On the public citation graph

NADPH oxidase regulates paraquat and maneb-induced dopaminergic neurodegeneration through ferroptosis

https://doi.org/10.1016/j.tox.2019.02.011

0 signed · 162 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

1 of the 56 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.3892/mmr.2017.6230 (notice 2025-06-02).

Dataset join, best-effort; this page does not check the publisher record. Retraction Watch data via Crossref Labs, used with credit; OpenCitations Index (CC0) and Meta (CC BY 4.0); dataset doi:10.7910/DVN/WT8VOA (CC BY 4.0).

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1007/s00401-017-1794-7openalex-snapshot

Neuronal complex I deficiency occurs throughout the Parkinson’s disease brain, but is not associated with neurodegeneration or mitochondrial DNA damage

inferredcites →https://doi.org/10.1007/s00441-004-0937-zopenalex-snapshot

Neurotoxicant-induced animal models of Parkinson?s disease: understanding the role of rotenone, maneb and paraquat in neurodegeneration

inferredcites →https://doi.org/10.1007/s10654-011-9574-5openalex-snapshot

Parkinson’s disease risk from ambient exposure to pesticides

inferredcites →https://doi.org/10.1007/s12035-015-9179-1openalex-snapshot

Formation and Implications of Alpha-Synuclein Radical in Maneb- and Paraquat-Induced Models of Parkinson’s Disease

inferredcites →https://doi.org/10.1016/j.bbadis.2013.01.021openalex-snapshot

Pro-inflammatory cytokines modulate iron regulatory protein 1 expression and iron transportation through reactive oxygen/nitrogen species production in ventral mesencephalic neurons

inferredcites →https://doi.org/10.1016/j.bbadis.2014.11.016openalex-snapshot

NADPH oxidase activation and 4-hydroxy-2-nonenal/aquaporin-4 adducts as possible new players in oxidative neuronal damage presents in drug-resistant epilepsy

inferredcites →https://doi.org/10.1016/j.brainres.2013.01.007openalex-snapshot

Post-treatment of an NADPH oxidase inhibitor prevents seizure-induced neuronal death

inferredcites →https://doi.org/10.1016/j.cell.2012.03.042openalex-snapshot

Ferroptosis: An Iron-Dependent Form of Nonapoptotic Cell Death

inferredcites →https://doi.org/10.1016/j.cell.2017.09.021openalex-snapshot

Ferroptosis: A Regulated Cell Death Nexus Linking Metabolism, Redox Biology, and Disease

inferredcites →https://doi.org/10.1016/j.celrep.2017.02.054openalex-snapshot

Oncogene-Selective Sensitivity to Synchronous Cell Death following Modulation of the Amino Acid Nutrient Cystine

inferredcites →https://doi.org/10.1016/j.nbd.2013.09.019openalex-snapshot

Pooled analysis of iron-related genes in Parkinson's disease: Association with transferrin

inferredcites →https://doi.org/10.1016/j.nbd.2016.05.011openalex-snapshot

Ferroptosis, a newly characterized form of cell death in Parkinson's disease that is regulated by PKC

inferredcites →https://doi.org/10.1016/j.neuron.2014.01.043openalex-snapshot

Microglial CR3 Activation Triggers Long-Term Synaptic Depression in the Hippocampus via NADPH Oxidase

inferredcites →https://doi.org/10.1016/j.neuroscience.2004.06.048openalex-snapshot

Proteasomal inhibition induced by manganese ethylene-bis-dithiocarbamate: Relevance to parkinson′s disease

inferredcites →https://doi.org/10.1016/j.neuroscience.2013.09.037openalex-snapshot

Pro-inflammatory cytokine-mediated ferroportin down-regulation contributes to the nigral iron accumulation in lipopolysaccharide-induced Parkinsonian models

inferredcites →https://doi.org/10.1016/j.neuroscience.2015.10.021openalex-snapshot

The impact of combined administration of paraquat and maneb on motor and non-motor functions in the rat

inferredcites →https://doi.org/10.1016/j.pestbp.2015.03.007openalex-snapshot

NADPH oxidase mediated maneb- and paraquat-induced oxidative stress in rat polymorphs: Crosstalk with mitochondrial dysfunction

inferredcites →https://doi.org/10.1016/j.pneurobio.2005.02.004openalex-snapshot

Oxidative stress in the brain: Novel cellular targets that govern survival during neurodegenerative disease

inferredcites →https://doi.org/10.1016/j.redox.2017.01.021openalex-snapshot

Ablation of ferroptosis regulator glutathione peroxidase 4 in forebrain neurons promotes cognitive impairment and neurodegeneration

inferredcites →https://doi.org/10.1016/j.redox.2017.02.016openalex-snapshot

NADPH oxidase-derived H2O2 mediates the regulatory effects of microglia on astrogliosis in experimental models of Parkinson's disease

inferredcites →https://doi.org/10.1016/j.redox.2017.09.017openalex-snapshot

Complement receptor 3 mediates NADPH oxidase activation and dopaminergic neurodegeneration through a Src-Erk-dependent pathway

inferredcites →https://doi.org/10.1016/j.redox.2017.11.001openalex-snapshot

α-Lipoic acid improves abnormal behavior by mitigation of oxidative stress, inflammation, ferroptosis, and tauopathy in P301S Tau transgenic mice

inferredcites →https://doi.org/10.1016/j.redox.2017.11.010openalex-snapshot

Integrin CD11b mediates α-synuclein-induced activation of NADPH oxidase through a Rho-dependent pathway

inferredcites →https://doi.org/10.1016/j.redox.2018.03.005openalex-snapshot

NADPH oxidases in traumatic brain injury – Promising therapeutic targets?

inferredcites →https://doi.org/10.1016/j.tox.2017.02.009openalex-snapshot

Paraquat and maneb co-exposure induces noradrenergic locus coeruleus neurodegeneration through NADPH oxidase-mediated microglial activation

inferredcites →https://doi.org/10.1016/j.toxlet.2005.07.001openalex-snapshot

In vitro cytotoxicity assays: Comparison of LDH, neutral red, MTT and protein assay in hepatoma cell lines following exposure to cadmium chloride

inferredcites →https://doi.org/10.1016/s0006-8993(01)02577-xopenalex-snapshot

Carrier-mediated processes in blood–brain barrier penetration and neural uptake of paraquat

inferredcites →https://doi.org/10.1023/a:1020884312053openalex-snapshot

Food Intake, Water Intake, and Drinking Spout Side Preference of 28 Mouse Strains

inferredcites →https://doi.org/10.1038/aps.2014.107openalex-snapshot

Protopanaxtriol protects against 3-nitropropionic acid-induced oxidative stress in a rat model of Huntington's disease

inferredcites →https://doi.org/10.1038/cdd.2015.158openalex-snapshot

Ferroptosis: process and function

inferredcites →https://doi.org/10.1038/nature05859openalex-snapshot

RAS–RAF–MEK-dependent oxidative cell death involving voltage-dependent anion channels

inferredcites →https://doi.org/10.1038/nri1312openalex-snapshot

NOX enzymes and the biology of reactive oxygen

inferredcites →https://doi.org/10.1038/nrn2038openalex-snapshot

Microglia-mediated neurotoxicity: uncovering the molecular mechanisms

inferredcites →https://doi.org/10.1038/s41419-018-0468-2openalex-snapshot

Taurine protects dopaminergic neurons in a mouse Parkinson’s disease model through inhibition of microglial M1 polarization

inferredcites →https://doi.org/10.1073/pnas.0807581105openalex-snapshot

Mitochondrial complex I inhibition is not required for dopaminergic neuron death induced by rotenone, MPP + , or paraquat

inferredcites →https://doi.org/10.1089/ars.2006.8.144openalex-snapshot

The Role of Oxidative Stress in the Dysregulation of Gene Expression and Protein Metabolism in Neurodegenerative Disease

inferredcites →https://doi.org/10.1093/aje/kwp006openalex-snapshot

Parkinson's Disease and Residential Exposure to Maneb and Paraquat From Agricultural Applications in the Central Valley of California

inferredcites →https://doi.org/10.1093/brain/awv034openalex-snapshot

Post-treatment with an ultra-low dose of NADPH oxidase inhibitor diphenyleneiodonium attenuates disease progression in multiple Parkinson’s disease models

inferredcites →https://doi.org/10.1097/wnr.0000000000000271openalex-snapshot

Maneb-induced dopaminergic neuronal death is not affected by loss of mitochondrial complex I activity

inferredcites →https://doi.org/10.1101/cshperspect.a001651openalex-snapshot

The Nuclear Factor NF- B Pathway in Inflammation

inferredcites →https://doi.org/10.1111/jnc.12244openalex-snapshot

Inflammation alters the expression of DMT 1, FPN 1 and hepcidin, and it causes iron accumulation in central nervous system cells

inferredcites →https://doi.org/10.1134/s0006297917060104openalex-snapshot

Disruption of functional activity of mitochondria during MTT assay of viability of cultured neurons

inferredcites →https://doi.org/10.1155/2014/581256openalex-snapshot

Nigral Iron Elevation Is an Invariable Feature of Parkinson’s Disease and Is a Sufficient Cause of Neurodegeneration

inferredcites →https://doi.org/10.1172/jci34060openalex-snapshot

SOD1 mutations disrupt redox-sensitive Rac regulation of NADPH oxidase in a familial ALS model

inferredcites →https://doi.org/10.1186/1742-2094-9-124openalex-snapshot

Endogenous dynorphin protects against neurotoxin-elicited nigrostriatal dopaminergic neuron damage and motor deficits in mice

inferredcites →https://doi.org/10.1186/s13024-017-0150-7openalex-snapshot

NADPH oxidase in brain injury and neurodegenerative disorders

inferredcites →https://doi.org/10.1248/bpb.23.1100openalex-snapshot

Phorbor Myristate Acetate Induces NADPH Oxidase Activity of Cytochalasin B-Primed Neutrophils through the Protein Kinase C-Independent Pathway.

inferredcites →https://doi.org/10.1271/bbb.120764openalex-snapshot

Application of LDH-Release Assay to Cellular-Level Evaluation of the Toxic Potential of Harmful Algal Species

inferredcites →https://doi.org/10.1523/jneurosci.20-24-09207.2000openalex-snapshot

The Nigrostriatal Dopaminergic System as a Preferential Target of Repeated Exposures to Combined Paraquat and Maneb: Implications for Parkinson's Disease

inferredcites →https://doi.org/10.1523/jneurosci.2238-14.2014openalex-snapshot

Substance P Exacerbates Dopaminergic Neurodegeneration through Neurokinin-1 Receptor-Independent Activation of Microglial NADPH Oxidase

inferredcites →https://doi.org/10.2174/157015912804143540openalex-snapshot

NADPH Oxidase and Neurodegeneration

inferredcites →https://doi.org/10.2174/157015912804499483openalex-snapshot

NADPH Oxidase and Neurodegeneration

inferredcites →https://doi.org/10.3389/fnins.2016.00408openalex-snapshot

Alpha-Synuclein Oligomers—Neurotoxic Molecules in Parkinson's Disease and Other Lewy Body Disorders

inferredcites →https://doi.org/10.3389/fphar.2014.00038openalex-snapshot

The interplay between iron accumulation, mitochondrial dysfunction, and inflammation during the execution step of neurodegenerative disorders

inferredcites →https://doi.org/10.3390/ijms19123824openalex-snapshot

The Role of NADPH Oxidases and Oxidative Stress in Neurodegenerative Disorders

inferredcites →https://doi.org/10.3892/mmr.2017.6230openalex-snapshot

Antiproliferation effect of the uremic toxin para-cresol on endothelial progenitor cells is related to its antioxidant activity

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.4567061openalex-extracted

inferred← citeshttps://doi.org/10.1002/cbdv.71676openalex-snapshot

Chronic Paraquat Neurotoxicity and Dopaminergic Degeneration: A Mechanistic Review

inferred← citeshttps://doi.org/10.1002/cbin.11443openalex-snapshot

ACADSB regulates ferroptosis and affects the migration, invasion, and proliferation of colorectal cancer cells

inferred← citeshttps://doi.org/10.1002/smtd.202001045openalex-snapshot

RNA m6A Modification Alteration by Black Phosphorus Quantum Dots Regulates Cell Ferroptosis: Implications for Nanotoxicological Assessment

inferred← citeshttps://doi.org/10.1007/978-981-97-9877-3_42openalex-snapshot

Nicotinamide Coenzyme II and Neuroexcitotoxicity

inferred← citeshttps://doi.org/10.1007/s00018-025-05841-3openalex-snapshot

Molecular components of the FPR2/ALX pathway participate in astrocyte-neuron resolution responses to afford maneb-induced toxicity

inferred← citeshttps://doi.org/10.1007/s00109-023-02346-zopenalex-snapshot

Molecular therapy of cardiac ischemia–reperfusion injury based on mitochondria and ferroptosis

inferred← citeshttps://doi.org/10.1007/s00204-022-03317-yopenalex-snapshot

Ferroptosis as a mechanism of non-ferrous metal toxicity

inferred← citeshttps://doi.org/10.1007/s10072-022-06302-6openalex-snapshot

Research progress on oxidative stress regulating different types of neuronal death caused by epileptic seizures

inferred← citeshttps://doi.org/10.1007/s11064-025-04348-4openalex-snapshot

The Interplay Between Endoplasmic Reticulum Stress and Ferroptosis in Neurological Diseases

inferred← citeshttps://doi.org/10.1007/s11481-025-10242-1openalex-snapshot

The Identification and Synthesis of New Sea Cucumber Peptides Leveraging Peptidomics Technology, along with their Anti-Parkinson’s Disease Efficacy

inferred← citeshttps://doi.org/10.1007/s12035-019-01832-1openalex-snapshot

The Role of Xenobiotics and Trace Metals in Parkinson’s Disease

inferred← citeshttps://doi.org/10.1007/s12035-023-03646-8openalex-snapshot

Oxytosis/Ferroptosis in Neurodegeneration: the Underlying Role of Master Regulator Glutathione Peroxidase 4 (GPX4)

inferred← citeshttps://doi.org/10.1007/s13346-024-01610-0openalex-snapshot

Brain targeted lactoferrin coated lipid nanocapsules for the combined effects of apocynin and lavender essential oil in PTZ induced seizures

inferred← citeshttps://doi.org/10.1007/s13577-020-00431-wopenalex-snapshot

Molecular characteristics associated with ferroptosis in hepatocellular carcinoma progression

inferred← citeshttps://doi.org/10.1007/s40242-021-1438-2openalex-snapshot

Maltol as a Novel Agent Protecting SH-SY5Y Cells Against Hemin-induced Ferroptosis

inferred← citeshttps://doi.org/10.1007/s41207-024-00537-9openalex-snapshot

Unveiling the hazards: comprehensive assessment of paraquat herbicide’s toxicity and health effects

inferred← citeshttps://doi.org/10.1016/b978-0-12-822120-4.00001-0openalex-snapshot

Parkinson's disease

inferred← citeshttps://doi.org/10.1016/j.bbr.2021.113699openalex-snapshot

Neuroprotective role of apocynin against pentylenetetrazole kindling epilepsy and associated comorbidities in mice by suppression of ROS/RNS

inferred← citeshttps://doi.org/10.1016/j.bbrc.2020.03.079openalex-snapshot

GDF15 knockdown promotes erastin-induced ferroptosis by decreasing SLC7A11 expression

inferred← citeshttps://doi.org/10.1016/j.canlet.2025.217696openalex-snapshot

Ferroptosis meets inflammation: A new frontier in cancer therapy

inferred← citeshttps://doi.org/10.1016/j.cbi.2023.110604openalex-snapshot

Dl-3-n-butylphthalide activates Nrf2, inhibits ferritinophagy, and protects MES23.5 dopaminergic neurons from ferroptosis

inferred← citeshttps://doi.org/10.1016/j.cca.2019.07.037openalex-snapshot

Lipid peroxidation in neurodegeneration

inferred← citeshttps://doi.org/10.1016/j.cellsig.2021.110098openalex-snapshot

G6PD inhibits ferroptosis in hepatocellular carcinoma by targeting cytochrome P450 oxidoreductase

inferred← citeshttps://doi.org/10.1016/j.chemosphere.2021.132982openalex-snapshot

Rotenone impairs learning and memory in mice through microglia-mediated blood brain barrier disruption and neuronal apoptosis

inferred← citeshttps://doi.org/10.1016/j.chemosphere.2026.144867openalex-snapshot

Maneb-induced neurotoxicity involves dopaminergic cell loss and impaired lipid metabolism

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.113972openalex-snapshot

Neurotoxicity of pesticides – A link to neurodegeneration

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118427openalex-snapshot

BECN1 regulates ferroptosis induced by 2,4-dichlorophenoxyacetic acid in SH-SY5Y cells

inferred← citeshttps://doi.org/10.1016/j.ejphar.2024.176402openalex-snapshot

Pentoxifylline protects against cerebral ischaemia-reperfusion injury through ferroptosis regulation via the Nrf2/SLC7A11/GPX4 signalling pathway

inferred← citeshttps://doi.org/10.1016/j.expneurol.2021.113828openalex-snapshot

Inhibition of TLR4 prevents hippocampal hypoxic-ischemic injury by regulating ferroptosis in neonatal rats

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2022.06.241openalex-snapshot

A novel synthetic peptide SVHRSP attenuates dopaminergic neurodegeneration by inhibiting NADPH oxidase-mediated neuroinflammation in experimental models of Parkinson's disease

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.12.045openalex-snapshot

Clozapine-N-oxide protects dopaminergic neurons against rotenone-induced neurotoxicity by preventing ferritinophagy-mediated ferroptosis

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2024.10.296openalex-snapshot

Role of ferroptosis in mitochondrial damage in diabetic retinopathy

inferred← citeshttps://doi.org/10.1016/j.jep.2023.116497openalex-snapshot

NLRP3 mediates the neuroprotective effects of SVHRSP derived from scorpion venom in rotenone-induced experimental Parkinson’s disease model

inferred← citeshttps://doi.org/10.1016/j.jhazmat.2021.125179openalex-snapshot

Combined exposure of alumina nanoparticles and chronic stress exacerbates hippocampal neuronal ferroptosis via activating IFN-γ/ASK1/JNK signaling pathway in rats

inferred← citeshttps://doi.org/10.1016/j.lddd.2025.100258openalex-snapshot

Paraquat-induced neurotoxicity: Mechanisms and potential therapies

inferred← citeshttps://doi.org/10.1016/j.molmet.2022.101502openalex-snapshot

Role and mechanism of ferroptosis in neurological diseases

inferred← citeshttps://doi.org/10.1016/j.mtchem.2021.100672openalex-snapshot

Inhibition of NADP(H) supply by highly active phosphatase-like ceria nanozymes to boost oxidative stress and ferroptosis

inferred← citeshttps://doi.org/10.1016/j.neuro.2026.103433openalex-snapshot

Paraquat-induced rodent models of Parkinson’s disease: A PRISMA-compliant systematic review and meta-analysis

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2019.09.006openalex-snapshot

Lesion of the Locus Coeruleus Damages Learning and Memory Performance in Paraquat and Maneb-induced Mouse Parkinson’s Disease Model

inferred← citeshttps://doi.org/10.1016/j.pestbp.2025.106838openalex-snapshot

Unveiling the crosslinks between pesticide exposure and the development of neurodegenerative disorders

inferred← citeshttps://doi.org/10.1016/j.plipres.2026.101395openalex-snapshot

Iron and lipid dysregulation as key determinants of ferroptosis in cardiometabolic disease

inferred← citeshttps://doi.org/10.1016/j.prp.2021.153576openalex-snapshot

Resveratrol attenuates rotenone-induced inflammation and oxidative stress via STAT1 and Nrf2/Keap1/SLC7A11 pathway in a microglia cell line

inferred← citeshttps://doi.org/10.1016/j.redox.2024.103369openalex-snapshot

Microglial CR3 promotes neuron ferroptosis via NOX2-mediated iron deposition in rotenone-induced experimental models of Parkinson's disease

inferred← citeshttps://doi.org/10.1016/j.taap.2025.117232openalex-snapshot

T-2 toxin triggers immunotoxic effects in goats by inducing ferroptosis and neutrophil extracellular traps

inferred← citeshttps://doi.org/10.1016/j.tiv.2023.105655openalex-snapshot

Paraquat-induced ferroptosis suppression via NRF2 expression regulation

inferred← citeshttps://doi.org/10.1016/j.tox.2020.152407openalex-snapshot

Where ferroptosis inhibitors and paraquat detoxification mechanisms intersect, exploring possible treatment strategies

inferred← citeshttps://doi.org/10.1021/acs.chemrestox.3c00389openalex-snapshot

Mechanisms Mediating the Combined Toxicity of Paraquat and Maneb in SH-SY5Y Neuroblastoma Cells

inferred← citeshttps://doi.org/10.1021/acs.est.3c06127openalex-snapshot

Ferroptosis Induced by Pollutants: An Emerging Mechanism in Environmental Toxicology

inferred← citeshttps://doi.org/10.1021/acs.jafc.3c00798openalex-snapshot

Heat Stress-Induced Intestinal Barrier Impairment: Current Insights into the Aspects of Oxidative Stress and Endoplasmic Reticulum Stress

inferred← citeshttps://doi.org/10.1021/acscentsci.3c00052openalex-snapshot

Dihydroxy-Metabolites of Dihomo-γ-linolenic Acid Drive Ferroptosis-Mediated Neurodegeneration

inferred← citeshttps://doi.org/10.1021/acschemneuro.3c00406openalex-snapshot

Ferroptosis-Regulated Cell Death as a Therapeutic Strategy for Neurodegenerative Diseases: Current Status and Future Prospects

inferred← citeshttps://doi.org/10.1038/s41401-021-00700-wopenalex-snapshot

ATF3 contributes to brucine-triggered glioma cell ferroptosis via promotion of hydrogen peroxide and iron

inferred← citeshttps://doi.org/10.1038/s41531-025-00892-6openalex-snapshot

SVHRSP protects against rotenone-induced neurodegeneration in mice by inhibiting TLR4/NF-κB-mediated neuroinflammation via gut microbiota

inferred← citeshttps://doi.org/10.1038/s41598-020-74916-xopenalex-snapshot

Endoplasmic reticulum stress-related neuroinflammation and neural stem cells decrease in mice exposure to paraquat

inferred← citeshttps://doi.org/10.1038/s41598-025-98679-5openalex-snapshot

TNF-α inhibits Epstein Barr virus reactivation through the GPX4 mediated glutathione pathway

inferred← citeshttps://doi.org/10.1038/s41598-026-54184-xopenalex-snapshot

Simulated microgravity induces a NOX-sensitive oxidative response that is attenuated by resveratrol in human endothelial cells

inferred← citeshttps://doi.org/10.1039/d3bm01000gopenalex-snapshot

GSH-depleting metal–polyphenol-network nanoparticles with dual enzyme activities induce enhanced ferroptosis

inferred← citeshttps://doi.org/10.1080/21655979.2022.2054194openalex-snapshot

RETRACTED ARTICLE: MiR-19a suppresses ferroptosis of colorectal cancer cells by targeting IREB2

inferred← citeshttps://doi.org/10.1089/ars.2019.8014openalex-snapshot

Nicotinamide Adenine Dinucleotide Phosphate Oxidase and Neurodegenerative Diseases: Mechanisms and Therapy

inferred← citeshttps://doi.org/10.1096/fj.202001290ropenalex-snapshot

The protective function of taurine on pesticide‐induced permanent neurodevelopmental toxicity in juvenile rats

inferred← citeshttps://doi.org/10.1111/jipb.13175openalex-snapshot

Tangeretin inhibits fungal ferroptosis to suppress rice blast

inferred← citeshttps://doi.org/10.1152/jn.00306.2022openalex-snapshot

HSPB1 overexpression improves hypoxic-ischemic brain damage by attenuating ferroptosis in rats through promoting G6PD expression

inferred← citeshttps://doi.org/10.1155/2020/6286984openalex-snapshot

Pretreatment with Roxadustat (FG-4592) Attenuates Folic Acid-Induced Kidney Injury through Antiferroptosis via Akt/GSK-3β/Nrf2 Pathway

inferred← citeshttps://doi.org/10.1155/2021/9912436openalex-snapshot

Reactive Oxygen Species (ROS) Regulates Different Types of Cell Death by Acting as a Rheostat

inferred← citeshttps://doi.org/10.1155/2022/1274550openalex-snapshot

Mechanism of Ferroptosis and Its Relationships with Other Types of Programmed Cell Death: Insights for Potential Therapeutic Benefits in Traumatic Brain Injury

inferred← citeshttps://doi.org/10.1155/2022/4914727openalex-snapshot

Exploring the Association between Glutathione Metabolism and Ferroptosis in Osteoblasts with Disuse Osteoporosis and the Key Genes Connecting them

inferred← citeshttps://doi.org/10.1155/2023/5803323openalex-snapshot

α-Synuclein Attenuates Maneb Neurotoxicity through the Modulation of Redox-Sensitive Transcription Factors

inferred← citeshttps://doi.org/10.1177/07482337221089585openalex-snapshot

Neurotoxicity associated with oxidative stress and inflammasome gene expression induced by allethrin in SH-SY5Y cells

inferred← citeshttps://doi.org/10.1177/09603271211052987openalex-snapshot

The role of ferroptosis in organ toxicity

inferred← citeshttps://doi.org/10.1177/09603271231167585openalex-snapshot

Treatment with paraquat affects the expression of ferroptosis-related genes

inferred← citeshttps://doi.org/10.1186/s10020-022-00494-5openalex-snapshot

Oxalate-induced apoptosis through ERS-ROS–NF-κB signalling pathway in renal tubular epithelial cell

inferred← citeshttps://doi.org/10.1186/s12974-020-02065-zopenalex-snapshot

Microglial activation contributes to cognitive impairments in rotenone-induced mouse Parkinson’s disease model

inferred← citeshttps://doi.org/10.12122/j.issn.1673-4254.2020.08.05openalex-snapshot

[Vitamin E reduces radiation injury of hippocampal neurons in mice by inhibiting ferroptosis].

inferred← citeshttps://doi.org/10.14670/hh-18-286openalex-snapshot

Targeting NRF2 to suppress ferroptosis in brain injury.

inferred← citeshttps://doi.org/10.18632/aging.103225openalex-snapshot

Clioquinol improves motor and non-motor deficits in MPTP-induced monkey model of Parkinson’s disease through AKT/mTOR pathway

inferred← citeshttps://doi.org/10.21037/tp-23-596openalex-snapshot

A ferroptosis-related ceRNA network for investigating the molecular mechanisms and the treatment of neonatal hypoxic-ischemic encephalopathy

inferred← citeshttps://doi.org/10.2147/dddt.s458026openalex-snapshot

Mapping the Research of Ferroptosis in Parkinson’s Disease from 2013 to 2023: A Scientometric Review

inferred← citeshttps://doi.org/10.2147/jir.s299927openalex-snapshot

Microglial Activation Mediates Noradrenergic Locus Coeruleus Neurodegeneration via Complement Receptor 3 in a Rotenone-Induced Parkinson’s Disease Mouse Model

inferred← citeshttps://doi.org/10.21608/aps.2021.92639.1068openalex-snapshot

Overview on Parkinson’s disease: pathophysiology, and experimental models

inferred← citeshttps://doi.org/10.2174/1386207325666220823122942openalex-snapshot

Integrative Multi-Omics Analysis of Identified Ferroptosis-Marker RPL8 as a Candidate Oncogene Correlates with Poor Prognosis and Immune Infiltration in Liver Cancer

inferred← citeshttps://doi.org/10.3389/fcell.2023.1083838openalex-snapshot

Role of ferroptosis in pregnancy related diseases and its therapeutic potential

inferred← citeshttps://doi.org/10.3389/fmolb.2022.890766openalex-snapshot

Therapeutic Implications of Ferroptosis in Renal Fibrosis

inferred← citeshttps://doi.org/10.3389/fnagi.2022.830569openalex-snapshot

Iron Dyshomeostasis and Ferroptosis: A New Alzheimer’s Disease Hypothesis?

inferred← citeshttps://doi.org/10.3389/fnagi.2022.904152openalex-snapshot

Mechanisms of Ferroptosis and Emerging Links to the Pathology of Neurodegenerative Diseases

inferred← citeshttps://doi.org/10.3389/fncel.2020.581191openalex-snapshot

Chemically Induced Models of Parkinson’s Disease: History and Perspectives for the Involvement of Ferroptosis

inferred← citeshttps://doi.org/10.3389/fncel.2021.819182openalex-snapshot

Sepsis-Exacerbated Brain Dysfunction After Intracerebral Hemorrhage

inferred← citeshttps://doi.org/10.3389/fncel.2022.1067570openalex-snapshot

Elucidating the progress and impact of ferroptosis in hemorrhagic stroke

inferred← citeshttps://doi.org/10.3389/fncel.2023.1080344openalex-snapshot

Ferroptosis: Underlying mechanism and the crosstalk with other modes of neuronal death after intracerebral hemorrhage

inferred← citeshttps://doi.org/10.3389/fnins.2020.00267openalex-snapshot

Nrf2 and Ferroptosis: A New Research Direction for Neurodegenerative Diseases

inferred← citeshttps://doi.org/10.3389/fnins.2020.589042openalex-snapshot

Mechanism of Ferroptosis and Its Relationships With Other Types of Programmed Cell Death: Insights for Potential Interventions After Intracerebral Hemorrhage

inferred← citeshttps://doi.org/10.3389/fphar.2023.1134895openalex-snapshot

Inhibitory effect and related mechanism of decitabine combined with gemcitabine on proliferation of NK/T cell lymphoma cells

inferred← citeshttps://doi.org/10.3389/fphys.2025.1641323openalex-snapshot

Targeting ferroptosis for neuroprotection: potential therapeutic avenues in neurodegenerative and neuropsychiatric diseases

inferred← citeshttps://doi.org/10.3390/antiox10010061openalex-snapshot

Inflaming the Brain with Iron

inferred← citeshttps://doi.org/10.3390/biomedicines9111679openalex-snapshot

Ferroptosis as a Major Factor and Therapeutic Target for Neuroinflammation in Parkinson’s Disease

inferred← citeshttps://doi.org/10.3390/diseases14030096openalex-snapshot

Pesticides Drive Liver Diseases Through Non-Apoptotic Regulated Cell Death Pathways

inferred← citeshttps://doi.org/10.3390/ijms21228765openalex-snapshot

Ferroptosis Mechanisms Involved in Neurodegenerative Diseases

inferred← citeshttps://doi.org/10.3390/ijms23052793openalex-snapshot

Microglial Activation Damages Dopaminergic Neurons through MMP-2/-9-Mediated Increase of Blood-Brain Barrier Permeability in a Parkinson’s Disease Mouse Model

inferred← citeshttps://doi.org/10.3390/ijms26146658openalex-snapshot

Ferroptosis in Toxicology: Present and Future

inferred← citeshttps://doi.org/10.3390/ijms262411953openalex-snapshot

Gestational and Lactational Exposure to BPS Triggers Microglial Ferroptosis via the SLC7A11/GPX4 Antioxidant Axis and Induces Memory Impairment in Offspring Mice

inferred← citeshttps://doi.org/10.3390/nu15122775openalex-snapshot

New Pieces for an Old Puzzle: Approaching Parkinson’s Disease from Translatable Animal Models, Gut Microbiota Modulation, and Lipidomics

inferred← citeshttps://doi.org/10.3920/wmj2020.2605openalex-snapshot

Apocynin attenuates patulin-induced cytotoxicity through reduction of oxidation stress and apoptosis in HEK293cells

inferred← citeshttps://doi.org/10.4103/1673-5374.332157openalex-snapshot

Oxidized low-density lipoprotein receptor 1: a novel potential therapeutic target for intracerebral hemorrhage

inferred← citeshttps://doi.org/10.5498/wjp.v13.i8.511openalex-snapshot

Dexmedetomidine mediates the mechanism of action of ferroptosis in mice with Alzheimer’s disease by regulating the mTOR-TFR1 pathway

inferred← citeshttps://doi.org/10.6084/m9.figshare.13525190openalex-snapshot

Additional file 1 of Microglial activation contributes to cognitive impairments in rotenone-induced mouse Parkinson’s disease model

inferred← citeshttps://doi.org/10.7150/ijbs.69714openalex-snapshot

Forsythoside A Mitigates Alzheimer's-like Pathology by Inhibiting Ferroptosis-mediated Neuroinflammation via Nrf2/GPX4 Axis Activation

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.