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The molecular mechanisms of diapause and diapause-like reversible arrest

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What this work says

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

inferredcites →https://doi.org/10.1002/arch.21400openalex-snapshot
Knockdown of TOR causing ovarian diapause in a genetically stable brachypterous strain of Nilaparvata lugens
inferredcites →https://doi.org/10.1016/0012-1606(75)90109-8openalex-snapshot
The dauerlarva, a post-embryonic developmental variant of the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/0022-1910(96)00003-0openalex-snapshot
Diapause hormone of the silkworm, Bombyx mori: Structure, gene expression and function
inferredcites →https://doi.org/10.1016/0896-6273(89)90069-xopenalex-snapshot
Molecular characterization of the drosophila trp locus: A putative integral membrane protein required for phototransduction
inferredcites →https://doi.org/10.1016/j.anireprosci.2018.09.009openalex-snapshot
Research advances on embryonic diapause in mammals
inferredcites →https://doi.org/10.1016/j.bbamcr.2022.119389openalex-snapshot
ROS elevate HIF-1α phosphorylation for insect lifespan through the CK2-MKP3-p38 pathway
inferredcites →https://doi.org/10.1016/j.ccell.2018.05.001openalex-snapshot
Cancer Cells Co-opt the Neuronal Redox-Sensing Channel TRPA1 to Promote Oxidative-Stress Tolerance
inferredcites →https://doi.org/10.1016/j.ccell.2020.12.002openalex-snapshot
An Embryonic Diapause-like Adaptation with Suppressed Myc Activity Enables Tumor Treatment Persistence
inferredcites →https://doi.org/10.1016/j.ccell.2021.01.013openalex-snapshot
A Malignant Case of Arrested Development: Cancer Cell Dormancy Mimics Embryonic Diapause
inferredcites →https://doi.org/10.1016/j.cell.2013.01.020openalex-snapshot
A Genetic Program Promotes C. elegans Longevity at Cold Temperatures via a Thermosensitive TRP Channel
inferredcites →https://doi.org/10.1016/j.cell.2015.12.033openalex-snapshot
Myc Depletion Induces a Pluripotent Dormant State Mimicking Diapause
inferredcites →https://doi.org/10.1016/j.cell.2018.12.024openalex-snapshot
Plasticity of the Electrical Connectome of C. elegans
inferredcites →https://doi.org/10.1016/j.cell.2020.11.018openalex-snapshot
Colorectal Cancer Cells Enter a Diapause-like DTP State to Survive Chemotherapy
inferredcites →https://doi.org/10.1016/j.cmet.2008.01.005openalex-snapshot
Insulin, cGMP, and TGF-β Signals Regulate Food Intake and Quiescence in C. elegans: A Model for Satiety
inferredcites →https://doi.org/10.1016/j.cub.2015.05.009openalex-snapshot
Turquoise killifish
inferredcites →https://doi.org/10.1016/j.cub.2018.04.043openalex-snapshot
Ecology of animal migration
inferredcites →https://doi.org/10.1016/j.cub.2022.01.061openalex-snapshot
Recovery from cold-induced reproductive dormancy is regulated by temperature-dependent AstC signaling
inferredcites →https://doi.org/10.1016/j.cub.2023.01.006openalex-snapshot
Seasonal cues act through the circadian clock and pigment-dispersing factor to control EYES ABSENT and downstream physiological changes
inferredcites →https://doi.org/10.1016/j.devcel.2018.05.028openalex-snapshot
A Temperature-Dependent Switch in Feeding Preference Improves Drosophila Development and Survival in the Cold
inferredcites →https://doi.org/10.1016/j.devcel.2019.12.018openalex-snapshot
Metabolic Control over mTOR-Dependent Diapause-like State
inferredcites →https://doi.org/10.1016/j.ibmb.2019.103262openalex-snapshot
P–S6K is associated with insect diapause via the ROS/AKT/ S6K/CREB/HIF-1 pathway in the cotton bollworm, Helicoverpa armigera
inferredcites →https://doi.org/10.1016/j.jinsphys.2007.03.018openalex-snapshot
Meeting the energetic demands of insect diapause: Nutrient storage and utilization
inferredcites →https://doi.org/10.1016/j.jinsphys.2018.04.006openalex-snapshot
Redefining reproductive dormancy in Drosophila as a general stress response to cold temperatures
inferredcites →https://doi.org/10.1016/j.resp.2004.03.014openalex-snapshot
Natural hypometabolism during hibernation and daily torpor in mammals
inferredcites →https://doi.org/10.1016/j.stem.2020.06.005openalex-snapshot
Histone Acetyltransferase MOF Blocks Acquisition of Quiescence in Ground-State ESCs through Activating Fatty Acid Oxidation
inferredcites →https://doi.org/10.1016/j.stemcr.2019.10.014openalex-snapshot
Genetic Deletion of Hesx1 Promotes Exit from the Pluripotent State and Impairs Developmental Diapause
inferredcites →https://doi.org/10.1016/j.stemcr.2020.01.001openalex-snapshot
Critical Role for P53 in Regulating the Cell Cycle of Ground State Embryonic Stem Cells
inferredcites →https://doi.org/10.1016/s0092-8674(00)81751-1openalex-snapshot
Cell Nonautonomy of C. elegans daf-2 Function in the Regulation of Diapause and Life Span
inferredcites →https://doi.org/10.1016/s0959-4388(03)00101-6openalex-snapshot
Lessons from peppers and peppermint: the molecular logic of thermosensation
inferredcites →https://doi.org/10.1038/39807openalex-snapshot
The capsaicin receptor: a heat-activated ion channel in the pain pathway
inferredcites →https://doi.org/10.1038/nature20578openalex-snapshot
Inhibition of mTOR induces a paused pluripotent state
inferredcites →https://doi.org/10.1038/s41467-021-26945-xopenalex-snapshot
Maintenance of quiescent oocytes by noradrenergic signals
inferredcites →https://doi.org/10.1038/s41467-022-28347-zopenalex-snapshot
Enhanced germline stem cell longevity in Drosophila diapause
inferredcites →https://doi.org/10.1038/s41467-022-28592-2openalex-snapshot
The insect somatostatin pathway gates vitellogenesis progression during reproductive maturation and the post-mating response
inferredcites →https://doi.org/10.1038/s41586-020-2387-5openalex-snapshot
Neurons that regulate mouse torpor
inferredcites →https://doi.org/10.1038/s41598-021-87590-4openalex-snapshot
Comparisons in temperature and photoperiodic-dependent diapause induction between domestic and wild mulberry silkworms
inferredcites →https://doi.org/10.1071/rd20256openalex-snapshot
Embryonic diapause in mammals and dormancy in embryonic stem cells with the European roe deer as experimental model
inferredcites →https://doi.org/10.1073/pnas.0604592103openalex-snapshot
Natural variation in Drosophila melanogaster diapause due to the insulin-regulated PI3-kinase
inferredcites →https://doi.org/10.1073/pnas.0704699104openalex-snapshot
The circadian clock stops ticking during deep hibernation in the European hamster
inferredcites →https://doi.org/10.1073/pnas.0802067105openalex-snapshot
Insulin signaling and FOXO regulate the overwintering diapause of the mosquito Culex pipiens
inferredcites →https://doi.org/10.1073/pnas.1322134111openalex-snapshot
Embryonic thermosensitive TRPA1 determines transgenerational diapause phenotype of the silkworm, Bombyx mori
inferredcites →https://doi.org/10.1073/pnas.1711042114openalex-snapshot
Reactive oxygen species extend insect life span using components of the insulin-signaling pathway
inferredcites →https://doi.org/10.1073/pnas.1804590115openalex-snapshot
Temperature-dependent vitamin D signaling regulates developmental trajectory associated with diapause in an annual killifish
inferredcites →https://doi.org/10.1073/pnas.1922747117openalex-snapshot
Photoperiod and temperature separately regulate nymphal development through JH and insulin/TOR signaling pathways in an insect
inferredcites →https://doi.org/10.1073/pnas.2004262117openalex-snapshot
EYES ABSENT and TIMELESS integrate photoperiodic and temperature cues to regulate seasonal physiology in Drosophila
inferredcites →https://doi.org/10.1073/pnas.2017603118openalex-snapshot
ROS and hypoxia signaling regulate periodic metabolic arousal during insect dormancy to coordinate glucose, amino acid, and lipid metabolism
inferredcites →https://doi.org/10.1073/pnas.2100500118openalex-snapshot
Amino acids activate mTORC1 to release roe deer embryos from decelerated proliferation during diapause
inferredcites →https://doi.org/10.1073/pnas.2210404119openalex-snapshot
FoxO induces pupal diapause by decreasing TGFβ signaling
inferredcites →https://doi.org/10.1073/pnas.2215214120openalex-snapshot
Mmp-induced fat body cell dissociation promotes pupal development and moderately averts pupal diapause by activating lipid metabolism
inferredcites →https://doi.org/10.1073/pnas.2315248121openalex-snapshot
Neuronal IL-17 controls Caenorhabditis elegans developmental diapause through CEP-1/p53
inferredcites →https://doi.org/10.1093/biolre/ioac135openalex-snapshot
Efficient cell chatting between embryo and uterus ensures embryo implantation
inferredcites →https://doi.org/10.1093/biolre/iox019openalex-snapshot
Embryo arrest and reactivation: potential candidates controlling embryonic diapause in the tammar wallaby and mink†
inferredcites →https://doi.org/10.1093/biolre/ioy112openalex-snapshot
The history of the discovery of embryonic diapause in mammals
inferredcites →https://doi.org/10.1093/genetics/156.3.1047openalex-snapshot
Dauer Formation Induced by High Temperatures in Caenorhabditis elegans
inferredcites →https://doi.org/10.1093/molehr/gaac043openalex-snapshot
Pre-implantation mouse embryo movement under hormonally altered conditions
inferredcites →https://doi.org/10.1111/1744-7917.13089openalex-snapshot
MicroRNA miR‐2765‐3p regulates reproductive diapause by targeting FoxO in Galeruca daurica
inferredcites →https://doi.org/10.1111/eea.12753openalex-snapshot
Diapause research in insects: historical review and recent work perspectives
inferredcites →https://doi.org/10.1126/sciadv.aaz7070openalex-snapshot
Let-7 derived from endometrial extracellular vesicles is an important inducer of embryonic diapause in mice
inferredcites →https://doi.org/10.1126/science.1178343openalex-snapshot
Starvation Protects Germline Stem Cells and Extends Reproductive Longevity in C. elegans
inferredcites →https://doi.org/10.1126/science.277.5328.942openalex-snapshot
daf-2 , an Insulin Receptor-Like Gene That Regulates Longevity and Diapause in Caenorhabditis elegans
inferredcites →https://doi.org/10.1126/science.3933112openalex-snapshot
Rescue of the Drosophila Phototransduction Mutation trp by Germline Transformation
inferredcites →https://doi.org/10.1126/science.6896933openalex-snapshot
A Pheromone Influences Larval Development in the Nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1126/science.aaw2601openalex-snapshot
Vertebrate diapause preserves organisms long term through Polycomb complex members
inferredcites →https://doi.org/10.1146/annurev-ento-011019-025116openalex-snapshot
Dormancy, Diapause, and the Role of the Circadian System in Insect Photoperiodism
inferredcites →https://doi.org/10.1146/annurev.physiol.66.032102.115105openalex-snapshot
Metabolic Rate and Body Temperature Reduction During Hibernation and Daily Torpor
inferredcites →https://doi.org/10.1186/1477-7827-11-92openalex-snapshot
Embryonic diapause in humans: time to consider?
inferredcites →https://doi.org/10.1186/gb-2004-6-1-202openalex-snapshot
Profiling gene expression in growth-arrested mouse embryos in diapause.
inferredcites →https://doi.org/10.1186/s12864-020-07285-4openalex-snapshot
High-throughput profiling of diapause regulated genes from Trichogramma dendrolimi (Hymenoptera: Trichogrammatidae)
inferredcites →https://doi.org/10.1242/dev.148213openalex-snapshot
The enigma of embryonic diapause
inferredcites →https://doi.org/10.1242/jeb.179812openalex-snapshot
Clocks and meals keep mice from being cool
inferredcites →https://doi.org/10.1242/jeb.205831openalex-snapshot
Selection for reproduction under short photoperiods changes diapause-associated traits and induces widespread genomic divergence
inferredcites →https://doi.org/10.1242/jeb.245329openalex-snapshot
Insect diapause: from a rich history to an exciting future
inferredcites →https://doi.org/10.1371/journal.pbio.3001734openalex-snapshot
Clock gene-dependent glutamate dynamics in the bean bug brain regulate photoperiodic reproduction
inferredcites →https://doi.org/10.1371/journal.pgen.1008158openalex-snapshot
Peptidergic signaling from clock neurons regulates reproductive dormancy in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1009678openalex-snapshot
CREB mediates the C. elegans dauer polyphenism through direct and cell-autonomous regulation of TGF-β expression
inferredcites →https://doi.org/10.1371/journal.pone.0113051openalex-snapshot
The Sleeping Beauty: How Reproductive Diapause Affects Hormone Signaling, Metabolism, Immune Response and Somatic Maintenance in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pone.0274076openalex-snapshot
Nutrient sensing pathways regulating adult reproductive diapause in C. elegans
inferredcites →https://doi.org/10.15252/emmm.202114903openalex-snapshot
Inhibition of NPC1L1 disrupts adaptive responses of drug‐tolerant persister cells to chemotherapy
inferredcites →https://doi.org/10.1534/genetics.118.301250openalex-snapshot
Transgenerational Effects of Extended Dauer Diapause on Starvation Survival and Gene Expression Plasticity in Caenorhabditis elegans
inferredcites →https://doi.org/10.1895/wormbook.1.144.1openalex-snapshot
Dauer
inferredcites →https://doi.org/10.3389/fphys.2016.00572openalex-snapshot
Characterization of Reproductive Dormancy in Male Drosophila melanogaster
inferredcites →https://doi.org/10.3389/fphys.2022.825057openalex-snapshot
Endocrine Regulation of Lifespan in Insect Diapause
inferredcites →https://doi.org/10.3389/fphys.2022.873580openalex-snapshot
Juvenile Hormone Is an Important Factor in Regulating Aspongopus chinensis Dallas Diapause
inferredcites →https://doi.org/10.3389/fphys.2022.877153openalex-snapshot
Enhanced Degradation of Juvenile Hormone Promotes Reproductive Diapause in the Predatory Ladybeetle Coccinella Septempunctata
inferredcites →https://doi.org/10.3390/biology10090842openalex-snapshot
Circadian Clock Gene Period Contributes to Diapause via GABAeric-Diapause Hormone Pathway in Bombyx mori
inferredcites →https://doi.org/10.3390/cells11192929openalex-snapshot
Molecular Regulators of Embryonic Diapause and Cancer Diapause-like State
inferredcites →https://doi.org/10.7554/elife.78277openalex-snapshot
Targeted depletion of uterine glandular Foxa2 induces embryonic diapause in mice

What points at this work

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

inferred← citeshttps://doi.org/10.55730/1300-0179.3209zenodo-depositor-declared
A study of the dormant period of Thaumetopoea pityocampa (Lepidoptera: Notodontidae) in Bulgaria
inferred← citeshttps://doi.org/10.1002/arch.70203openalex-snapshot
Characterization and Seasonal Expression Profiling of a Takeout/Juvenile Hormone‐Binding Protein‐Family Gene Associated With Diapause in Eurygaster integriceps
inferred← citeshttps://doi.org/10.1007/978-3-031-87707-0_2openalex-snapshot
Reproductive Strategies and Their Relevance to Vertebrate Conservation
inferred← citeshttps://doi.org/10.1007/s11357-024-01401-yopenalex-snapshot
Post-senescence reproductive rebound in Daphnia associated with reversal of age-related transcriptional changes
inferred← citeshttps://doi.org/10.1007/s12672-024-01049-2openalex-snapshot
Advances in the molecular regulation mechanism of tumor dormancy and its therapeutic strategy
inferred← citeshttps://doi.org/10.1016/j.arr.2025.102998openalex-snapshot
Diapause and aging: Two opposing yet intertwined biological phenomena
inferred← citeshttps://doi.org/10.1016/j.biopha.2026.119821openalex-snapshot
PARP inhibition induces a redox-dependent dormant reservoir vulnerable to disulfiram in high-grade serous ovarian cancer
inferred← citeshttps://doi.org/10.1016/j.cobeha.2025.101595openalex-snapshot
Facing the heat: behavioral and molecular underpinnings of heat stress in bumblebees
inferred← citeshttps://doi.org/10.1016/j.ibmb.2025.104305openalex-snapshot
The role of insulin receptor InR in photoperiod-regulated reproductive diapause of Chrysoperla nipponensis
inferred← citeshttps://doi.org/10.1016/j.ibmb.2025.104417openalex-snapshot
A conserved Piezo–mRPL2/Jun axis controls reproduction via mitochondrial bioenergetics
inferred← citeshttps://doi.org/10.1016/j.tig.2024.08.005openalex-snapshot
Hypertranscription: the invisible hand in stem cell biology
inferred← citeshttps://doi.org/10.1038/s41392-024-01891-4openalex-snapshot
Drug tolerant persister cell plasticity in cancer: a revolutionary strategy for more effective anticancer therapies
inferred← citeshttps://doi.org/10.1038/s41598-025-21239-4openalex-snapshot
Prepupal diapause reduces adult lifespan in the solitary alfalfa leafcutter bee
inferred← citeshttps://doi.org/10.1038/s41598-025-27154-yopenalex-snapshot
Tissue-specific transcriptomic and endocrine signatures of obligatory reproductive diapause in Eurygaster integriceps
inferred← citeshttps://doi.org/10.1073/pnas.2400964121openalex-snapshot
Altered circadian rhythm, sleep, and rhodopsin 7 –dependent shade preference during diapause in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1093/aesa/saag026openalex-snapshot
Crosstalk in the cold: host–microbe interactions in insect diapause
inferred← citeshttps://doi.org/10.1093/gbe/evae255openalex-snapshot
Convergent Evolution Associated with the Loss of Developmental Diapause May Promote Extended Lifespan in Bees
inferred← citeshttps://doi.org/10.1101/2025.01.26.634899openalex-snapshot
BubR1 and Mad2 regulate adult midgut remodeling in Drosophila diapause
inferred← citeshttps://doi.org/10.1111/rda.14576openalex-snapshot
Effect of cryopreservation on Odc1 and RhoA genes expression in diapausing mouse blastocysts
inferred← citeshttps://doi.org/10.1126/sciimmunol.adu9280openalex-snapshot
Transient disruption of T cell help impairs germinal center dynamics and memory responses
inferred← citeshttps://doi.org/10.1134/s1062360425700018openalex-snapshot
Embryonic Diapause in Mammals: Current State of the Problem
inferred← citeshttps://doi.org/10.1134/s1067413624700097openalex-snapshot
Experimental Approaches to Controlled Diapause in Mammals
inferred← citeshttps://doi.org/10.1186/s12864-025-12163-yopenalex-snapshot
Genome-wide identification and multi-level analysis of the HSP gene superfamily in Aphidoletes aphidimyza: sHSP gene family expansion and its role in diapause regulation
inferred← citeshttps://doi.org/10.1186/s40779-025-00595-2openalex-snapshot
Tumor dormancy and relapse: understanding the molecular mechanisms of cancer recurrence
inferred← citeshttps://doi.org/10.18632/aging.206135openalex-snapshot
Longevity biotechnology: bridging AI, biomarkers, geroscience and clinical applications for healthy longevity
inferred← citeshttps://doi.org/10.26508/lsa.202403147openalex-snapshot
DAF-18/PTEN protects LIN-35/Rb from CLP-1/CAPN-mediated cleavage to promote starvation resistance
inferred← citeshttps://doi.org/10.3354/meps15182openalex-snapshot
Microbial community reshuffling during diapause in a scyphozoan jellyfish
inferred← citeshttps://doi.org/10.3389/fceld.2024.1477346openalex-snapshot
Not dead yet: cell death and survival in cancer and normal physiology
inferred← citeshttps://doi.org/10.3389/fmicb.2026.1810191openalex-snapshot
Temperature regulation mechanisms of diapause in Coridius chinensis revealed by multi-omics integration: coordinated responses of Brain-Gut-Fat Body
inferred← citeshttps://doi.org/10.3390/biology15181587openalex-snapshot
Mechanisms of Diapause in Major Crustacean Taxa: Environmental Cues, Gene Regulation, and Adaptive Strategies
inferred← citeshttps://doi.org/10.64898/2026.05.18.726068openalex-snapshot
Dynamic polyadenylation safeguards developmental trajectories during paused embryogenesis
inferred← citeshttps://doi.org/10.64898/2026.09.04.749554openalex-snapshot
An atlas of the C. elegans starvation response reveals that transcription is necessary to initiate transcriptional silencing in quiescent primordial germ cells
inferred← citeshttps://doi.org/10.7554/elife.98142openalex-snapshot
A genome-wide association study implicates the olfactory system in Drosophila melanogaster diapause-associated lifespan extension and fecundity
inferred← citeshttps://doi.org/10.7554/elife.98142.1openalex-snapshot
A genome-wide association study implicates the olfactory system in Drosophila melanogaster diapause-associated lifespan extension and fecundity
inferred← citeshttps://doi.org/10.7554/elife.98142.1.sa0openalex-snapshot
Reviewer #3 (Public Review): A genome-wide association study implicates the olfactory system in Drosophila melanogaster diapause-associated lifespan extension and fecundity
inferred← citeshttps://doi.org/10.7554/elife.98142.1.sa1openalex-snapshot
Reviewer #2 (Public Review): A genome-wide association study implicates the olfactory system in Drosophila melanogaster diapause-associated lifespan extension and fecundity
inferred← citeshttps://doi.org/10.7554/elife.98142.1.sa2openalex-snapshot
Reviewer #1 (Public Review): A genome-wide association study implicates the olfactory system in Drosophila melanogaster diapause-associated lifespan extension and fecundity
inferred← citeshttps://doi.org/10.7554/elife.98142.1.sa3openalex-snapshot
eLife Assessment: A genome-wide association study implicates the olfactory system in Drosophila melanogaster diapause-associated lifespan extension and fecundity
inferred← citeshttps://doi.org/10.7554/elife.98142.1.sa4openalex-snapshot
Author response: A genome-wide association study implicates the olfactory system in Drosophila melanogaster diapause-associated lifespan extension and fecundity
inferred← citeshttps://doi.org/10.7554/elife.98142.2openalex-snapshot
A genome-wide association study implicates the olfactory system in Drosophila melanogaster diapause-associated lifespan extension and fecundity
inferred← citeshttps://doi.org/10.7554/elife.98142.3openalex-snapshot
A genome-wide association study implicates the olfactory system in Drosophila melanogaster diapause-associated lifespan extension and fecundity
inferred← citeshttps://doi.org/10.7554/elife.98142.4openalex-snapshot
A genome-wide association study implicates the olfactory system in Drosophila melanogaster diapause-associated lifespan extension and fecundity
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