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The transcription factor ATF-3 promotes neurite outgrowth
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Outgoing claims: the papers this work cites, builds on, or argues with.
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NT-3 delivered by an adenoviral vector induces injured dorsal root axons to regenerate into the spinal cord of adult rats
inferredcites →https://doi.org/10.1002/jnr.10176openalex-snapshot
Promoting axonal regeneration in the central nervous system by enhancing the cell body response to axotomy
inferredcites →https://doi.org/10.1002/jnr.490390603openalex-snapshot
Neurite outgrowth and GAP‐43 mRNA expression in cultured adult rat dorsal root ganglion neurons: Effects of NGF or prior peripheral axotomy
inferredcites →https://doi.org/10.1002/jnr.490420314openalex-snapshot
Comparison of c‐jun, junB, and junD mRNA expression and protein in the rat dorsal root ganglia following sciatic nerve transection
inferredcites →https://doi.org/10.1002/neu.480240709openalex-snapshot
Injury‐associated induction of GAP‐43 expression displays axon branch specificity in rat dorsal root ganglion neurons
inferredcites →https://doi.org/10.1002/neu.480251209openalex-snapshot
Gap‐43 immunoreactivity and axon regeneration in retinal ganglion cells of the rat
inferredcites →https://doi.org/10.1006/exnr.1993.1040openalex-snapshot
Differential Regenerative Growth of CNS Axons into Tibial and Peroneal Nerve Grafts in the Thalamus of Adult Rats
inferredcites →https://doi.org/10.1006/exnr.1994.1161openalex-snapshot
Regeneration of Adult Rat Sensory Axons into Intraspinal Nerve Grafts: Promoting Effects of Conditioning Lesion and Graft Predegeneration
inferredcites →https://doi.org/10.1006/jmcc.2002.2091openalex-snapshot
ATF3 Inhibits Doxorubicin-induced Apoptosis in Cardiac Myocytes: A Novel Cardioprotective Role of ATF3
inferredcites →https://doi.org/10.1006/mcne.1999.0814openalex-snapshot
Activating Transcription Factor 3 (ATF3) Induction by Axotomy in Sensory and Motoneurons: A Novel Neuronal Marker of Nerve Injury
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Improved Helper Virus-Free Packaging System for HSV Amplicon Vectors Using an ICP27-Deleted, Oversized HSV-1 DNA in a Bacterial Artificial Chromosome
inferredcites →https://doi.org/10.1007/bf00228507openalex-snapshot
GAP-43 in the axons of mammalian CNS neurons regenerating into peripheral nerve grafts
inferredcites →https://doi.org/10.1007/bf01148324openalex-snapshot
Regeneration of long spinal axons in the rat
inferredcites →https://doi.org/10.1007/bf01611859openalex-snapshot
The induction of a regenerative propensity in sensory neurons following peripheral axonal injury
inferredcites →https://doi.org/10.1016/0006-8993(85)91047-9openalex-snapshot
Lengthy regrowth of cut axons from ganglion cells after peripheral nerve transplantation into the retina of adult rats
inferredcites →https://doi.org/10.1016/0006-8993(91)91699-2openalex-snapshot
Selective expression of Jun proteins following axotomy and axonal transport block in peripheral nerves in the rat: evidence for a role in the regeneration process
inferredcites →https://doi.org/10.1016/0092-8674(95)90168-xopenalex-snapshot
Overexpression of the neural growth-associated protein GAP-43 induces nerve sprouting in the adult nervous system of transgenic mice
inferredcites →https://doi.org/10.1016/0169-328x(93)90083-2openalex-snapshot
Colocalisation and covariation of c-JUN transcription factor with galanin in primary afferent neurons and with CGRP in spinal motoneurons following transection of rat sciatic nerve
inferredcites →https://doi.org/10.1016/j.conb.2004.01.004openalex-snapshot
Nogo and axon regeneration
inferredcites →https://doi.org/10.1016/j.expneurol.2004.11.026openalex-snapshot
Upregulation of activating transcription factor 3 (ATF3) by intrinsic CNS neurons regenerating axons into peripheral nerve grafts
inferredcites →https://doi.org/10.1016/j.jneumeth.2003.09.027openalex-snapshot
Utilization of an HSV-based amplicon vector encoding the axonal marker hPLAP to follow neurite outgrowth in cultured DRG neurons
inferredcites →https://doi.org/10.1016/j.mcn.2004.07.001openalex-snapshot
Inhibition of c-Jun phosphorylation reduces axonal outgrowth of adult rat nodose ganglia and dorsal root ganglia sensory neurons
inferredcites →https://doi.org/10.1016/j.molbrainres.2003.09.014openalex-snapshot
ATF3 enhances c-Jun-mediated neurite sprouting
inferredcites →https://doi.org/10.1016/j.molbrainres.2003.10.027openalex-snapshot
Over expression of ATF-3 protects rat hippocampal neurons from in vivo injection of kainic acid
inferredcites →https://doi.org/10.1016/j.nbd.2003.11.015openalex-snapshot
Degenerative and regenerative mechanisms governing spinal cord injury
inferredcites →https://doi.org/10.1016/j.neuron.2004.06.005openalex-snapshot
The AP-1 Transcription Factor c-Jun Is Required for Efficient Axonal Regeneration
inferredcites →https://doi.org/10.1016/j.pneurobio.2003.06.001openalex-snapshot
Role of semaphorins in the adult nervous system
inferredcites →https://doi.org/10.1016/j.tins.2003.08.004openalex-snapshot
Inflammation, degeneration and regeneration in the injured spinal cord: insights from DNA microarrays
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Transgenic Mice with Cardiac-Specific Expression of Activating Transcription Factor 3, a Stress-Inducible Gene, Have Conduction Abnormalities and Contractile Dysfunction
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Enhanced functional recovery after proximal nerve root injury by vector-mediated gene transfer
inferredcites →https://doi.org/10.1016/s0074-7696(08)62224-xopenalex-snapshot
Cytoplasmic Mechanisms of Axonal and Dendritic Growth in Neurons
inferredcites →https://doi.org/10.1016/s0092-8674(02)00934-0openalex-snapshot
Translating Axon Guidance Cues
inferredcites →https://doi.org/10.1016/s0166-2236(02)02188-4openalex-snapshot
Axonal and presynaptic protein synthesis: new insights into the biology of the neuron
inferredcites →https://doi.org/10.1016/s0166-2236(96)01000-4openalex-snapshot
The c-Jun transcription factor – bipotential mediator of neuronal death, survival and regeneration
inferredcites →https://doi.org/10.1016/s0166-2236(96)10072-2openalex-snapshot
GAP-43: an intrinsic determinant of neuronal development and plasticity
inferredcites →https://doi.org/10.1016/s0169-328x(03)00181-5openalex-snapshot
Biphasic expression of activating transcription factor-3 in neurons after cerebral infarction
inferredcites →https://doi.org/10.1016/s0301-0082(97)00043-9openalex-snapshot
B-50, the growth associated protein-43: modulation of cell morphology and communication in the nervous system
inferredcites →https://doi.org/10.1016/s0378-1119(01)00551-0openalex-snapshot
The molecular biology and nomenclature of the activating transcription factor/cAMP responsive element binding family of transcription factors: activating transcription factor proteins and homeostasis
inferredcites →https://doi.org/10.1016/s0896-6273(00)80039-2openalex-snapshot
Neurotrophins Cause a New Sensation
inferredcites →https://doi.org/10.1016/s0896-6273(00)80681-9openalex-snapshot
Prior Exposure to Neurotrophins Blocks Inhibition of Axonal Regeneration by MAG and Myelin via a cAMP-Dependent Mechanism
inferredcites →https://doi.org/10.1016/s0896-6273(00)80755-2openalex-snapshot
Regeneration of Dorsal Column Fibers into and beyond the Lesion Site following Adult Spinal Cord Injury
inferredcites →https://doi.org/10.1016/s0896-6273(02)00702-xopenalex-snapshot
Regeneration of Sensory Axons within the Injured Spinal Cord Induced by Intraganglionic cAMP Elevation
inferredcites →https://doi.org/10.1016/s0896-6273(02)00730-4openalex-snapshot
Spinal Axon Regeneration Induced by Elevation of Cyclic AMP
inferredcites →https://doi.org/10.1016/s0896-6273(02)00762-6openalex-snapshot
Signaling the Pathway to Regeneration
inferredcites →https://doi.org/10.1016/s0896-6273(02)00826-7openalex-snapshot
Arginase I and Polyamines Act Downstream from Cyclic AMP in Overcoming Inhibition of Axonal Growth MAG and Myelin In Vitro
inferredcites →https://doi.org/10.1016/s0896-6273(02)00941-8openalex-snapshot
Hsp27 Upregulation and Phosphorylation Is Required for Injured Sensory and Motor Neuron Survival
inferredcites →https://doi.org/10.1016/s0959-437x(02)00321-0openalex-snapshot
Pax genes and eye organogenesis
inferredcites →https://doi.org/10.1023/a:1023941421781openalex-snapshot
The Nogo receptor, its ligands and axonal regeneration in the spinal cord; A review
inferredcites →https://doi.org/10.1038/309791a0openalex-snapshot
Peripheral injury enhances central regeneration of primary sensory neurones
inferredcites →https://doi.org/10.1038/35002084openalex-snapshot
Functional regeneration of sensory axons into the adult spinal cord
inferredcites →https://doi.org/10.1038/82881openalex-snapshot
Spinal axon regeneration evoked by replacing two growth cone proteins in adult neurons
inferredcites →https://doi.org/10.1038/nn1193openalex-snapshot
PKC mediates inhibitory effects of myelin and chondroitin sulfate proteoglycans on axonal regeneration
inferredcites →https://doi.org/10.1038/nrn1195openalex-snapshot
Myelin-associated inhibitors of axonal regeneration in the adult mammalian CNS
inferredcites →https://doi.org/10.1038/sj.onc.1204200openalex-snapshot
Transcription factor ATF3 partially transforms chick embryo fibroblasts by promoting growth factor-independent proliferation
inferredcites →https://doi.org/10.1038/sj.onc.1205896openalex-snapshot
ATF3 induction following DNA damage is regulated by distinct signaling pathways and over-expression of ATF3 protein suppresses cells growth
inferredcites →https://doi.org/10.1038/sj.onc.1207676openalex-snapshot
Runx2 control of organization, assembly and activity of the regulatory machinery for skeletal gene expression
inferredcites →https://doi.org/10.1046/j.1460-9568.1999.00756.xopenalex-snapshot
Growth responses of different subpopulations of adult sensory neurons to neurotrophic factors in vitro
inferredcites →https://doi.org/10.1046/j.1460-9568.2003.02809.xopenalex-snapshot
Corticospinal neurons up‐regulate a range of growth‐associated genes following intracortical, but not spinal, axotomy
inferredcites →https://doi.org/10.1046/j.1469-7580.2003.00139.xopenalex-snapshot
The formation of skeletal muscle: from somite to limb
inferredcites →https://doi.org/10.1073/pnas.122231899openalex-snapshot
Identification of gene expression profile of dorsal root ganglion in the rat peripheral axotomy model of neuropathic pain
inferredcites →https://doi.org/10.1073/pnas.88.9.3720openalex-snapshot
Cross-family dimerization of transcription factors Fos/Jun and ATF/CREB alters DNA binding specificity.
inferredcites →https://doi.org/10.1073/pnas.89.2.693openalex-snapshot
A recombinant retrovirus encoding alkaline phosphatase confirms clonal boundary assignment in lineage analysis of murine retina.
inferredcites →https://doi.org/10.1074/jbc.m100986200openalex-snapshot
The Roles of ATF3 in Glucose Homeostasis
inferredcites →https://doi.org/10.1074/jbc.m202974200openalex-snapshot
Transcriptional Repressor Activating Transcription Factor 3 Protects Human Umbilical Vein Endothelial Cells from Tumor Necrosis Factor-α-induced Apoptosis through Down-regulation ofp53 Transcription
inferredcites →https://doi.org/10.1111/j.1460-9568.2004.03262.xopenalex-snapshot
Dynamic changes in glypican‐1 expression in dorsal root ganglion neurons after peripheral and central axonal injury
inferredcites →https://doi.org/10.1126/science.274.5290.1123openalex-snapshot
The Molecular Biology of Axon Guidance
inferredcites →https://doi.org/10.1126/science.6171034openalex-snapshot
Axonal Elongation into Peripheral Nervous System "Bridges" After Central Nervous System Injury in Adult Rats
inferredcites →https://doi.org/10.1128/mcb.12.10.4654openalex-snapshot
Interactions among LRF-1, JunB, c-Jun, and c-Fos define a regulatory program in the G1 phase of liver regeneration.
inferredcites →https://doi.org/10.1128/mcb.24.13.5721-5732.2004openalex-snapshot
Role for Activating Transcription Factor 3 in Stress-Induced β-Cell Apoptosis
inferredcites →https://doi.org/10.1146/annurev.cellbio.18.012502.105758openalex-snapshot
Myogenic Regulatory Factors and the Specification of Muscle Progenitors in Vertebrate Embryos
inferredcites →https://doi.org/10.1159/000068405openalex-snapshot
Regeneration of Primary Sensory Neurons
inferredcites →https://doi.org/10.1186/1471-2202-3-16openalex-snapshot
Replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury.
inferredcites →https://doi.org/10.1523/jneurosci.05-06-01616.1985openalex-snapshot
Injured neurons in the olfactory bulb of the adult rat grow axons along grafts of peripheral nerve
inferredcites →https://doi.org/10.1523/jneurosci.08-07-02394.1988openalex-snapshot
Nerve growth factors (NGF, BDNF) enhance axonal regeneration but are not required for survival of adult sensory neurons
inferredcites →https://doi.org/10.1523/jneurosci.14-07-04375.1994openalex-snapshot
GAP-43 expression in primary sensory neurons following central axotomy
inferredcites →https://doi.org/10.1523/jneurosci.17-02-00646.1997openalex-snapshot
A Transcription-Dependent Switch Controls Competence of Adult Neurons for Distinct Modes of Axon Growth
inferredcites →https://doi.org/10.1523/jneurosci.17-04-01425.1997openalex-snapshot
The Expression and Function of Notch Pathway Genes in the Developing Rat Eye
inferredcites →https://doi.org/10.1523/jneurosci.19-20-08945.1999openalex-snapshot
A Role for HSP27 in Sensory Neuron Survival
inferredcites →https://doi.org/10.1523/jneurosci.22-04-01303.2002openalex-snapshot
Small Proline-Rich Repeat Protein 1A Is Expressed by Axotomized Neurons and Promotes Axonal Outgrowth
inferredcites →https://doi.org/10.1523/jneurosci.23-12-05187.2003openalex-snapshot
Expression of the Activating Transcription Factor 3 Prevents c-Jun N-Terminal Kinase-Induced Neuronal Death by Promoting Heat Shock Protein 27 Expression and Akt Activation
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.4786379openalex-extracted
Linc00894 Inhibited Neuron Cellular Apoptosis Via Regulating Activating Transcription Factor 3 Expression
inferred← citeshttps://doi.org/10.1002/9783527622467.ch2openalex-snapshot
A Meta‐Analysis of Large‐Scale Gene Expression Studies of the Injured PNS: Toward the Genetic Networks That Govern Successful Regeneration
inferred← citeshttps://doi.org/10.1002/9783527622467.ch5openalex-snapshot
The Role of Gene Expression Dependent Molecular Pathways in Axon Plasticity and Neuron Repair Following Acute CNS Injury
inferred← citeshttps://doi.org/10.1002/advs.202301367openalex-snapshot
The Lysine Demethylase KDM7A Regulates Immediate Early Genes in Neurons
inferred← citeshttps://doi.org/10.1002/ana.25209openalex-snapshot
The nerve conditioning lesion: A strategy to enhance nerve regeneration
inferred← citeshttps://doi.org/10.1002/ar.23843openalex-snapshot
Expression of Regeneration‐Associated Proteins in Primary Sensory Neurons and Regenerating Axons After Nerve Injury—An Overview
inferred← citeshttps://doi.org/10.1002/art.23063openalex-snapshot
Collagen‐induced arthritis as a model of hyperalgesia: Functional and cellular analysis of the analgesic actions of tumor necrosis factor blockade
inferred← citeshttps://doi.org/10.1002/cne.21944openalex-snapshot
Expression of the regeneration‐associated protein SPRR1A in primary sensory neurons and spinal cord of the adult mouse following peripheral and central injury
inferred← citeshttps://doi.org/10.1002/cne.22714openalex-snapshot
Peripheral nerve graft with immunosuppression modifies gene expression in axotomized CNS neurons
inferred← citeshttps://doi.org/10.1002/cne.23749openalex-snapshot
Phenotypic changes in dorsal root ganglion and spinal cord in the collagen antibody‐induced arthritis mouse model
inferred← citeshttps://doi.org/10.1002/ctm2.1650openalex-snapshot
ATF3 is a neuron‐specific biomarker for spinal cord injury and ischaemic stroke
inferred← citeshttps://doi.org/10.1002/dneu.20934openalex-snapshot
Multiple transcription factor families regulate axon growth and regeneration
inferred← citeshttps://doi.org/10.1002/dneu.22312openalex-snapshot
Contrasting developmental axon regrowth and neurite sprouting of Drosophila mushroom body neurons reveals shared and unique molecular mechanisms
inferred← citeshttps://doi.org/10.1002/glia.22571openalex-snapshot
Satellite glial cell proliferation in the trigeminal ganglia after chronic constriction injury of the infraorbital nerve
inferred← citeshttps://doi.org/10.1002/jnr.22439openalex-snapshot
Involvement of nerve injury and activation of peripheral glial cells in tetanic sciatic stimulation‐induced persistent pain in rats
inferred← citeshttps://doi.org/10.1002/mus.23631openalex-snapshot
Shock wave treatment improves nerve regeneration in the rat
inferred← citeshttps://doi.org/10.1002/mus.26879openalex-snapshot
Differentiated adipose‐derived stem cells promote peripheral nerve regeneration
inferred← citeshttps://doi.org/10.1002/reg2.99openalex-snapshot
Axonal regeneration in zebrafish spinal cord
inferred← citeshttps://doi.org/10.1007/400_2009_14openalex-snapshot
Retrograde Injury Signaling in Lesioned Axons
inferred← citeshttps://doi.org/10.1007/400_2009_19openalex-snapshot
Axon Regeneration in the Peripheral and Central Nervous Systems
inferred← citeshttps://doi.org/10.1007/978-1-4614-4090-1_1openalex-snapshot
Frontiers Of Spinal Cord And Spine Repair: Experimental Approaches for Repair of Spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/978-1-4899-7654-3_8openalex-snapshot
Gene Therapy for Spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/978-1-4939-2306-9_6openalex-snapshot
Gene Therapy Approaches to Promoting Axonal Regeneration After Spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/978-3-031-89307-0_10openalex-snapshot
Gene Therapy for Spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/978-3-319-41406-5_27openalex-snapshot
Spinal Cord and Peripheral Nerve Regeneration Current Research and Future Possibilities
inferred← citeshttps://doi.org/10.1007/978-3-319-70049-6_7openalex-snapshot
Electrospun Nanofibrous Nerve Conduits
inferred← citeshttps://doi.org/10.1007/s00586-013-2733-5openalex-snapshot
Expression of activating transcription factor 3 (ATF3) in uninjured dorsal root ganglion neurons in a lower trunk avulsion pain model in rats
inferred← citeshttps://doi.org/10.1007/s10495-008-0266-xopenalex-snapshot
Apoptosis-related genes change their expression with age and hearing loss in the mouse cochlea
inferred← citeshttps://doi.org/10.1007/s10571-023-01361-5openalex-snapshot
A Carboxy-terminal Smarcb1 Point Mutation Induces Hydrocephalus Formation and Affects AP-1 and Neuronal Signalling Pathways in Mice
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The Effects of IGF-1 on TNF-α-Treated DRG Neurons by Modulating ATF3 and GAP-43 Expression via PI3K/Akt/S6K Signaling Pathway
inferred← citeshttps://doi.org/10.1007/s12017-013-8236-zopenalex-snapshot
Mechanism of Action for NNZ-2566 Anti-inflammatory Effects Following PBBI Involves Upregulation of Immunomodulator ATF3
inferred← citeshttps://doi.org/10.1007/s12017-014-8329-3openalex-snapshot
Spinal Cord Injury and the Neuron-Intrinsic Regeneration-Associated Gene Program
inferred← citeshttps://doi.org/10.1007/s12031-010-9359-4openalex-snapshot
PACAP Expression in Explant Cultured Mouse Major Pelvic Ganglia
inferred← citeshttps://doi.org/10.1007/s12031-010-9481-3openalex-snapshot
Distinct Expression of c-Jun and HSP27 in Axotomized and Spared Bulbospinal Neurons After Cervical Spinal Cord Injury
inferred← citeshttps://doi.org/10.1007/s12035-009-8083-yopenalex-snapshot
Central Nervous System Regeneration Inhibitors and their Intracellular Substrates
inferred← citeshttps://doi.org/10.1007/s12035-015-9397-6openalex-snapshot
Inhibitory Injury Signaling Represses Axon Regeneration After Dorsal Root Injury
inferred← citeshttps://doi.org/10.1007/s12035-022-03090-0openalex-snapshot
Transcriptional Control of Peripheral Nerve Regeneration
inferred← citeshttps://doi.org/10.1007/s12035-023-03887-7openalex-snapshot
Brachial Plexus Root Avulsion Injury-Induced Endothelin-Converting Enzyme-Like 1 Overexpression Is Associated with Injured Motor Neurons Survival
inferred← citeshttps://doi.org/10.1007/s12264-016-0071-4openalex-snapshot
Transcriptional and Epigenetic Regulation in Injury-Mediated Neuronal Dendritic Plasticity
inferred← citeshttps://doi.org/10.1007/s12519-017-0002-0openalex-snapshot
Identifying key genes associated with Hirschsprung’s disease based on bioinformatics analysis of RNA-sequencing data
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Induction of activating transcription factor 3 (ATF3) in the cerebral cortex of a mouse model of blast-induced traumatic brain injury
inferred← citeshttps://doi.org/10.1016/b978-0-12-801732-6.00001-xopenalex-snapshot
Advances and Challenges for Neural Regeneration Research
inferred← citeshttps://doi.org/10.1016/b978-0-12-801732-6.00002-1openalex-snapshot
Functional Regeneration and Remyelination in the Zebrafish Optic Nerve
inferred← citeshttps://doi.org/10.1016/b978-0-323-55140-3.00014-xopenalex-snapshot
Biologic Augmentation in Peripheral Nerve Repair
inferred← citeshttps://doi.org/10.1016/b978-0-444-52137-8.00035-8openalex-snapshot
Gene therapy, neurotrophic factors and spinal cord regeneration
inferred← citeshttps://doi.org/10.1016/b978-012373994-0.50003-8openalex-snapshot
INTRINSIC DETERMINANTS OF AXON REGENERATION
inferred← citeshttps://doi.org/10.1016/b978-012373994-0.50019-1openalex-snapshot
CYCLIC AMP MODULATION OF AXONAL REGENERATION FOLLOWING SPINAL CORD INJURY
inferred← citeshttps://doi.org/10.1016/j.aanat.2011.01.010openalex-snapshot
Transcribing the path to neurological recovery—From early signals through transcription factors to downstream effectors of successful regeneration
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.114544openalex-snapshot
The potential roles of ATF family in the treatment of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.brainres.2007.06.066openalex-snapshot
An evolving cellular pathology occurs in dorsal root ganglia, peripheral nerve and spinal cord following intravenous administration of paclitaxel in the rat
inferred← citeshttps://doi.org/10.1016/j.brainres.2008.10.050openalex-snapshot
Identification of new Nerve Growth Factor-responsive immediate-early genes
inferred← citeshttps://doi.org/10.1016/j.brainres.2008.12.032openalex-snapshot
Sox11 transcription factor modulates peripheral nerve regeneration in adult mice
inferred← citeshttps://doi.org/10.1016/j.brainres.2009.11.011openalex-snapshot
Peripherin and ATF3 genes are differentially regulated in regenerating and non-regenerating primary sensory neurons
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.03.058openalex-snapshot
Functional Genome-wide Screen Identifies Pathways Restricting Central Nervous System Axonal Regeneration
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109666openalex-snapshot
Topoisomerase I inhibition and peripheral nerve injury induce DNA breaks and ATF3-associated axon regeneration in sensory neurons
inferred← citeshttps://doi.org/10.1016/j.conb.2010.03.013openalex-snapshot
Neuronal intrinsic barriers for axon regeneration in the adult CNS
inferred← citeshttps://doi.org/10.1016/j.conb.2018.02.024openalex-snapshot
Cytoskeleton dynamics in axon regeneration
inferred← citeshttps://doi.org/10.1016/j.cub.2009.04.017openalex-snapshot
Chronically CNS-Injured Adult Sensory Neurons Gain Regenerative Competence upon a Lesion of Their Peripheral Axon
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ATF3: Friend or foe in cellular stress and repair? A context-dependent stress rheostat framework
inferred← citeshttps://doi.org/10.1016/j.ejpb.2017.02.007openalex-snapshot
Lidocaine/multivalent ion complex as a potential strategy for prolonged local anesthesia
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Evidence for a phenotypic switch in corneal afferents after lacrimal gland excision
inferred← citeshttps://doi.org/10.1016/j.expneurol.2006.07.022openalex-snapshot
Intravenous paclitaxel administration in the rat induces a peripheral sensory neuropathy characterized by macrophage infiltration and injury to sensory neurons and their supporting cells
inferred← citeshttps://doi.org/10.1016/j.expneurol.2007.05.025openalex-snapshot
Rewiring the injured CNS: Lessons from the optic nerve
inferred← citeshttps://doi.org/10.1016/j.expneurol.2007.06.020openalex-snapshot
The role of cyclic AMP signaling in promoting axonal regeneration after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2009.12.001openalex-snapshot
Introduction to special issue: Challenges and opportunities for regeneration in the peripheral nervous system
inferred← citeshttps://doi.org/10.1016/j.expneurol.2011.01.015openalex-snapshot
Gene therapy approaches to enhancing plasticity and regeneration after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2011.12.037openalex-snapshot
Conditioning lesions before or after spinal cord injury recruit broad genetic mechanisms that sustain axonal regeneration: Superiority to camp-mediated effects
inferred← citeshttps://doi.org/10.1016/j.expneurol.2015.02.026openalex-snapshot
Regeneration of sensory but not motor axons following visceral nerve injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2015.09.018openalex-snapshot
Overexpression of the monocyte chemokine CCL2 in dorsal root ganglion neurons causes a conditioning-like increase in neurite outgrowth and does so via a STAT3 dependent mechanism
inferred← citeshttps://doi.org/10.1016/j.expneurol.2016.03.012openalex-snapshot
The multiple sclerosis drug fingolimod (FTY720) stimulates neuronal gene expression, axonal growth and regeneration
inferred← citeshttps://doi.org/10.1016/j.expneurol.2016.06.002openalex-snapshot
Cutaneous tissue damage induces long-lasting nociceptive sensitization and regulation of cellular stress- and nerve injury-associated genes in sensory neurons
inferred← citeshttps://doi.org/10.1016/j.expneurol.2017.01.009openalex-snapshot
Surgical repair in humans after traumatic nerve injury provides limited functional neural regeneration in adults
inferred← citeshttps://doi.org/10.1016/j.expneurol.2020.113215openalex-snapshot
NeuroD1 overexpression in spinal neurons accelerates axonal regeneration after sciatic nerve injury
inferred← citeshttps://doi.org/10.1016/j.expneurol.2022.114025openalex-snapshot
Unfolded protein response-induced expression of long noncoding RNA Ngrl1 supports peripheral axon regeneration by activating the PI3K-Akt pathway
inferred← citeshttps://doi.org/10.1016/j.expneurol.2022.114157openalex-snapshot
Gas5 inhibition promotes the axon regeneration in the adult mammalian nervous system
inferred← citeshttps://doi.org/10.1016/j.expneurol.2023.114368openalex-snapshot
Pyruvate dehydrogenase beta subunit (Pdhb) promotes peripheral axon regeneration by regulating energy supply and gene expression
inferred← citeshttps://doi.org/10.1016/j.febslet.2015.04.046openalex-snapshot
Growth control mechanisms in neuronal regeneration
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148670openalex-snapshot
LINC00894 inhibited neuron cellular apoptosis and regulated activating transcription factor 3 expression
inferred← citeshttps://doi.org/10.1016/j.jpain.2008.05.010openalex-snapshot
Dermatomal Scratching After Intramedullary Quisqualate Injection: Correlation With Cutaneous Denervation
inferred← citeshttps://doi.org/10.1016/j.jpain.2010.02.001openalex-snapshot
Skin Incision Induces Expression of Axonal Regeneration-Related Genes in Adult Rat Spinal Sensory Neurons
inferred← citeshttps://doi.org/10.1016/j.lfs.2010.05.015openalex-snapshot
The sensitization of peripheral C-fibers to lysophosphatidic acid in bone cancer pain
inferred← citeshttps://doi.org/10.1016/j.mcn.2007.06.011openalex-snapshot
GDNF selectively promotes regeneration of injury-primed sensory neurons in the lesioned spinal cord
inferred← citeshttps://doi.org/10.1016/j.mcn.2017.04.004openalex-snapshot
Crosstalk control and limits of physiological c-Jun N-terminal kinase activity for cell viability and neurite stability in differentiated PC12 cells
inferred← citeshttps://doi.org/10.1016/j.neuint.2017.05.007openalex-snapshot
Microglia support ATF3-positive neurons following hypoglossal nerve axotomy
inferred← citeshttps://doi.org/10.1016/j.neulet.2010.08.058openalex-snapshot
Injury-induced CRMP4 expression in adult sensory neurons; a possible target gene for ciliary neurotrophic factor
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.03.006openalex-snapshot
Serum Response Factor Mediates NGF-Dependent Target Innervation by Embryonic DRG Sensory Neurons
inferred← citeshttps://doi.org/10.1016/j.neuron.2016.01.034openalex-snapshot
A Systems-Level Analysis of the Peripheral Nerve Intrinsic Axonal Growth Program
inferred← citeshttps://doi.org/10.1016/j.neuron.2020.03.031openalex-snapshot
Macrophages Expressing GALC Improve Peripheral Krabbe Disease by a Mechanism Independent of Cross-Correction
inferred← citeshttps://doi.org/10.1016/j.neuron.2020.07.026openalex-snapshot
Transcriptional Reprogramming of Distinct Peripheral Sensory Neuron Subtypes after Axonal Injury
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2007.10.008openalex-snapshot
Activating transcription factor 3 induction in sympathetic neurons after axotomy: Response to decreased neurotrophin availability
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2009.12.019openalex-snapshot
Conditioning lesions enhance growth state only in sensory neurons lacking calcitonin gene-related peptide and isolectin B4-binding
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2014.09.027openalex-snapshot
The neuroimmunology of degeneration and regeneration in the peripheral nervous system
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2018.04.037openalex-snapshot
Increased Expression of Transcription Factor SRY-box-Containing Gene 11 (Sox11) Enhances Neurite Growth by Regulating Neurotrophic Factor Responsiveness
inferred← citeshttps://doi.org/10.1016/j.pain.2007.02.015openalex-snapshot
Pharmacological, behavioural and mechanistic analysis of HIV-1 gp120 induced painful neuropathy
inferred← citeshttps://doi.org/10.1016/j.pain.2009.09.030openalex-snapshot
Peripheral and central sensitization in remote spinal cord regions contribute to central neuropathic pain after spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2007.06.005openalex-snapshot
Neural plasticity after peripheral nerve injury and regeneration
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2018.05.002openalex-snapshot
The intriguing nature of dorsal root ganglion neurons: Linking structure with polarity and function
inferred← citeshttps://doi.org/10.1016/j.scr.2014.03.006openalex-snapshot
ATF3 is a novel nuclear marker for migrating ependymal stem cells in the rat spinal cord
inferred← citeshttps://doi.org/10.1016/j.sjpain.2015.10.006openalex-snapshot
Analgesic properties of intrathecal glucocorticoids in three well established preclinical pain models
inferred← citeshttps://doi.org/10.1016/s0074-7742(09)87028-1openalex-snapshot
Chapter 28 Future Perspective in Peripheral Nerve Reconstruction
inferred← citeshttps://doi.org/10.1017/s1462399409001288openalex-snapshot
Extrinsic and intrinsic factors controlling axonal regeneration after spinal cord injury
inferred← citeshttps://doi.org/10.1021/acschemneuro.2c00189openalex-snapshot
Microtubule Dynamics Following Central and Peripheral Nervous System Axotomy
inferred← citeshttps://doi.org/10.1038/cddis.2017.212openalex-snapshot
Damage-induced neuronal endopeptidase (DINE) enhances axonal regeneration potential of retinal ganglion cells after optic nerve injury
inferred← citeshttps://doi.org/10.1038/cgt.2009.71openalex-snapshot
Imaging and therapy of experimental schwannomas using HSV amplicon vector-encoding apoptotic protein under Schwann cell promoter
inferred← citeshttps://doi.org/10.1038/gt.2010.14openalex-snapshot
A dual promoter lentiviral vector for the in vivo evaluation of gene therapeutic approaches to axon regeneration after spinal cord injury
inferred← citeshttps://doi.org/10.1038/s41419-020-2722-7openalex-snapshot
Correction: Damage-induced neuronal endopeptidase (DINE) enhances axonal regeneration potential of retinal ganglion cells after optic nerve injury
inferred← citeshttps://doi.org/10.1038/s41467-018-03496-2openalex-snapshot
Inhibition of neuronal FLT3 receptor tyrosine kinase alleviates peripheral neuropathic pain in mice
inferred← citeshttps://doi.org/10.1038/s41467-024-55275-xopenalex-snapshot
Defects in hair cells disrupt the development of auditory peripheral circuitry
inferred← citeshttps://doi.org/10.1038/s41467-026-72397-6openalex-snapshot
Self-assembling scaffolds epigenetically reactivate and electroactively guide neuronal regeneration to restore central neural circuits
inferred← citeshttps://doi.org/10.1038/s41583-018-0001-8openalex-snapshot
Intrinsic mechanisms of neuronal axon regeneration
inferred← citeshttps://doi.org/10.1038/s41598-017-18757-1openalex-snapshot
Highly conserved molecular pathways, including Wnt signaling, promote functional recovery from spinal cord injury in lampreys
inferred← citeshttps://doi.org/10.1038/s41598-018-34510-8openalex-snapshot
The ALS-inducing factors, TDP43A315T and SOD1G93A, directly affect and sensitize sensory neurons to stress
inferred← citeshttps://doi.org/10.1038/s41598-020-79624-0openalex-snapshot
Ascending dorsal column sensory neurons respond to spinal cord injury and downregulate genes related to lipid metabolism
inferred← citeshttps://doi.org/10.1073/pnas.1314826111openalex-snapshot
ATF3 expression improves motor function in the ALS mouse model by promoting motor neuron survival and retaining muscle innervation
inferred← citeshttps://doi.org/10.1074/jbc.m113.502914openalex-snapshot
The Nuclear Calcium Signaling Target, Activating Transcription Factor 3 (ATF3), Protects against Dendrotoxicity and Facilitates the Recovery of Synaptic Transmission after an Excitotoxic Insult
inferred← citeshttps://doi.org/10.1074/jbc.m114.582460openalex-snapshot
cAMP-responsive Element-binding Protein (CREB) and cAMP Co-regulate Activator Protein 1 (AP1)-dependent Regeneration-associated Gene Expression and Neurite Growth
inferred← citeshttps://doi.org/10.1074/mcp.r115.053751openalex-snapshot
Molecular and Cellular Mechanisms of Axonal Regeneration After Spinal Cord Injury
inferred← citeshttps://doi.org/10.1080/02844310701318288openalex-snapshot
Induction of activating transcription factor 3 after different sciatic nerve injuries in adult rats
inferred← citeshttps://doi.org/10.1080/17590914.2024.2440299openalex-snapshot
Neurons Are Not All the Same: Diversity in Neuronal Populations and Their Intrinsic Responses to Spinal Cord Injury
inferred← citeshttps://doi.org/10.1089/neu.2016.4789openalex-snapshot
Activation of KCNQ Channels Suppresses Spontaneous Activity in Dorsal Root Ganglion Neurons and Reduces Chronic Pain after Spinal Cord Injury
inferred← citeshttps://doi.org/10.1089/neu.2017.5593openalex-snapshot
Neuroinflammation after Traumatic Brain Injury Is Enhanced in Activating Transcription Factor 3 Mutant Mice
inferred← citeshttps://doi.org/10.1093/brain/awac415openalex-snapshot
Promoting regeneration while blocking cell death preserves motor neuron function in a model of ALS
inferred← citeshttps://doi.org/10.1093/hmg/ddv383openalex-snapshot
Overexpression of ATF3 or the combination of ATF3, c-Jun, STAT3 and Smad1 promotes regeneration of the central axon branch of sensory neurons but without synergistic effects
inferred← citeshttps://doi.org/10.1093/humrep/deaa061openalex-snapshot
Activation of ATF3/AP-1 signaling pathway is required for P2X3-induced endometriosis pain
inferred← citeshttps://doi.org/10.1093/jnen/nlz008openalex-snapshot
Axotomy Induces Phasic Alterations in Luman/CREB3 Expression and Nuclear Localization in Injured and Contralateral Uninjured Sensory Neurons: Correlation With Intrinsic Axon Growth Capacity
inferred← citeshttps://doi.org/10.1093/toxsci/kfaa063openalex-snapshot
Aryl Hydrocarbon Receptor Mediates Larval Zebrafish Fin Duplication Following Exposure to Benzofluoranthenes
inferred← citeshttps://doi.org/10.1097/00007632-200112151-00003openalex-snapshot
Spinal Cord Regeneration
inferred← citeshttps://doi.org/10.1097/aco.0b013e32834871dfopenalex-snapshot
A brief comparison of the pathophysiology of inflammatory versus neuropathic pain
inferred← citeshttps://doi.org/10.1097/j.pain.0000000000002704openalex-snapshot
Resurgent neuropathic discharge: an obstacle to the therapeutic use of neuroma resection?
inferred← citeshttps://doi.org/10.1097/wnr.0b013e32833e787fopenalex-snapshot
Impaired nerve regeneration and Schwann cell activation after repair with tension
inferred← citeshttps://doi.org/10.1098/rsob.160091openalex-snapshot
Atf3 mutant mice show reduced axon regeneration and impaired regeneration-associated gene induction after peripheral nerve injury
inferred← citeshttps://doi.org/10.1111/ejn.13737openalex-snapshot
Sustained cell body reactivity and loss of NeuN in a subset of axotomized bulbospinal neurons after a chronic high cervical spinal cord injury
inferred← citeshttps://doi.org/10.1111/j.1460-9568.2006.05284.xopenalex-snapshot
The characteristics of neuronal injury in a static compression model of spinal cord injury in adult rats
inferred← citeshttps://doi.org/10.1111/j.1460-9568.2007.05597.xopenalex-snapshot
Identification of candidate transcriptional modulators involved in successful regeneration after nerve injury
inferred← citeshttps://doi.org/10.1111/j.1460-9568.2009.06920.xopenalex-snapshot
Preconditioning selective ventral root injury promotes plasticity of ascending sensory neurons in the injured spinal cord of adult rats – possible roles of brain‐derived neurotrophic factor, TrkB and p75 neurotrophin receptor
inferred← citeshttps://doi.org/10.1111/j.1460-9568.2011.07958.xopenalex-snapshot
Cysteine‐ and glycine‐rich protein 1a is involved in spinal cord regeneration in adult zebrafish
inferred← citeshttps://doi.org/10.1111/j.1471-4159.2006.04089.xopenalex-snapshot
Retrograde signaling in injured nerve – the axon reaction revisited
inferred← citeshttps://doi.org/10.1136/annrheumdis-2011-201233.3openalex-snapshot
Phenotypic changes in dorsal root ganglion and spinal cord in the collagen antibody-induced arthritis model
inferred← citeshttps://doi.org/10.1152/jn.00560.2013openalex-snapshot
Distinct subclassification of DRG neurons innervating the distal colon and glans penis/distal urethra based on the electrophysiological current signature
inferred← citeshttps://doi.org/10.1155/2014/392971openalex-snapshot
Nerve Injury-Induced c-Jun Activation in Schwann Cells Is JNK Independent
inferred← citeshttps://doi.org/10.1155/2015/251204openalex-snapshot
Neurotrauma and Inflammation: CNS and PNS Responses
inferred← citeshttps://doi.org/10.1155/2016/7692602openalex-snapshot
Neuroprotective and Neurorestorative Processes after Spinal Cord Injury: The Case of the Bulbospinal Respiratory Neurons
inferred← citeshttps://doi.org/10.1159/000330195openalex-snapshot
Neuronal Injury Marker ATF-3 Is Induced in Primary Afferent Neurons of Monoarthritic Rats
inferred← citeshttps://doi.org/10.1167/iovs.61.2.31openalex-snapshot
Activating Transcription Factor 3 (ATF3) Protects Retinal Ganglion Cells and Promotes Functional Preservation After Optic Nerve Crush
inferred← citeshttps://doi.org/10.1177/1744806918787427openalex-snapshot
ATF2, but not ATF3, participates in the maintenance of nerve injury-induced tactile allodynia and thermal hyperalgesia
inferred← citeshttps://doi.org/10.1177/24725552211026270openalex-snapshot
Phenotypic Screening Following Transcriptomic Deconvolution to Identify Transcription Factors Mediating Axon Growth Induced by a Kinase Inhibitor
inferred← citeshttps://doi.org/10.1186/1471-2202-11-69openalex-snapshot
Intrinsic response of thoracic propriospinal neurons to axotomy
inferred← citeshttps://doi.org/10.1186/1471-2202-15-92openalex-snapshot
Time-specific microRNA changes during spinal motoneuron degeneration in adult rats following unilateral brachial plexus root avulsion: ipsilateral vs. contralateral changes
inferred← citeshttps://doi.org/10.1186/1471-2202-8-100openalex-snapshot
Analysis of gene expression during neurite outgrowth and regeneration
inferred← citeshttps://doi.org/10.1186/1471-2202-9-88openalex-snapshot
Expression of ATF3 and axonal outgrowth are impaired after delayed nerve repair
inferred← citeshttps://doi.org/10.1186/1744-8069-4-10openalex-snapshot
Vascularization of the Dorsal Root Ganglia and Peripheral Nerve of the Mouse: Implications for Chemical-Induced Peripheral Sensory Neuropathies
inferred← citeshttps://doi.org/10.1186/1744-8069-6-76openalex-snapshot
Prevention of Paclitaxel-Induced Allodynia by Minocycline: Effect on Loss of Peripheral Nerve Fibers and Infiltration of Macrophages in Rats
inferred← citeshttps://doi.org/10.1186/1744-8069-6-94openalex-snapshot
Ablation of Rat TRPV1-Expressing Adelta/C-Fibers with Resiniferatoxin: Analysis of Withdrawal Behaviors, Recovery of Function and Molecular Correlates
inferred← citeshttps://doi.org/10.1186/1744-8069-7-30openalex-snapshot
TRESK Channel Contribution to Nociceptive Sensory Neurons Excitability: Modulation by Nerve Injury
inferred← citeshttps://doi.org/10.1186/s13024-025-00805-4openalex-snapshot
The transcription factor combination MEF2 and KLF7 promotes axonal sprouting in the injured spinal cord with functional improvement and regeneration-associated gene expression
inferred← citeshttps://doi.org/10.1186/s13287-023-03395-4openalex-snapshot
The activation of dormant ependymal cells following spinal cord injury
inferred← citeshttps://doi.org/10.1186/s13578-021-00646-wopenalex-snapshot
Dexibuprofen ameliorates peripheral and central risk factors associated with Alzheimer’s disease in metabolically stressed APPswe/PS1dE9 mice
inferred← citeshttps://doi.org/10.1186/s40478-015-0255-6openalex-snapshot
Tamoxifen induces cellular stress in the nervous system by inhibiting cholesterol synthesis
inferred← citeshttps://doi.org/10.1242/dev.204563openalex-snapshot
Distinct BMP-Smad signaling outputs confer diverse functions in dental mesenchyme
inferred← citeshttps://doi.org/10.1242/jcs.024943openalex-snapshot
Enhancement of axonal regeneration by in vitro conditioning and its inhibition by cyclopentenone prostaglandins
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011969openalex-snapshot
DLK orchestrates a modular transcriptional response to axon injury with separate roles for Fos and Jun
inferred← citeshttps://doi.org/10.1371/journal.pone.0021754openalex-snapshot
Transcriptional Responses of Cultured Rat Sympathetic Neurons during BMP-7-Induced Dendritic Growth
inferred← citeshttps://doi.org/10.1517/14728220903307517openalex-snapshot
Molecular targets for axon regeneration: focus on the intrinsic pathways
inferred← citeshttps://doi.org/10.1523/eneuro.0044-14.2015openalex-snapshot
The Acquisition of Target Dependence by Developing Rat Retinal Ganglion Cells
inferred← citeshttps://doi.org/10.1523/eneuro.0182-22.2022openalex-snapshot
Identification of a Novel Axon Regeneration Role for Noncanonical Wnt Signaling in the Adult Retina after Injury
inferred← citeshttps://doi.org/10.1523/jneurosci.0304-12.2012openalex-snapshot
Sodium Channel Nav1.7 Is Essential for Lowering Heat Pain Threshold after Burn Injury
inferred← citeshttps://doi.org/10.1523/jneurosci.0403-12.2012openalex-snapshot
Cannabinoid Type-1 Receptor Reduces Pain and Neurotoxicity Produced by Chemotherapy
inferred← citeshttps://doi.org/10.1523/jneurosci.1175-09.2009openalex-snapshot
Increased Synthesis of Spermidine as a Result of Upregulation of Arginase I Promotes Axonal Regeneration in Culture andIn Vivo
inferred← citeshttps://doi.org/10.1523/jneurosci.1337-07.2007openalex-snapshot
NKCC1 Phosphorylation Stimulates Neurite Growth of Injured Adult Sensory Neurons
inferred← citeshttps://doi.org/10.1523/jneurosci.3371-11.2012openalex-snapshot
Improved Outcome after Peripheral Nerve Injury in Mice with Increased Levels of Endogenous Omega-3 Polyunsaturated Fatty Acids
inferred← citeshttps://doi.org/10.1523/jneurosci.3938-09.2009openalex-snapshot
NFIL3 and cAMP Response Element-Binding Protein Form a Transcriptional Feedforward Loop that Controls Neuronal Regeneration-Associated Gene Expression
inferred← citeshttps://doi.org/10.1523/jneurosci.4550-11.2011openalex-snapshot
The BMP Coreceptor RGMb Promotes While the Endogenous BMP Antagonist Noggin Reduces Neurite Outgrowth and Peripheral Nerve Regeneration by Modulating BMP Signaling
inferred← citeshttps://doi.org/10.1523/jneurosci.5103-10.2011openalex-snapshot
Diffuse Traumatic Axonal Injury in the Mouse Induces Atrophy, c-Jun Activation, and Axonal Outgrowth in the Axotomized Neuronal Population
inferred← citeshttps://doi.org/10.1523/jneurosci.5313-06.2007openalex-snapshot
ATF3 Increases the Intrinsic Growth State of DRG Neurons to Enhance Peripheral Nerve Regeneration
inferred← citeshttps://doi.org/10.1523/jneurosci.6156-10.2011openalex-snapshot
The Basis for Diminished Functional Recovery after Delayed Peripheral Nerve Repair
inferred← citeshttps://doi.org/10.15252/embj.2021110486openalex-snapshot
Impaired disassembly of the axon initial segment restricts mitochondrial entry into damaged axons
inferred← citeshttps://doi.org/10.2147/jpr.s15452openalex-snapshot
Pharmacological evaluation of rat dorsal root ganglion neurons as an in vitro model for diabetic neuropathy
inferred← citeshttps://doi.org/10.2147/jpr.s317877openalex-snapshot
TLR4 Antagonism Reduces Movement-Induced Nociception and ATF-3 Expression in Experimental Osteoarthritis
inferred← citeshttps://doi.org/10.2174/1568009618666181003170027openalex-snapshot
The Association of Neuronal Stress with Activating Transcription Factor 3 in Dorsal Root Ganglion of in vivo and in vitro Models of Bortezomib- Induced Neuropathy
inferred← citeshttps://doi.org/10.3389/fcell.2022.824036openalex-snapshot
Activating Transcription Factor 3 (ATF3) is a Highly Conserved Pro-regenerative Transcription Factor in the Vertebrate Nervous System
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1700109openalex-snapshot
Integrated machine learning and transcriptomics reveal immune infiltration-related orthologous transcription genes in cerebral ischemic injury
inferred← citeshttps://doi.org/10.3389/fncel.2019.00420openalex-snapshot
The ATP-P2X7 Signaling Pathway Participates in the Regulation of Slit1 Expression in Satellite Glial Cells
inferred← citeshttps://doi.org/10.3389/fneur.2011.00030openalex-snapshot
Activating Transcription Factor 3, a Useful Marker for Regenerative Response after Nerve Root Injury
inferred← citeshttps://doi.org/10.3389/fnmol.2011.00046openalex-snapshot
A Gene Network Perspective on Axonal Regeneration
inferred← citeshttps://doi.org/10.3389/fnmol.2011.00053openalex-snapshot
The nuclear events guiding successful nerve regeneration
inferred← citeshttps://doi.org/10.3389/fnmol.2012.00007openalex-snapshot
Activating Transcription Factor 3 and the Nervous System
inferred← citeshttps://doi.org/10.3389/fnmol.2012.00008openalex-snapshot
Role of Transcription Factors in Peripheral Nerve Regeneration
inferred← citeshttps://doi.org/10.3389/fnmol.2015.00043openalex-snapshot
What makes a RAG regeneration associated?
inferred← citeshttps://doi.org/10.3389/fnmol.2016.00049openalex-snapshot
Expressing Constitutively Active Rheb in Adult Dorsal Root Ganglion Neurons Enhances the Integration of Sensory Axons that Regenerate Across a Chondroitinase-Treated Dorsal Root Entry Zone Following Dorsal Root Crush
inferred← citeshttps://doi.org/10.3389/fnmol.2022.967472openalex-snapshot
Analysis of neuronal injury transcriptional response identifies CTCF and YY1 as co-operating factors regulating axon regeneration
inferred← citeshttps://doi.org/10.3389/fnmol.2024.1484487openalex-snapshot
Editorial: ATF3: a crucial stress-responsive gene of glia and neurons in CNS
inferred← citeshttps://doi.org/10.3390/cells9112355openalex-snapshot
Deletion of Acid-Sensing Ion Channel 3 Relieves the Late Phase of Neuropathic Pain by Preventing Neuron Degeneration and Promoting Neuron Repair
inferred← citeshttps://doi.org/10.3390/genes17091034openalex-snapshot
Activating Transcription Factor 3 in Pain: A Molecular Regulator and Emerging Biomarker
inferred← citeshttps://doi.org/10.3390/ijms222413380openalex-snapshot
New Frontiers in Peripheral Nerve Regeneration: Concerns and Remedies
inferred← citeshttps://doi.org/10.3390/ijms23094964openalex-snapshot
The Role of ATF3 in Neuronal Differentiation and Development of Neuronal Networks in Opossum Postnatal Cortical Cultures
inferred← citeshttps://doi.org/10.3390/ijms232113566openalex-snapshot
Unleashing Intrinsic Growth Pathways in Regenerating Peripheral Neurons
inferred← citeshttps://doi.org/10.3390/ijms242015359openalex-snapshot
Inflammatory Mediators of Axon Regeneration in the Central and Peripheral Nervous Systems
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