On the public citation graph

The Mysterious Food-Entrainable Oscillator: Insights from Mutant and Engineered Mouse Models

https://doi.org/10.1177/0748730418789043

0 signed · 236 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/cne.21777openalex-snapshot

Distribution of Wfs1 protein in the central nervous system of the mouse and its relation to clinical symptoms of the Wolfram syndrome

inferredcites →https://doi.org/10.1002/gene.20102openalex-snapshot

Progressive arthropathy in mice with a targeted disruption of theMop3/Bmal-1 locus

inferredcites →https://doi.org/10.1006/bbrc.1998.9750openalex-snapshot

Independent Feeding and Metabolic Actions of Orexins in Mice

inferredcites →https://doi.org/10.1007/978-3-319-27069-2_2openalex-snapshot

Molecular Architecture of the Circadian Clock in Mammals

inferredcites →https://doi.org/10.1007/978-3-319-27069-2_6openalex-snapshot

Redox and Metabolic Oscillations in the Clockwork

inferredcites →https://doi.org/10.1007/s00360-010-0451-4openalex-snapshot

Interactions between light, mealtime and calorie restriction to control daily timing in mammals

inferredcites →https://doi.org/10.1007/s41105-016-0050-1openalex-snapshot

Unique food-entrained circadian rhythm in cysteine414-alanine mutant mCRY1 transgenic mice

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/10.1016/0031-9384(86)90422-1openalex-snapshot

Coupling between feeding- and light-entrainable circadian pacemakers in the rat

inferredcites →https://doi.org/10.1016/0031-9384(87)90356-8openalex-snapshot

Palatable daily meals entrain anticipatory activity rhythms in free-feeding rats: Dependence on meal size and nutrient content

inferredcites →https://doi.org/10.1016/0031-9384(92)90381-bopenalex-snapshot

Resetting of a feeding-entrainable circadian clock in the rat

inferredcites →https://doi.org/10.1016/0092-8674(95)90145-0openalex-snapshot

Dopamine-deficient mice are severely hypoactive, adipsic, and aphagic

inferredcites →https://doi.org/10.1016/0149-7634(80)90010-xopenalex-snapshot

Food availability and daily biological rhythms

inferredcites →https://doi.org/10.1016/0149-7634(94)90023-xopenalex-snapshot

Circadian food-anticipatory activity: Formal models and physiological mechanisms

inferredcites →https://doi.org/10.1016/j.bbrc.2012.07.017openalex-snapshot

Circadian rhythms and food anticipatory behavior in Wfs1-deficient mice

inferredcites →https://doi.org/10.1016/j.brainres.2008.02.026openalex-snapshot

Entrainment of temperature and activity rhythms to restricted feeding in orexin knock out mice

inferredcites →https://doi.org/10.1016/j.cell.2010.08.016openalex-snapshot

Poly(ADP-Ribose) Polymerase 1 Participates in the Phase Entrainment of Circadian Clocks to Feeding

inferredcites →https://doi.org/10.1016/j.conb.2013.04.008openalex-snapshot

Control of arousal by the orexin neurons

inferredcites →https://doi.org/10.1016/j.cub.2006.02.023openalex-snapshot

Synchronization and Maintenance of Timekeeping in Suprachiasmatic Circadian Clock Cells by Neuropeptidergic Signaling

inferredcites →https://doi.org/10.1016/j.cub.2006.08.053openalex-snapshot

Lack of Food Anticipation in Per2 Mutant Mice

inferredcites →https://doi.org/10.1016/j.euroneuro.2010.06.005openalex-snapshot

Acute and chronic suppression of the central ghrelin signaling system reveals a role in food anticipatory activity

inferredcites →https://doi.org/10.1016/j.neures.2005.03.003openalex-snapshot

Altered food-anticipatory activity rhythm in Cryptochrome-deficient mice

inferredcites →https://doi.org/10.1016/j.neuroscience.2005.03.057openalex-snapshot

Rapid damping of food-entrained circadian rhythm of clock gene expression in clock-defective peripheral tissues under fasting conditions

inferredcites →https://doi.org/10.1016/j.neuroscience.2009.04.007openalex-snapshot

Feeding-elicited cataplexy in orexin knockout mice

inferredcites →https://doi.org/10.1016/j.neuroscience.2009.08.009openalex-snapshot

Reduced anticipatory locomotor responses to scheduled meals in ghrelin receptor deficient mice

inferredcites →https://doi.org/10.1016/j.pbb.2013.05.011openalex-snapshot

Time of day influences the voluntary intake and behavioral response to methamphetamine and food reward

inferredcites →https://doi.org/10.1016/j.physbeh.2010.10.017openalex-snapshot

Signaling through the ghrelin receptor modulates hippocampal function and meal anticipation in mice

inferredcites →https://doi.org/10.1016/j.physbeh.2014.01.021openalex-snapshot

Effects of light, food, and methamphetamine on the circadian activity rhythm in mice

inferredcites →https://doi.org/10.1016/j.regpep.2004.06.026openalex-snapshot

Enhanced running wheel activity of both Mch1r- and Pmch-deficient mice

inferredcites →https://doi.org/10.1016/j.tem.2013.10.006openalex-snapshot

BDNF mediates adaptive brain and body responses to energetic challenges

inferredcites →https://doi.org/10.1016/j.tem.2015.01.003openalex-snapshot

Regulation of energy homeostasis by the NPY system

inferredcites →https://doi.org/10.1016/j.tips.2010.02.003openalex-snapshot

Ten years of NAD-dependent SIR2 family deacetylases: implications for metabolic diseases

inferredcites →https://doi.org/10.1016/j.yhbeh.2015.02.004openalex-snapshot

Sex-related difference in food-anticipatory activity of mice

inferredcites →https://doi.org/10.1016/s0006-8993(98)00847-6openalex-snapshot

Role of the cerebellum in exploration behavior

inferredcites →https://doi.org/10.1016/s0014-2999(02)01429-2openalex-snapshot

Orexins and the treatment of obesity

inferredcites →https://doi.org/10.1016/s0092-8674(00)00205-1openalex-snapshot

Mop3 Is an Essential Component of the Master Circadian Pacemaker in Mammals

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/s0092-8674(00)81369-0openalex-snapshot

Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic Mice

inferredcites →https://doi.org/10.1016/s0168-1591(00)00204-5openalex-snapshot

A concept of welfare based on reward evaluating mechanisms in the brain: anticipatory behaviour as an indicator for the state of reward systems

inferredcites →https://doi.org/10.1037/bne0000058openalex-snapshot

A sex difference in circadian food-anticipatory rhythms in mice: Interaction with dopamine D1 receptor knockout.

inferredcites →https://doi.org/10.1038/372425a0openalex-snapshot

Positional cloning of the mouse obese gene and its human homologue

inferredcites →https://doi.org/10.1038/374542a0openalex-snapshot

Eating disorder and epilepsy in mice lacking 5-HT2C serotonin receptors

inferredcites →https://doi.org/10.1038/385165a0openalex-snapshot

Role of melanocortinergic neurons in feeding and the agouti obesity syndrome

inferredcites →https://doi.org/10.1038/417405aopenalex-snapshot

Prokineticin 2 transmits the behavioural circadian rhythm of the suprachiasmatic nucleus

inferredcites →https://doi.org/10.1038/ncomms10580openalex-snapshot

Liver-derived ketone bodies are necessary for food anticipation

inferredcites →https://doi.org/10.1038/nn1419openalex-snapshot

Vasoactive intestinal polypeptide mediates circadian rhythmicity and synchrony in mammalian clock neurons

inferredcites →https://doi.org/10.1038/nn1651openalex-snapshot

The dorsomedial hypothalamic nucleus is critical for the expression of food-entrainable circadian rhythms

inferredcites →https://doi.org/10.1038/nrm1963openalex-snapshot

Poly(ADP-ribose): novel functions for an old molecule

inferredcites →https://doi.org/10.1038/s41598-017-15332-6openalex-snapshot

mPeriod2 Brdm1 and other single Period mutant mice have normal food anticipatory activity

inferredcites →https://doi.org/10.1038/srep21945openalex-snapshot

Period-independent novel circadian oscillators revealed by timed exercise and palatable meals

inferredcites →https://doi.org/10.1038/srep29386openalex-snapshot

Rev-erbα in the brain is essential for circadian food entrainment

inferredcites →https://doi.org/10.1073/pnas.052706899openalex-snapshot

Melanin-concentrating hormone 1 receptor-deficient mice are lean, hyperactive, and hyperphagic and have altered metabolism

inferredcites →https://doi.org/10.1073/pnas.0604189103openalex-snapshot

The dorsomedial hypothalamic nucleus as a putative food-entrainable circadian pacemaker

inferredcites →https://doi.org/10.1073/pnas.0902063106openalex-snapshot

Daily rhythms of food-anticipatory behavioral activity do not require the known circadian clock

inferredcites →https://doi.org/10.1073/pnas.0906426106openalex-snapshot

Stomach ghrelin-secreting cells as food-entrainable circadian clocks

inferredcites →https://doi.org/10.1073/pnas.1015551108openalex-snapshot

Interaction between hypothalamic dorsomedial nucleus and the suprachiasmatic nucleus determines intensity of food anticipatory behavior

inferredcites →https://doi.org/10.1073/pnas.1206213109openalex-snapshot

Period determination in the food-entrainable and methamphetamine-sensitive circadian oscillator(s)

inferredcites →https://doi.org/10.1073/pnas.1218699110openalex-snapshot

PKCγ participates in food entrainment by regulating BMAL1

inferredcites →https://doi.org/10.1073/pnas.90.19.8856openalex-snapshot

Identification of a receptor for gamma melanotropin and other proopiomelanocortin peptides in the hypothalamus and limbic system.

inferredcites →https://doi.org/10.1073/pnas.96.21.12138openalex-snapshot

Feeding behavior in dopamine-deficient mice

inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a003274openalex-snapshot

Protein Kinase C (PKC ): Function of Neuron Specific Isotype

inferredcites →https://doi.org/10.1098/rstb.2006.1861openalex-snapshot

The role of the central melanocortin system in the regulation of food intake and energy homeostasis: lessons from mouse models

inferredcites →https://doi.org/10.1101/gad.1432206openalex-snapshot

Early aging and age-related pathologies in mice deficient in BMAL1, the core componentof the circadian clock

inferredcites →https://doi.org/10.1111/ejn.12390openalex-snapshot

Ghrelin receptor‐knockout mice display alterations in circadian rhythms of activity and feeding under constant lighting conditions

inferredcites →https://doi.org/10.1111/j.1460-9568.2004.03581.xopenalex-snapshot

Mu‐opioid receptor knockout mice show diminished food‐anticipatory activity

inferredcites →https://doi.org/10.1111/j.1460-9568.2004.03749.xopenalex-snapshot

Reduced food anticipatory activity in genetically orexin (hypocretin) neuron‐ablated mice

inferredcites →https://doi.org/10.1111/j.1460-9568.2009.06697.xopenalex-snapshot

The dorsomedial hypothalamic nucleus is not necessary for food‐anticipatory circadian rhythms of behavior, temperature or clock gene expression in mice

inferredcites →https://doi.org/10.1111/j.1460-9568.2009.06789.xopenalex-snapshot

Deletion of TASK1 and TASK3 channels disrupts intrinsic excitability but does not abolish glucose or pH responses of orexin/hypocretin neurons

inferredcites →https://doi.org/10.1111/j.1460-9568.2009.06960.xopenalex-snapshot

Food‐entrainable circadian oscillators in the brain

inferredcites →https://doi.org/10.1111/j.1460-9568.2009.06961.xopenalex-snapshot

Lesion studies targeting food‐anticipatory activity

inferredcites →https://doi.org/10.1111/j.1460-9568.2009.06962.xopenalex-snapshot

Neurogenetics of food anticipation

inferredcites →https://doi.org/10.1111/j.1460-9568.2009.06965.xopenalex-snapshot

Food‐anticipatory circadian rhythms: concepts and methods

inferredcites →https://doi.org/10.1111/j.1601-183x.2010.00576.xopenalex-snapshot

Behavioural food anticipation in clock genes deficient mice: confirming old phenotypes, describing new phenotypes

inferredcites →https://doi.org/10.1111/jnc.14128openalex-snapshot

Deleting the Arntl clock gene in the granular layer of the mouse cerebellum: impact on the molecular circadian clockwork

inferredcites →https://doi.org/10.1126/science.1082795openalex-snapshot

Altered Patterns of Sleep and Behavioral Adaptability in NPAS2-Deficient Mice

inferredcites →https://doi.org/10.1126/science.1100135openalex-snapshot

Cleavage of proBDNF by tPA/Plasmin Is Essential for Long-Term Hippocampal Plasticity

inferredcites →https://doi.org/10.1126/science.1118357openalex-snapshot

Increase in Activity During Calorie Restriction Requires Sirt1

inferredcites →https://doi.org/10.1126/science.1153277openalex-snapshot

Differential Rescue of Light- and Food-Entrainable Circadian Rhythms

inferredcites →https://doi.org/10.1126/science.1161284openalex-snapshot

Comment on "Differential Rescue of Light- and Food-Entrainable Circadian Rhythms"

inferredcites →https://doi.org/10.1126/science.1161387openalex-snapshot

Response to Comment on "Differential Rescue of Light- and Food-Entrainable Circadian Rhythms"

inferredcites →https://doi.org/10.1126/science.8171325openalex-snapshot

Mutagenesis and Mapping of a Mouse Gene, Clock , Essential for Circadian Behavior

inferredcites →https://doi.org/10.1152/ajpendo.1996.270.4.e589openalex-snapshot

Effects of restricted daily feeding on neuropeptide Y release in the rat paraventricular nucleus

inferredcites →https://doi.org/10.1152/ajpregu.00023.2003openalex-snapshot

Food-entrained circadian rhythms are sustained in arrhythmic Clk/Clk mutant mice

inferredcites →https://doi.org/10.1152/ajpregu.00294.2004openalex-snapshot

Rhythms of ghrelin, leptin, and sleep in rats: effects of the normal diurnal cycle, restricted feeding, and sleep deprivation

inferredcites →https://doi.org/10.1152/ajpregu.00557.2009openalex-snapshot

Restricted feeding-induced sleep, activity, and body temperature changes in normal and preproghrelin-deficient mice

inferredcites →https://doi.org/10.1152/ajpregu.00874.2005openalex-snapshot

Persistence of a behavioral food-anticipatory circadian rhythm following dorsomedial hypothalamic ablation in rats

inferredcites →https://doi.org/10.1152/ajpregu.1990.258.4.r994openalex-snapshot

Phase-shifting the light-dark cycle resets the food-entrainable circadian pacemaker

inferredcites →https://doi.org/10.1159/000334144openalex-snapshot

Anorexigenic and Orexigenic Hormone Modulation of Mammalian Target of Rapamycin Complex 1 Activity and the Regulation of Hypothalamic Agouti-Related Protein mRNA Expression

inferredcites →https://doi.org/10.1172/jci1176openalex-snapshot

Postnatal leptin surge and regulation of circadian rhythm of leptin by feeding. Implications for energy homeostasis and neuroendocrine function.

inferredcites →https://doi.org/10.1172/jci26002openalex-snapshot

Mice lacking ghrelin receptors resist the development of diet-induced obesity

inferredcites →https://doi.org/10.1172/jci29867openalex-snapshot

Ghrelin modulates the activity and synaptic input organization of midbrain dopamine neurons while promoting appetite

inferredcites →https://doi.org/10.1177/0748730412455913openalex-snapshot

Dopamine Is Involved in Food-Anticipatory Activity in Mice

inferredcites →https://doi.org/10.1186/1476-5926-5-8openalex-snapshot

Feeding and fasting controls liver expression of a regulator of G protein signaling (Rgs16) in periportal hepatocytes

inferredcites →https://doi.org/10.1186/1740-3391-7-11openalex-snapshot

Food anticipation in Bmal1-/- and AAV-Bmal1 rescued mice: a reply to Fuller et al

inferredcites →https://doi.org/10.1186/1740-3391-7-3openalex-snapshot

Standards of evidence in chronobiology: critical review of a report that restoration of Bmal1 expression in the dorsomedial hypothalamus is sufficient to restore circadian food anticipatory rhythms in Bmal1-/- mice

inferredcites →https://doi.org/10.1186/1740-3391-7-9openalex-snapshot

Standards of evidence in chronobiology: A response

inferredcites →https://doi.org/10.1186/s12899-018-0036-0openalex-snapshot

Regulation of Locomotor activity in fed, fasted, and food-restricted mice lacking tissue-type plasminogen activator

inferredcites →https://doi.org/10.1210/en.143.7.2469openalex-snapshot

Targeted Disruption of the Melanin-Concentrating Hormone Receptor-1 Results in Hyperphagia and Resistance to Diet-Induced Obesity

inferredcites →https://doi.org/10.1371/journal.pbio.0020377openalex-snapshot

BMAL1 and CLOCK, Two Essential Components of the Circadian Clock, Are Involved in Glucose Homeostasis

inferredcites →https://doi.org/10.1371/journal.pone.0004860openalex-snapshot

Robust Food Anticipatory Activity in BMAL1-Deficient Mice

inferredcites →https://doi.org/10.1371/journal.pone.0011802openalex-snapshot

Enhanced Food Anticipatory Activity Associated with Enhanced Activation of Extrahypothalamic Neural Pathways in Serotonin2C Receptor Null Mutant Mice

inferredcites →https://doi.org/10.1371/journal.pone.0017655openalex-snapshot

Attenuated Food Anticipatory Activity and Abnormal Circadian Locomotor Rhythms in Rgs16 Knockdown Mice

inferredcites →https://doi.org/10.1371/journal.pone.0018377openalex-snapshot

Single Gene Deletions of Orexin, Leptin, Neuropeptide Y, and Ghrelin Do Not Appreciably Alter Food Anticipatory Activity in Mice

inferredcites →https://doi.org/10.1371/journal.pone.0023364openalex-snapshot

Contrasting Effects of Leptin on Food Anticipatory and Total Locomotor Activity

inferredcites →https://doi.org/10.1371/journal.pone.0025079openalex-snapshot

Rhythmic Leptin Is Required for Weight Gain from Circadian Desynchronized Feeding in the Mouse

inferredcites →https://doi.org/10.1371/journal.pone.0048892openalex-snapshot

Circadian Regulation of Food-Anticipatory Activity in Molecular Clock–Deficient Mice

inferredcites →https://doi.org/10.1371/journal.pone.0146981openalex-snapshot

Altered Circadian Food Anticipatory Activity Rhythms in PACAP Receptor 1 (PAC1) Deficient Mice

inferredcites →https://doi.org/10.1371/journal.pone.0199586openalex-snapshot

Food anticipatory activity on a calorie-restricted diet is independent of Sirt1

inferredcites →https://doi.org/10.1523/jneurosci.1385-10.2010openalex-snapshot

SIRT1 Promotes the Central Adaptive Response to Diet Restriction through Activation of the Dorsomedial and Lateral Nuclei of the Hypothalamus

inferredcites →https://doi.org/10.1523/jneurosci.1694-10.2010openalex-snapshot

Disruption of Peripheral Circadian Timekeeping in a Mouse Model of Huntington's Disease and Its Restoration by Temporally Scheduled Feeding

inferredcites →https://doi.org/10.1523/jneurosci.23-18-07143.2003openalex-snapshot

Transgenic Mice Expressing Green Fluorescent Protein under the Control of the Melanocortin-4 Receptor Promoter

inferredcites →https://doi.org/10.1523/jneurosci.2801-11.2011openalex-snapshot

Bmal1in the Nervous System Is Essential for Normal Adaptation of Circadian Locomotor Activity and Food Intake to Periodic Feeding

inferredcites →https://doi.org/10.1523/jneurosci.3171-04.2004openalex-snapshot

Orexin Neurons Function in an Efferent Pathway of a Food-Entrainable Circadian Oscillator in Eliciting Food-Anticipatory Activity and Wakefulness

inferredcites →https://doi.org/10.1523/jneurosci.3615-08.2008openalex-snapshot

The Melanocortin-3 Receptor Is Required for Entrainment to Meal Intake

inferredcites →https://doi.org/10.1523/jneurosci.3679-06.2006openalex-snapshot

Attenuated Circadian Rhythms in Mice Lacking theProkineticin 2Gene

inferredcites →https://doi.org/10.1523/jneurosci.3842-04.2005openalex-snapshot

Disintegration of the Sleep-Wake Cycle and Circadian Timing in Huntington's Disease

inferredcites →https://doi.org/10.1523/jneurosci.4843-06.2007openalex-snapshot

Entrainment to Feeding but Not to Light: Circadian Phenotype of VPAC2Receptor-Null Mice

inferredcites →https://doi.org/10.1523/jneurosci.5855-09.2010openalex-snapshot

The Cerebellum Harbors a Circadian Oscillator Involved in Food Anticipation

inferredcites →https://doi.org/10.1530/jme-16-0014openalex-snapshot

60 YEARS OF POMC: Regulation of feeding and energy homeostasis by α-MSH

inferredcites →https://doi.org/10.1677/joe.0.1810053openalex-snapshot

Dissociation between adipose tissue signals, behavior and the food-entrained oscillator

inferredcites →https://doi.org/10.3109/07420528.2012.667467openalex-snapshot

Circadian Discrimination of Reward: Evidence for Simultaneous Yet Separable Food- and Drug-Entrained Rhythms in the Rat

inferredcites →https://doi.org/10.3389/fnbeh.2016.00143openalex-snapshot

The Running Wheel Enhances Food Anticipatory Activity: An Exploratory Study

inferredcites →https://doi.org/10.3389/fncir.2013.00152openalex-snapshot

Dopamine Signaling in reward-related behaviors

inferredcites →https://doi.org/10.5962/bhl.title.151527openalex-snapshot

A behavioristic study of the activity of the rat,

inferredcites →https://doi.org/10.7554/elife.03781openalex-snapshot

Dopamine receptor 1 neurons in the dorsal striatum regulate food anticipatory circadian activity rhythms in mice

inferredcites →https://doi.org/10.7554/elife.04617openalex-snapshot

Differential effects of light and feeding on circadian organization of peripheral clocks in a forebrain Bmal1 mutant

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.3941714openalex-extracted

inferred← citeshttps://doi.org/10.1007/978-3-030-28008-6_38openalex-snapshot

Night, Darkness, Sleep, and Cardiovascular Activity

inferred← citeshttps://doi.org/10.1007/978-3-031-32729-2_9openalex-snapshot

Integral Analysis of Circadian Rhythms

inferred← citeshttps://doi.org/10.1007/978-3-319-90305-7_38-1openalex-snapshot

Night, Darkness, Sleep, and Cardiovascular Activity

inferred← citeshttps://doi.org/10.1007/s10522-025-10298-9openalex-snapshot

Light phase feeding and estradiol reverse ovariectomy-induced alterations in metabolism and liver clock gene expression in rat

inferred← citeshttps://doi.org/10.1016/b978-0-12-823453-2.00009-6openalex-snapshot

Circadian circuits

inferred← citeshttps://doi.org/10.1016/j.bbih.2022.100412openalex-snapshot

Circadian rhythm disruption in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Implications for the post-acute sequelae of COVID-19

inferred← citeshttps://doi.org/10.1016/j.beproc.2019.05.017openalex-snapshot

Circadian entrainment by food and drugs of abuse

inferred← citeshttps://doi.org/10.1016/j.bj.2025.100827openalex-snapshot

Circadian disruption of feeding-fasting rhythm and its consequences for metabolic, immune, cancer, and cognitive processes

inferred← citeshttps://doi.org/10.1016/j.cell.2019.02.017openalex-snapshot

Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time

inferred← citeshttps://doi.org/10.1016/j.celrep.2019.11.027openalex-snapshot

Hypomorphic Expression of Pitx3 Disrupts Circadian Clocks and Prevents Metabolic Entrainment of Energy Expenditure

inferred← citeshttps://doi.org/10.1016/j.celrep.2021.110241openalex-snapshot

Restricting feeding to dark phase fails to entrain circadian activity and energy expenditure oscillations in Pitx3-mutant Aphakia mice

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.113933openalex-snapshot

Development of activity-based anorexia requires PKC-δ neurons in two central extended amygdala nuclei

inferred← citeshttps://doi.org/10.1016/j.cmet.2024.11.009openalex-snapshot

Acute and circadian feedforward regulation of agouti-related peptide hunger neurons

inferred← citeshttps://doi.org/10.1016/j.cnd.2020.02.003openalex-snapshot

Interactions réciproques entre prise alimentaire et horloges circadiennes : mécanismes et conséquences physiopathologiques

inferred← citeshttps://doi.org/10.1016/j.cub.2023.10.027openalex-snapshot

A time memory engram embedded in a light-entrainable circadian clock

inferred← citeshttps://doi.org/10.1016/j.cub.2024.02.042openalex-snapshot

Pheromone-mediated command from the female to male clock induces and synchronizes circadian rhythms of the moth Spodoptera littoralis

inferred← citeshttps://doi.org/10.1016/j.cub.2026.08.061openalex-snapshot

A population of dopaminergic neurons in the substantia nigra is required for food-anticipatory activity

inferred← citeshttps://doi.org/10.1016/j.isci.2021.103142openalex-snapshot

Zfhx3-mediated genetic ablation of the SCN abolishes light entrainable circadian activity while sparing food anticipatory activity

inferred← citeshttps://doi.org/10.1016/j.isci.2022.104267openalex-snapshot

Time-restricted feeding entrains long-term behavioral changes through the IGF2-KCC2 pathway

inferred← citeshttps://doi.org/10.1016/j.isci.2025.113292openalex-snapshot

A novel circadian behavior rhythm in arrhythmic Period triple knockout mice revealed by constant light exposure

inferred← citeshttps://doi.org/10.1016/j.molmet.2025.102171openalex-snapshot

IL-6 decodes sex and diet-dependent circadian and metabolic rhythms

inferred← citeshttps://doi.org/10.1016/j.nbscr.2025.100116openalex-snapshot

Multiple oscillators underlie circadian food anticipation in mice

inferred← citeshttps://doi.org/10.1016/j.neubiorev.2026.106945openalex-snapshot

Time as a cue for human hunger

inferred← citeshttps://doi.org/10.1016/j.neulet.2022.136462openalex-snapshot

Secretin Receptor-Deficient Mice Exhibit Robust Food Anticipatory Activity

inferred← citeshttps://doi.org/10.1016/j.physbeh.2020.112939openalex-snapshot

Food anticipatory circadian rhythms in mice entrained to long or short day photoperiods

inferred← citeshttps://doi.org/10.1016/j.xpro.2024.102935openalex-snapshot

Protocol to study circadian food-anticipatory poking in mice using the feeding experimentation device version 3

inferred← citeshttps://doi.org/10.1038/s41586-020-2204-1openalex-snapshot

Retinal innervation tunes circuits that drive nonphotic entrainment to food

inferred← citeshttps://doi.org/10.1038/s41598-017-15332-6openalex-snapshot

mPeriod2 Brdm1 and other single Period mutant mice have normal food anticipatory activity

inferred← citeshttps://doi.org/10.1038/s41598-020-66538-0openalex-snapshot

Synchronization of the circadian clock by time-restricted feeding with progressive increasing calorie intake. Resemblances and differences regarding a sustained hypocaloric restriction

inferred← citeshttps://doi.org/10.1038/s41598-025-13194-xopenalex-snapshot

Food reward entrainment increases mealtime anxiety in goldfish via a ghrelin-dependent mechanism

inferred← citeshttps://doi.org/10.1038/s42003-025-07932-0openalex-snapshot

The metabolic significance of peripheral tissue clocks

inferred← citeshttps://doi.org/10.1038/s42255-025-01237-6openalex-snapshot

The time is now: accounting for time-of-day effects to improve reproducibility and translation of metabolism research

inferred← citeshttps://doi.org/10.1038/s44323-026-00093-1openalex-snapshot

Timing of feeding mitigates metabolic effects of circadian disruption

inferred← citeshttps://doi.org/10.1039/bk9781839167553-00222openalex-snapshot

Circadian Rhythms and the Gastrointestinal System

inferred← citeshttps://doi.org/10.1073/pnas.2506313123openalex-snapshot

Gut microbiome–produced bile acid metabolite lengthens the circadian period in host intestinal cells

inferred← citeshttps://doi.org/10.1080/07420528.2021.1994984openalex-snapshot

New integrative approaches to discovery of pathophysiological mechanisms triggered by night shift work

inferred← citeshttps://doi.org/10.1080/07420528.2025.2574851openalex-snapshot

Intestinal production of melatonin and its putative role as a circadian organizer

inferred← citeshttps://doi.org/10.1080/07420528.2026.2636037openalex-snapshot

Effect of nocturnal feeding on locomotor activity and rumination rhythms, and sleep/wake cycle in diurnal dromedary camels

inferred← citeshttps://doi.org/10.1080/19420889.2024.2341050openalex-snapshot

A single incidental dark pulse during daytime attenuated food anticipatory behavior

inferred← citeshttps://doi.org/10.1093/9780197639979.003.0001openalex-snapshot

Introduction to Circadian Rhythms

inferred← citeshttps://doi.org/10.1093/advances/nmac011openalex-snapshot

Satiety Associated with Calorie Restriction and Time-Restricted Feeding: Central Neuroendocrine Integration

inferred← citeshttps://doi.org/10.1093/function/zqaa034openalex-snapshot

Timing of Food Intake Drives the Circadian Rhythm of Blood Pressure

inferred← citeshttps://doi.org/10.1093/pnasnexus/pgaf070openalex-snapshot

Methamphetamine alters the circadian oscillator and its couplings on multiple scales in Per1/2/3 knockout mice

inferred← citeshttps://doi.org/10.1093/sleep/zsz157openalex-snapshot

Sleep homeostasis during daytime food entrainment in mice

inferred← citeshttps://doi.org/10.1096/fj.202401536ropenalex-snapshot

Impacts of circadian disruptions on behavioral rhythms in mice

inferred← citeshttps://doi.org/10.1101/2022.09.26.509442openalex-snapshot

Age-associated sleep-wake patterns are altered with Prdm13 signaling in the dorsomedial hypothalamus and dietary restriction in mice

inferred← citeshttps://doi.org/10.1101/2023.02.24.529901openalex-snapshot

A leptin-responsive hypothalamic circuit inputs to the circadian feeding network

inferred← citeshttps://doi.org/10.1111/cen.14607openalex-snapshot

Sleep, circadian rhythms, and type 2 diabetes mellitus

inferred← citeshttps://doi.org/10.1111/ejn.14219openalex-snapshot

Overexpression of striatal D2 receptors reduces motivation thereby decreasing food anticipatory activity

inferred← citeshttps://doi.org/10.1111/febs.16320openalex-snapshot

Many faces of sleep regulation: beyond the time of day and prior wake time

inferred← citeshttps://doi.org/10.1111/jnc.15246openalex-snapshot

Chrono‐nutrition: From molecular and neuronal mechanisms to human epidemiology and timed feeding patterns

inferred← citeshttps://doi.org/10.1126/sciadv.adh9570openalex-snapshot

Leptin receptor neurons in the dorsomedial hypothalamus input to the circadian feeding network

inferred← citeshttps://doi.org/10.1134/s0022093023010210openalex-snapshot

The Effects of Insulin on Spike Activity of the Suprachiasmatic Nucleus Neurones and Functional State of Afferent Inputs from the Arcuate Nucleus in Rats

inferred← citeshttps://doi.org/10.1134/s0022093024030189openalex-snapshot

The Effects of Ghrelin on Spike Activity of the Suprachiasmatic Nucleus Neurones of the Rat

inferred← citeshttps://doi.org/10.1152/ajpgi.00368.2025openalex-snapshot

Elucidation of daily timed-palatable meal-anticipatory activity in the circadian system of mice

inferred← citeshttps://doi.org/10.1159/000542557openalex-snapshot

The Anti-Elixir Triad: Non-Synced Circadian Rhythm, Gut Dysbiosis, and Telomeric Damage

inferred← citeshttps://doi.org/10.1161/circresaha.123.323513openalex-snapshot

Circadian Regulation of Cardiac Arrhythmias and Electrophysiology

inferred← citeshttps://doi.org/10.1177/07487304221111287openalex-snapshot

Effects of Food Availability Cycles on Phase and Period of Activity-rest Rhythm in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1177/07487304251346606openalex-snapshot

TRPV1 Desensitization Abolishes Metabolic Effects of Time-Restricted Feeding in Rats

inferred← citeshttps://doi.org/10.1177/07487304251359349openalex-snapshot

Antibiotic-induced Dysbiosis of Gut Microbiota Increases Food Motivation and Anticipatory Activity Under a Time-restricted Feeding Protocol

inferred← citeshttps://doi.org/10.1210/endocr/bqab199openalex-snapshot

Metabolic Homeostasis: It’s All in the Timing

inferred← citeshttps://doi.org/10.12688/f1000research.20829.1openalex-snapshot

Food as circadian time cue for appetitive behavior

inferred← citeshttps://doi.org/10.1371/journal.pone.0242897openalex-snapshot

Type 1 dopamine receptor (D1R)-independent circadian food anticipatory activity in mice

inferred← citeshttps://doi.org/10.1371/journal.pone.0332295openalex-snapshot

Time-restricted feeding leads to sex- and organ-specific responses in the murine digestive system

inferred← citeshttps://doi.org/10.1523/jneurosci.1886-23.2024openalex-snapshot

Deletion of the Clock Gene Bmal2 Leads to Alterations in Hypothalamic Clocks, Circadian Regulation of Feeding, and Energy Balance

inferred← citeshttps://doi.org/10.1530/joe-20-0011openalex-snapshot

Night-time feeding of Bmal1−/− mice restores SCFA rhythms and their effect on ghrelin

inferred← citeshttps://doi.org/10.2174/1381612826666200310145006openalex-snapshot

Interaction Between Circadian Rhythms, Energy Metabolism, and Cognitive Function

inferred← citeshttps://doi.org/10.2337/db20-0910openalex-snapshot

Insulin Directly Regulates the Circadian Clock in Adipose Tissue

inferred← citeshttps://doi.org/10.2486/indhealth.2018-0173openalex-snapshot

Working against the biological clock: a review for the Occupational Physician

inferred← citeshttps://doi.org/10.26508/lsa.202301992openalex-snapshot

Sleep–wake patterns are altered with age, Prdm13 signaling in the DMH, and diet restriction in mice

inferred← citeshttps://doi.org/10.31857/s086981392302005xopenalex-snapshot

The Effects of Insulin on Spike Activity of the Suprachiasmatic Nucleus Neurones and Functional State of Afferent Inputs from the Arcuate Nucleus in Rats

inferred← citeshttps://doi.org/10.31857/s0869813924060088openalex-snapshot

The Effects of Ghrelin on Spike Activity of the Suprachiasmatic Nucleus Neurones of the Rat

inferred← citeshttps://doi.org/10.3389/fendo.2022.975509openalex-snapshot

Chrono-communication and cardiometabolic health: The intrinsic relationship and therapeutic nutritional promises

inferred← citeshttps://doi.org/10.3389/fgene.2024.1343030openalex-snapshot

Histone methylation: at the crossroad between circadian rhythms in transcription and metabolism

inferred← citeshttps://doi.org/10.3389/fnins.2021.745227openalex-snapshot

Effect of Restricted Feeding on Metabolic Health and Sleep-Wake Rhythms in Aging Mice

inferred← citeshttps://doi.org/10.3389/fnint.2022.957193openalex-snapshot

Dopamine systems and biological rhythms: Let’s get a move on

inferred← citeshttps://doi.org/10.3389/fnmol.2020.534238openalex-snapshot

Food Anticipatory Activity on Circadian Time Scales Is Not Dependent on Central Serotonin: Evidence From Tryptophan Hydroxylase-2 and Serotonin Transporter Knockout Mice

inferred← citeshttps://doi.org/10.3389/fnut.2022.998331openalex-snapshot

Studying food entrainment: Models, methods, and musings

inferred← citeshttps://doi.org/10.3389/fphar.2022.910195openalex-snapshot

Time Restricted Feeding to the Light Cycle Dissociates Canonical Circadian Clocks and Physiological Rhythms in Heart Rate

inferred← citeshttps://doi.org/10.3389/fphys.2019.00682openalex-snapshot

New Insights Into the Circadian Rhythm and Its Related Diseases

inferred← citeshttps://doi.org/10.3389/fphys.2023.1239278openalex-snapshot

Circadian rhythms in colonic function

inferred← citeshttps://doi.org/10.3389/fphys.2023.1299474openalex-snapshot

Gut microbiota depletion minimally affects the daily voluntary wheel running activity and food anticipatory activity in female and male C57BL/6J mice

inferred← citeshttps://doi.org/10.3390/antiox14060649openalex-snapshot

Transcriptomic Analysis of the Liver Redox Response During Food-Anticipatory Activity Under a Time-Restricted Feeding Protocol in Rats

inferred← citeshttps://doi.org/10.3390/bioengineering12020192openalex-snapshot

Visible Exocytosis of the Non-Photic Signal Neuropeptide Y to the Suprachiasmatic Nucleus in Fasted Transgenic Mice Throughout Their Circadian Rhythms

inferred← citeshttps://doi.org/10.3390/biom14050559openalex-snapshot

Biological Rhythms, Chrono-Nutrition, and Gut Microbiota: Epigenomics Insights for Precision Nutrition and Metabolic Health

inferred← citeshttps://doi.org/10.3390/biomedicines11051463openalex-snapshot

Restricted Feeding Resets the Peripheral Clocks of the Digestive System

inferred← citeshttps://doi.org/10.3390/clockssleep1010007openalex-snapshot

Measuring Food Anticipation in Mice

inferred← citeshttps://doi.org/10.3390/clockssleep3010012openalex-snapshot

Circadian Rhythms of the Hypothalamus: From Function to Physiology

inferred← citeshttps://doi.org/10.3390/fishes10110564openalex-snapshot

Three Non-Invasive Tests Reveal Anxiety-like Responses During Food Anticipation in Rainbow Trout

inferred← citeshttps://doi.org/10.3390/ijms23052778openalex-snapshot

The Effects of Light and the Circadian System on Rhythmic Brain Function

inferred← citeshttps://doi.org/10.5935/1984-0063.20200005openalex-snapshot

XV Latin-American Symposium on Chronobiology

inferred← citeshttps://doi.org/10.5935/1984-0063.20200006openalex-snapshot

Circadian modulation of motivation-related behavior

inferred← citeshttps://doi.org/10.5935/1984-0063.20200007openalex-snapshot

From the ruler to the smartphone tasks applied to identify sleep deprivation

inferred← citeshttps://doi.org/10.5935/1984-0063.20200008openalex-snapshot

The effect of pubertal development on the sleep-wake cycle

inferred← citeshttps://doi.org/10.5935/1984-0063.20200009openalex-snapshot

Shift work-related health problems: causes, effects, and light-based interventions

inferred← citeshttps://doi.org/10.5935/1984-0063.20200010openalex-snapshot

The impact of training shifts in dancers’ chronotype and sleep patterns

inferred← citeshttps://doi.org/10.5935/1984-0063.20200011openalex-snapshot

Characterization of the circadian expression profile of clock genes in Aag2 cell line infected and uninfected by Dengue 2 virus (DENV2)

inferred← citeshttps://doi.org/10.5935/1984-0063.20200012openalex-snapshot

Social modulation on daily variability in electric behavior

inferred← citeshttps://doi.org/10.5935/1984-0063.20200013openalex-snapshot

Electrocortical temporal complexity during wakefulness and sleep: an updated account

inferred← citeshttps://doi.org/10.5935/1984-0063.20200014openalex-snapshot

Fetal programming of adipose tissue function by gestational chronodisruption

inferred← citeshttps://doi.org/10.5935/1984-0063.20200015openalex-snapshot

Annual variation of daily activity patterns and its dependence on photoperiod: a quick overview

inferred← citeshttps://doi.org/10.5935/1984-0063.20200016openalex-snapshot

Different latitude influences the habitat and reproductive patterns of Pinnipeds

inferred← citeshttps://doi.org/10.5935/1984-0063.20200018openalex-snapshot

Chikungunya infection modulates the locomotor/flight activity of Aedes aegypti

inferred← citeshttps://doi.org/10.5935/1984-0063.20200019openalex-snapshot

Sleep and maternal behavior in the postpartum rat after haloperidol and midazolam treatments

inferred← citeshttps://doi.org/10.5935/1984-0063.20200020openalex-snapshot

Chronobiology in the wild: toolkit to study daily rhythms in free-living animals

inferred← citeshttps://doi.org/10.5935/1984-0063.20200021openalex-snapshot

What, how and (especially) when: chronoparmacological approach in cancer therapies

inferred← citeshttps://doi.org/10.70675/aa2d51b1zf20dz4abdz8160ze3c91dd95623openalex-snapshot

Les phéromones sexuelles redéfinissent les rythmes quotidiens d'activité et de repos des insectes

inferred← citeshttps://doi.org/10.7554/elife.52623openalex-snapshot

The p75 neurotrophin receptor in AgRP neurons is necessary for homeostatic feeding and food anticipation

inferred← citeshttps://doi.org/10.7759/cureus.61694openalex-snapshot

Vulnerable Hours of the Day for Severe Iatrogenic Hypoglycaemia in Type 2 Diabetes: A Single-Centre Retrospective Study

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.