On the public citation graph
4-Hydroxynonenal induces p53-mediated apoptosis in retinal pigment epithelial cells
0 signed · 161 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.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/hep.510290510openalex-snapshot
Regulation of Rat Hepatocyte Protein Kinase C β Isoenzymes by the Lipid Peroxidation Product 4–Hydroxy–2,3–Nonenal: A Signaling Pathway to Modulate Vesicular Transport of Glycoproteins
inferredcites →https://doi.org/10.1006/abbi.1995.1028openalex-snapshot
The Hepatocellular Metabolism of 4-Hydroxynonenal by Alcohol Dehydrogenase, Aldehyde Dehydrogenase, and Glutathione S-Transferase
inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot
A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
inferredcites →https://doi.org/10.1006/bbrc.1999.0389openalex-snapshot
The Influence of SV40 Immortalization of Human Fibroblasts on p53-Dependent Radiation Responses
inferredcites →https://doi.org/10.1006/bbrc.2001.4707openalex-snapshot
Two Distinct 4-Hydroxynonenal Metabolizing Glutathione S-Transferase Isozymes Are Differentially Expressed in Human Tissues
inferredcites →https://doi.org/10.1006/taap.1996.0152openalex-snapshot
4-Hydroxynonenal-Induced Cell Death in Murine Alveolar Macrophages
inferredcites →https://doi.org/10.1006/taap.1996.8070openalex-snapshot
Increased Resistance to Oxidative Stress in Transfected Cultured Cells Overexpressing GlutathioneS-Transferase mGSTA4-4
inferredcites →https://doi.org/10.1007/978-3-642-65340-7_19openalex-snapshot
Retinal Metabolism in Dark and Light
inferredcites →https://doi.org/10.1007/s10384-003-0043-xopenalex-snapshot
Ionizing Radiation Induces a p53-dependent Apoptotic Mechanism in ARPE-19 Cells
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/0092-8674(92)90593-2openalex-snapshot
A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia-telangiectasia
inferredcites →https://doi.org/10.1016/0092-8674(93)90500-popenalex-snapshot
WAF1, a potential mediator of p53 tumor suppression
inferredcites →https://doi.org/10.1016/0092-8674(94)90543-6openalex-snapshot
Cyclins and cancer II: Cyclin D and CDK inhibitors come of age
inferredcites →https://doi.org/10.1016/0092-8674(95)90412-3openalex-snapshot
Tumor suppressor p53 is a direct transcriptional activator of the human bax gene
inferredcites →https://doi.org/10.1016/0092-8674(95)90513-8openalex-snapshot
A novel form of Epstein-Barr virus latency in normal B cells in vivo
inferredcites →https://doi.org/10.1016/0891-5849(91)90192-6openalex-snapshot
Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes
inferredcites →https://doi.org/10.1016/j.bbrc.2005.06.099openalex-snapshot
Depletion of 4-hydroxynonenal in hGSTA4-transfected HLE B-3 cells results in profound changes in gene expression
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.05.033openalex-snapshot
Regulation of 4-hydroxynonenal-mediated signaling by glutathione S-transferases
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.08.027openalex-snapshot
Signaling kinases modulated by 4-hydroxynonenal
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.10.014openalex-snapshot
4-Hydroxynonenal modulation of p53 family gene expression in the SK-N-BE neuroblastoma cell line
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2006.04.005openalex-snapshot
c-Jun N-terminal kinase upregulation as a key event in the proapoptotic interaction between transforming growth factor-β1 and 4-hydroxynonenal in colon mucosa
inferredcites →https://doi.org/10.1016/j.taap.2003.10.001openalex-snapshot
Physiological role of mGSTA4-4, a glutathione S-transferase metabolizing 4-hydroxynonenal: generation and analysis of mGsta4 null mouse
inferredcites →https://doi.org/10.1016/s0014-4835(03)00023-xopenalex-snapshot
Oxidative stress-induced mitochondrial DNA damage in human retinal pigment epithelial cells: a possible mechanism for RPE aging and age-related macular degeneration
inferredcites →https://doi.org/10.1016/s0021-9258(18)47344-9openalex-snapshot
CPP32, a novel human apoptotic protein with homology to Caenorhabditis elegans cell death protein Ced-3 and mammalian interleukin-1 beta-converting enzyme.
inferredcites →https://doi.org/10.1016/s0092-8674(00)80416-xopenalex-snapshot
DNA Damage-Induced Phosphorylation of p53 Alleviates Inhibition by MDM2
inferredcites →https://doi.org/10.1016/s0092-8674(00)81871-1openalex-snapshot
p53, the Cellular Gatekeeper for Growth and Division
inferredcites →https://doi.org/10.1016/s0098-2997(03)00017-7openalex-snapshot
Role of 4-hydroxynonenal in stress-mediated apoptosis signaling
inferredcites →https://doi.org/10.1016/s0098-2997(03)00020-7openalex-snapshot
Oxidized LDL and 4-hydroxynonenal modulate tyrosine kinase receptor activity
inferredcites →https://doi.org/10.1016/s0098-2997(03)00021-9openalex-snapshot
4-Hydroxynonenal from pathology to physiology
inferredcites →https://doi.org/10.1016/s0169-328x(98)00339-8openalex-snapshot
Hydrogen peroxide induces nuclear translocation of p53 and apoptosis in cells of oligodendroglia origin
inferredcites →https://doi.org/10.1021/bi701559fopenalex-snapshot
4-Hydroxynonenal Self-Limits Fas-Mediated DISC-Independent Apoptosis by Promoting Export of Daxx from the Nucleus to the Cytosol and Its Binding to Fas
inferredcites →https://doi.org/10.1021/ja057358lopenalex-snapshot
Inhibition of Thioredoxin and Thioredoxin Reductase by 4-Hydroxy-2-nonenal in Vitro and in Vivo
inferredcites →https://doi.org/10.1038/nrm2395openalex-snapshot
Transcriptional control of human p53-regulated genes
inferredcites →https://doi.org/10.1038/sj.onc.1201404openalex-snapshot
DNA-damage-inducible p53 activity in SV40-transformed cells
inferredcites →https://doi.org/10.1038/sj.onc.1208615openalex-snapshot
The p53 pathway: positive and negative feedback loops
inferredcites →https://doi.org/10.1042/bj20020041openalex-snapshot
Cloning and expression of a novel Mu class murine glutathione transferase isoenzyme
inferredcites →https://doi.org/10.1074/jbc.274.4.2234openalex-snapshot
Activation of Stress Signaling Pathways by the End Product of Lipid Peroxidation
inferredcites →https://doi.org/10.1074/jbc.m106838200openalex-snapshot
Accelerated Metabolism and Exclusion of 4-Hydroxynonenal through Induction of RLIP76 and hGST5.8 Is an Early Adaptive Response of Cells to Heat and Oxidative Stress
inferredcites →https://doi.org/10.1074/jbc.m211134200openalex-snapshot
Electrophilic Prostaglandins and Lipid Aldehydes Repress Redox-sensitive Transcription Factors p53 and Hypoxia-inducible Factor by Impairing the Selenoprotein Thioredoxin Reductase
inferredcites →https://doi.org/10.1074/jbc.m305766200openalex-snapshot
Cells Preconditioned with Mild, Transient UVA Irradiation Acquire Resistance to Oxidative Stress and UVA-induced Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m509065200openalex-snapshot
Identification of a Lipid Peroxidation Product as a Potential Trigger of the p53 Pathway
inferredcites →https://doi.org/10.1076/ceyr.22.3.165.5517openalex-snapshot
Hydrogen peroxide stimulates apoptosis in cultured human retinal pigment epithelial cells
inferredcites →https://doi.org/10.1083/jcb.33.1.61openalex-snapshot
THE RENEWAL OF PHOTORECEPTOR CELL OUTER SEGMENTS
inferredcites →https://doi.org/10.1093/carcin/bgl111openalex-snapshot
Thioredoxin reductase is required for the inactivation of tumor suppressor p53 and for apoptosis induced by endogenous electrophiles
inferredcites →https://doi.org/10.1101/gad.11.24.3471openalex-snapshot
DNA damage induces phosphorylation of the amino terminus of p53
inferredcites →https://doi.org/10.1111/j.1432-1033.2004.04067.xopenalex-snapshot
Transfection with 4‐hydroxynonenal‐metabolizing glutathione S‐transferase isozymes leads to phenotypic transformation and immortalization of adherent cells
inferredcites →https://doi.org/10.1126/science.281.5383.1677openalex-snapshot
Activation of the ATM Kinase by Ionizing Radiation and Phosphorylation of p53
inferredcites →https://doi.org/10.1126/science.290.5493.989openalex-snapshot
Role of BAX in the Apoptotic Response to Anticancer Agents
inferredcites →https://doi.org/10.1126/science.7878464openalex-snapshot
Apoptosis in the Pathogenesis and Treatment of Disease
inferredcites →https://doi.org/10.1128/jvi.65.12.6447-6453.1991openalex-snapshot
The ability of large T antigen to complex with p53 is necessary for the increased life span and partial transformation of human cells by simian virus 40
inferredcites →https://doi.org/10.1136/bjo.59.2.111-copenalex-snapshot
Handbook of Sensory Physiology
inferredcites →https://doi.org/10.1159/000479441openalex-snapshot
Anti-Vascular Endothelial Growth Factors Protect Retinal Pigment Epithelium Cells Against Oxidation by Modulating Nitric Oxide Release and Autophagy
inferredcites →https://doi.org/10.1242/jcs.113.4.635openalex-snapshot
4-hydroxynonenal induces a cellular redox status-related activation of the caspase cascade for apoptotic cell death
inferredcites →https://doi.org/10.1523/jneurosci.17-13-05089.1997openalex-snapshot
Evidence that 4-Hydroxynonenal Mediates Oxidative Stress-Induced Neuronal Apoptosis
inferredcites →https://doi.org/10.4161/cc.4.5.1672openalex-snapshot
Inhibition of p53 by Lentiviral Mediated sh RNA Abrogates G1 Arrest and Apoptosis in Retinal Pigmented Epithelial Cell Line
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.4794612openalex-extracted
Molecular Mechanism of 4-Hydroxynonenal Induced Cell Death
inferred← citeshttps://doi.org/10.1002/9781119374947.ch12openalex-snapshot
Adipose Carbonylation and Mitochondrial Dysfunction
inferred← citeshttps://doi.org/10.1002/iub.2544openalex-snapshot
Identification of novel key molecular signatures in the pathogenesis of experimental diabetic retinopathy
inferred← citeshttps://doi.org/10.1002/jcp.28246openalex-snapshot
Glutathione transferase P silencing promotes neuronal differentiation of retinal R28 cells
inferred← citeshttps://doi.org/10.1002/ptr.3297openalex-snapshot
Role of alpha class glutathione transferases (GSTs) in chemoprevention: GSTA1 and A4 overexpressing human leukemia (HL60) cells resist sulforaphane and curcumin induced toxicity
inferred← citeshttps://doi.org/10.1007/978-81-322-1533-2_8openalex-snapshot
Mechanisms of Chemopreventive Activity of Sulforaphane
inferred← citeshttps://doi.org/10.1007/978-981-13-6260-6_5openalex-snapshot
Aldehyde Dehydrogenase 2 and Heart Failure
inferred← citeshttps://doi.org/10.1007/s12015-026-11113-9openalex-snapshot
Differential Effects of Retinal Fatty Acids Under Oxidative Stress Reveal DHA’s Susceptibility to Ferroptosis and Polarity Disruption in iPSC Derived RPE Cells
inferred← citeshttps://doi.org/10.1007/s12017-011-8164-8openalex-snapshot
Naturally Occurring Genetic Variability in Expression of Gsta4 is Associated with Differential Survival of Axotomized Rat Motoneurons
inferred← citeshttps://doi.org/10.1016/b978-0-12-819672-4.00008-8openalex-snapshot
Microbiota, mucosal immunity, and Colon cancer
inferred← citeshttps://doi.org/10.1016/j.abb.2014.07.021openalex-snapshot
High-glucose-induced CARM1 expression regulates apoptosis of human retinal pigment epithelial cells via histone 3 arginine 17 dimethylation: Role in diabetic retinopathy
inferred← citeshttps://doi.org/10.1016/j.aninu.2021.08.003openalex-snapshot
Hydroxyproline alleviates 4-hydroxy-2-nonenal-induced DNA damage and apoptosis in porcine intestinal epithelial cells
inferred← citeshttps://doi.org/10.1016/j.arr.2015.09.002openalex-snapshot
RPE necroptosis in response to oxidative stress and in AMD
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.11.113openalex-snapshot
The expression and function of vascular endothelial growth factor in retinal pigment epithelial (RPE) cells is regulated by 4-hydroxynonenal (HNE) and glutathione S-transferaseA4-4
inferred← citeshttps://doi.org/10.1016/j.cbi.2010.12.018openalex-snapshot
Protective effect of rat aldo-keto reductase (AKR1C15) on endothelial cell damage elicited by 4-hydroxy-2-nonenal
inferred← citeshttps://doi.org/10.1016/j.exer.2010.10.007openalex-snapshot
Differential roles of AMPKα1 and AMPKα2 in regulating 4-HNE-induced RPE cell death and permeability
inferred← citeshttps://doi.org/10.1016/j.exer.2010.11.010openalex-snapshot
Role of 4-hydroxynonenal in epidermal growth factor receptor-mediated signaling in retinal pigment epithelial cells
inferred← citeshttps://doi.org/10.1016/j.exer.2013.10.018openalex-snapshot
Lens specific RLIP76 transgenic mice show a phenotype similar to microphthalmia
inferred← citeshttps://doi.org/10.1016/j.exer.2014.04.014openalex-snapshot
Protective effect of a laser-induced sub-lethal temperature rise on RPE cells from oxidative stress
inferred← citeshttps://doi.org/10.1016/j.exer.2015.02.001openalex-snapshot
Quercetin alleviates 4-hydroxynonenal-induced cytotoxicity and inflammation in ARPE-19 cells
inferred← citeshttps://doi.org/10.1016/j.exer.2018.08.019openalex-snapshot
Oxidative stress induces ferroptotic cell death in retinal pigment epithelial cells
inferred← citeshttps://doi.org/10.1016/j.exer.2018.12.011openalex-snapshot
A derivative of betulinic acid protects human Retinal Pigment Epithelial (RPE) cells from cobalt chloride-induced acute hypoxic stress
inferred← citeshttps://doi.org/10.1016/j.exer.2021.108902openalex-snapshot
Altered transsulfuration pathway enzymes and redox homeostasis in inherited retinal degenerative diseases
inferred← citeshttps://doi.org/10.1016/j.fct.2024.115095openalex-snapshot
The interplay of oxidative stress, apoptotic signaling, and impaired mitochondrial function in the pyrethroid-induced cardiac injury: Alleviative role of curcumin-loaded chitosan nanoparticle
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.04.012openalex-snapshot
Role of 4-hydroxynonenal in chemopreventive activities of sulforaphane
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.04.021openalex-snapshot
Inhibition of Hydrogen peroxide signaling by 4-hydroxynonenal due to differential regulation of Akt1 and Akt2 contributes to decreases in cell survival and proliferation in hepatocellular carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.10.493openalex-snapshot
Regulatory roles of glutathione-S-transferases and 4-hydroxynonenal in stress-mediated signaling and toxicity
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.11.027openalex-snapshot
Ptgr1 expression is regulated by NRF2 in rat hepatocarcinogenesis and promotes cell proliferation and resistance to oxidative stress
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.11.032openalex-snapshot
4-hydroxynonenal-mediated signaling and aging
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2020.03.017openalex-snapshot
4-Hydroxy-7-oxo-5-heptenoic acid (HOHA) lactone induces apoptosis in retinal pigment epithelial cells
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2020.09.009openalex-snapshot
4-Hydroxy-7-oxo-5-heptenoic acid lactone can induce mitochondrial dysfunction in retinal pigmented epithelial cells
inferred← citeshttps://doi.org/10.1016/j.gendis.2026.102454openalex-snapshot
Molecular mechanisms of autologous ozonized blood transfusion: Antioxidant and anti-inflammatory effects
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.145082openalex-snapshot
Extracellular GMFB activates the non-canonical FAS-FAF1 pathway to induce lysosomal dysfunction in early diabetic retinopathy
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.150272openalex-snapshot
Oxidative stress in diabetic retinopathy: Metabolic triggers, molecular pathways and emerging antioxidant therapies
inferred← citeshttps://doi.org/10.1016/j.jgo.2014.04.005openalex-snapshot
Determinants of short- and long-term survival from colorectal cancer in very elderly patients
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2014.07.016openalex-snapshot
Docosahexaenoic acid aggravates photooxidative damage in retinal pigment epithelial cells via lipid peroxidation
inferred← citeshttps://doi.org/10.1016/j.kjms.2013.06.002openalex-snapshot
Pharmacological implications from the adhesion‐induced signaling profiles in cultured human retinal pigment epithelial cells
inferred← citeshttps://doi.org/10.1016/j.labinv.2022.100058openalex-snapshot
p53 Activates the Lipoxygenase Activity of ALOX15B via Inhibiting SLC7A11 to Induce Ferroptosis in Bladder Cancer Cells
inferred← citeshttps://doi.org/10.1016/j.labinv.2024.102027openalex-snapshot
Mediation of Ferroptosis Suppressor Protein 1 Expression via 4-Hydroxy-2-Nonenal Accumulation Contributes to Acquisition of Resistance to Apoptosis and Ferroptosis in Diffuse Large B-Cell Lymphoma
inferred← citeshttps://doi.org/10.1016/j.molcel.2019.12.027openalex-snapshot
Candidate Cancer Driver Mutations in Distal Regulatory Elements and Long-Range Chromatin Interaction Networks
inferred← citeshttps://doi.org/10.1016/j.neuint.2021.105118openalex-snapshot
Lipid peroxidation in brain tumors
inferred← citeshttps://doi.org/10.1016/j.redox.2020.101799openalex-snapshot
Oxidative stress and diabetic retinopathy: Molecular mechanisms, pathogenetic role and therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.redox.2022.102292openalex-snapshot
Glia maturation factor-β induces ferroptosis by impairing chaperone-mediated autophagic degradation of ACSL4 in early diabetic retinopathy
inferred← citeshttps://doi.org/10.1016/j.redox.2023.102840openalex-snapshot
Comparative mechanistic study of RPE cell death induced by different oxidative stresses
inferred← citeshttps://doi.org/10.1016/j.redox.2023.102967openalex-snapshot
Oxidative stress in the eye and its role in the pathophysiology of ocular diseases
inferred← citeshttps://doi.org/10.1016/j.taap.2015.10.006openalex-snapshot
Antioxidant role of glutathione S-transferases: 4-Hydroxynonenal, a key molecule in stress-mediated signaling
inferred← citeshttps://doi.org/10.1016/j.yexcr.2017.03.004openalex-snapshot
Nrf-2/Gst-α mediated imatinib resistance through rapid 4-HNE clearance
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.5b00485openalex-snapshot
Covalent Modification of CDK2 by 4-Hydroxynonenal as a Mechanism of Inhibition of Cell Cycle Progression
inferred← citeshttps://doi.org/10.1021/acs.jafc.5b04341openalex-snapshot
Visible Light-Induced Lipid Peroxidation of Unsaturated Fatty Acids in the Retina and the Inhibitory Effects of Blueberry Polyphenols
inferred← citeshttps://doi.org/10.1021/bi100517xopenalex-snapshot
Mechanisms of 4-Hydroxy-2-nonenal Induced Pro- and Anti-Apoptotic Signaling
inferred← citeshttps://doi.org/10.1038/cdd.2013.138openalex-snapshot
Cell death and diseases related to oxidative stress:4-hydroxynonenal (HNE) in the balance
inferred← citeshttps://doi.org/10.1038/nri3459openalex-snapshot
Immunology of age-related macular degeneration
inferred← citeshttps://doi.org/10.1038/onc.2016.113openalex-snapshot
Glutathione S-transferase alpha 4 induction by activator protein 1 in colorectal cancer
inferred← citeshttps://doi.org/10.1038/srep10630openalex-snapshot
The Oxidant Role of 4-Hydroxynonenal in Corneal Epithelium
inferred← citeshttps://doi.org/10.1038/srep17645openalex-snapshot
Fisetin and luteolin protect human retinal pigment epithelial cells from oxidative stress-induced cell death and regulate inflammation
inferred← citeshttps://doi.org/10.1038/srep32929openalex-snapshot
4-Hydroxy-2-nonenal induces apoptosis by activating ERK1/2 signaling and depleting intracellular glutathione in intestinal epithelial cells
inferred← citeshttps://doi.org/10.1039/c3mb70114jopenalex-snapshot
RNA-seq data analysis at the gene and CDS levels provides a comprehensive view of transcriptome responses induced by 4-hydroxynonenal
inferred← citeshttps://doi.org/10.1039/c7cc03387gopenalex-snapshot
Lipid radicals cause light-induced retinal degeneration
inferred← citeshttps://doi.org/10.1053/j.gastro.2011.11.020openalex-snapshot
4-Hydroxy-2-Nonenal Mediates Genotoxicity and Bystander Effects Caused by Enterococcus faecalis–Infected Macrophages
inferred← citeshttps://doi.org/10.1074/jbc.m109.023572openalex-snapshot
Increased Lipid Oxidation Causes Oxidative Stress, Increased Peroxisome Proliferator-activated Receptor-γ Expression, and Diminished Pro-osteogenic Wnt Signaling in the Skeleton
inferred← citeshttps://doi.org/10.1074/jbc.m113.467662openalex-snapshot
4-Hydroxynonenal Induces G2/M Phase Cell Cycle Arrest by Activation of the Ataxia Telangiectasia Mutated and Rad3-related Protein (ATR)/Checkpoint Kinase 1 (Chk1) Signaling Pathway
inferred← citeshttps://doi.org/10.1080/10715762.2026.2667438openalex-snapshot
Proteomic insights into nepetin-mediated protection against oxidative stress in ARPE-19 cells
inferred← citeshttps://doi.org/10.1093/pnasnexus/pgac056openalex-snapshot
Aldehyde dehydrogenase 3A1 deficiency leads to mitochondrial dysfunction and impacts salivary gland stem cell phenotype
inferred← citeshttps://doi.org/10.1096/fj.202402612rrropenalex-snapshot
Rhodopsin Induces Myopia via Lipid Peroxidation in Zebrafish Reared in a Dark Environment
inferred← citeshttps://doi.org/10.1111/ceo.13834openalex-snapshot
Retinal pigment epithelium and age‐related macular degeneration: A review of major disease mechanisms
inferred← citeshttps://doi.org/10.1111/opo.12198openalex-snapshot
Glutathione attenuates nitric oxide‐induced retinal lipid and protein changes
inferred← citeshttps://doi.org/10.1155/2014/360438openalex-snapshot
Lipid Peroxidation: Production, Metabolism, and Signaling Mechanisms of Malondialdehyde and 4-Hydroxy-2-Nonenal
inferred← citeshttps://doi.org/10.1155/2014/427318openalex-snapshot
Oxidative Stress in Alzheimer’s Disease: Why Did Antioxidant Therapy Fail?
inferred← citeshttps://doi.org/10.1155/2015/402386openalex-snapshot
Cytotoxic and Antitumor Activity of Sulforaphane: The Role of Reactive Oxygen Species
inferred← citeshttps://doi.org/10.1155/2015/617919openalex-snapshot
PRMT1 and PRMT4 Regulate Oxidative Stress-Induced Retinal Pigment Epithelial Cell Damage in SIRT1-Dependent and SIRT1-Independent Manners
inferred← citeshttps://doi.org/10.1155/2019/5937326openalex-snapshot
4-Hydroxy-Trans-2-Nonenal in the Regulation of Anti-Oxidative and Pro-Inflammatory Signaling Pathways
inferred← citeshttps://doi.org/10.1155/2023/5513507openalex-snapshot
Aldehyde Dehydrogenase 2 Ameliorates LPS-Induced Acute Kidney Injury through Detoxification of 4-HNE and Suppression of the MAPK Pathway
inferred← citeshttps://doi.org/10.1161/jaha.113.000779openalex-snapshot
Mitochondrial Aldehyde Dehydrogenase 2 Plays Protective Roles in Heart Failure After Myocardial Infarction via Suppression of the Cytosolic JNK/p53 Pathway in Mice
inferred← citeshttps://doi.org/10.1167/iovs.10-6991openalex-snapshot
Inhibition of Mdm2 Sensitizes Human Retinal Pigment Epithelial Cells to Apoptosis
inferred← citeshttps://doi.org/10.1167/iovs.12-10079openalex-snapshot
Elucidation of the Pathogenic Mechanism of Rhegmatogenous Retinal Detachment with Proliferative Vitreoretinopathy by Proteomic Analysis
inferred← citeshttps://doi.org/10.1167/iovs.15-16401openalex-snapshot
4-Acetoxyphenol Prevents RPE Oxidative Stress–Induced Necrosis by Functioning as an NRF2 Stabilizer
inferred← citeshttps://doi.org/10.1167/iovs.61.10.1openalex-snapshot
Gradual Increase in Environmental Light Intensity Induces Oxidative Stress and Inflammation and Accelerates Retinal Neurodegeneration
inferred← citeshttps://doi.org/10.1371/journal.pone.0301239openalex-snapshot
Phenotypic high-throughput screening identifies aryl hydrocarbon receptor agonism as common inhibitor of toxin-induced retinal pigment epithelium cell death
inferred← citeshttps://doi.org/10.1515/bmc.2011.002openalex-snapshot
Aldose reductase: new insights for an old enzyme
inferred← citeshttps://doi.org/10.18632/oncotarget.6131openalex-snapshot
4-Hydroxynonenal regulates mitochondrial function in human small airway epithelial cells
inferred← citeshttps://doi.org/10.2147/jir.s347231openalex-snapshot
Long-Chain Polyunsaturated Fatty Acids and Their Metabolites Regulate Inflammation in Age-Related Macular Degeneration
inferred← citeshttps://doi.org/10.29413/abs.2022-7.4.2openalex-snapshot
The role of some lipids and their metabolites in programmed cell death (lipoapoptosis).
inferred← citeshttps://doi.org/10.3109/10715762.2010.498477openalex-snapshot
Chemistry and biochemistry of lipid peroxidation products
inferred← citeshttps://doi.org/10.3389/fcell.2020.591067openalex-snapshot
Not All Stressors Are Equal: Mechanism of Stressors on RPE Cell Degeneration
inferred← citeshttps://doi.org/10.3389/fcvm.2017.00038openalex-snapshot
Cardiac Cell Senescence and Redox Signaling
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1571576openalex-snapshot
Targeting oxidative stress in diabetic retinopathy: mechanisms, pathology, and novel treatment approaches
inferred← citeshttps://doi.org/10.3389/fnut.2022.844757openalex-snapshot
Molecular Mechanisms of Iron Mediated Programmed Cell Death and Its Roles in Eye Diseases
inferred← citeshttps://doi.org/10.3389/fphar.2023.1122632openalex-snapshot
Acetaminophen-induced liver injury: Molecular mechanism and treatments from natural products
inferred← citeshttps://doi.org/10.3390/antiox10050653openalex-snapshot
Oxidative and Nitrosative Stress in Age-Related Macular Degeneration: A Review of Their Role in Different Stages of Disease
inferred← citeshttps://doi.org/10.3390/antiox9020150openalex-snapshot
In Vitro Aging of Human Skin Fibroblasts: Age-Dependent Changes in 4-Hydroxynonenal Metabolism
inferred← citeshttps://doi.org/10.3390/biom10030402openalex-snapshot
Involvement of Metabolic Lipid Mediators in the Regulation of Apoptosis
inferred← citeshttps://doi.org/10.3390/biom10050770openalex-snapshot
Proeryptotic Activity of 4-Hydroxynonenal: A New Potential Physiopathological Role for Lipid Peroxidation Products
inferred← citeshttps://doi.org/10.3390/cancers13246377openalex-snapshot
Anticancer Activity of Ω-6 Fatty Acids through Increased 4-HNE in Breast Cancer Cells
inferred← citeshttps://doi.org/10.3390/cells10071763openalex-snapshot
Extracellular Vesicles under Oxidative Stress Conditions: Biological Properties and Physiological Roles
inferred← citeshttps://doi.org/10.3390/ijms22031361openalex-snapshot
Spermidine Attenuates Oxidative Stress-Induced Apoptosis via Blocking Ca2+ Overload in Retinal Pigment Epithelial Cells Independently of ROS
inferred← citeshttps://doi.org/10.3390/jdad2020017openalex-snapshot
Oxidative Stress and Mitochondrial Dysfunction in Alzheimer’s Disease: Insights into Pathophysiology and Treatment
inferred← citeshttps://doi.org/10.3390/medsci13030087openalex-snapshot
Pathophysiological Mechanisms of Diabetes-Induced Macrovascular and Microvascular Complications: The Role of Oxidative Stress
inferred← citeshttps://doi.org/10.3390/nu15051255openalex-snapshot
Gamma-Muricholic Acid Inhibits Nonalcoholic Steatohepatitis: Abolishment of Steatosis-Dependent Peroxidative Impairment by FXR/SHP/LXRα/FASN Signaling
inferred← citeshttps://doi.org/10.3892/mmr.2021.11855openalex-snapshot
Potassium bromate-induced cell model of age-related macular degeneration in vitro
inferred← citeshttps://doi.org/10.4236/ojapo.2013.21001openalex-snapshot
Gsta4 Null Mouse Embryonic Fibroblasts Exhibit Enhanced Sensitivity to Oxidants: Role of 4-Hydroxynonenal in Oxidant Toxicity
inferred← citeshttps://doi.org/10.4239/wjd.v12.i9.1442openalex-snapshot
Cellular targets in diabetic retinopathy therapy
inferred← citeshttps://doi.org/10.5114/wo.2014.40456openalex-snapshot
Comparison of 4-hydroxynonenal induced p53-mediated apoptosis in prostate cancer cells LNCaP and DU145
inferred← citeshttps://doi.org/10.70675/3474a8e0zbde2z43f5za2aazac54d227d0d7openalex-snapshot
Dégénérescence maculaire liée à l'âge (DMLA) et voie du complément : rôle de la voie alterne du complément dans la pathologie
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.