulated transcript and Agouti- related peptide levels associated Eating behavior in medication-free children with attention deficit and hyperactivity disorder?
inferred← citeshttps://doi.org/10.1016/j.psj.2025.106331openalex-snapshot
Effects of commercial genetic selection on gene expression in the developing neuroendocrine system of broilers
inferred← citeshttps://doi.org/10.1016/j.semcancer.2025.05.013openalex-snapshot
The intricate role of adipokines in cancer-related signaling and the tumor microenvironment: Insights for future research
inferred← citeshttps://doi.org/10.1016/j.tifs.2025.104976openalex-snapshot
Role of plant-derived protein hydrolysates and peptides in appetite regulation
inferred← citeshttps://doi.org/10.1016/j.vph.2025.107553openalex-snapshot
Hypothalamic regulation of obesity: Revealing the therapeutic potential of a novel anti-obesity peptide
inferred← citeshttps://doi.org/10.1016/j.ygcen.2024.114658openalex-snapshot
Neuromodulation in the fish brain for reproductive success
inferred← citeshttps://doi.org/10.1017/s0029665123002203openalex-snapshot
How can physical activity facilitate a sustainable future? Reducing obesity and chronic disease
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.3c01822openalex-snapshot
Novel Cocrystal Structures of Peptide Antagonists Bound to the Human Melanocortin Receptor 4 Unveil Unexplored Grounds for Structure-Based Drug Design
inferred← citeshttps://doi.org/10.1038/s41398-026-03970-2openalex-snapshot
The mitigation of activity-based anorexia by obese adipose tissue transplant is abolished by neonatal AgRP neuron ablation
inferred← citeshttps://doi.org/10.1038/s41467-025-61499-2openalex-snapshot
Body temperature regulates glucose metabolism and torpid behavior
inferred← citeshttps://doi.org/10.1038/s41583-023-00736-3openalex-snapshot
Defensive responses: behaviour, the brain and the body
inferred← citeshttps://doi.org/10.1038/s41586-024-08164-8openalex-snapshot
Stochastic neuropeptide signals compete to calibrate the rate of satiation
inferred← citeshttps://doi.org/10.1038/s41593-023-01482-6openalex-snapshot
AgRP neurons encode circadian feeding time
inferred← citeshttps://doi.org/10.1038/s41598-025-03040-5openalex-snapshot
Optogenetic activation of hypothalamic AgRP neurons in transgenic zebrafish larvae increased food intake
inferred← citeshttps://doi.org/10.1038/s41598-025-27087-6openalex-snapshot
The effect of alpha lipoic acid and caffeine loaded into chitosan nanoparticles on the hypothalamic amino acid neurotransmitters in a rat model of obesity
inferred← citeshttps://doi.org/10.1038/s42003-025-08620-9openalex-snapshot
AgRP neuron activity enhances reward-related consummatory behaviors during energy deficit in mice
inferred← citeshttps://doi.org/10.1038/s42255-022-00673-yopenalex-snapshot
Food odor perception promotes systemic lipid utilization
inferred← citeshttps://doi.org/10.1038/s42255-024-01168-8openalex-snapshot
Molecular connectomics reveals a glucagon-like peptide 1-sensitive neural circuit for satiety
inferred← citeshttps://doi.org/10.1038/s42255-025-01405-8openalex-snapshot
Fat sensory cues in early life program central response to food and obesity
inferred← citeshttps://doi.org/10.1039/d4fo04024dopenalex-snapshot
Bioactive compounds regulate appetite through the melanocortin system: a review
inferred← citeshttps://doi.org/10.1073/pnas.2300015120openalex-snapshot
A small-molecule degrader of TET3 as treatment for anorexia nervosa in an animal model
inferred← citeshttps://doi.org/10.1073/pnas.2411069122openalex-snapshot
Dopaminergic neurons in the paraventricular hypothalamus extend the food consumption phase
inferred← citeshttps://doi.org/10.1073/pnas.2524926123openalex-snapshot
Olfactory inputs to appetite neurons in the hypothalamus
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/ejendo/lvaf226openalex-snapshot
Agouti-related peptide: a promising prognostic biomarker in adrenocortical carcinoma. Results from a large single-centre cross-sectional analysis
inferred← citeshttps://doi.org/10.1096/fj.202600683ropenalex-snapshot
Molecular and Cellular Mechanisms of Anti‐Obesity Agents: An Integrative Review
inferred← citeshttps://doi.org/10.1101/2023.05.03.538908openalex-snapshot
A brainstem to hypothalamic arcuate nucleus GABAergic circuit drives feeding
inferred← citeshttps://doi.org/10.1101/2024.04.23.590824openalex-snapshot
The attenuation of activity-based anorexia by obese adipose tissue transplant is AgRP neuron-dependent
inferred← citeshttps://doi.org/10.1101/2025.04.29.651295openalex-snapshot
Dopamine signaling tracks naturalistic short-term fluctuations in hunger-satiety
inferred← citeshttps://doi.org/10.1101/2025.07.13.664597openalex-snapshot
Diet context gates AgRP neuron involvement in Semaglutide-induced weight loss
inferred← citeshttps://doi.org/10.1101/2025.09.17.676826openalex-snapshot
Pharmacological Modulation of MC4R in the Periaqueductal Gray Does Not Alter Social Behavior
inferred← citeshttps://doi.org/10.1101/2025.11.25.690337openalex-snapshot
The fat-body secreted neuropeptide CCHa2 signals insulin-producing cells in the brain to promote sleep
inferred← citeshttps://doi.org/10.1111/acel.14047openalex-snapshot
Cpt1a silencing in AgRP neurons improves cognitive and physical capacity and promotes healthy aging in male mice
inferred← citeshttps://doi.org/10.1111/age.13331openalex-snapshot
Whole genome sequencing identifies candidate genes and mutations that can explain diluted and other colour varieties of domestic canaries (Serinus canaria)
inferred← citeshttps://doi.org/10.1111/dom.70154openalex-snapshot
Shared and divergent acute cardiovascular risk protein responses to lipid infusion in women with and without PCOS
inferred← citeshttps://doi.org/10.1111/dom.70722openalex-snapshot
SemaGBA : A System Dynamics Model of the Semaglutide‐Responsive Gut‐Brain Axis A Model of How the Brain and Semaglutide Regulate Appetite and Weight
inferred← citeshttps://doi.org/10.1111/ejn.15498openalex-snapshot
AgRP neuronal activity across feeding‐related behaviours
inferred← citeshttps://doi.org/10.1111/febs.16436openalex-snapshot
The brain—from neurodevelopment to neurodegeneration
inferred← citeshttps://doi.org/10.1111/jne.13248openalex-snapshot
Neuroendocrine control of brown adipocyte function by prolactin and growth hormone
inferred← citeshttps://doi.org/10.1111/jne.70099openalex-snapshot
The adverse effect of a hypercaloric high‐fat diet feeding on hypothalamic cellular energy homeostasis is attenuated by a hypoglycemiant
inferred← citeshttps://doi.org/10.1111/jne.70202openalex-snapshot
Altered responses to ghrelin and food cues in AgRP neurons during pregnancy and lactation
inferred← citeshttps://doi.org/10.1111/jne.70290openalex-snapshot
Acute ayahuasca administration attenuates binge‐like eating and anxiety‐related behaviors in mice subjected to intermittent fasting
inferred← citeshttps://doi.org/10.1111/raq.12982openalex-snapshot
The Effect of Probiotics and Prebiotics on Feed Intake in Cultured Fish
inferred← citeshttps://doi.org/10.1124/pharmrev.121.000302openalex-snapshot
β−Arrestins: Structure, Function, Physiology, and Pharmacological Perspectives
inferred← citeshttps://doi.org/10.1126/sciadv.ado1820openalex-snapshot
A normative framework dissociates need and motivation in hypothalamic neurons
inferred← citeshttps://doi.org/10.1126/sciimmunol.aed0186openalex-snapshot
Androgen signaling via sympathetic neurons regulates allergic pulmonary inflammation
inferred← citeshttps://doi.org/10.1134/s0022093026040228openalex-snapshot
The Role of T1R3 Receptor Protein in Lipid Synthesis Regulation in the Liver during Energy Metabolism
inferred← citeshttps://doi.org/10.1146/annurev-nutr-061824-054717openalex-snapshot
Lac-Phe: An Exercise Hormone for Metabolic Regulation
inferred← citeshttps://doi.org/10.1152/ajpregu.00128.2024openalex-snapshot
Mitragynine and morphine produce dose-dependent bimodal action on food but not water intake in rats
inferred← citeshttps://doi.org/10.1152/physiolgenomics.00042.2023openalex-snapshot
Krüppel-like factor 4 in transcriptional control of the three unique isoforms of Agouti-related peptide in mice
inferred← citeshttps://doi.org/10.1159/000530804openalex-snapshot
Alpha-Melanocyte-Stimulating Hormone-Mediated Appetite Regulation in the Central Nervous System
inferred← citeshttps://doi.org/10.1161/jaha.125.042144openalex-snapshot
Association of Inflammatory and Cardiovascular Proteomics Biomarkers With Indices of Heart Rate Variability in the General Population: KORA S4/FF4 Study
inferred← citeshttps://doi.org/10.1172/jci.insight.160891openalex-snapshot
Sustained inhibition of NPY/AgRP neuronal activity by FGF1
inferred← citeshttps://doi.org/10.1172/jci162365openalex-snapshot
TET3 epigenetically controls feeding and stress response behaviors via AGRP neurons
inferred← citeshttps://doi.org/10.1172/jci174597openalex-snapshot
How should we think about the unprecedented weight loss efficacy of incretin-mimetic drugs?
inferred← citeshttps://doi.org/10.1186/s12929-026-01264-9openalex-snapshot
Primary cilia and neural computation
inferred← citeshttps://doi.org/10.1186/s40337-026-01582-1openalex-snapshot
Changes in agouti-related protein and symptom improvement in drug-naïve Chinese female patients with anorexia nervosa: a 6-month real-world longitudinal study
inferred← citeshttps://doi.org/10.1186/s40478-025-02201-xopenalex-snapshot
Differential effects of overexpression of mutant huntingtin and TDP-43 in agouti-related protein neurons in the arcuate nucleus of the hypothalamus in mice
inferred← citeshttps://doi.org/10.1186/s43045-025-00578-yopenalex-snapshot
The relationship between Agouti related protein and leptin in patients with methamphetamine use disorder
inferred← citeshttps://doi.org/10.1186/s43556-025-00324-0openalex-snapshot
Iron accumulation in hypothalamus promotes age-dependent obesity and metabolic dysfunction of male mice
inferred← citeshttps://doi.org/10.1360/tb-2024-0706openalex-snapshot
Hypothalamic astrocytes and metabolism homeostasis
inferred← citeshttps://doi.org/10.14218/ge.2023.00202openalex-snapshot
(Epi)genetic Aspects of Metabolic Syndrome Pathogenesis in Relation to Brain-derived Neurotrophic Factor Expression: A Review
inferred← citeshttps://doi.org/10.14744/sigma.2023.00072openalex-snapshot
Variation of NPY and AGRP MRNA expression in Syrian hamsters according to feeding times
inferred← citeshttps://doi.org/10.1590/1806-9282.20241836openalex-snapshot
Investigation of serum agouti-related peptide levels in women with polycystic ovary syndrome
inferred← citeshttps://doi.org/10.20944/preprints202504.0717.v1openalex-snapshot
A Critical Analysis of Dietetics: Part 3, Dietary Ratios: Amino Acids, Fatty Acids, Hormones
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7207699/v1openalex-snapshot
The metabolic response to high fat intake depends on dietary fatty acid composition and sex
inferred← citeshttps://doi.org/10.21608/jabps.2023.225432.1194openalex-snapshot
Pharmacotherapeutic options for the management of obesity in children
inferred← citeshttps://doi.org/10.22215/etd/2024-16006openalex-snapshot
Ghrelin Regulates Food Intake in the Ventral Tegmental Area During Chronic Psychosocial Stress
inferred← citeshttps://doi.org/10.22365/jpsych.2023.002openalex-snapshot
Modelling disruptions of intentionality in psychosis
inferred← citeshttps://doi.org/10.2337/db22-0002openalex-snapshot
Forkhead Box i2 Transcription Factor Regulates Systemic Energy Metabolism Via Neuropeptide AgRP
inferred← citeshttps://doi.org/10.3389/fcell.2022.979251openalex-snapshot
Reciprocal signaling between adipose tissue depots and the central nervous system
inferred← citeshttps://doi.org/10.3389/fendo.2022.1010472openalex-snapshot
Agouti-related protein as the glucose signaling sensor in the central melanocortin circuits in regulating fish food intake
inferred← citeshttps://doi.org/10.3389/fendo.2025.1726498openalex-snapshot
The endocrine disruptor chlorpyrifos alters hypothalamic Npy and Agrp expression via ERβ-dependent regulation in vitro and in vivo
inferred← citeshttps://doi.org/10.3389/fgene.2024.1411931openalex-snapshot
Effect modification by sex of genetic associations of vitamin C related metabolites in the Canadian Longitudinal study on aging
inferred← citeshttps://doi.org/10.3389/fnmol.2025.1536577openalex-snapshot
GPCRs in hypothalamic neurons and their roles in controlling food intake and metabolism
inferred← citeshttps://doi.org/10.3389/fnut.2023.1094616openalex-snapshot
Emerging role of hypothalamus in the metabolic regulation in the offspring of maternal obesity
inferred← citeshttps://doi.org/10.3389/fnut.2023.1143613openalex-snapshot
Longan extract suppresses food intake through regulation of POMC/AgRP neuronal activities and endoplasmic reticulum stress in hypothalamus of db/db mice
inferred← citeshttps://doi.org/10.3389/fnut.2026.1745358openalex-snapshot
Maternal docosahexaenoic acid and eicosapentaenoic acid supplementation: effects and mechanisms on lipid metabolism in the offspring
inferred← citeshttps://doi.org/10.3389/fphar.2025.1730786openalex-snapshot
Setmelanotide-mediated MC4R activation improves hypothalamic obesity via CaMKK2/AMPK pathways
inferred← citeshttps://doi.org/10.3390/biom16071016openalex-snapshot
Molecular Mechanisms and Targeted Therapies of PTPN2 in Metabolic Diseases: A Review
inferred← citeshttps://doi.org/10.3390/cells12131801openalex-snapshot
Neurochemical Basis of Inter-Organ Crosstalk in Health and Obesity: Focus on the Hypothalamus and the Brainstem
inferred← citeshttps://doi.org/10.3390/cells12141822openalex-snapshot
Neural Progenitor Cells and the Hypothalamus
inferred← citeshttps://doi.org/10.3390/ijms222011010openalex-snapshot
Female Mice with Selenocysteine tRNA Deletion in Agrp Neurons Maintain Leptin Sensitivity and Resist Weight Gain While on a High-Fat Diet
inferred← citeshttps://doi.org/10.3390/ijms23010495openalex-snapshot
The Two β-Arrestins Regulate Distinct Metabolic Processes: Studies with Novel Mutant Mouse Models
inferred← citeshttps://doi.org/10.3390/ijms23052609openalex-snapshot
Distinct Firing Activities of the Hypothalamic Arcuate Nucleus Neurons to Appetite Hormones
inferred← citeshttps://doi.org/10.3390/ijms23169438openalex-snapshot
TRIM67 Deficiency Exacerbates Hypothalamic Inflammation and Fat Accumulation in Obese Mice
inferred← citeshttps://doi.org/10.3390/ijms232315445openalex-snapshot
Selenium in Bodily Homeostasis: Hypothalamus, Hormones, and Highways of Communication
inferred← citeshttps://doi.org/10.3390/ijms25084511openalex-snapshot
Mechanisms Involved in the Link between Depression, Antidepressant Treatment, and Associated Weight Change
inferred← citeshttps://doi.org/10.3390/ijms25137398openalex-snapshot
Mechanisms and Functions of Sweet Reception in Oral and Extraoral Organs
inferred← citeshttps://doi.org/10.3390/ijms262210974openalex-snapshot
Neurobiological Mechanisms and Therapeutic Potential of Glucagon-like Peptide-1 Receptor Agonists in Binge Eating Disorder: A Narrative Review
inferred← citeshttps://doi.org/10.3390/ijms27115056openalex-snapshot
Maternal Separation Differentially Programs Structural and Functional Remodeling of Visceral Adipose Tissue Depots in Mice Exposed to a Post-Weaning High-Fat Diet
inferred← citeshttps://doi.org/10.3390/mps7060086openalex-snapshot
Methodology for Studying Hypothalamic Regulation of Feeding Behaviors
inferred← citeshttps://doi.org/10.3390/nu18111767openalex-snapshot
Emotional Eating and Abdominal Obesity: A Narrative Review of the Potential Mechanisms Underlying Their Relationship and Emerging Interventions for Their Management
inferred← citeshttps://doi.org/10.3390/nu18172832openalex-snapshot
The Effects of Dietary Fiber and High-Dietary-Fiber Diets on Body Weight Regulation and Lipid Metabolism in Athletes: A Narrative Review
inferred← citeshttps://doi.org/10.36233/0372-9311-830openalex-snapshot
Features of the gut microbiome in mice with polygenic disorders of energy metabolism
inferred← citeshttps://doi.org/10.4239/wjd.v14.i2.76openalex-snapshot
Insulin: A connection between pancreatic β cells and the hypothalamus
inferred← citeshttps://doi.org/10.5772/intechopen.1006504openalex-snapshot
Regenerative Medicine for the Hypothalamic-Pituitary Axis: Current Progress and Future Challenges
inferred← citeshttps://doi.org/10.64898/2026.01.15.699765openalex-snapshot
THIK-1 channel mediates microglial glucose sensing and modulates AgRP neurons
inferred← citeshttps://doi.org/10.64898/2026.03.26.714551openalex-snapshot
Molecularly defined subpopulations of leptin receptor neurons dissociate the control of food intake from blood pressure
inferred← citeshttps://doi.org/10.64898/2026.06.25.733229openalex-snapshot
HIV-1 Infection in Humanized Microglial Mice Disrupts Feeding Behavior and Circadian Rhythms with Cortical Neuroinflammation
inferred← citeshttps://doi.org/10.70675/31092b82za087z48dczb698z1409347feb21openalex-snapshot
Role of PTH and PTHrP in the central regulation of energy metabolism
inferred← citeshttps://doi.org/10.70675/e375f801z0fd1z4fc6z9d73zc74380dd25f4openalex-snapshot
Reward abnormalities in the genetics of addictive disorders
inferred← citeshttps://doi.org/10.7554/elife.108551openalex-snapshot
Hugin-AstA circuitry is a novel central energy sensor that directly regulates sweet sensation in Drosophila and mouse
inferred← citeshttps://doi.org/10.7554/elife.108551.2openalex-snapshot
Hugin-AstA circuitry is a novel central energy sensor that directly regulates sweet sensation in Drosophila and mouse
inferred← citeshttps://doi.org/10.7554/elife.108551.4openalex-snapshot
Hugin-AstA circuitry is a novel central energy sensor that directly regulates sweet sensation in Drosophila and mouse
inferred← citeshttps://doi.org/10.7555/jbr.39.20250114openalex-snapshot
RAF1 in AgRP neurons involved in the regulation of energy metabolism via the MAPK signaling pathway
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