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Emerging roles for lipids in non-apoptotic cell death
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/emmm.201201283openalex-snapshot
Sphingosine analogue drug FTY720 targets I2PP2A/SET and mediates lung tumour suppression via activation of PP2A‐RIPK1‐dependent necroptosis
inferredcites →https://doi.org/10.1002/jnr.10257openalex-snapshot
Studies on neuronal death in the mouse model of Niemann‐Pick C disease
inferredcites →https://doi.org/10.1016/j.bbabio.2010.10.022openalex-snapshot
Inhibition of fatty acid oxidation by etomoxir impairs NADPH production and increases reactive oxygen species resulting in ATP depletion and cell death in human glioblastoma cells
inferredcites →https://doi.org/10.1016/j.bbalip.2011.06.009openalex-snapshot
Lipid classification, structures and tools
inferredcites →https://doi.org/10.1016/j.bbalip.2014.01.001openalex-snapshot
Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency
inferredcites →https://doi.org/10.1016/j.bbalip.2014.11.012openalex-snapshot
Targeted lipidomic strategies for oxygenated metabolites of polyunsaturated fatty acids
inferredcites →https://doi.org/10.1016/j.cell.2004.11.046openalex-snapshot
Growth Factor Regulation of Autophagy and Cell Survival in the Absence of Apoptosis
inferredcites →https://doi.org/10.1016/j.cell.2006.07.033openalex-snapshot
Caspase-1 Activation of Lipid Metabolic Pathways in Response to Bacterial Pore-Forming Toxins Promotes Cell Survival
inferredcites →https://doi.org/10.1016/j.cell.2011.10.033openalex-snapshot
Programmed Cell Death in Animal Development and Disease
inferredcites →https://doi.org/10.1016/j.cell.2011.11.031openalex-snapshot
Mixed Lineage Kinase Domain-like Protein Mediates Necrosis Signaling Downstream of RIP3 Kinase
inferredcites →https://doi.org/10.1016/j.cell.2011.12.017openalex-snapshot
Mutant p53 Disrupts Mammary Tissue Architecture via the Mevalonate Pathway
inferredcites →https://doi.org/10.1016/j.cell.2012.01.038openalex-snapshot
Sphingolipid Metabolism Cooperates with BAK and BAX to Promote the Mitochondrial Pathway of Apoptosis
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.2013.12.010openalex-snapshot
Regulation of Ferroptotic Cancer Cell Death by GPX4
inferredcites →https://doi.org/10.1016/j.cell.2013.12.015openalex-snapshot
Dividing Cells Regulate Their Lipid Composition and Localization
inferredcites →https://doi.org/10.1016/j.cell.2015.04.026openalex-snapshot
Acyl-CoA Dehydrogenase Drives Heat Adaptation by Sequestering Fatty Acids
inferredcites →https://doi.org/10.1016/j.cell.2015.05.051openalex-snapshot
A Conserved Circular Network of Coregulated Lipids Modulates Innate Immune Responses
inferredcites →https://doi.org/10.1016/j.cell.2015.05.056openalex-snapshot
Elucidating Compound Mechanism of Action by Network Perturbation Analysis
inferredcites →https://doi.org/10.1016/j.celrep.2014.04.026openalex-snapshot
MLKL Compromises Plasma Membrane Integrity by Binding to Phosphatidylinositol Phosphates
inferredcites →https://doi.org/10.1016/j.celrep.2015.01.043openalex-snapshot
Analysis of p53 Transactivation Domain Mutants Reveals Acad11 as a Metabolic Target Important for p53 Pro-Survival Function
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Synthetic Lethal Screening Identifies Compounds Activating Iron-Dependent, Nonapoptotic Cell Death in Oncogenic-RAS-Harboring Cancer Cells
inferredcites →https://doi.org/10.1016/j.chembiol.2015.09.010openalex-snapshot
Profiling of Free Fatty Acids Using Stable Isotope Tagging Uncovers a Role for Saturated Fatty Acids in Neuroexocytosis
inferredcites →https://doi.org/10.1016/j.chembiol.2015.11.004openalex-snapshot
Differential Regulation of Specific Sphingolipids in Colon Cancer Cells during Staurosporine-Induced Apoptosis
inferredcites →https://doi.org/10.1016/j.chemphyslip.2013.11.010openalex-snapshot
Cardiolipin asymmetry, oxidation and signaling
inferredcites →https://doi.org/10.1016/j.cmet.2013.05.017openalex-snapshot
Cellular Fatty Acid Metabolism and Cancer
inferredcites →https://doi.org/10.1016/j.ijdevneu.2005.11.002openalex-snapshot
Mechanism of toxicity of the branched‐chain fatty acid phytanic acid, a marker of Refsum disease, in astrocytes involves mitochondrial impairment
inferredcites →https://doi.org/10.1016/j.mito.2014.06.006openalex-snapshot
Lysosomal membrane permeabilization in cell death: Concepts and challenges
inferredcites →https://doi.org/10.1016/j.molcel.2014.03.003openalex-snapshot
Mixed Lineage Kinase Domain-like Protein MLKL Causes Necrotic Membrane Disruption upon Phosphorylation by RIP3
inferredcites →https://doi.org/10.1016/j.molcel.2015.06.011openalex-snapshot
Glutaminolysis and Transferrin Regulate Ferroptosis
inferredcites →https://doi.org/10.1016/j.plipres.2013.09.001openalex-snapshot
The eosinophil chemoattractant 5-oxo-ETE and the OXE receptor
inferredcites →https://doi.org/10.1016/j.semcdb.2014.07.013openalex-snapshot
Necroptosis in health and diseases
inferredcites →https://doi.org/10.1016/j.steroids.2015.02.007openalex-snapshot
24(S)-Hydroxycholesterol induces RIPK1-dependent but MLKL-independent cell death in the absence of caspase-8
inferredcites →https://doi.org/10.1016/j.tcb.2015.10.014openalex-snapshot
Ferroptosis: Death by Lipid Peroxidation
inferredcites →https://doi.org/10.1016/j.tem.2012.06.007openalex-snapshot
Regulation of lipid metabolism by p53 – fighting two villains with one sword
inferredcites →https://doi.org/10.1021/ac501395gopenalex-snapshot
Raman Imaging Providing Insights into Chemical Composition of Lipid Droplets of Different Size and Origin: In Hepatocytes and Endothelium
inferredcites →https://doi.org/10.1021/acschembio.5b00245openalex-snapshot
Human Haploid Cell Genetics Reveals Roles for Lipid Metabolism Genes in Nonapoptotic Cell Death
inferredcites →https://doi.org/10.1021/cr200246dopenalex-snapshot
Lipoxygenase and Leukotriene Pathways: Biochemistry, Biology, and Roles in Disease
inferredcites →https://doi.org/10.1021/cr2002799openalex-snapshot
Endocannabinoid Oxygenation by Cyclooxygenases, Lipoxygenases, and Cytochromes P450: Cross-Talk between the Eicosanoid and Endocannabinoid Signaling Pathways
inferredcites →https://doi.org/10.1021/ja411006aopenalex-snapshot
Ferrostatins Inhibit Oxidative Lipid Damage and Cell Death in Diverse Disease Models
inferredcites →https://doi.org/10.1038/cdd.2008.150openalex-snapshot
Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009
inferredcites →https://doi.org/10.1038/cdd.2010.81openalex-snapshot
Blebbing confers resistance against cell lysis
inferredcites →https://doi.org/10.1038/cdd.2012.34openalex-snapshot
Apoptosis-induced mitochondrial dysfunction causes cytoplasmic lipid droplet formation
inferredcites →https://doi.org/10.1038/cdd.2012.63openalex-snapshot
Regulation of lipid stores and metabolism by lipophagy
inferredcites →https://doi.org/10.1038/cdd.2014.137openalex-snapshot
Essential versus accessory aspects of cell death: recommendations of the NCCD 2015
inferredcites →https://doi.org/10.1038/cdd.2014.4openalex-snapshot
High sphingomyelin levels induce lysosomal damage and autophagy dysfunction in Niemann Pick disease type A
inferredcites →https://doi.org/10.1038/cdd.2015.122openalex-snapshot
The phospholipid code: a key component of dying cell recognition, tumor progression and host–microbe interactions
inferredcites →https://doi.org/10.1038/cddis.2013.524openalex-snapshot
Induction of apoptosis and necroptosis by 24(S)-hydroxycholesterol is dependent on activity of acyl-CoA:cholesterol acyltransferase 1
inferredcites →https://doi.org/10.1038/cr.2013.171openalex-snapshot
Translocation of mixed lineage kinase domain-like protein to plasma membrane leads to necrotic cell death
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/nature07976openalex-snapshot
Autophagy regulates lipid metabolism
inferredcites →https://doi.org/10.1038/nature08710openalex-snapshot
Hsp70 stabilizes lysosomes and reverts Niemann–Pick disease-associated lysosomal pathology
inferredcites →https://doi.org/10.1038/nature09583openalex-snapshot
Calcium-dependent phospholipid scrambling by TMEM16F
inferredcites →https://doi.org/10.1038/nature09663openalex-snapshot
A role for mitochondria in NLRP3 inflammasome activation
inferredcites →https://doi.org/10.1038/nature11351openalex-snapshot
Rapid induction of inflammatory lipid mediators by the inflammasome in vivo
inferredcites →https://doi.org/10.1038/nature11689openalex-snapshot
Metabolic control of adult neural stem cell activity by Fasn-dependent lipogenesis
inferredcites →https://doi.org/10.1038/nature14344openalex-snapshot
Ferroptosis as a p53-mediated activity during tumour suppression
inferredcites →https://doi.org/10.1038/nature15514openalex-snapshot
Cleavage of GSDMD by inflammatory caspases determines pyroptotic cell death
inferredcites →https://doi.org/10.1038/nature15541openalex-snapshot
Caspase-11 cleaves gasdermin D for non-canonical inflammasome signalling
inferredcites →https://doi.org/10.1038/nbt.2488openalex-snapshot
A community-driven global reconstruction of human metabolism
inferredcites →https://doi.org/10.1038/ncb2171openalex-snapshot
Stat3 controls lysosomal-mediated cell death in vivo
inferredcites →https://doi.org/10.1038/ncb3043openalex-snapshot
Stat3 controls cell death during mammary gland involution by regulating uptake of milk fat globules and lysosomal membrane permeabilization
inferredcites →https://doi.org/10.1038/ncb3064openalex-snapshot
Inactivation of the ferroptosis regulator Gpx4 triggers acute renal failure in mice
inferredcites →https://doi.org/10.1038/nchembio711openalex-snapshot
Chemical inhibitor of nonapoptotic cell death with therapeutic potential for ischemic brain injury
inferredcites →https://doi.org/10.1038/nchembio727openalex-snapshot
Cytochrome c acts as a cardiolipin oxygenase required for release of proapoptotic factors
inferredcites →https://doi.org/10.1038/ncomms6646openalex-snapshot
Mechanism of Ca2+-triggered ESCRT assembly and regulation of cell membrane repair
inferredcites →https://doi.org/10.1038/ni.2022openalex-snapshot
Fatty acid–induced NLRP3-ASC inflammasome activation interferes with insulin signaling
inferredcites →https://doi.org/10.1038/nmeth.2878openalex-snapshot
Live-cell imaging of alkyne-tagged small biomolecules by stimulated Raman scattering
inferredcites →https://doi.org/10.1038/nri3743openalex-snapshot
Regulated cell death and inflammation: an auto-amplification loop causes organ failure
inferredcites →https://doi.org/10.1038/nri3859openalex-snapshot
Eicosanoid storm in infection and inflammation
inferredcites →https://doi.org/10.1038/nrm2952openalex-snapshot
Mitochondria and cell death: outer membrane permeabilization and beyond
inferredcites →https://doi.org/10.1038/nrm3737openalex-snapshot
Regulated necrosis: the expanding network of non-apoptotic cell death pathways
inferredcites →https://doi.org/10.1038/nrmicro2070openalex-snapshot
Pyroptosis: host cell death and inflammation
inferredcites →https://doi.org/10.1038/onc.2008.310openalex-snapshot
Lysosomal membrane permeabilization in cell death
inferredcites →https://doi.org/10.1038/onc.2011.168openalex-snapshot
Association and dissociation of autophagy, apoptosis and necrosis by systematic chemical study
inferredcites →https://doi.org/10.1038/onc.2014.338openalex-snapshot
Impairment of antioxidant defense via glutathione depletion sensitizes acute lymphoblastic leukemia cells for Smac mimetic-induced cell death
inferredcites →https://doi.org/10.1046/j.1365-2958.2000.02103.xopenalex-snapshot
Salmonella induces macrophage death by caspase‐1‐dependent necrosis
inferredcites →https://doi.org/10.1073/pnas.0630588100openalex-snapshot
Triglyceride accumulation protects against fatty acid-induced lipotoxicity
inferredcites →https://doi.org/10.1073/pnas.0709747104openalex-snapshot
Beyond aerobic glycolysis: Transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis
inferredcites →https://doi.org/10.1073/pnas.1408987111openalex-snapshot
Activation of the pseudokinase MLKL unleashes the four-helix bundle domain to induce membrane localization and necroptotic cell death
inferredcites →https://doi.org/10.1073/pnas.1415518111openalex-snapshot
Synchronized renal tubular cell death involves ferroptosis
inferredcites →https://doi.org/10.1074/jbc.272.6.3324openalex-snapshot
Inhibition of Carnitine Palmitoyltransferase I Augments Sphingolipid Synthesis and Palmitate-induced Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m006655200openalex-snapshot
The Reactive Oxygen Species- and Michael Acceptor-inducible Human Aldo-Keto Reductase AKR1C1 Reduces the α,β-Unsaturated Aldehyde 4-Hydroxy-2-nonenal to 1,4-Dihydroxy-2-nonene
inferredcites →https://doi.org/10.1074/jbc.m111.230870openalex-snapshot
Ceramide Synthase-dependent Ceramide Generation and Programmed Cell Death
inferredcites →https://doi.org/10.1074/jbc.m111.236273openalex-snapshot
24(S)-Hydroxycholesterol Induces Neuronal Cell Death through Necroptosis, a Form of Programmed Necrosis
inferredcites →https://doi.org/10.1074/jbc.m111.272393openalex-snapshot
Cathepsin B Overexpression Due to Acid Sphingomyelinase Ablation Promotes Liver Fibrosis in Niemann-Pick Disease
inferredcites →https://doi.org/10.1074/jbc.m111.319129openalex-snapshot
Inhibition of Autophagy Rescues Palmitic Acid-induced Necroptosis of Endothelial Cells
inferredcites →https://doi.org/10.1074/jbc.m113.531202openalex-snapshot
Lysosomes Integrate Metabolic-Inflammatory Cross-talk in Primary Macrophage Inflammasome Activation
inferredcites →https://doi.org/10.1074/jbc.m114.583419openalex-snapshot
Exposure of Phosphatidylserine by Xk-related Protein Family Members during Apoptosis
inferredcites →https://doi.org/10.1074/jbc.m115.641191openalex-snapshot
Inhibition of Caspase-1 Activation in Endothelial Cells Improves Angiogenesis
inferredcites →https://doi.org/10.1091/mbc.e13-09-0516openalex-snapshot
Lipids in cell biology: how can we understand them better?
inferredcites →https://doi.org/10.1093/hmg/ddn066openalex-snapshot
Toxic effects of X-linked adrenoleukodystrophy-associated, very long chain fatty acids on glial cells and neurons from rat hippocampus in culture
inferredcites →https://doi.org/10.1093/hmg/dds090openalex-snapshot
Disruption and therapeutic rescue of autophagy in a human neuronal model of Niemann Pick type C1
inferredcites →https://doi.org/10.1101/gad.198630.112openalex-snapshot
Dysregulated mTORC1 renders cells critically dependent on desaturated lipids for survival under tumor-like stress
inferredcites →https://doi.org/10.1111/j.1462-5822.2006.00751.xopenalex-snapshot
Caspase-1-dependent pore formation during pyroptosis leads to osmotic lysis of infected host macrophages
inferredcites →https://doi.org/10.1111/j.1463-1326.2010.01279.xopenalex-snapshot
Causes and cures for endoplasmic reticulum stress in lipotoxic β ‐cell dysfunction
inferredcites →https://doi.org/10.1126/science.1236758openalex-snapshot
Xk-Related Protein 8 and CED-8 Promote Phosphatidylserine Exposure in Apoptotic Cells
inferredcites →https://doi.org/10.1126/science.1247005openalex-snapshot
Genome-Scale CRISPR-Cas9 Knockout Screening in Human Cells
inferredcites →https://doi.org/10.1126/science.1250256openalex-snapshot
Metabolic control of cell death
inferredcites →https://doi.org/10.1126/science.1252809openalex-snapshot
Caspase-mediated cleavage of phospholipid flippase for apoptotic phosphatidylserine exposure
inferredcites →https://doi.org/10.1126/science.8456305openalex-snapshot
Programmed Cell Death Induced by Ceramide
inferredcites →https://doi.org/10.1146/annurev-cellbio-100913-013226openalex-snapshot
Regulated Cell Death: Signaling and Mechanisms
inferredcites →https://doi.org/10.1152/ajpgi.00509.2005openalex-snapshot
Bax inhibition protects against free fatty acid-induced lysosomal permeabilization
inferredcites →https://doi.org/10.1152/physrev.00037.2014openalex-snapshot
Membrane Repair: Mechanisms and Pathophysiology
inferredcites →https://doi.org/10.1159/000373980openalex-snapshot
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
inferredcites →https://doi.org/10.1161/circresaha.113.279984openalex-snapshot
Combined Deficiency in Glutathione Peroxidase 4 and Vitamin E Causes Multiorgan Thrombus Formation and Early Death in Mice
inferredcites →https://doi.org/10.1172/jci68506openalex-snapshot
Cholestenoic acids regulate motor neuron survival via liver X receptors
inferredcites →https://doi.org/10.1172/jci78253openalex-snapshot
UCP2-induced fatty acid synthase promotes NLRP3 inflammasome activation during sepsis
inferredcites →https://doi.org/10.1182/blood-2015-06-654194openalex-snapshot
Glutathione peroxidase 4 prevents necroptosis in mouse erythroid precursors
inferredcites →https://doi.org/10.1194/jlr.m059105openalex-snapshot
Enhancement of lipid peroxidation and its amelioration by vitamin E in a subject with mutations in the SBP2 gene
inferredcites →https://doi.org/10.1194/jlr.r800095-jlr200openalex-snapshot
Update of the LIPID MAPS comprehensive classification system for lipids
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TLR4 Activation Under Lipotoxic Conditions Leads to Synergistic Macrophage Cell Death through a TRIF-Dependent Pathway
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Pharmacological inhibition of cystine–glutamate exchange induces endoplasmic reticulum stress and ferroptosis
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/s11064-024-04286-7openalex-snapshot
Neuroprotective Effects of Chaperonin Containing TCP1 Subunit 2 (CCT2) on Motor Neurons Following Oxidative or Ischemic Stress
inferred← citeshttps://doi.org/10.1007/s12035-020-02277-7openalex-snapshot
New Insights into the Role of Ferritin in Iron Homeostasis and Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.1007/s12035-024-04288-0openalex-snapshot
Mitochondrial Uncoupling Protein-2 Ameliorates Ischemic Stroke by Inhibiting Ferroptosis-Induced Brain Injury and Neuroinflammation
inferred← citeshttps://doi.org/10.1016/bs.enz.2023.07.003openalex-snapshot
Sphingolipids: From structural components to signaling hubs
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2019.11.004openalex-snapshot
A lipid perspective on regulated cell death
inferred← citeshttps://doi.org/10.1016/j.ajpath.2024.01.013openalex-snapshot
Ninjurin 2 Modulates Tumorigenesis, Inflammation, and Metabolism via Pyroptosis
inferred← citeshttps://doi.org/10.1016/j.amjms.2025.10.001openalex-snapshot
Targeting the ROS-ferroptosis axis: A clinical perspective on oxidative stress management in systemic lupus erythematosus
inferred← citeshttps://doi.org/10.1016/j.bbalip.2020.158728openalex-snapshot
Lipidomic analysis of epithelial corneal cells following hyperosmolarity and benzalkonium chloride exposure: New insights in dry eye disease
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.08.034openalex-snapshot
CISD1 inhibits ferroptosis by protection against mitochondrial lipid peroxidation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.08.124openalex-snapshot
Identification of ACSL4 as a biomarker and contributor of ferroptosis
inferred← citeshttps://doi.org/10.1016/j.biochi.2020.07.015openalex-snapshot
Lipidomic analysis of human corneal epithelial cells exposed to ocular irritants highlights the role of phospholipid and sphingolipid metabolisms in detergent toxicity mechanisms
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.114849openalex-snapshot
Ferroptosis: A new mechanism of traditional Chinese medicine compounds for treating acute kidney injury
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.116057openalex-snapshot
Ferroptosis in cardiovascular disease
inferred← citeshttps://doi.org/10.1016/j.biopha.2024.117513openalex-snapshot
Nuclear factor erythroid 2-related factor-mediated signaling alleviates ferroptosis during cerebral ischemia-reperfusion injury
inferred← citeshttps://doi.org/10.1016/j.cbpa.2017.06.002openalex-snapshot
Lipid homeostasis and regulated cell death
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114636openalex-snapshot
Inherent preference for polyunsaturated fatty acids instigates ferroptosis of Treg cells that aggravates high-fat-diet-related colitis
inferred← citeshttps://doi.org/10.1016/j.chembiol.2017.08.026openalex-snapshot
Very Long Chain Fatty Acids Are Functionally Involved in Necroptosis
inferred← citeshttps://doi.org/10.1016/j.chembiol.2018.11.016openalex-snapshot
Exogenous Monounsaturated Fatty Acids Promote a Ferroptosis-Resistant Cell State
inferred← citeshttps://doi.org/10.1016/j.chembiol.2019.01.008openalex-snapshot
Imidazole Ketone Erastin Induces Ferroptosis and Slows Tumor Growth in a Mouse Lymphoma Model
inferred← citeshttps://doi.org/10.1016/j.chembiol.2023.10.012openalex-snapshot
Ferroptosis inhibition by oleic acid mitigates iron-overload-induced injury
inferred← citeshttps://doi.org/10.1016/j.cmet.2022.09.023openalex-snapshot
The role of lipids in cancer progression and metastasis
inferred← citeshttps://doi.org/10.1016/j.dadm.2019.07.002openalex-snapshot
Sets of coregulated serum lipids are associated with Alzheimer's disease pathophysiology
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.06.020openalex-snapshot
Very long-chain fatty acids control peroxisome dynamics via a feedback loop in intestinal stem cells during gut regeneration
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2019.110039openalex-snapshot
The toxic effect of triclosan and methyl-triclosan on biological pathways revealed by metabolomics and gene expression in zebrafish embryos
inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.174319openalex-snapshot
Ferroptosis as a new therapeutic opportunity for nonviral liver disease
inferred← citeshttps://doi.org/10.1016/j.ejphar.2022.175175openalex-snapshot
Proteomic analysis reveals that ACSL4 activation during reflux esophagitis contributes to ferroptosis-mediated esophageal mucosal damage
inferred← citeshttps://doi.org/10.1016/j.envint.2025.109367openalex-snapshot
Polystyrene nanoplastics trigger ferroptosis in Nrf2-deficient gut via ether phospholipid accumulation
inferred← citeshttps://doi.org/10.1016/j.foodchem.2022.132051openalex-snapshot
Supercritical CO2 extraction of fermented soybean lipids against erastin-induced ferroptosis in rat pheochromocytoma cells
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2021.02.026openalex-snapshot
Physical plasma-derived oxidants sensitize pancreatic cancer cells to ferroptotic cell death
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2025.01.010openalex-snapshot
Downregulation of the SREBP pathways and disruption of redox status by 25-hydroxycholesterol predispose cells to ferroptosis
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2026.10.015openalex-snapshot
GLS2 Promotes Early Ferroptosis Followed by Apoptosis and p53 Signaling in Renal Ischemia–Reperfusion Injury
inferred← citeshttps://doi.org/10.1016/j.ghir.2022.101513openalex-snapshot
Biomarkers of growth and carbohydrate metabolism in neonatal rats supplemented with fish oil and/or antioxidants during intermittent hypoxia
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2022.06.064openalex-snapshot
Microwave assisted extraction, characterization of a polysaccharide from Salvia miltiorrhiza Bunge and its antioxidant effects via ferroptosis-mediated activation of the Nrf2/HO-1 pathway
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.109981openalex-snapshot
Matrine alleviates oxidative stress and ferroptosis in severe acute pancreatitis-induced acute lung injury by activating the UCP2/SIRT3/PGC1α pathway
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.112155openalex-snapshot
Oxidative medicine and cellular longevity the role and mechanism of NCOA4 in ferroptosis induced by intestinal ischemia reperfusion
inferred← citeshttps://doi.org/10.1016/j.jcis.2020.05.002openalex-snapshot
Toxicity and cellular uptake of lipid nanoparticles of different structure and composition
inferred← citeshttps://doi.org/10.1016/j.jconrel.2022.01.034openalex-snapshot
Nanodrug delivery systems for ferroptosis-based cancer therapy
inferred← citeshttps://doi.org/10.1016/j.jddst.2024.105998openalex-snapshot
Ferroptosis: Molecular perspective, cellular influence, cancer manifestation, and therapeutic potentials
inferred← citeshttps://doi.org/10.1016/j.jep.2024.117868openalex-snapshot
Integration of metabolomics and transcriptomics reveals that Da Chuanxiong Formula improves vascular cognitive impairment via ACSL4/GPX4 mediated ferroptosis
inferred← citeshttps://doi.org/10.1016/j.jff.2021.104620openalex-snapshot
The phytochemical vitexin and syringic acid derived from foxtail fillet bran inhibit breast cancer cells proliferation via GRP78/SREBP-1/SCD1 signaling axis
inferred← citeshttps://doi.org/10.1016/j.jhip.2024.08.001openalex-snapshot
Ferroptosis: A prospective therapeutic target for radiotherapy- and chemotherapy-induced gastrointestinal inflammation
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2022.109018openalex-snapshot
Docosahexaenoic acid enrichment of tumor phospholipid membranes increases tumor necroptosis in mice bearing triple negative breast cancer patient-derived xenografts
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2022.109255openalex-snapshot
Differential effects of oleate on vascular endothelial and liver sinusoidal endothelial cells reveal its toxic features in vitro
inferred← citeshttps://doi.org/10.1016/j.jss.2019.07.050openalex-snapshot
Protective Effect of Phosphatidylserine Blockade in Hemorrhagic Shock
inferred← citeshttps://doi.org/10.1016/j.molmet.2023.101865openalex-snapshot
Sestrin2 maintains hepatic immune homeostasis and redox balance partially via inhibiting RIPK3-mediated necroptosis in metabolic dysfunction-associated steatohepatitis
inferred← citeshttps://doi.org/10.1016/j.neures.2022.04.003openalex-snapshot
cPKCγ ameliorates ischemic injury in cultured neurons exposed to oxygen glucose deprivation/reoxygenation by inhibiting ferroptosis
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2024.01.021openalex-snapshot
Faecal Microbiota Transplantation Alleviates Ferroptosis after Ischaemic Stroke
inferred← citeshttps://doi.org/10.1016/j.phrs.2026.108442openalex-snapshot
Neural–metabolic crosstalk governing cell death and therapy resistance in tumors
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2022.106651openalex-snapshot
Lipidomics characterization of the lipid metabolism profiles in a cystinuria rat model: Precalculus damage in the kidney of cystinuria
inferred← citeshttps://doi.org/10.1016/j.saa.2022.122180openalex-snapshot
Spectroscopic signature of ZnO NP-induced cell death modalities assessed by non-negative PCA
inferred← citeshttps://doi.org/10.1016/j.yexcr.2024.114272openalex-snapshot
Emerging insights: miRNA modulation of ferroptosis pathways in lung cancer
inferred← citeshttps://doi.org/10.1016/j.yjmcc.2017.06.008openalex-snapshot
Suppression of autophagic flux contributes to cardiomyocyte death by activation of necroptotic pathways
inferred← citeshttps://doi.org/10.1016/j.ymthe.2021.03.022openalex-snapshot
Emerging mechanisms and targeted therapy of ferroptosis in cancer
inferred← citeshttps://doi.org/10.1021/acs.biochem.7b00862openalex-snapshot
Noncanonical Roles of Lipids in Different Cellular Fates
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.1c00281openalex-snapshot
Dose-Dependent Molecular Responses of Labeo rohita to Triphenyl Phosphate
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c09001openalex-snapshot
miR-145 Modulates Fatty Acid Metabolism by Targeting FOXO1 to Affect SERBP1 Activity in Bovine Mammary Epithelial Cells
inferred← citeshttps://doi.org/10.1021/acs.jpclett.9b02531openalex-snapshot
Phospholipid Scramblases Remodel the Shape of Asymmetric Membranes
inferred← citeshttps://doi.org/10.1021/acs.jproteome.4c00123openalex-snapshot
Taurine Alleviates Ferroptosis-Induced Metabolic Impairments in C2C12 Myoblasts by Stabilizing the Labile Iron Pool and Improving Redox Homeostasis
inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.2c00642openalex-snapshot
Unsaturated Fatty Acid Liposomes Selectively Regulate Glutathione Peroxidase 4 to Exacerbate Lipid Peroxidation as an Adaptable Liposome Platform for Anti-Tumor Therapy
inferred← citeshttps://doi.org/10.1021/acschembio.7b01082openalex-snapshot
Turning the Spotlight on Lipids in Non-Apoptotic Cell Death
inferred← citeshttps://doi.org/10.1021/acschembio.9b00616openalex-snapshot
Membrane Disruption by Very Long Chain Fatty Acids during Necroptosis
inferred← citeshttps://doi.org/10.1038/bcj.2017.61openalex-snapshot
MYC is a positive regulator of choline metabolism and impedes mitophagy-dependent necroptosis in diffuse large B-cell lymphoma
inferred← citeshttps://doi.org/10.1038/s12276-023-01083-0openalex-snapshot
Recent advances in cell death
inferred← citeshttps://doi.org/10.1038/s41392-020-00216-5openalex-snapshot
The interaction between ferroptosis and lipid metabolism in cancer
inferred← citeshttps://doi.org/10.1038/s41418-019-0299-4openalex-snapshot
Ischemia-induced ACSL4 activation contributes to ferroptosis-mediated tissue injury in intestinal ischemia/reperfusion
inferred← citeshttps://doi.org/10.1038/s41419-019-2115-yopenalex-snapshot
Modulation of the extrinsic cell death signaling pathway by viral Flip induces acute-death mediated liver failure
inferred← citeshttps://doi.org/10.1038/s41419-020-03275-2openalex-snapshot
Distinct photo-oxidation-induced cell death pathways lead to selective killing of human breast cancer cells
inferred← citeshttps://doi.org/10.1038/s41419-021-04406-zopenalex-snapshot
Chemotoxicity-induced exosomal lncFERO regulates ferroptosis and stemness in gastric cancer stem cells
inferred← citeshttps://doi.org/10.1038/s41419-023-05601-wopenalex-snapshot
3-Carboxy-4-methyl-5-propyl-2-furanpropanoic acid (CMPF) induces cell death through ferroptosis and acts as a trigger of apoptosis in kidney cells
inferred← citeshttps://doi.org/10.1038/s41419-024-07244-xopenalex-snapshot
Emerging mechanisms of lipid peroxidation in regulated cell death and its physiological implications
inferred← citeshttps://doi.org/10.1038/s41420-021-00656-0openalex-snapshot
Inhibition of DNMT-1 alleviates ferroptosis through NCOA4 mediated ferritinophagy during diabetes myocardial ischemia/reperfusion injury
inferred← citeshttps://doi.org/10.1038/s41420-025-02633-3openalex-snapshot
Emerging regulated cell death mechanisms in bone remodeling: decoding ferroptosis, cuproptosis, disulfidptosis, and PANoptosis as therapeutic targets for skeletal disorders
inferred← citeshttps://doi.org/10.1038/s41420-026-03115-wopenalex-snapshot
Regulation of lipid droplets accumulation by the Hippo–YAP/COX2 signaling pathway in neomycin-induced ototoxicity
inferred← citeshttps://doi.org/10.1038/s41467-020-15646-6openalex-snapshot
Dietary lipids fuel GPX4-restricted enteritis resembling Crohn’s disease
inferred← citeshttps://doi.org/10.1038/s41467-020-16220-wopenalex-snapshot
Dietary serine-microbiota interaction enhances chemotherapeutic toxicity without altering drug conversion
inferred← citeshttps://doi.org/10.1038/s41556-024-01405-yopenalex-snapshot
LPCAT1-mediated membrane phospholipid remodelling promotes ferroptosis evasion and tumour growth
inferred← citeshttps://doi.org/10.1038/s41598-025-88917-1openalex-snapshot
Cannabidiol attenuates lipid metabolism and induces CB1 receptor-mediated ER stress associated apoptosis in ovarian cancer cells
inferred← citeshttps://doi.org/10.1038/s43018-023-00702-zopenalex-snapshot
Lipids as mediators of cancer progression and metastasis
inferred← citeshttps://doi.org/10.1038/s44324-025-00092-zopenalex-snapshot
Parkin–ACSL4 axis in ferroptosis regulation: a narrative review on therapeutic insights from exercise in aging cardiomyocytes
inferred← citeshttps://doi.org/10.1039/c6mb00842aopenalex-snapshot
Regulation of lipids is central to replicative senescence
inferred← citeshttps://doi.org/10.1039/d2cb00172aopenalex-snapshot
SREBP activation contributes to fatty acid accumulations in necroptosis
inferred← citeshttps://doi.org/10.1039/d2na00719copenalex-snapshot
Recent trends in emerging strategies for ferroptosis-based cancer therapy
inferred← citeshttps://doi.org/10.1039/d4sc02129kopenalex-snapshot
Current progress in the regulation of endogenous molecules for enhanced chemodynamic therapy
inferred← citeshttps://doi.org/10.1042/bcj20170604openalex-snapshot
Metabolic profiling of visceral adipose tissue from obese subjects with or without metabolic syndrome
inferred← citeshttps://doi.org/10.1042/bsr20180764openalex-snapshot
Dropping in on lipid droplets: insights into cellular stress and cancer
inferred← citeshttps://doi.org/10.1063/5.0121995openalex-snapshot
Sperm fatty acid composition in infertile men
inferred← citeshttps://doi.org/10.1073/pnas.1710733114openalex-snapshot
Optimal nutrient exchange and immune responses operate in partner specificity in the cnidarian-dinoflagellate symbiosis
inferred← citeshttps://doi.org/10.1080/08830185.2021.2016739openalex-snapshot
Molecular mechanisms of ferroptosis and their role in inflammation
inferred← citeshttps://doi.org/10.1080/17568919.2025.2602422openalex-snapshot
Small molecule inhibitors of HG-induced VEC ferroptosis: synthetic advances and therapeutic applications
inferred← citeshttps://doi.org/10.1093/biolre/iox005openalex-snapshot
Inhibition of arachidonate 15-lipoxygenase prevents 4-hydroxynonenal-induced protein damage in male germ cells†
inferred← citeshttps://doi.org/10.1093/jmcb/mjac044openalex-snapshot
AIM-CICs: an automatic identification method for cell-in-cell structures based on convolutional neural network
inferred← citeshttps://doi.org/10.1096/fj.202400721ropenalex-snapshot
SREBP‐1‐mediated lipogenesis confers resistance to ferroptosis and improves endothelial injury
inferred← citeshttps://doi.org/10.1097/cad.0000000000000841openalex-snapshot
Heterocyclic organobismuth(III) compound induces nonapoptotic cell death via lipid peroxidation
inferred← citeshttps://doi.org/10.1101/2020.06.26.174110openalex-snapshot
WNT6-ACC2-induced accumulation of triacylglycerol rich lipid droplets is exploited by M. tuberculosis
inferred← citeshttps://doi.org/10.1101/2021.04.07.438684openalex-snapshot
Selective abrogation of S6K2 maps lipid homeostasis as a survival vulnerability in MAPKi-resistant NRAS MUT melanoma
inferred← citeshttps://doi.org/10.1101/2022.08.22.504843openalex-snapshot
SREBP1 Activation Contributes to Fatty Acid Accumulations in Necroptosis
inferred← citeshttps://doi.org/10.1101/2025.09.11.675514openalex-snapshot
FERROPTOSIS GENE SIGNATURES REVEAL DISTINCT REGULATORY LANDSCAPES IN GASTRIC ADENOCARCINOMA AND OTHER TISSUES
inferred← citeshttps://doi.org/10.1101/550723openalex-snapshot
Sets of Co-regulated Serum Lipids are Associated with Alzheimer Disease Pathophysiology
inferred← citeshttps://doi.org/10.1101/gad.314674.118openalex-snapshot
Regulation of lipid peroxidation and ferroptosis in diverse species
inferred← citeshttps://doi.org/10.1111/cas.13380openalex-snapshot
Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3
inferred← citeshttps://doi.org/10.1111/cmi.13317openalex-snapshot
Intracellular Staphylococcus aureus and host cell death pathways
inferred← citeshttps://doi.org/10.1111/cpr.13376openalex-snapshot
Comprehensive analysis of pyroptosis‐related gene signatures for glioblastoma immune microenvironment and target therapy
inferred← citeshttps://doi.org/10.1111/imr.12583openalex-snapshot
Necroptotic cell death in anti‐cancer therapy
inferred← citeshttps://doi.org/10.1111/jcmm.70410openalex-snapshot
DDR1 Targeting HOXA6 Facilitates Bladder Cancer Progression via Inhibiting Ferroptosis
inferred← citeshttps://doi.org/10.1111/jcmm.71002openalex-snapshot
Oxidative Stress‐Related Programmed Cell Death in Male Infertility: Focussing on Ferroptosis
inferred← citeshttps://doi.org/10.1111/jfbc.14040openalex-snapshot
Xylitol improves antioxidant, purinergic and cholinergic dysfunction, and lipid metabolic homeostasis in hepatic injury in type 2 diabetic rats
inferred← citeshttps://doi.org/10.1111/jnc.15807openalex-snapshot
Iron, ferroptosis, and ischemic stroke
inferred← citeshttps://doi.org/10.1126/science.adt8307openalex-snapshot
Epigenetic and 3D genome reprogramming during the aging of the human hippocampus
inferred← citeshttps://doi.org/10.1126/scitranslmed.aaz6314openalex-snapshot
Reprogramming lipid metabolism prevents effector T cell senescence and enhances tumor immunotherapy
inferred← citeshttps://doi.org/10.1126/scitranslmed.adp8913openalex-snapshot
Selective abrogation of S6K2 identifies lipid homeostasis as a survival vulnerability in MAPK inhibitor–resistant NRAS -mutant melanoma
inferred← citeshttps://doi.org/10.1128/aac.00835-21openalex-snapshot
Polymyxin-Induced Metabolic Perturbations in Human Lung Epithelial Cells
inferred← citeshttps://doi.org/10.1128/iai.00299-24openalex-snapshot
Host cell-specific metabolism of linoleic acid controls Toxoplasma gondii growth in cell culture
inferred← citeshttps://doi.org/10.1139/cjpp-2018-0490openalex-snapshot
Oxidized lipids: not just another brick in the wall
inferred← citeshttps://doi.org/10.1146/annurev-cancerbio-030518-055844openalex-snapshot
The Hallmarks of Ferroptosis
inferred← citeshttps://doi.org/10.1152/ajpheart.00076.2019openalex-snapshot
Phospholipid oxidation products in ferroptotic myocardial cell death
inferred← citeshttps://doi.org/10.1152/ajpheart.00237.2020openalex-snapshot
Oxidized phosphatidylcholines trigger ferroptosis in cardiomyocytes during ischemia-reperfusion injury
inferred← citeshttps://doi.org/10.1152/ajpheart.00452.2017openalex-snapshot
Protective effects of the mechanistic target of rapamycin against excess iron and ferroptosis in cardiomyocytes
inferred← citeshttps://doi.org/10.1155/2020/5146982openalex-snapshot
Nrf2 and STAT3 Alleviates Ferroptosis-Mediated IIR-ALI by Regulating SLC7A11
inferred← citeshttps://doi.org/10.1155/2020/6375938openalex-snapshot
The Latest View on the Mechanism of Ferroptosis and Its Research Progress in Spinal Cord Injury
inferred← citeshttps://doi.org/10.1155/2021/9074206openalex-snapshot
Positive and Negative Regulation of Ferroptosis and Its Role in Maintaining Metabolic and Redox Homeostasis
inferred← citeshttps://doi.org/10.1155/2022/9678625openalex-snapshot
Inhibiting Ferroptosis: A Novel Approach for Ulcerative Colitis Therapeutics
inferred← citeshttps://doi.org/10.1155/2023/6144967openalex-snapshot
Punica granatum L. Polyphenolic Extract as an Antioxidant to Prevent Kidney Injury in Metabolic Syndrome Rats
inferred← citeshttps://doi.org/10.1158/0008-5472.c.6513228.v1openalex-snapshot
Data from Ferroptosis Inducers Are a Novel Therapeutic Approach for Advanced Prostate Cancer
inferred← citeshttps://doi.org/10.1158/0008-5472.can-19-0369openalex-snapshot
Stearoyl-CoA Desaturase 1 Protects Ovarian Cancer Cells from Ferroptotic Cell Death
inferred← citeshttps://doi.org/10.1158/0008-5472.can-20-3477openalex-snapshot
Ferroptosis Inducers Are a Novel Therapeutic Approach for Advanced Prostate Cancer
inferred← citeshttps://doi.org/10.1158/0008-5472.can-21-4369openalex-snapshot
Monounsaturated and Diunsaturated Fatty Acids Sensitize Cervical Cancer to Radiation Therapy
inferred← citeshttps://doi.org/10.1158/1541-7786.mcr-18-0055openalex-snapshot
Ferroptosis-Induced Endoplasmic Reticulum Stress: Cross-talk between Ferroptosis and Apoptosis
inferred← citeshttps://doi.org/10.1158/1541-7786.mcr-21-0038openalex-snapshot
Cell-Intrinsic Mechanisms of Drug Tolerance to Systemic Therapies in Cancer
inferred← citeshttps://doi.org/10.1172/jci.insight.136676openalex-snapshot
Fbxo2 mediates clearance of damaged lysosomes and modifies neurodegeneration in the Niemann-Pick C brain
inferred← citeshttps://doi.org/10.1172/jci.insight.97102openalex-snapshot
RIPK3 mediates pathogenesis of experimental ventilator-induced lung injury
inferred← citeshttps://doi.org/10.1177/17590914211037505openalex-snapshot
Emerging Role of Ferroptosis in the Pathogenesis of Ischemic Stroke: A New Therapeutic Target?
inferred← citeshttps://doi.org/10.1186/s10020-025-01250-1openalex-snapshot
Lipocalin-2-mediated ferroptosis as a target for protection against light-induced photoreceptor degeneration
inferred← citeshttps://doi.org/10.1186/s12864-018-4603-3openalex-snapshot
Integrative analysis reveals ncRNA-mediated molecular regulatory network driving secondary hair follicle regression in cashmere goats
inferred← citeshttps://doi.org/10.1186/s12933-025-02614-xopenalex-snapshot
Ferroptosis: mechanism and role in diabetes-related cardiovascular diseases
inferred← citeshttps://doi.org/10.1186/s12938-024-01288-yopenalex-snapshot
Ferroptosis in radiation-induced brain injury: roles and clinical implications
inferred← citeshttps://doi.org/10.1186/s12964-024-01862-wopenalex-snapshot
Peroxisomal homeostasis in metabolic diseases and its implication in ferroptosis
inferred← citeshttps://doi.org/10.1186/s13048-024-01508-yopenalex-snapshot
Research progress of ferroptosis in female infertility
inferred← citeshttps://doi.org/10.1186/s13098-026-02193-1openalex-snapshot
Advances in targeted treatment of ferroptosis in diabetic kidney disease with SGLT2 inhibitors
inferred← citeshttps://doi.org/10.1186/s13567-026-01814-xopenalex-snapshot
Hemolysin EthA is an Edwardsiella T3SS effector that induces PANoptosis in macrophages
inferred← citeshttps://doi.org/10.1186/s40170-026-00428-3openalex-snapshot
Tumor cell death by ferroptosis contributes to an immunosuppressive tumor microenvironment in syngeneic murine models of cancer
inferred← citeshttps://doi.org/10.1186/s43556-026-00420-9openalex-snapshot
Ferroptosis in cardiovascular diseases: molecular mechanisms and a novel therapeutic target
inferred← citeshttps://doi.org/10.1212/nxg.0000000000200061openalex-snapshot
A Phase 1 Study of Oral Vitamin D 3 in Boys and Young Men With X-Linked Adrenoleukodystrophy
inferred← citeshttps://doi.org/10.1364/boe.9.002095openalex-snapshot
Selective delivery of laser energy to ester bonds of triacylglycerol in lipid droplets of adipocyte using a quantum cascade laser
inferred← citeshttps://doi.org/10.1371/journal.pbio.2006203openalex-snapshot
Unsolved mysteries: How does lipid peroxidation cause ferroptosis?
inferred← citeshttps://doi.org/10.14715/cmb/2022.68.2.31openalex-snapshot
Frontiers of Ferroptosis in Cancer Treatment
inferred← citeshttps://doi.org/10.14735/amko20182s21openalex-snapshot
Ferroptosis as a New Type of Cell Death and its Role in Cancer Treatment
inferred← citeshttps://doi.org/10.15212/bioi-2020-0039openalex-snapshot
Ferroptosis Resistance in Cancer: An Emerging Crisis of New Hope
inferred← citeshttps://doi.org/10.15406/ijcam.2019.12.00453openalex-snapshot
Anticancer activity of Giloe, Tinospora Cordifoila (Willd.) Miers Ex Hook F & Thoms
inferred← citeshttps://doi.org/10.15406/mojap.2019.06.00261openalex-snapshot
Alteration in the activities of antioxidant enzymes and lipid peroxidation in mice transplanted with Dalton’s lymphoma ascites tumor by Helicia Nilagirica Bedd
inferred← citeshttps://doi.org/10.17116/repro20202606197openalex-snapshot
Comparative study of the efficacy and safety of the use of the vitamin-mineral complex L-carnitine and the complex of acetyl-L-carnitine, L-carnitine fumarate, alpha-lipoic acid in the treatment of male infertility
inferred← citeshttps://doi.org/10.18632/oncotarget.11687openalex-snapshot
RSL3 and Erastin differentially regulate redox signaling to promote Smac mimetic-induced cell death
inferred← citeshttps://doi.org/10.18632/oncotarget.23046openalex-snapshot
Molecular crosstalk between ferroptosis and apoptosis: emerging role of ER stress-induced p53-independent PUMA expression
inferred← citeshttps://doi.org/10.21203/rs.3.rs-11156074/v1openalex-snapshot
Spermine inhibits ferroptosis in vascular dementia rats by intervening Nrf2/SLC7A11/GPX4 expression in chondriosome
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3336330/v1openalex-snapshot
CXCL14 Accelerates Fibroblast Ferroptosis in Inflammatory Bowel Disease by Regulating Lipid Metabolism via SCD1
inferred← citeshttps://doi.org/10.2147/ijn.s548090openalex-snapshot
Silica-Coated SPIONs Induce Ferroptosis in Endothelial Cells While Oleic Acid Mitigates Their Cytotoxic Effects
inferred← citeshttps://doi.org/10.2147/jhc.s616354openalex-snapshot
Subgroup-Specific Nomogram for Refined Risk Stratification in Hepatocellular Carcinoma Patients with Low LDL-C
inferred← citeshttps://doi.org/10.2174/011573403x370981250618074406openalex-snapshot
Phytoconstituents-mediated Targeting of Ferroptosis for the Treatment of Cardiovascular Disease
inferred← citeshttps://doi.org/10.2174/0929867330666230223103524openalex-snapshot
Enlightening the Mechanism of Ferroptosis in Epileptic Heart
inferred← citeshttps://doi.org/10.2174/1386207326666230328123223openalex-snapshot
The Potential of Lipid Droplet-associated Genes as Diagnostic and Prognostic Biomarkers in Head and Neck Squamous Cell Carcinoma
inferred← citeshttps://doi.org/10.23880/jonam-16000111openalex-snapshot
Dichloromethane Extract of Giloe (Tinospora Cordifolia, Wild) Increases the Radiosensitivity of Cultured Hela Cells Exposed to Different Doses of Γ-Radiation
inferred← citeshttps://doi.org/10.24272/j.issn.2095-8137.2024.028openalex-snapshot
Integrated multi-omics analysis reveals liver metabolic reprogramming by fish iridovirus and antiviral function of alpha-linolenic acid
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