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Peroxiredoxins are conserved markers of circadian rhythms

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What this work says

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

inferredcites →https://doi.org/10.1006/jmbi.2001.4853openalex-snapshot
Crystal structure of human peroxiredoxin 5, a novel type of mammalian peroxiredoxin at 1.5 Å resolution
inferredcites →https://doi.org/10.1007/s00203-008-0438-7openalex-snapshot
Functional characterisation of the peroxiredoxin gene family members of Synechococcus elongatus PCC 7942
inferredcites →https://doi.org/10.1007/s00442-007-0744-9openalex-snapshot
Dynamics of dissolved oxygen isotopic ratios: a transient model to quantify primary production, community respiration, and air–water exchange in aquatic ecosystems
inferredcites →https://doi.org/10.1007/s11910-009-0024-7openalex-snapshot
Neurobehavioral, health, and safety consequences associated with shift work in safety-sensitive professions
inferredcites →https://doi.org/10.1016/j.cell.2010.03.008openalex-snapshot
SnapShot: Reactive Oxygen Intermediates (ROI)
inferredcites →https://doi.org/10.1016/j.cub.2004.08.023openalex-snapshot
The Adaptive Value of Circadian Clocks
inferredcites →https://doi.org/10.1016/j.cub.2005.08.019openalex-snapshot
The Circadian Timekeeping System of Drosophila
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.2006.04.026openalex-snapshot
Circadian Orchestration of the Hepatic Proteome
inferredcites →https://doi.org/10.1016/j.cub.2008.07.012openalex-snapshot
A Cyanobacterial Circadian Clockwork
inferredcites →https://doi.org/10.1016/j.ecolind.2005.03.004openalex-snapshot
Stream diurnal dissolved oxygen profiles as indicators of in-stream metabolism and disturbance effects: Fort Benning as a case study
inferredcites →https://doi.org/10.1016/j.febslet.2009.05.029openalex-snapshot
The oligomeric conformation of peroxiredoxins links redox state to function
inferredcites →https://doi.org/10.1016/j.fgb.2010.08.001openalex-snapshot
A role in the regulation of transcription by light for RCO-1 and RCM-1, the Neurospora homologs of the yeast Tup1–Ssn6 repressor
inferredcites →https://doi.org/10.1016/j.mib.2006.10.008openalex-snapshot
How fungi keep time: circadian system in Neurospora and other fungi
inferredcites →https://doi.org/10.1016/j.tcb.2009.10.005openalex-snapshot
Healthy clocks, healthy body, healthy mind
inferredcites →https://doi.org/10.1016/s0076-6879(05)93030-9openalex-snapshot
Analysis of Circadian Mechanisms in the Suprachiasmatic Nucleus by Transgenesis and Biolistic Transfection
inferredcites →https://doi.org/10.1016/s0092-8674(00)80566-8openalex-snapshot
Molecular Bases for Circadian Clocks
inferredcites →https://doi.org/10.1016/s0092-8674(00)81440-3openalex-snapshot
A Mutant Drosophila Homolog of Mammalian Clock Disrupts Circadian Rhythms and Transcription of period and timeless
inferredcites →https://doi.org/10.1016/s0891-5849(02)00905-xopenalex-snapshot
Superoxide dismutase multigene family: a comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression
inferredcites →https://doi.org/10.1016/s0969-2126(00)00147-7openalex-snapshot
Crystal structure of decameric 2-Cys peroxiredoxin from human erythrocytes at 1.7Å resolution
inferredcites →https://doi.org/10.1038/21190openalex-snapshot
Assignment of circadian function for the Neurospora clock gene frequency
inferredcites →https://doi.org/10.1038/35088576openalex-snapshot
Time zones: a comparative genetics of circadian clocks
inferredcites →https://doi.org/10.1038/nature09654openalex-snapshot
Circadian rhythms persist without transcription in a eukaryote
inferredcites →https://doi.org/10.1038/nature09702openalex-snapshot
Circadian clocks in human red blood cells
inferredcites →https://doi.org/10.1038/nprot.2006.79openalex-snapshot
Analysis of locomotor activity rhythms in Drosophila
inferredcites →https://doi.org/10.1042/bst0320269openalex-snapshot
Hyperthermophilic and salt-dependent formyltransferase from Methanopyrus kandleri
inferredcites →https://doi.org/10.1046/j.1365-2826.1998.00272.xopenalex-snapshot
Stationary Organotypic Cultures of Oxytocin and Vasopressin Magnocellular Neurones from Rat and Mouse Hypothalamus
inferredcites →https://doi.org/10.1073/pnas.0130099100openalex-snapshot
Origin and evolution of circadian clock genes in prokaryotes
inferredcites →https://doi.org/10.1073/pnas.0308709101openalex-snapshot
PERIOD2::LUCIFERASE real-time reporting of circadian dynamics reveals persistent circadian oscillations in mouse peripheral tissues
inferredcites →https://doi.org/10.1073/pnas.1002119107openalex-snapshot
Intermolecular associations determine the dynamics of the circadian KaiABC oscillator
inferredcites →https://doi.org/10.1073/pnas.93.19.10183openalex-snapshot
Circadian gating of cell division in cyanobacteria growing with average doubling times of less than 24 hours.
inferredcites →https://doi.org/10.1074/jbc.c300428200openalex-snapshot
Reversible Oxidation of the Active Site Cysteine of Peroxiredoxins to Cysteine Sulfinic Acid
inferredcites →https://doi.org/10.1093/bioinformatics/btq137openalex-snapshot
Studying the co-evolution of protein families with the Mirrortree web server
inferredcites →https://doi.org/10.1093/emboj/16.22.6762openalex-snapshot
The DBP gene is expressed according to a circadian rhythm in the suprachiasmatic nucleus and influences circadian behavior
inferredcites →https://doi.org/10.1093/emboj/cdg168openalex-snapshot
Cyanobacterial circadian clockwork: roles of KaiA, KaiB and the kaiBC promoter in regulating KaiC
inferredcites →https://doi.org/10.1093/jxb/erq218openalex-snapshot
Functional analysis of the pathways for 2-Cys peroxiredoxin reduction in Arabidopsis thaliana chloroplasts
inferredcites →https://doi.org/10.1093/molbev/msq232openalex-snapshot
A Universal Molecular Clock of Protein Folds and Its Power in Tracing the Early History of Aerobic Metabolism and Planet Oxygenation
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a039993openalex-snapshot
Molecular evolution of a repetitive region within the per gene of Drosophila.
inferredcites →https://doi.org/10.1093/protein/14.9.609openalex-snapshot
Similarity of phylogenetic trees as indicator of protein–protein interaction
inferredcites →https://doi.org/10.1099/mic.0.28030-0openalex-snapshot
Stability of the Synechococcus elongatus PCC 7942 circadian clock under directed anti-phase expression of the kai genes
inferredcites →https://doi.org/10.1105/tpc.006734openalex-snapshot
Dual Role of TOC1 in the Control of Circadian and Photomorphogenic Responses in Arabidopsis[W]
inferredcites →https://doi.org/10.1105/tpc.109.068825openalex-snapshot
Clocks in the Green Lineage: Comparative Functional Analysis of the Circadian Architecture of the Picoeukaryote Ostreococcus
inferredcites →https://doi.org/10.1111/j.1365-313x.2009.03819.xopenalex-snapshot
Delayed fluorescence as a universal tool for the measurement of circadian rhythms in higher plants
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.06985.xopenalex-snapshot
Typical 2‐Cys peroxiredoxins – structures, mechanisms and functions
inferredcites →https://doi.org/10.1126/science.1060698openalex-snapshot
Regulation of Clock and NPAS2 DNA Binding by the Redox State of NAD Cofactors
inferredcites →https://doi.org/10.1126/science.1080405openalex-snapshot
Peroxiredoxin Evolution and the Regulation of Hydrogen Peroxide Signaling
inferredcites →https://doi.org/10.1126/science.1108451openalex-snapshot
Reconstitution of Circadian Oscillation of Cyanobacterial KaiC Phosphorylation in Vitro
inferredcites →https://doi.org/10.1126/science.1115581openalex-snapshot
Plant Circadian Clocks Increase Photosynthesis, Growth, Survival, and Competitive Advantage
inferredcites →https://doi.org/10.1126/science.281.5382.1519openalex-snapshot
Expression of a Gene Cluster kaiABC as a Circadian Feedback Process in Cyanobacteria
inferredcites →https://doi.org/10.1126/science.8128244openalex-snapshot
Negative Feedback Defining a Circadian Clock: Autoregulation of the Clock Gene frequency
inferredcites →https://doi.org/10.1146/annurev-physiol-021909-135922openalex-snapshot
Mammalian Per-Arnt-Sim Proteins in Environmental Adaptation
inferredcites →https://doi.org/10.1146/annurev.biochem.67.1.135openalex-snapshot
THE MOLECULAR CONTROL OF CIRCADIAN BEHAVIORAL RHYTHMS AND THEIR ENTRAINMENT IN DROSOPHILA
inferredcites →https://doi.org/10.1146/annurev.biochem.71.090501.142857openalex-snapshot
Metabolism and the Control of Circadian Rhythms
inferredcites →https://doi.org/10.1146/annurev.genet.40.110405.090603openalex-snapshot
Interplay of Circadian Clocks and Metabolic Rhythms
inferredcites →https://doi.org/10.1146/annurev.micro.58.030603.123744openalex-snapshot
Circadian Rhythms in Microorganisms: New Complexities
inferredcites →https://doi.org/10.1146/annurev.neuro.24.1.1091openalex-snapshot
Stopping Time: The Genetics of Fly and Mouse Circadian Clocks
inferredcites →https://doi.org/10.1159/000337115openalex-snapshot
Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity
inferredcites →https://doi.org/10.1177/0748730403255934openalex-snapshot
Circadian Rhythms in Neurospora Crassa: Farnesol or Geraniol Allow Expression of Rhythmicity in the Otherwise Arrhythmic Strains frq 10, wc-1, and wc-2
inferredcites →https://doi.org/10.1177/0748730405286102openalex-snapshot
Transcriptional Feedback Oscillators: Maybe, Maybe Not...
inferredcites →https://doi.org/10.1177/0748730406293053openalex-snapshot
Transcriptional Profiling in the Adrenal Gland Reveals Circadian Regulation of Hormone Biosynthesis Genes and Nucleosome Assembly Genes
inferredcites →https://doi.org/10.1371/journal.pbio.1000062openalex-snapshot
The Implications of Multiple Circadian Clock Origins
inferredcites →https://doi.org/10.1371/journal.pone.0005485openalex-snapshot
Diurnally Entrained Anticipatory Behavior in Archaea
inferredcites →https://doi.org/10.1371/journal.pone.0007509openalex-snapshot
Intramolecular Regulation of Phosphorylation Status of the Circadian Clock Protein KaiC
inferredcites →https://doi.org/10.1371/journal.pone.0028227openalex-snapshot
Cross-Talk between the Cellular Redox State and the Circadian System in Neurospora
inferredcites →https://doi.org/10.1534/genetics.107.088658openalex-snapshot
Probing the Relative Importance of Molecular Oscillations in the Circadian Clock
inferredcites →https://doi.org/10.4319/lo.1962.7.3.0348openalex-snapshot
DIURNAL CHANGES IN SHALLOW AQUATIC HABITATS

What points at this work

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

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Regulation of the Cyanobacterial Circadian Clock by Electrochemically Controlled Extracellular Electron Transfer
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Regulation of the Cyanobacterial Circadian Clock by Electrochemically Controlled Extracellular Electron Transfer
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The cost of circadian desynchrony: Evidence, insights and open questions
inferred← citeshttps://doi.org/10.1002/bies.201500056openalex-snapshot
Cross‐talk between circadian clocks, sleep‐wake cycles, and metabolic networks: Dispelling the darkness
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Temperature‐controlled Rhythmic Gene Expression in Endothermic Mammals: All Diurnal Rhythms are Equal, but Some are Circadian
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CBC‐Clock Theory of Life – Integration of cellular circadian clocks and cellular sentience is essential for cognitive basis of life
inferred← citeshttps://doi.org/10.1002/bies.70157openalex-snapshot
The Temporal Architecture of Human Cells: Organelle Clocks and Distributed Circadian Time
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Protocols for in vitro reconstitution of the cyanobacterial circadian clock
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Extensive soma‐soma plate‐like contact sites (ephapses) connect suprachiasmatic nucleus neurons
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Circadian Rhythms in Adipose Tissue Physiology
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In vitro characterisation of murine pre‐adipose nucleated cells reveals electrophysiological cycles associated with biological clocks
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miR‐455‐5p regulates circadian rhythms by accelerating the degradation of Clock mRNA
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Circadian Rhythms in Adipose Tissue Physiology
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Cross‐species complementation reveals conserved functions for EARLY FLOWERING 3 between monocots and dicots
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Proteomics and circadian rhythms: It's all about signaling!
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Redox‐Active Polymers Connecting Living Microbial Cells to an Extracellular Electrical Circuit
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Circadian rhythms and the HPA axis: A systems view
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The Clock Keeps on Ticking: Emerging Roles for Circadian Regulation in the Control of Fungal Physiology and Pathogenesis
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Neuroanatomy of the Suprachiasmatic Nucleus (SCN): Multicolor Immunohistochemistry and 3D Reconstruction
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Cell Cycle Regulation in Plasmodium
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Biomedical Effects of Circadian Rhythm Disturbances
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Assessing Redox State and Reactive Oxygen Species in Circadian Rhythmicity
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The Perennial Clock Is an Essential Timer for Seasonal Growth Events and Cold Hardiness
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Daily Rhythmicity in Coastal Microbial Mats
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Redox and Metabolic Oscillations in the Clockwork
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Free-Running Cycle
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KaiC-like ATPases as Signal Transduction Hubs in Archaea
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Variability in Digestive Enzyme Capacity in Early Stages of Marine Fish Larvae: Ontogenetic Variations, Biorhythms, Hormonal Control and Nutrient Sensing Mechanisms
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Behavioral Risk Factors
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Interactions Between Circadian Rhythms, ROS and Redox
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Molecular Components of the Mammalian Circadian Clock
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Small molecule modifiers of circadian clocks
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Rhythms in lipid droplet content driven by a metabolic oscillator are conserved throughout evolution
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Yeast engineered translucent cell wall to provide its endosymbiont cyanobacteria with light
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Circadian regulation of innate immunity in animals and humans and implications for human disease
inferred← citeshttps://doi.org/10.1007/s00294-018-0897-6openalex-snapshot
Circadian rhythms, metabolic oscillators, and the target of rapamycin (TOR) pathway: the Neurospora connection
inferred← citeshttps://doi.org/10.1007/s00335-016-9643-xopenalex-snapshot
Ageing in relation to skeletal muscle dysfunction: redox homoeostasis to regulation of gene expression
inferred← citeshttps://doi.org/10.1007/s00344-026-12053-xopenalex-snapshot
The Regulatory Functions of Thiol-Based Redoxins in Plant Cellular Physiology
inferred← citeshttps://doi.org/10.1007/s00360-016-1000-6openalex-snapshot
Life in a dark biosphere: a review of circadian physiology in “arrhythmic” environments
inferred← citeshttps://doi.org/10.1007/s00424-016-1820-yopenalex-snapshot
Post-transcriptional control of the mammalian circadian clock: implications for health and disease
inferred← citeshttps://doi.org/10.1007/s00775-013-0988-2openalex-snapshot
Insertion mutants in Drosophila melanogaster Hsc20 halt larval growth and lead to reduced iron–sulfur cluster enzyme activities and impaired iron homeostasis
inferred← citeshttps://doi.org/10.1007/s10123-026-00875-4openalex-snapshot
Diurnal dynamics of maize gene expression is associated with phyllosphere microbiome composition
inferred← citeshttps://doi.org/10.1007/s10126-025-10418-zopenalex-snapshot
Photoperiod and Light Spectrum Modulate Daily Rhythms and Expression of Genes Involved in Cell Proliferation, DNA Repair, Apoptosis and Oxidative Stress in a Seabream Embryonic Stem Cell Line
inferred← citeshttps://doi.org/10.1007/s10522-025-10281-4openalex-snapshot
Circadian clock and its effect on aging and lifespan
inferred← citeshttps://doi.org/10.1007/s10535-015-0568-0openalex-snapshot
BvPRR7 is a cold responsive gene with a clock function in beet
inferred← citeshttps://doi.org/10.1007/s11084-026-09743-7openalex-snapshot
Magnesium at the dawn of life from geochemistry to cell biology
inferred← citeshttps://doi.org/10.1007/s11120-019-00667-0openalex-snapshot
The endogenous redox rhythm is controlled by a central circadian oscillator in cyanobacterium Synechococcus elongatus PCC7942
inferred← citeshttps://doi.org/10.1007/s11120-022-00956-1openalex-snapshot
The circadian night depression of photosynthesis analyzed in a herb, Pulmonaria vallarsae. Day/night quantitative relationships
inferred← citeshttps://doi.org/10.1007/s11427-021-2064-7openalex-snapshot
Integration of rhythmic metabolome and transcriptome provides insights into the transmission of rhythmic fluctuations and temporal diversity of metabolism in rice
inferred← citeshttps://doi.org/10.1007/s11515-017-1460-4openalex-snapshot
Salicylic acid-mediated plant defense: Recent developments, missing links, and future outlook
inferred← citeshttps://doi.org/10.1007/s12015-024-10761-zopenalex-snapshot
Role of Neurotransmitters in Steady State Hematopoiesis, Aging, and Leukemia
inferred← citeshttps://doi.org/10.1007/s12035-018-1152-3openalex-snapshot
Proliferative Glioblastoma Cancer Cells Exhibit Persisting Temporal Control of Metabolism and Display Differential Temporal Drug Susceptibility in Chemotherapy
inferred← citeshttps://doi.org/10.1007/s12035-021-02595-4openalex-snapshot
Circadian Regulation and Clock-Controlled Mechanisms of Glycerophospholipid Metabolism from Neuronal Cells and Tissues to Fibroblasts
inferred← citeshttps://doi.org/10.1007/s12042-013-9124-2openalex-snapshot
Thermal-Stable Proteins of Fruit of Long-Living Sacred Lotus Nelumbo nucifera Gaertn var. China Antique
inferred← citeshttps://doi.org/10.1007/s12374-025-09467-7openalex-snapshot
Pseudo-Response Regulators: Molecular Mediators Transducing NTRC-Dependent Metabolic Oscillatory Signals to the Nuclear Clocks in Plants
inferred← citeshttps://doi.org/10.1007/s12561-019-09236-4openalex-snapshot
Joint and Individual Representation of Domains of Physical Activity, Sleep, and Circadian Rhythmicity
inferred← citeshttps://doi.org/10.1007/s13562-020-00612-6openalex-snapshot
Regulatory mechanisms across networks of the circadian clock and senescence pathways
inferred← citeshttps://doi.org/10.1007/s13752-022-00426-wopenalex-snapshot
Many Paths to Anticipatory Behavior: Anticipatory Model Acquisition Across Phylogenetic and Ontogenetic Timescales
inferred← citeshttps://doi.org/10.1007/s40610-015-0001-7openalex-snapshot
Chromatin Dynamics of Circadian Transcription
inferred← citeshttps://doi.org/10.1007/s40614-018-00178-8openalex-snapshot
An Inconvenient Truth: Some Neglected Issues in Invertebrate Learning
inferred← citeshttps://doi.org/10.1007/s40675-017-0072-5openalex-snapshot
Circadian Rhythms in AD Pathogenesis: a Critical Appraisal
inferred← citeshttps://doi.org/10.1007/s41048-015-0007-yopenalex-snapshot
Detecting peroxiredoxin hyperoxidation by one-dimensional isoelectric focusing
inferred← citeshttps://doi.org/10.1016/b978-0-12-394807-6.00101-5openalex-snapshot
The Regulation of Circadian Rhythms in Plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-396971-2.00004-xopenalex-snapshot
Peripheral Circadian Oscillators
inferred← citeshttps://doi.org/10.1016/b978-0-12-396971-2.00005-1openalex-snapshot
Circadian Clocks, Food Intake, and Metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-12-396971-2.00010-5openalex-snapshot
Health Consequences of Circadian Disruption in Humans and Animal Models
inferred← citeshttps://doi.org/10.1016/b978-0-12-405882-8.00002-7openalex-snapshot
Evaluating Peroxiredoxin Sensitivity Toward Inactivation by Peroxide Substrates
inferred← citeshttps://doi.org/10.1016/b978-0-12-405882-8.00006-4openalex-snapshot
Peroxiredoxins and Sulfiredoxin at the Crossroads of the NO and H2O2 Signaling Pathways
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.20670-5openalex-snapshot
Circadian Rhythmicity in Prokaryotes ☆
inferred← citeshttps://doi.org/10.1016/b978-0-323-65403-6.00011-1openalex-snapshot
History of sleep medicine and physiology
inferred← citeshttps://doi.org/10.1016/b978-0-323-90219-9.00006-6openalex-snapshot
A thiol chemistry perspective on redox medicine
inferred← citeshttps://doi.org/10.1016/b978-0-323-90219-9.00025-xopenalex-snapshot
Thiols in blood
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00031-0openalex-snapshot
Peroxidases
inferred← citeshttps://doi.org/10.1016/b978-0-323-96106-6.00018-6openalex-snapshot
Circadian clock in cyanobacteria
inferred← citeshttps://doi.org/10.1016/bs.adgen.2015.09.003openalex-snapshot
Around the Fungal Clock
inferred← citeshttps://doi.org/10.1016/bs.adgen.2017.05.001openalex-snapshot
Sleeping Beauty? Developmental Timing, Sleep, and the Circadian Clock in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2024.01.017openalex-snapshot
Circadian timing of satellite cell function and muscle regeneration
inferred← citeshttps://doi.org/10.1016/bs.mie.2014.10.007openalex-snapshot
Analysis of the Redox Oscillations in the Circadian Clockwork
inferred← citeshttps://doi.org/10.1016/bs.mie.2014.10.018openalex-snapshot
Photic Regulation of Clock Systems
inferred← citeshttps://doi.org/10.1016/bs.mim.2018.07.004openalex-snapshot
Measuring Microbial Metabolism in Atypical Environments
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2022.737950openalex-snapshot
Changes in daylength and temperature from April until August for Atlantic salmon (Salmo salar) reared in sea cages, increase growth, and may cause consumption of antioxidants, onset of cataracts and increased oxidation of fillet astaxanthin
inferred← citeshttps://doi.org/10.1016/j.aquatox.2014.11.006openalex-snapshot
Hypoxia and the pharmaceutical diclofenac influence the circadian responses of three-spined stickleback
inferred← citeshttps://doi.org/10.1016/j.arr.2016.12.006openalex-snapshot
Circadian rhythms, time-restricted feeding, and healthy aging
inferred← citeshttps://doi.org/10.1016/j.arr.2018.03.005openalex-snapshot
Beyond ROS clearance: Peroxiredoxins in stress signaling and aging
inferred← citeshttps://doi.org/10.1016/j.arr.2023.101928openalex-snapshot
Aryl hydrocarbon receptor (AhR) impairs circadian regulation: Impact on the aging process
inferred← citeshttps://doi.org/10.1016/j.bbagen.2014.10.025openalex-snapshot
The circadian clock and hypoxia in tumor cell de-differentiation and metastasis
inferred← citeshttps://doi.org/10.1016/j.bbagen.2016.09.006openalex-snapshot
S-nitrosylation of peroxiredoxin 1 contributes to viability of lung epithelial cells during Bacillus anthracis infection
inferred← citeshttps://doi.org/10.1016/j.bbagen.2017.08.012openalex-snapshot
The reversible function switching of the circadian clock protein KaiA is encoded in its structure
inferred← citeshttps://doi.org/10.1016/j.bbagen.2018.08.017openalex-snapshot
Structural properties of the peroxiredoxin AhpC2 from the hyperthermophilic eubacterium Aquifex aeolicus
inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.158533openalex-snapshot
Circadian profiling reveals distinct regulation of endocannabinoid system in the rat plasma, liver and adrenal glands by light-dark and feeding cycles
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.04.009openalex-snapshot
BMAL1 regulates transcription initiation and activates circadian clock gene expression in mammals
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.10.081openalex-snapshot
Possible molecular mechanism underlying cadmium-induced circadian rhythms disruption in zebrafish
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.04.095openalex-snapshot
Light exposure influences the diurnal oscillation of gut microbiota in mice
inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.01.072openalex-snapshot
The recovery of KaiA’s activity depends on its N-terminal domain and KaiB in the cyanobacterial circadian clock
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.06.081openalex-snapshot
Disulfide reductase activity of thioredoxin-h2 imparts cold tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.bbrep.2026.102643openalex-snapshot
Evolutionary divergence of nocturnin led to redox regulation in mammalian orthologs
inferred← citeshttps://doi.org/10.1016/j.bcp.2025.117034openalex-snapshot
Madecassoside exerts anti-neurodegeneration effects in protein l-isoaspartyl methyltransferase deficient mice via targeting PRDX2-mediated oxidative stress and inflammation
inferred← citeshttps://doi.org/10.1016/j.biocel.2014.04.024openalex-snapshot
Peroxiredoxin 2 nuclear levels are regulated by circadian clock synchronization in human keratinocytes
inferred← citeshttps://doi.org/10.1016/j.biocel.2015.05.018openalex-snapshot
Nuclear redox imbalance affects circadian oscillation in HaCaT keratinocytes
inferred← citeshttps://doi.org/10.1016/j.biochi.2015.04.014openalex-snapshot
Redox regulation and pro-oxidant reactions in the physiology of circadian systems
inferred← citeshttps://doi.org/10.1016/j.bj.2018.02.003openalex-snapshot
The discoveries of molecular mechanisms for the circadian rhythm: The 2017 Nobel Prize in Physiology or Medicine
inferred← citeshttps://doi.org/10.1016/j.cbpa.2018.03.009openalex-snapshot
Phylogenetic analysis of cnidarian peroxiredoxins and stress-responsive expression in the estuarine sea anemone Nematostella vectensis
inferred← citeshttps://doi.org/10.1016/j.cbpa.2021.111020openalex-snapshot
Comparison of effects in sustained and diel-cycling hypoxia on hypoxia tolerance, histology, physiology and expression of clock genes in high latitude fish Phoxinus lagowskii
inferred← citeshttps://doi.org/10.1016/j.cbpc.2016.04.003openalex-snapshot
The effects of the painkiller diclofenac and hypoxia on gene transcription and antioxidant system in the gills of three-spined stickleback
inferred← citeshttps://doi.org/10.1016/j.cbpc.2022.109420openalex-snapshot
Altered mitochondria oscillations and circadian changes in NADH levels in freshwaters mussels exposed to cadmium
inferred← citeshttps://doi.org/10.1016/j.ceb.2013.01.003openalex-snapshot
The circadian epigenome: how metabolism talks to chromatin remodeling
inferred← citeshttps://doi.org/10.1016/j.cell.2014.03.057openalex-snapshot
Interaction of Circadian Clock Proteins CRY1 and PER2 Is Modulated by Zinc Binding and Disulfide Bond Formation
inferred← citeshttps://doi.org/10.1016/j.cell.2014.09.048openalex-snapshot
Transkingdom Control of Microbiota Diurnal Oscillations Promotes Metabolic Homeostasis
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.11.031openalex-snapshot
Controlling the Cyanobacterial Clock by Synthetically Rewiring Metabolism
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.03.041openalex-snapshot
FAD Regulates CRYPTOCHROME Protein Stability and Circadian Clock in Mice
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110703openalex-snapshot
The role of cell-autonomous circadian oscillation of Cry transcription in circadian rhythm generation
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.110787openalex-snapshot
Mitochondrial LETM1 Drives Ionic and Molecular Clock Rhythms in Circadian Pacemaker Neurons
inferred← citeshttps://doi.org/10.1016/j.chom.2020.01.005openalex-snapshot
Periodic Parasites and Daily Host Rhythms
inferred← citeshttps://doi.org/10.1016/j.cities.2019.102523openalex-snapshot
The geography of human activity and land use: A big data approach
inferred← citeshttps://doi.org/10.1016/j.cmet.2016.07.024openalex-snapshot
The Pentose Phosphate Pathway Regulates the Circadian Clock
inferred← citeshttps://doi.org/10.1016/j.cmet.2025.04.016openalex-snapshot
Hydrogen peroxide in midbrain sleep neurons regulates sleep homeostasis
inferred← citeshttps://doi.org/10.1016/j.conb.2013.02.012openalex-snapshot
A circadian clock nanomachine that runs without transcription or translation
inferred← citeshttps://doi.org/10.1016/j.conb.2013.05.002openalex-snapshot
A role for clock genes in sleep homeostasis
inferred← citeshttps://doi.org/10.1016/j.conb.2013.05.004openalex-snapshot
Circadian clocks and neurodegenerative diseases: time to aggregate?
inferred← citeshttps://doi.org/10.1016/j.coph.2020.10.006openalex-snapshot
Molecular link between circadian clocks and cardiac function: a network of core clock, slave clock, and effectors
inferred← citeshttps://doi.org/10.1016/j.coviro.2020.12.003openalex-snapshot
Transmembrane redox regulation of genome replication functions in positive-strand RNA viruses
inferred← citeshttps://doi.org/10.1016/j.csbj.2023.08.035openalex-snapshot
Dominant constraints on the evolution of rhythmic gene expression
inferred← citeshttps://doi.org/10.1016/j.cub.2012.06.023openalex-snapshot
Circadian Biology: A 2.5 Billion Year Old Clock
inferred← citeshttps://doi.org/10.1016/j.cub.2015.02.035openalex-snapshot
Metabolic Cycles in Yeast Share Features Conserved among Circadian Rhythms
inferred← citeshttps://doi.org/10.1016/j.cub.2015.02.052openalex-snapshot
Metabolic molecular markers of the tidal clock in the marine crustacean Eurydice pulchra
inferred← citeshttps://doi.org/10.1016/j.cub.2023.10.051openalex-snapshot
Biological clocks: Hungry on time
inferred← citeshttps://doi.org/10.1016/j.dcit.2025.100050openalex-snapshot
Circadian rhythm of mosquitoes: Blood feeding and disease transmission
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2021.104756openalex-snapshot
Rhythmical redox homeostasis can be restored by exogenous melatonin in hulless barley (Hordeum vulgare L.var. nudum) under cold stress
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105683openalex-snapshot
Genome-wide identification and expression profiling of Pseudo-Response Regulator (PRR) gene family in tomato
inferred← citeshttps://doi.org/10.1016/j.euprot.2013.11.010openalex-snapshot
Proteomic analysis of the purple sulfur bacterium Candidatus “Thiodictyon syntrophicum” strain Cad16T isolated from Lake Cadagno
inferred← citeshttps://doi.org/10.1016/j.expneurol.2013.01.014openalex-snapshot
Circadian dysfunction may be a key component of the non-motor symptoms of Parkinson's disease: Insights from a transgenic mouse model
inferred← citeshttps://doi.org/10.1016/j.febslet.2012.07.041openalex-snapshot
Systems biology of cellular rhythms
inferred← citeshttps://doi.org/10.1016/j.febslet.2014.06.005openalex-snapshot
Molecular mechanisms of the circadian clockwork in mammals
inferred← citeshttps://doi.org/10.1016/j.febslet.2015.05.024openalex-snapshot
How is the inner circadian clock controlled by interactive clock proteins?
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.12.016openalex-snapshot
Reactive oxygen species can modulate circadian phase and period in Neurospora crassa
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2015.03.022openalex-snapshot
The cysteine proteome
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2015.04.030openalex-snapshot
Plasmodium falciparum antioxidant protein reveals a novel mechanism for balancing turnover and inactivation of peroxiredoxins
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.02.004openalex-snapshot
The circadian gene Rev-erbα improves cellular bioenergetics and provides preconditioning for protection against oxidative stress
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.02.035openalex-snapshot
Increasing extracellular H2O2 produces a bi-phasic response in intracellular H2O2, with peroxiredoxin hyperoxidation only triggered once the cellular H2O2-buffering capacity is overwhelmed
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.02.037openalex-snapshot
Circadian modulation of proteasome activity and accumulation of oxidized protein in human embryonic kidney HEK 293 cells and primary dermal fibroblasts
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.04.199openalex-snapshot
Quantitative measures for redox signaling
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.05.022openalex-snapshot
Redox biology and the interface between bioenergetics, autophagy and circadian control of metabolism
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.10.383openalex-snapshot
Redox regulation of circadian molecular clock in chronic airway diseases
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.11.023openalex-snapshot
Neuroprotection afforded by circadian regulation of intracellular glutathione levels: A key role for miRNAs
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.12.024openalex-snapshot
Redox and the circadian clock in plant immunity: A balancing act
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.12.025openalex-snapshot
Circadian regulation of metabolism and healthspan in Drosophila
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.12.033openalex-snapshot
Redox clocks: Time to rethink redox interventions
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