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Gap junctions in the C. elegans nervous system regulate ageing and lifespan
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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/bies.201200092openalex-snapshot
On the cause of aging and control of lifespan
inferredcites →https://doi.org/10.1002/cne.901600305openalex-snapshot
Electron microscopical reconstruction of the anterior sensory anatomy of the nematode caenorhabditis elegans
inferredcites →https://doi.org/10.1002/cne.901620106openalex-snapshot
The nerve ring of the nematode Caenorhabditis elegans: Sensory input and motor output
inferredcites →https://doi.org/10.1002/cne.901630207openalex-snapshot
Dopaminergic neurons in the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1002/dvdy.22025openalex-snapshot
High resolution map of Caenorhabditis elegans gap junction proteins
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb04966.xopenalex-snapshot
Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences.
inferredcites →https://doi.org/10.1002/wmts.72openalex-snapshot
Gap junctions and Bystander effects: Good Samaritans and executioners
inferredcites →https://doi.org/10.1007/978-1-4419-7002-2_14openalex-snapshot
Sensory Influence on Homeostasis and Lifespan: Molecules and Circuits
inferredcites →https://doi.org/10.1007/978-1-62703-239-1_31openalex-snapshot
Assessing Aging and Senescent Decline in Caenorhabditis elegans: Cohort Survival Analysis
inferredcites →https://doi.org/10.1016/0012-1606(81)90459-0openalex-snapshot
Developmental genetics of the mechanosensory neurons of Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/0012-1606(86)90314-3openalex-snapshot
Mutant sensory cilia in the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/0047-6374(81)90136-6openalex-snapshot
Quantitative measures of aging in the nematode Caenorhabditis elegans. I. Population and longitudinal studies of two behavioral parameters
inferredcites →https://doi.org/10.1016/0891-5849(89)90066-xopenalex-snapshot
The antioxidant action of N-acetylcysteine: Its reaction with hydrogen peroxide, hydroxyl radical, superoxide, and hypochlorous acid
inferredcites →https://doi.org/10.1016/b978-0-12-394620-1.00006-0openalex-snapshot
Laser Microsurgery in Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/j.bbamem.2004.10.004openalex-snapshot
Innexins: members of an evolutionarily conserved family of gap-junction proteins
inferredcites →https://doi.org/10.1016/j.bbamem.2011.10.016openalex-snapshot
Functional redundancy and compensation among members of gap junction protein families?
inferredcites →https://doi.org/10.1016/j.cell.2007.02.052openalex-snapshot
An Innexin-Dependent Cell Network Establishes Left-Right Neuronal Asymmetry in C. elegans
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.2013.08.001openalex-snapshot
Serotonin and the Neuropeptide PDF Initiate and Extend Opposing Behavioral States in C. elegans
inferredcites →https://doi.org/10.1016/j.cell.2013.09.052openalex-snapshot
Modular Control of Glutamatergic Neuronal Identity in C. elegans by Distinct Homeodomain Proteins
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.celrep.2017.03.062openalex-snapshot
How a Mutation that Slows Aging Can Also Disproportionately Extend End-of-Life Decrepitude
inferredcites →https://doi.org/10.1016/j.cels.2016.09.003openalex-snapshot
Extended Twilight among Isogenic C. elegans Causes a Disproportionate Scaling between Lifespan and Health
inferredcites →https://doi.org/10.1016/j.cmet.2013.08.007openalex-snapshot
Functional Aging in the Nervous System Contributes to Age-Dependent Motor Activity Decline in C. elegans
inferredcites →https://doi.org/10.1016/j.cub.2007.06.060openalex-snapshot
UNC-1 Regulates Gap Junctions Important to Locomotion in C. elegans
inferredcites →https://doi.org/10.1016/j.cub.2007.08.031openalex-snapshot
A Calcium Wave Mediated by Gap Junctions Coordinates a Rhythmic Behavior in C. elegans
inferredcites →https://doi.org/10.1016/j.cub.2009.03.041openalex-snapshot
Regulation of the Longevity Response to Temperature by Thermosensory Neurons in Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/j.cub.2013.04.030openalex-snapshot
A Gap Junction Circuit Enhances Processing of Coincident Mechanosensory Inputs
inferredcites →https://doi.org/10.1016/j.cub.2018.06.035openalex-snapshot
C. elegans Eats Its Own Intestine to Make Yolk Leading to Multiple Senescent Pathologies
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2011.10.445openalex-snapshot
The redox stress hypothesis of aging
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2007.12.007openalex-snapshot
Identification by machine vision of the rate of motor activity decline as a lifespan predictor in C. elegans
inferredcites →https://doi.org/10.1016/j.neuron.2003.08.015openalex-snapshot
In Vivo Imaging of C. elegans Mechanosensory Neurons Demonstrates a Specific Role for the MEC-4 Channel in the Process of Gentle Touch Sensation
inferredcites →https://doi.org/10.1016/j.neuron.2011.09.005openalex-snapshot
An Imbalancing Act: Gap Junctions Reduce the Backward Motor Circuit Activity to Bias C. elegans for Forward Locomotion
inferredcites →https://doi.org/10.1016/j.redox.2016.12.020openalex-snapshot
Caenorhabditis elegans as a model for understanding ROS function in physiology and disease
inferredcites →https://doi.org/10.1016/j.tins.2012.11.001openalex-snapshot
Neuronal gap junctions: making and breaking connections during development and injury
inferredcites →https://doi.org/10.1016/j.ymeth.2014.04.002openalex-snapshot
The C. elegans lifespan assay toolkit
inferredcites →https://doi.org/10.1016/j.ymeth.2014.04.003openalex-snapshot
The C. elegans healthspan and stress-resistance assay toolkit
inferredcites →https://doi.org/10.1016/s0012-1606(02)00116-1openalex-snapshot
The caenorhabditis elegans innexin INX-3 is localized to gap junctions and is essential for embryonic development
inferredcites →https://doi.org/10.1016/s0074-7696(05)43004-1openalex-snapshot
Insulin-Like Growth Factor Signaling in Fish
inferredcites →https://doi.org/10.1016/s0168-9525(98)01547-9openalex-snapshot
Innexins: a family of invertebrate gap-junction proteins
inferredcites →https://doi.org/10.1016/s0378-1119(00)00579-5openalex-snapshot
Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/s0896-6273(03)00816-xopenalex-snapshot
Regulation of C. elegans Longevity by Specific Gustatory and Olfactory Neurons
inferredcites →https://doi.org/10.1016/s0925-4773(02)00293-9openalex-snapshot
MTD-1, a touch-cell-specific membrane protein with a subtle effect on touch sensitivity
inferredcites →https://doi.org/10.1038/15693openalex-snapshot
Selective transfer of endogenous metabolites through gap junctions composed of different connexins
inferredcites →https://doi.org/10.1038/349588a0openalex-snapshot
The mec-4 gene is a member of a family of Caenorhabditis elegans genes that can mutate to induce neuronal degeneration
inferredcites →https://doi.org/10.1038/378082a0openalex-snapshot
Synaptic code for sensory modalities revealed by C. elegans GLR-1 glutamate receptor
inferredcites →https://doi.org/10.1038/45544openalex-snapshot
Regulation of lifespan by sensory perception in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/emboj.2013.75openalex-snapshot
Counterbalance between BAG and URX neurons via guanylate cyclases controls lifespan homeostasis in C. elegans
inferredcites →https://doi.org/10.1038/nature00891openalex-snapshot
Identification of genes expressed in C. elegans touch receptor neurons
inferredcites →https://doi.org/10.1038/nature01135openalex-snapshot
Stochastic and genetic factors influence tissue-specific decline in ageing C. elegans
inferredcites →https://doi.org/10.1038/nature03809openalex-snapshot
Systematic analysis of genes required for synapse structure and function
inferredcites →https://doi.org/10.1038/nature08983openalex-snapshot
Neural mechanisms of ageing and cognitive decline
inferredcites →https://doi.org/10.1038/ncomms1308openalex-snapshot
The neural circuits and sensory channels mediating harsh touch sensation in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/ncomms14818openalex-snapshot
Antidromic-rectifying gap junctions amplify chemical transmission at functionally mixed electrical-chemical synapses
inferredcites →https://doi.org/10.1038/ncomms9919openalex-snapshot
C. elegans maximum velocity correlates with healthspan and is maintained in worms with an insulin receptor mutation
inferredcites →https://doi.org/10.1038/nmeth.1445openalex-snapshot
Conditional gene expression and RNAi using MEC-8–dependent splicing in C. elegans
inferredcites →https://doi.org/10.1038/nn.3061openalex-snapshot
Tonic signaling from O2 sensors sets neural circuit activity and behavioral state
inferredcites →https://doi.org/10.1038/nn1362openalex-snapshot
The MEC-4 DEG/ENaC channel of Caenorhabditis elegans touch receptor neurons transduces mechanical signals
inferredcites →https://doi.org/10.1038/nn1886openalex-snapshot
Caenorhabditis elegans TRPA-1 functions in mechanosensation
inferredcites →https://doi.org/10.1038/srep42295openalex-snapshot
Polymodal Responses in C. elegans Phasmid Neurons Rely on Multiple Intracellular and Intercellular Signaling Pathways
inferredcites →https://doi.org/10.1046/j.1471-4159.1997.69062251.xopenalex-snapshot
The Caenorhabditis elegans Avermectin Resistance and Anesthetic Response Gene unc‐9 Encodes a Member of a Protein Family Implicated in Electrical Coupling of Excitable Cells
inferredcites →https://doi.org/10.1073/pnas.0400848101openalex-snapshot
Measurements of age-related changes of physiological processes that predict lifespan of Caenorhabditis elegans
inferredcites →https://doi.org/10.1073/pnas.1011711108openalex-snapshot
Genetic analysis of age-dependent defects of the Caenorhabditis elegans touch receptor neurons
inferredcites →https://doi.org/10.1073/pnas.1412192112openalex-snapshot
Uncoupling lifespan and healthspan in Caenorhabditis elegans longevity mutants
inferredcites →https://doi.org/10.1073/pnas.1524727113openalex-snapshot
Roles for ROS and hydrogen sulfide in the longevity response to germline loss in Caenorhabditis elegans
inferredcites →https://doi.org/10.1073/pnas.1621274114openalex-snapshot
Dissection of neuronal gap junction circuits that regulate social behavior in Caenorhabditis elegans
inferredcites →https://doi.org/10.1073/pnas.1717022115openalex-snapshot
Descending pathway facilitates undulatory wave propagation in Caenorhabditis elegans through gap junctions
inferredcites →https://doi.org/10.1073/pnas.95.15.8761openalex-snapshot
unc - 1 : A stomatin homologue controls sensitivity to volatile anesthetics in Caenorhabditis elegans
inferredcites →https://doi.org/10.1073/pnas.95.22.13091openalex-snapshot
The genetics of caloric restriction in Caenorhabditis elegans
inferredcites →https://doi.org/10.1073/pnas.97.6.2674openalex-snapshot
The genetics of ivermectin resistance in Caenorhabditis elegans
inferredcites →https://doi.org/10.1080/09687680210139839openalex-snapshot
Gap junctions: structure and function (Review)
inferredcites →https://doi.org/10.1083/jcb.134.2.537openalex-snapshot
eat-5 and unc-7 represent a multigene family in Caenorhabditis elegans involved in cell-cell coupling.
inferredcites →https://doi.org/10.1083/jcb.144.1.45openalex-snapshot
A Conserved LIM Protein That Affects Muscular Adherens Junction Integrity and Mechanosensory Function in Caenorhabditis elegans
inferredcites →https://doi.org/10.1091/mbc.e02-11-0716openalex-snapshot
Regulation of Intermuscular Electrical Coupling by theCaenorhabditis elegansInnexininx-6
inferredcites →https://doi.org/10.1093/genetics/113.4.821openalex-snapshot
MUTATIONS WITH DOMINANT EFFECTS ON THE BEHAVIOR AND MORPHOLOGY OF THE NEMATODE CAENORHABDITIS ELEGANS
inferredcites →https://doi.org/10.1093/genetics/139.3.1247openalex-snapshot
Mutations in the clk-1 gene of Caenorhabditis elegans affect developmental and behavioral timing.
inferredcites →https://doi.org/10.1093/genetics/150.1.129openalex-snapshot
Two Pleiotropic Classes of daf-2 Mutation Affect Larval Arrest, Adult Behavior, Reproduction and Longevity in Caenorhabditis elegans
inferredcites →https://doi.org/10.1093/genetics/154.4.1597openalex-snapshot
Genetic, Behavioral and Environmental Determinants of Male Longevity in Caenorhabditis elegans
inferredcites →https://doi.org/10.1093/genetics/77.1.95openalex-snapshot
THE DNA OF CAENORHABDITIS ELEGANS
inferredcites →https://doi.org/10.1093/gerona/gls088openalex-snapshot
Genetics, Life Span, Health Span, and the Aging Process in Caenorhabditis elegans
inferredcites →https://doi.org/10.1093/gerona/glw248openalex-snapshot
Assessing Health Span in Caenorhabditis elegans: Lessons From Short-Lived Mutants
inferredcites →https://doi.org/10.1098/rstb.1986.0056openalex-snapshot
The structure of the nervous system of the nematode Caenorhabditis elegans
inferredcites →https://doi.org/10.1098/rstb.1997.0169openalex-snapshot
Ageing and physiological functions
inferredcites →https://doi.org/10.1101/gad.3.12a.1823openalex-snapshot
The mec-3 gene of Caenorhabditis elegans requires its own product for maintained expression and is expressed in three neuronal cell types.
inferredcites →https://doi.org/10.1101/gad.309625.117openalex-snapshot
Brain–gut communications via distinct neuroendocrine signals bidirectionally regulate longevity in C. elegans
inferredcites →https://doi.org/10.1111/acel.12569openalex-snapshot
Synergism between soluble guanylate cyclase signaling and neuropeptides extends lifespan in the nematodeCaenorhabditis elegans
inferredcites →https://doi.org/10.1111/acel.12704openalex-snapshot
Movement decline across lifespan of Caenorhabditis elegans mutants in the insulin/insulin‐like signaling pathway
inferredcites →https://doi.org/10.1126/science.8103239openalex-snapshot
Cooperative Interactions Between the Caenorhabditis elegans Homeoproteins UNC-86 and MEC-3
inferredcites →https://doi.org/10.1146/annurev-biochem-060815-014451openalex-snapshot
Signaling Networks Determining Life Span
inferredcites →https://doi.org/10.1146/annurev-bioeng-071114-040829openalex-snapshot
The Mechanobiology of Aging
inferredcites →https://doi.org/10.1146/annurev.neuro.26.041002.131128openalex-snapshot
ELECTRICAL SYNAPSES IN THE MAMMALIAN BRAIN
inferredcites →https://doi.org/10.1152/ajpcell.00220.2004openalex-snapshot
Connexins are mechanosensitive
inferredcites →https://doi.org/10.1186/1471-2180-12-49openalex-snapshot
Control of intestinal bacterial proliferation in regulation of lifespan in Caenorhabditis elegans
inferredcites →https://doi.org/10.1186/1471-2202-14-156openalex-snapshot
The Caenorhabditis elegans interneuron ALA is (also) a high-threshold mechanosensor
inferredcites →https://doi.org/10.1186/1749-8104-4-16openalex-snapshot
Interactions between innexins UNC-7 and UNC-9 mediate electrical synapse specificity in the Caenorhabditis elegans locomotory nervous system
inferredcites →https://doi.org/10.1186/s12860-016-0091-yopenalex-snapshot
Characteristics and plasticity of electrical synaptic transmission
inferredcites →https://doi.org/10.1186/s12860-016-0120-xopenalex-snapshot
Gap junctions and hemichannels: communicating cell death in neurodevelopment and disease
inferredcites →https://doi.org/10.1242/jeb.02165openalex-snapshot
Evolution of pharyngeal behaviors and neuronal functions in free-living soil nematodes
inferredcites →https://doi.org/10.1371/journal.pbio.1000556openalex-snapshot
A Mitochondrial Superoxide Signal Triggers Increased Longevity in Caenorhabditis elegans
inferredcites →https://doi.org/10.1371/journal.pgen.0030129openalex-snapshot
Genetics of Aging in Caenorhabditis elegans
inferredcites →https://doi.org/10.1371/journal.pgen.1003921openalex-snapshot
Neuron-Specific Feeding RNAi in C. elegans and Its Use in a Screen for Essential Genes Required for GABA Neuron Function
inferredcites →https://doi.org/10.1371/journal.pone.0041633openalex-snapshot
Local Oxidative Stress Expansion through Endothelial Cells – A Key Role for Gap Junction Intercellular Communication
inferredcites →https://doi.org/10.1371/journal.pone.0076877openalex-snapshot
Six Innexins Contribute to Electrical Coupling of C. elegans Body-Wall Muscle
inferredcites →https://doi.org/10.1523/jneurosci.0022-14.2014openalex-snapshot
Modulation of C. elegans Touch Sensitivity Is Integrated at Multiple Levels
inferredcites →https://doi.org/10.1523/jneurosci.0637-09.2009openalex-snapshot
Caenorhabditis elegansInnexins Regulate Active Zone Differentiation
inferredcites →https://doi.org/10.1523/jneurosci.1494-11.2012openalex-snapshot
Neurite Sprouting and Synapse Deterioration in the Aging Caenorhabditis elegans Nervous System
inferredcites →https://doi.org/10.1523/jneurosci.20-07-02575.2000openalex-snapshot
In VivoStructure–Function Analyses ofCaenorhabditis elegansMEC-4, a Candidate Mechanosensory Ion Channel Subunit
inferredcites →https://doi.org/10.1523/jneurosci.22-03-00644.2002openalex-snapshot
Specific Gap Junctions Enhance the Neuronal Vulnerability to Brain Traumatic Injury
inferredcites →https://doi.org/10.1523/jneurosci.6606-10.2011openalex-snapshot
Spontaneous Age-Related Neurite Branching in Caenorhabditis elegans
inferredcites →https://doi.org/10.1534/g3.112.003830openalex-snapshot
Large-Scale Screening for Targeted Knockouts in the Caenorhabditis elegans Genome
inferredcites →https://doi.org/10.1534/genetics.107.083923openalex-snapshot
DAF-16-Dependent Suppression of Immunity During Reproduction inCaenorhabditis elegans
inferredcites →https://doi.org/10.1534/genetics.113.152660openalex-snapshot
Defining Specificity Determinants of cGMP Mediated Gustatory Sensory Transduction inCaenorhabditis elegans
inferredcites →https://doi.org/10.1534/genetics.114.168815openalex-snapshot
Two Classes of Gap Junction Channels Mediate Soma-Germline Interactions Essential for Germline Proliferation and Gametogenesis in Caenorhabditis elegans
inferredcites →https://doi.org/10.1534/genetics.117.202127openalex-snapshot
A Neurotransmitter Atlas of theCaenorhabditis elegansMale Nervous System Reveals Sexually Dimorphic Neurotransmitter Usage
inferredcites →https://doi.org/10.1534/genetics.118.300241openalex-snapshot
How Caenorhabditis elegans Senses Mechanical Stress, Temperature, and Other Physical Stimuli
inferredcites →https://doi.org/10.1895/wormbook.1.164.1openalex-snapshot
Insulin/insulin-like growth factor signaling in C. elegans
inferredcites →https://doi.org/10.2183/pjab.93.036openalex-snapshot
Comprehensive functional genomics using Caenorhabditis elegans as a model organism
inferredcites →https://doi.org/10.3389/fgene.2012.00222openalex-snapshot
Neuronal Responses to Physiological Stress
inferredcites →https://doi.org/10.3389/fgene.2013.00071openalex-snapshot
Neuronal Inputs and Outputs of Aging and Longevity
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1101/2025.09.14.675793openalex-snapshot
Molecular Configuration, Regulation and Function of Heterochannel Electrical Synapses
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1249436openalex-snapshot
A gonadal gap junction INX-14/Notch GLP-1 signaling axis suppresses gut defense through an intestinal lysosome pathway
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