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Dissecting the role of redox signaling in neuronal development

https://doi.org/10.1111/jnc.13581
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Glucose and NADPH oxidase drive neuronal superoxide formation in stroke
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Expression dynamics of NADPH oxidases during early zebrafish development
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A role for prolyl hydroxylase domain proteins in hippocampal synaptic plasticity
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The Nox1/4 Dual Inhibitor GKT137831 or Nox4 Knockdown Inhibits Angiotensin‐II‐Induced Adult Mouse Cardiac Fibroblast Proliferation and Migration. AT1 Physically Associates With Nox4
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Copper signaling in the mammalian nervous system: Synaptic effects
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Assembly of the phagocyte NADPH oxidase
inferredcites →https://doi.org/10.1007/s00702-006-0500-zopenalex-snapshot
Staurosporin induces neurite outgrowth through ROS generation in HN33 hippocampal cell lines
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Iron toxicity in neurodegeneration
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Directed differentiation of embryonic P19 cells and neural stem cells into neural lineage on conducting PEDOT–PEG and ITO glass substrates
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Localization of NADPH oxidase in sympathetic and sensory ganglion neurons and perivascular nerve fibers
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Molecular composition and regulation of the Nox family NAD(P)H oxidases
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Immunohistochemical study of p47Phox and gp91Phox distributions in rat brain
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Newborn neurons acquire high levels of reactive oxygen species and increased mitochondrial proteins upon differentiation from progenitors
inferredcites →https://doi.org/10.1016/j.ceca.2006.10.001openalex-snapshot
Calcium release by ryanodine receptors mediates hydrogen peroxide-induced activation of ERK and CREB phosphorylation in N2a cells and hippocampal neurons
inferredcites →https://doi.org/10.1016/j.cell.2013.12.035openalex-snapshot
Redox Modification of Nuclear Actin by MICAL-2 Regulates SRF Signaling
inferredcites →https://doi.org/10.1016/j.cellsig.2010.01.007openalex-snapshot
PKC delta and NADPH oxidase in retinoic acid-induced neuroblastoma cell differentiation
inferredcites →https://doi.org/10.1016/j.cub.2011.04.030openalex-snapshot
Rab6, Rab8, and MICAL3 Cooperate in Controlling Docking and Fusion of Exocytotic Carriers
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2008.06.027openalex-snapshot
Role of NADPH oxidase in the apoptotic death of cultured cerebellar granule neurons
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The redox stress hypothesis of aging
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Synaptic localization of a functional NADPH oxidase in the mouse hippocampus
inferredcites →https://doi.org/10.1016/j.mcn.2006.08.005openalex-snapshot
Reactive oxygen species modulate the differentiation of neurons in clonal cortical cultures
inferredcites →https://doi.org/10.1016/j.mcn.2015.06.007openalex-snapshot
Reactive oxygen species are involved in BMP-induced dendritic growth in cultured rat sympathetic neurons
inferredcites →https://doi.org/10.1016/j.molcel.2013.06.019openalex-snapshot
MsrB1 and MICALs Regulate Actin Assembly and Macrophage Function via Reversible Stereoselective Methionine Oxidation
inferredcites →https://doi.org/10.1016/j.neuint.2009.11.018openalex-snapshot
Endogenous reactive oxygen species are essential for proliferation of neural stem/progenitor cells
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Localization of NADPH oxidase subunits in neonatal sympathetic neurons
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p53-mediated regulation of neuronal differentiation via regulation of dual oxidase maturation factor 1
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NMDA Receptor-Nitric Oxide Transmission Mediates Neuronal Iron Homeostasis via the GTPase Dexras1
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From Synapse to Nucleus: Calcium-Dependent Gene Transcription in the Control of Synapse Development and Function
inferredcites →https://doi.org/10.1016/j.neuroscience.2004.12.038openalex-snapshot
Neuronal expression of the NADPH oxidase NOX4, and its regulation in mouse experimental brain ischemia
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Neuronal polarization and the cytoskeleton
inferredcites →https://doi.org/10.1016/j.stem.2010.11.028openalex-snapshot
Proliferative Neural Stem Cells Have High Endogenous ROS Levels that Regulate Self-Renewal and Neurogenesis in a PI3K/Akt-Dependant Manner
inferredcites →https://doi.org/10.1016/j.stem.2012.06.016openalex-snapshot
VCAM1 Is Essential to Maintain the Structure of the SVZ Niche and Acts as an Environmental Sensor to Regulate SVZ Lineage Progression
inferredcites →https://doi.org/10.1016/j.tcb.2012.08.002openalex-snapshot
Redox control of cell proliferation
inferredcites →https://doi.org/10.1016/j.tins.2004.05.010openalex-snapshot
Receptor compartmentalization and trafficking at glutamate synapses: a developmental proposal
inferredcites →https://doi.org/10.1016/j.yexcr.2010.03.021openalex-snapshot
Nox4-dependent H2O2 production contributes to chronic glutamate toxicity in primary cortical neurons
inferredcites →https://doi.org/10.1016/s0006-8993(03)03364-xopenalex-snapshot
NADPH oxidase immunoreactivity in the mouse brain
inferredcites →https://doi.org/10.1016/s0021-9258(19)38951-3openalex-snapshot
Evidence for a functional cytoplasmic domain of phagocyte oxidase cytochrome b558.
inferredcites →https://doi.org/10.1016/s0092-8674(02)00794-8openalex-snapshot
MICALs, a Family of Conserved Flavoprotein Oxidoreductases, Function in Plexin-Mediated Axonal Repulsion
inferredcites →https://doi.org/10.1016/s0166-2236(02)00040-1openalex-snapshot
The Yin and Yang of NMDA receptor signalling
inferredcites →https://doi.org/10.1016/s0896-6273(00)80052-5openalex-snapshot
Requirement for Superoxide in Excitotoxic Cell Death
inferredcites →https://doi.org/10.1016/s0896-6273(00)80683-2openalex-snapshot
Single Synaptic Events Evoke NMDA Receptor–Mediated Release of Calcium from Internal Stores in Hippocampal Dendritic Spines
inferredcites →https://doi.org/10.1016/s0968-0004(02)02191-6openalex-snapshot
Nanotransducers in cellular redox signaling: modification of thiols by reactive oxygen and nitrogen species
inferredcites →https://doi.org/10.1023/a:1015108306171openalex-snapshot
Neuregulin Induces Sustained Reactive Oxygen Species Generation to Mediate Neuronal Differentiation
inferredcites →https://doi.org/10.1038/327717a0openalex-snapshot
The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complex
inferredcites →https://doi.org/10.1038/364535a0openalex-snapshot
NMDA-dependent superoxide production and neurotoxicity
inferredcites →https://doi.org/10.1038/cddis.2011.96openalex-snapshot
Hydrogen peroxide: a Jekyll and Hyde signalling molecule
inferredcites →https://doi.org/10.1038/cddis.2013.50openalex-snapshot
Redox homeostasis: the linchpin in stem cell self-renewal and differentiation
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The ground state of embryonic stem cell self-renewal
inferredcites →https://doi.org/10.1038/nature08724openalex-snapshot
Mical links semaphorins to F-actin disassembly
inferredcites →https://doi.org/10.1038/ncb2871openalex-snapshot
SelR reverses Mical-mediated oxidation of actin to regulate F-actin dynamics
inferredcites →https://doi.org/10.1038/nchembio.1416openalex-snapshot
The role of iron and reactive oxygen species in cell death
inferredcites →https://doi.org/10.1038/nchembio.497openalex-snapshot
Nox2 redox signaling maintains essential cell populations in the brain
inferredcites →https://doi.org/10.1038/nchembio.607openalex-snapshot
Chemistry and biology of reactive oxygen species in signaling or stress responses
inferredcites →https://doi.org/10.1038/nchembio.85openalex-snapshot
Reconciling the chemistry and biology of reactive oxygen species
inferredcites →https://doi.org/10.1038/ncomms5317openalex-snapshot
The intracellular redox protein MICAL-1 regulates the development of hippocampal mossy fibre connections
inferredcites →https://doi.org/10.1038/nm979openalex-snapshot
Maintenance of pluripotency in human and mouse embryonic stem cells through activation of Wnt signaling by a pharmacological GSK-3-specific inhibitor
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NADPH oxidase is the primary source of superoxide induced by NMDA receptor activation
inferredcites →https://doi.org/10.1038/nn.2408openalex-snapshot
GSK-3 is a master regulator of neural progenitor homeostasis
inferredcites →https://doi.org/10.1038/nrd2803openalex-snapshot
Targeting cancer cells by ROS-mediated mechanisms: a radical therapeutic approach?
inferredcites →https://doi.org/10.1038/nrn1434openalex-snapshot
Oxidative stress in neurodegeneration: cause or consequence?
inferredcites →https://doi.org/10.1038/nrn3192openalex-snapshot
Mechanisms of CaMKII action in long-term potentiation
inferredcites →https://doi.org/10.1038/nrn3302openalex-snapshot
Getting neural circuits into shape with semaphorins
inferredcites →https://doi.org/10.1038/onc.2013.39openalex-snapshot
Constitutively active TrkB confers an aggressive transformed phenotype to a neural crest-derived cell line
inferredcites →https://doi.org/10.1042/bj20040954openalex-snapshot
Localization of Nox2 N-terminus using polyclonal antipeptide antibodies
inferredcites →https://doi.org/10.1042/bj20041835openalex-snapshot
Activation and assembly of the NADPH oxidase: a structural perspective
inferredcites →https://doi.org/10.1042/bj2270783openalex-snapshot
Cytochrome b-245 from human neutrophils is a glycoprotein
inferredcites →https://doi.org/10.1055/s-0033-1333875openalex-snapshot
Cognitive Ability in Children with Chronic Granulomatous Disease: A Comparison of Those Managed Conservatively with Those Who Have Undergone Hematopoietic Stem Cell Transplant
inferredcites →https://doi.org/10.1073/pnas.85.10.3319openalex-snapshot
Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b.
inferredcites →https://doi.org/10.1074/jbc.274.24.17297openalex-snapshot
Further Characterization of the Type 3 Ryanodine Receptor (RyR3) Purified from Rabbit Diaphragm
inferredcites →https://doi.org/10.1074/jbc.275.18.13175openalex-snapshot
Nerve Growth Factor-induced Neuronal Differentiation Requires Generation of Rac1-regulated Reactive Oxygen Species
inferredcites →https://doi.org/10.1074/jbc.m110.192138openalex-snapshot
The E-loop Is Involved in Hydrogen Peroxide Formation by the NADPH Oxidase Nox4
inferredcites →https://doi.org/10.1074/jbc.m110.213785openalex-snapshot
Iron Mediates N-Methyl-d-aspartate Receptor-dependent Stimulation of Calcium-induced Pathways and Hippocampal Synaptic Plasticity
inferredcites →https://doi.org/10.1074/jbc.m111899200openalex-snapshot
Reversible Inactivation of the Tumor Suppressor PTEN by H2O2
inferredcites →https://doi.org/10.1074/jbc.m313891200openalex-snapshot
Antagonistic Cross-talk between Rac and Cdc42 GTPases Regulates Generation of Reactive Oxygen Species
inferredcites →https://doi.org/10.1074/jbc.m406486200openalex-snapshot
Direct Interaction of the Novel Nox Proteins with p22phox Is Required for the Formation of a Functionally Active NADPH Oxidase
inferredcites →https://doi.org/10.1074/jbc.m708281200openalex-snapshot
Stimulus-dependent Regulation of the Phagocyte NADPH Oxidase by a VAV1, Rac1, and PAK1 Signaling Axis
inferredcites →https://doi.org/10.1080/15216540500092328openalex-snapshot
The Ryanodine Receptors Ca2 + Release Channels: Cellular Redox Sensors?
inferredcites →https://doi.org/10.1089/ars.2006.8.1533openalex-snapshot
Regulation of the Phagocyte NADPH Oxidase by Rac GTPase
inferredcites →https://doi.org/10.1089/ars.2006.8.1583openalex-snapshot
NADPH Oxidases of the Brain: Distribution, Regulation, and Function
inferredcites →https://doi.org/10.1089/ars.2006.8.1819openalex-snapshot
Regulation of Signal Transduction Through Protein Cysteine Oxidation
inferredcites →https://doi.org/10.1089/ars.2007.9.245openalex-snapshot
A Role for Reactive Oxygen/Nitrogen Species and Iron on Neuronal Synaptic Plasticity
inferredcites →https://doi.org/10.1089/ars.2008.2203openalex-snapshot
Role of Nox4 and Nox2 in Hyperoxia-Induced Reactive Oxygen Species Generation and Migration of Human Lung Endothelial Cells
inferredcites →https://doi.org/10.1089/ars.2009.2578openalex-snapshot
NOX Enzymes in the Central Nervous System: From Signaling to Disease
inferredcites →https://doi.org/10.1089/ars.2010.3208openalex-snapshot
Reactive Oxygen Species in the Regulation of Synaptic Plasticity and Memory
inferredcites →https://doi.org/10.1089/ars.2011.3960openalex-snapshot
NADPH Oxidase 1-Mediated Oxidative Stress Leads to Dopamine Neuron Death in Parkinson's Disease
inferredcites →https://doi.org/10.1089/ars.2012.4963openalex-snapshot
Roles of Reactive Oxygen Species in the Fate of Stem Cells
inferredcites →https://doi.org/10.1089/ars.2013.5487openalex-snapshot
MICAL-Family Proteins: Complex Regulators of the Actin Cytoskeleton
inferredcites →https://doi.org/10.1089/ars.2013.5703openalex-snapshot
New Insights on NOX Enzymes in the Central Nervous System
inferredcites →https://doi.org/10.1089/ars.2013.5713openalex-snapshot
NADPH Oxidase Complex-Derived Reactive Oxygen Species, the Actin Cytoskeleton, and Rho GTPases in Cell Migration
inferredcites →https://doi.org/10.1089/ars.2013.5814openalex-snapshot
Evolution of NADPH Oxidase Inhibitors: Selectivity and Mechanisms for Target Engagement
inferredcites →https://doi.org/10.1093/jb/mvs006openalex-snapshot
Regulation of intracellular signalling through cysteine oxidation by reactive oxygen species
inferredcites →https://doi.org/10.1096/fj.02-1104fjeopenalex-snapshot
Dual oxidases represent novel hydrogen peroxide sources supporting mucosal surface host defense
inferredcites →https://doi.org/10.1096/fj.12-208587openalex-snapshot
Expression of constitutively active FoxO3 in murine forebrain leads to a loss of neural progenitors
inferredcites →https://doi.org/10.1097/nen.0b013e3182358e4eopenalex-snapshot
Activation of NOX2 by the Stimulation of Ionotropic and Metabotropic Glutamate Receptors Contributes to Glutamate Neurotoxicity In Vivo Through the Production of Reactive Oxygen Species and Calpain Activation
inferredcites →https://doi.org/10.1111/j.1471-4159.2008.05787.xopenalex-snapshot
Reactive oxygen species regulate F‐actin dynamics in neuronal growth cones and neurite outgrowth
inferredcites →https://doi.org/10.1111/jnc.12676openalex-snapshot
Rab‐mediated trafficking role in neurite formation
inferredcites →https://doi.org/10.1111/jnc.12734openalex-snapshot
Bidirectional interactions between NOX 2‐type NADPH oxidase and the F‐actin cytoskeleton in neuronal growth cones
inferredcites →https://doi.org/10.1126/science.1211956openalex-snapshot
Direct Redox Regulation of F-Actin Assembly and Disassembly by Mical
inferredcites →https://doi.org/10.1126/science.274.5290.1123openalex-snapshot
The Molecular Biology of Axon Guidance
inferredcites →https://doi.org/10.1126/science.285.5435.1870openalex-snapshot
Long-Term Potentiation--A Decade of Progress?
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Thioredoxin Mediates Oxidation-Dependent Phosphorylation of CRMP2 and Growth Cone Collapse
inferredcites →https://doi.org/10.1128/mcb.00269-06openalex-snapshot
Synaptic Plasticity Deficits and Mild Memory Impairments in Mouse Models of Chronic Granulomatous Disease
inferredcites →https://doi.org/10.1152/ajpcell.00457.2011openalex-snapshot
Angiotensin II stimulates superoxide production in the thick ascending limb by activating NOX4
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Redox signaling: thiol chemistry defines which reactive oxygen and nitrogen species can act as second messengers
inferredcites →https://doi.org/10.1152/ajpheart.00974.2012openalex-snapshot
Mitochondrial-localized NADPH oxidase 4 is a source of superoxide in angiotensin II-stimulated neurons
inferredcites →https://doi.org/10.1152/ajprenal.00414.2002openalex-snapshot
Nox4 mediates angiotensin II-induced activation of Akt/protein kinase B in mesangial cells
inferredcites →https://doi.org/10.1152/jn.00659.2007openalex-snapshot
Superoxide-Induced Potentiation in the Hippocampus Requires Activation of Ryanodine Receptor Type 3 and ERK
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Cell-Permeable Scavengers of Superoxide Prevent Long-Term Potentiation in Hippocampal Area CA1
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The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
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Nox4-Generated Superoxide Drives Angiotensin II-Induced Neural Stem Cell Proliferation
inferredcites →https://doi.org/10.1161/atvbaha.108.164277openalex-snapshot
Nox4 and Nox2 NADPH Oxidases Mediate Distinct Cellular Redox Signaling Responses to Agonist Stimulation
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Cognitive Function in Patients With Chronic Granulomatous Disease: A Preliminary Report
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Cross Talk between Cellular Redox Status, Metabolism, and p53 in Neural Stem Cell Biology
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ROS Produced by NOX2 Controls In Vitro Development of Cerebellar Granule Neurons Development
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Ultrastructural Correlates of Enhanced Norepinephrine and Neuropeptide Y Cotransmission in the Spontaneously Hypertensive Rat Brain
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NADPH Oxidase: An Update
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Stem cells and the impact of ROS signaling
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mTOR regulates brain morphogenesis by mediating GSK3 signaling
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Contribution of NADPH-oxidase to the establishment of hippocampal neuronal polarity in culture
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Reactive Oxygen Species Regulate the Levels of Dual Oxidase (Duox1-2) in Human Neuroblastoma Cells
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Angiotensin II Increased Neuronal Stem Cell Proliferation: Role of AT2R
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NMDA Receptor Activation Increases Free Radical Production through Nitric Oxide and NOX2
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Neurotrophin-Dependent Dendritic Filopodial Motility: A Convergence on PI3K Signaling
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The Tumor Suppressor p53 Fine-Tunes Reactive Oxygen Species Levels and Neurogenesis via PI3 Kinase Signaling
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Mitochondrial production of reactive oxygen species in cortical neurons following exposure to N-methyl-D-aspartate
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Activation of Neuronal NMDA Receptors Induces Superoxide-Mediated Oxidative Stress in Neighboring Neurons and Astrocytes
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Superoxide production in rat hippocampal neurons: selective imaging with hydroethidine
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Impairment of Long-term Potentiation and Associative Memory in Mice That Overexpress Extracellular Superoxide Dismutase
inferredcites →https://doi.org/10.1523/jneurosci.5646-07.2008openalex-snapshot
Release of MICAL Autoinhibition by Semaphorin-Plexin Signaling Promotes Interaction with Collapsin Response Mediator Protein
inferredcites →https://doi.org/10.1523/jneurosci.6227-11.2012openalex-snapshot
NADPH Oxidase-4 Maintains Neuropathic Pain after Peripheral Nerve Injury
inferredcites →https://doi.org/10.2174/1381612821666151029112624openalex-snapshot
The role of Nox-mediated oxidation in the regulation of cytoskeletal dynamics
inferredcites →https://doi.org/10.3109/10715762.2012.748193openalex-snapshot
Activation of Rac1-dependent redox signaling is critically involved in staurosporine-induced neurite outgrowth in PC12 cells
inferredcites →https://doi.org/10.3389/fncel.2015.00381openalex-snapshot
Regulation of cytoskeletal dynamics by redox signaling and oxidative stress: implications for neuronal development and trafficking
inferredcites →https://doi.org/10.3390/biom5020472openalex-snapshot
Biological Activities of Reactive Oxygen and Nitrogen Species: Oxidative Stress versus Signal Transduction
inferredcites →https://doi.org/10.3892/mmr.2013.1628openalex-snapshot
Neuroprotective effect of brain-derived neurotrophic factor mediated by autophagy through the PI3K/Akt/mTOR pathway
inferredcites →https://doi.org/10.4049/jimmunol.170.11.5652openalex-snapshot
Rac1 Deletion in Mouse Neutrophils Has Selective Effects on Neutrophil Functions

What points at this work

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

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Dual roles of reactive oxygen species in ascidian brain regeneration and degeneration
inferred← citeshttps://doi.org/10.1016/j.ejphar.2025.177782openalex-snapshot
Teneligliptin, a DPP4 inhibitor protects dopaminergic neurons in PD models via inhibiting of oxidative stress and ferroptosis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2018.01.008openalex-snapshot
Crosstalk between Rac1-mediated actin regulation and ROS production
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2018.01.025openalex-snapshot
Circadian redox rhythms in the regulation of neuronal excitability
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2020.04.027openalex-snapshot
The role of NADPH oxidases in neuronal development
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2022.02.004openalex-snapshot
Oxidative stress and regeneration
inferred← citeshttps://doi.org/10.1016/j.gene.2021.145972openalex-snapshot
Tau and amyloid beta differentially affect the innate immune genes expression in Drosophila models of Alzheimer’s disease and β- D Mannuronic acid (M2000) modulates the dysregulation
inferred← citeshttps://doi.org/10.1016/j.mad.2016.07.009openalex-snapshot
Neurological disorders associated with DNA strand-break processing enzymes
inferred← citeshttps://doi.org/10.1016/j.mad.2022.111686openalex-snapshot
Redox modulation of stress resilience by Crocus sativus L. for potential neuroprotective and anti-neuroinflammatory applications in brain disorders: From molecular basis to therapy
inferred← citeshttps://doi.org/10.1016/j.mad.2023.111802openalex-snapshot
Sex differences in antioxidant defence and the regulation of redox homeostasis in physiology and pathology
inferred← citeshttps://doi.org/10.1016/j.mam.2016.10.004openalex-snapshot
Neuroglobin: From structure to function in health and disease
inferred← citeshttps://doi.org/10.1016/j.molcel.2021.08.018openalex-snapshot
Redox metabolism: ROS as specific molecular regulators of cell signaling and function
inferred← citeshttps://doi.org/10.1016/j.nbd.2024.106550openalex-snapshot
Brain development and bioenergetic changes
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2018.12.027openalex-snapshot
Action of Hydrogen Peroxide on Synaptic Transmission at the Mouse Neuromuscular Junction
inferred← citeshttps://doi.org/10.1016/j.placenta.2022.08.002openalex-snapshot
Downregulation of krüppel-like factor 6 expression modulates extravillous trophoblast cell behavior by increasing reactive oxygen species
inferred← citeshttps://doi.org/10.1016/j.redox.2026.104027openalex-snapshot
NMDAR and glutamate control axon growth by regulating Rac1-dependent actin dynamics and H2O2 production
inferred← citeshttps://doi.org/10.1016/j.semcdb.2017.09.012openalex-snapshot
From birth to death: A role for reactive oxygen species in neuronal development
inferred← citeshttps://doi.org/10.1016/j.tem.2019.02.006openalex-snapshot
Reactive Oxygen Comes of Age: Mechanism-Based Therapy of Diabetic End-Organ Damage
inferred← citeshttps://doi.org/10.1021/acsami.0c05497openalex-snapshot
Polydopamine Nanoparticles as an Organic and Biodegradable Multitasking Tool for Neuroprotection and Remote Neuronal Stimulation
inferred← citeshttps://doi.org/10.1021/acsnano.5c04181openalex-snapshot
Cellular Activity Modulation Mediated by Near Infrared-Irradiated Polydopamine Nanoparticles: In Vitro and Ex Vivo Investigation
inferred← citeshttps://doi.org/10.1038/s41418-018-0226-0openalex-snapshot
Novel crosstalk between Vps26a and Nox4 signaling during neurogenesis
inferred← citeshttps://doi.org/10.1038/s41419-020-03167-5openalex-snapshot
Parp3 promotes astrocytic differentiation through a tight regulation of Nox4-induced ROS and mTorc2 activation
inferred← citeshttps://doi.org/10.1038/s41598-021-82388-wopenalex-snapshot
Cerebrospinal fluid proteome shows disrupted neuronal development in multiple sclerosis
inferred← citeshttps://doi.org/10.1038/s41598-026-35597-0openalex-snapshot
Mitochondrial dysfunction and Ca2+ dysregulation in human iPSC-derived neurons carrying presenilin-1 mutation arise under stress via an MCU-1-independent mechanism
inferred← citeshttps://doi.org/10.1039/d2nr05256copenalex-snapshot
Engineering graphene-based electrodes for optical neural stimulation
inferred← citeshttps://doi.org/10.1042/bsr20211191openalex-snapshot
Dopamine signaling impairs ROS modulation by mitochondrial hexokinase in human neural progenitor cells
inferred← citeshttps://doi.org/10.1055/a-2429-4023openalex-snapshot
Activation of Hippocampal Neuronal NADPH Oxidase NOX2 Promotes Depressive-Like Behaviour and Cognition Deficits in Chronic Restraint Stress Mouse Model
inferred← citeshttps://doi.org/10.1080/14756366.2016.1205047openalex-snapshot
The role of modulation of antioxidant enzyme systems in the treatment of neurodegenerative diseases
inferred← citeshttps://doi.org/10.1083/jcb.202509200openalex-snapshot
Redox-dependent S -glutathionylation of Aurora-A kinase by Gstp promotes postsynaptic maturation
inferred← citeshttps://doi.org/10.1089/ars.2018.7606openalex-snapshot
Mitochondria, Metabolism, and Redox Mechanisms in Psychiatric Disorders
inferred← citeshttps://doi.org/10.1089/ars.2019.7763openalex-snapshot
Central and Peripheral Metabolic Defects Contribute to the Pathogenesis of Alzheimer's Disease: Targeting Mitochondria for Diagnosis and Prevention
inferred← citeshttps://doi.org/10.1089/ars.2019.8004openalex-snapshot
Mitochondrial and Redox-Based Therapeutic Strategies in Huntington's Disease
inferred← citeshttps://doi.org/10.1093/hmg/ddw234openalex-snapshot
Huntingtin N17 domain is a reactive oxygen species sensor regulating huntingtin phosphorylation and localization
inferred← citeshttps://doi.org/10.1101/2022.11.06.515333openalex-snapshot
Awakening adult neural stem cells: NOX signalling as a positive regulator of quiescence to proliferation transition in the Xenopus retina
inferred← citeshttps://doi.org/10.1101/2025.02.18.638875openalex-snapshot
Glutamate and early functional NMDA Receptors promote axonal elongation modulating both actin cytoskeleton dynamics and H 2 O 2 production dependent on Rac1 activity
inferred← citeshttps://doi.org/10.1101/2025.09.08.674945openalex-snapshot
Dysregulation of energy metabolism and calcium homeostasis in iPSC-derived neurons carrying Presenilin-1 M146L gene mutation
inferred← citeshttps://doi.org/10.1111/jnc.14705openalex-snapshot
Mitochondria‐coupled glucose phosphorylation develops after birth to modulate H2O2 release and calcium handling in rat brain
inferred← citeshttps://doi.org/10.1134/s106236042001004xopenalex-snapshot
Role of the Redox System in Initiation of a Regenerative Response of Neural Eye Tissues in Vertebrates
inferred← citeshttps://doi.org/10.1139/cjpp-2025-0153openalex-snapshot
Redox homeostasis and therapeutic modulation: the central role of oxidative stress and nuclear factor erythroid 2-related factor 2 (Nrf2) activation in systemic diseases and reproductive dysfunction
inferred← citeshttps://doi.org/10.1186/s40359-025-02586-3openalex-snapshot
Relationship between different physical activity parameters and cognitive impairment in middle-aged and older adults: insights from a 4-year longitudinal study
inferred← citeshttps://doi.org/10.1242/dev.201463openalex-snapshot
Awakening adult neural stem cells: NOX signalling as a positive regulator of the quiescence-to-proliferation transition in the Xenopus retina
inferred← citeshttps://doi.org/10.1371/journal.pbio.2005594openalex-snapshot
The mammalian decidual cell evolved from a cellular stress response
inferred← citeshttps://doi.org/10.1523/jneurosci.1065-19.2023openalex-snapshot
A Role for Second Messengers in Axodendritic Neuronal Polarity
inferred← citeshttps://doi.org/10.2139/ssrn.5399288openalex-snapshot
Minocycline-Mediated Redox Modulation Enhances Survival But Disrupts Neurobehavioral Outcomes in Drosophila Melanogaster
inferred← citeshttps://doi.org/10.24275/uami.7d278t04popenalex-snapshot
Efectos del sulforafano sobre la velocidad de conducción nerviosa y su relación con el estado redox en la corteza cerebral e hipocampo de ratas viejas
inferred← citeshttps://doi.org/10.3389/fcell.2020.586631openalex-snapshot
CAPt’n of Actin Dynamics: Recent Advances in the Molecular, Developmental and Physiological Functions of Cyclase-Associated Protein (CAP)
inferred← citeshttps://doi.org/10.3389/fcell.2022.820949openalex-snapshot
A possible connection between reactive oxygen species and the unfolded protein response in lens development: From insight to foresight
inferred← citeshttps://doi.org/10.3389/fphys.2018.00065openalex-snapshot
TNF-α Increases Production of Reactive Oxygen Species through Cdk5 Activation in Nociceptive Neurons
inferred← citeshttps://doi.org/10.3390/antiox11081456openalex-snapshot
The Hidden Notes of Redox Balance in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.3390/antiox14091041openalex-snapshot
Antioxidant Molecules in the Human Vitreous Body During Prenatal Eye Development
inferred← citeshttps://doi.org/10.3390/antiox14121415openalex-snapshot
Neuron–Glia Crosstalk in the Regulation of Astrocytic Antioxidative Mechanisms Following CNS Injury
inferred← citeshttps://doi.org/10.3390/biomedicines8090348openalex-snapshot
Utility of Reactive Species Generation in Plasma Medicine for Neuronal Development
inferred← citeshttps://doi.org/10.3390/cells11142211openalex-snapshot
Potential Cross Talk between Autism Risk Genes and Neurovascular Molecules: A Pilot Study on Impact of Blood Brain Barrier Integrity
inferred← citeshttps://doi.org/10.3390/cimb46070410openalex-snapshot
Interplay among Oxidative Stress, Autophagy, and the Endocannabinoid System in Neurodegenerative Diseases: Role of the Nrf2- p62/SQSTM1 Pathway and Nutraceutical Activation
inferred← citeshttps://doi.org/10.3390/gels8020065openalex-snapshot
Analysis of Three-Dimensional Cell Migration in Dopamine-Modified Poly(aspartic acid)-Based Hydrogels
inferred← citeshttps://doi.org/10.3390/ijms21218164openalex-snapshot
In Vivo Imaging with Genetically Encoded Redox Biosensors
inferred← citeshttps://doi.org/10.3390/ijms24010308openalex-snapshot
Metal Profiles in Autism Spectrum Disorders: A Crosstalk between Toxic and Essential Metals
inferred← citeshttps://doi.org/10.3390/medicina59112045openalex-snapshot
Polyphenols in Inner Ear Neurobiology, Health and Disease: From Bench to Clinics
inferred← citeshttps://doi.org/10.3390/nu18020362openalex-snapshot
Garlic-Derived S-allylcysteine Improves Functional Recovery and Neurotrophin Signaling After Brain Ischemia in Female Rats
inferred← citeshttps://doi.org/10.3390/ph16081077openalex-snapshot
Endogenous and Exogenous Antioxidants as Agents Preventing the Negative Effects of Contrast Media (Contrast-Induced Nephropathy)
inferred← citeshttps://doi.org/10.3791/62165openalex-snapshot
ROS Live Cell Imaging During Neuronal Development
inferred← citeshttps://doi.org/10.4103/1673-5374.205088openalex-snapshot
Nerves and hydrogen peroxide: how old enemies become new friends
inferred← citeshttps://doi.org/10.4137/jen.s39887openalex-snapshot
Reactive Oxygen Species: Physiological and Physiopathological Effects on Synaptic Plasticity
inferred← citeshttps://doi.org/10.70675/50b46ad5z2cd5z4d89z981cz414d4af4e046openalex-snapshot
Utilisation des cellules souches pluripotentes pour le criblage à haut débit de molécules thérapeutiques dans la maladie de Lesch-Nyhan
inferred← citeshttps://doi.org/10.70675/71c15a42zb6d9z4edazb7c1zd3f51e09c949openalex-snapshot
Mitochondrial physiology within myelinated axons in health and disease : an energetic interplay between counterparts
inferred← citeshttps://doi.org/10.70675/a9e8c6faze8d0z44d4zb97dzcacb09c83ffdopenalex-snapshot
La relation symbiotique
inferred← citeshttps://doi.org/10.7287/peerj.5048v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Pathway analysis identifies altered mitochondrial metabolism, neurotransmission, structural pathways and complement cascade in retina/RPE/ choroid in chick model of form-deprivation myopia (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5048v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Pathway analysis identifies altered mitochondrial metabolism, neurotransmission, structural pathways and complement cascade in retina/RPE/ choroid in chick model of form-deprivation myopia (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5048v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Pathway analysis identifies altered mitochondrial metabolism, neurotransmission, structural pathways and complement cascade in retina/RPE/ choroid in chick model of form-deprivation myopia (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.5048v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Pathway analysis identifies altered mitochondrial metabolism, neurotransmission, structural pathways and complement cascade in retina/RPE/ choroid in chick model of form-deprivation myopia (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.5048openalex-snapshot
Pathway analysis identifies altered mitochondrial metabolism, neurotransmission, structural pathways and complement cascade in retina/RPE/ choroid in chick model of form-deprivation myopia
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.