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Gliotransmission and adenosine signaling promote axon regeneration
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Lin28 Signaling Supports Mammalian PNS and CNS Axon Regeneration
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Nociceptive Neurons Protect Drosophila Larvae from Parasitoid Wasps
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Trim9 Regulates Activity-Dependent Fine-Scale Topography in Drosophila
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Stimulation of the adenosine A3 receptor, not the A1 or A2 receptors, promote neurite outgrowth of retinal ganglion cells
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A Drosophila adenosine receptor activates cAMP and calcium signaling
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Vimentin-Dependent Spatial Translocation of an Activated MAP Kinase in Injured Nerve
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Gliotransmitters Travel in Time and Space
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Injury-Induced Decline of Intrinsic Regenerative Ability Revealed by Quantitative Proteomics
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Intrinsic Control of Axon Regeneration
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The Calcium Channel Subunit Alpha2delta2 Suppresses Axon Regeneration in the Adult CNS
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The Mechanosensitive Ion Channel Piezo Inhibits Axon Regeneration
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Glia–neuron interactions in the mammalian retina
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Dendrites of Distinct Classes of Drosophila Sensory Neurons Show Different Capacities for Homotypic Repulsion
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Glia: listening and talking to the synapse
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Adenosine signaling and function in glial cells
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Light-avoidance-mediating photoreceptors tile the Drosophila larval body wall
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Adenosine receptors as therapeutic targets
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Glial inhibition of CNS axon regeneration
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Cortical astrocytes regulate ethanol consumption and intoxication in mice
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Single cell transcriptomics of primate sensory neurons identifies cell types associated with chronic pain
inferredcites →https://doi.org/10.1038/s41583-018-0001-8openalex-snapshot
Intrinsic mechanisms of neuronal axon regeneration
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Induction of corticospinal regeneration by lentiviral trkB-induced Erk activation
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Enhancer-driven membrane markers for analysis of nonautonomous mechanisms reveal neuron–glia interactions in Drosophila
inferredcites →https://doi.org/10.1073/pnas.1523645113openalex-snapshot
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inferredcites →https://doi.org/10.1073/pnas.1814456116openalex-snapshot
Glial ensheathment of the somatodendritic compartment regulates sensory neuron structure and activity
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An in vivo RNAi screen uncovers the role of AdoR signaling and adenosine deaminase in controlling intestinal stem cell activity
inferredcites →https://doi.org/10.1073/pnas.2113645119openalex-snapshot
Nociception and hypersensitivity involve distinct neurons and molecular transducers in Drosophila
inferredcites →https://doi.org/10.1074/jbc.m110.125336openalex-snapshot
Mammalian Target of Rapamycin (mTOR) Activation Increases Axonal Growth Capacity of Injured Peripheral Nerves
inferredcites →https://doi.org/10.1084/jem.20131780openalex-snapshot
B-RAF kinase drives developmental axon growth and promotes axon regeneration in the injured mature CNS
inferredcites →https://doi.org/10.1093/ilar/ilt057openalex-snapshot
Drosophila Models of Neuronal Injury
inferredcites →https://doi.org/10.1098/rstb.2014.0195openalex-snapshot
Glial cell regulation of neuronal activity and blood flow in the retina by release of gliotransmitters
inferredcites →https://doi.org/10.1101/gad.193243.112openalex-snapshot
Regeneration of Drosophila sensory neuron axons and dendrites is regulated by the Akt pathway involving Pten and microRNA bantam
inferredcites →https://doi.org/10.1101/gad.282848.116openalex-snapshot
In vivo dendrite regeneration after injury is different from dendrite development
inferredcites →https://doi.org/10.1126/science.1116916openalex-snapshot
Astrocytic Purinergic Signaling Coordinates Synaptic Networks
inferredcites →https://doi.org/10.1126/science.1144640openalex-snapshot
Astrocytes Potentiate Transmitter Release at Single Hippocampal Synapses
inferredcites →https://doi.org/10.1126/science.1161566openalex-snapshot
Promoting Axon Regeneration in the Adult CNS by Modulation of the PTEN/mTOR Pathway
inferredcites →https://doi.org/10.1126/science.277.5329.1103openalex-snapshot
In Situ Activation Pattern of Drosophila EGF Receptor Pathway During Development
inferredcites →https://doi.org/10.1126/science.abb0556openalex-snapshot
Regulation of sleep homeostasis mediator adenosine by basal forebrain glutamatergic neurons
inferredcites →https://doi.org/10.1126/science.abh2858openalex-snapshot
Astrocyte Ca 2+ -evoked ATP release regulates myelinated axon excitability and conduction speed
inferredcites →https://doi.org/10.1146/annurev-neuro-060909-153248openalex-snapshot
Wallerian Degeneration, WldS, and Nmnat
inferredcites →https://doi.org/10.1146/annurev-neuro-061010-113817openalex-snapshot
The Development and Application of Optogenetics
inferredcites →https://doi.org/10.1146/annurev.neuro.051508.135531openalex-snapshot
Neuropathic Pain: A Maladaptive Response of the Nervous System to Damage
inferredcites →https://doi.org/10.1242/dev.118.2.401openalex-snapshot
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
inferredcites →https://doi.org/10.1523/jneurosci.23-05-01659.2003openalex-snapshot
Glial Cell Inhibition of Neurons by Release of ATP
inferredcites →https://doi.org/10.1523/jneurosci.2510-13.2013openalex-snapshot
Short Hairpin RNA against PTEN Enhances Regenerative Growth of Corticospinal Tract Axons after Spinal Cord Injury
inferredcites →https://doi.org/10.1523/jneurosci.4238-13.2014openalex-snapshot
Neuronal Regeneration inC. elegansRequires Subcellular Calcium Release by Ryanodine Receptor Channels and Can Be Enhanced by Optogenetic Stimulation
inferredcites →https://doi.org/10.1523/jneurosci.4844-08.2008openalex-snapshot
Organization and Postembryonic Development of Glial Cells in the Adult Central Brain of Drosophila
inferredcites →https://doi.org/10.1523/jneurosci.5464-09.2010openalex-snapshot
Calcium and Cyclic AMP Promote Axonal Regeneration in Caenorhabditis elegans and Require DLK-1 Kinase
inferredcites →https://doi.org/10.7554/elife.18716openalex-snapshot
Direct modulation of GFAP-expressing glia in the arcuate nucleus bi-directionally regulates feeding
inferredcites →https://doi.org/10.7554/elife.57395openalex-snapshot
Optical control of ERK and AKT signaling promotes axon regeneration and functional recovery of PNS and CNS in Drosophila
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.4646302openalex-extracted
Calcium Plays an Essential Role in Early-Stage Dendrite Injury Detection
inferred← citeshttps://doi.org/10.1002/glia.24593openalex-snapshot
Adenosine A2B receptors differently modulate oligodendrogliogenesis and myelination depending on their cellular localization
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Carbohydrate and protein metabolism
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Retinal glia regulate development of the circadian photoentrainment circuit
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Advanced dECM-based bioprinting strategy for tissue regeneration
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Tafluprost promotes axon regeneration after optic nerve crush via Zn2+-mTOR pathway
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2024.102635openalex-snapshot
Calcium plays an essential role in early-stage dendrite injury detection and regeneration
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2025.101361openalex-snapshot
The neuroimmune interface in retinal regeneration
inferred← citeshttps://doi.org/10.1021/acsabm.5c01269openalex-snapshot
Engineered Hydrogels as Functional Components in Controllable Neuromodulation for Translational Therapeutics
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Aorticorenal ganglion ablation for blood pressure lowering in canine models
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Glia instruct axon regeneration via a ternary modulation of neuronal calcium channels in Drosophila
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Dynamics of glia and neurons regulate homeostatic rest, sleep and feeding behavior in Drosophila
inferred← citeshttps://doi.org/10.1038/s44386-025-00012-7openalex-snapshot
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Insect adenosine receptors: physiology, pharmacology, and structure–function
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Dynamics of sleep, feeding, and metabolic homeostasis in Drosophila ensheathing glia, astrocytes, and neurons
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Heat-off responses of epidermal cells sensitize Drosophila larvae to noxious inputs
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inferred← citeshttps://doi.org/10.4103/nrr.nrr-d-23-02049openalex-snapshot
Calcium channels caught in peripheral glia’s tug-of-war on axon regeneration in Drosophila
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