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Contribution of redox-active iron and copper to oxidative damage in Alzheimer disease

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What this work says

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

inferredcites →https://doi.org/10.1001/archneur.60.12.1685openalex-snapshot
Metal-Protein Attenuation With Iodochlorhydroxyquin (Clioquinol) Targeting Aβ Amyloid Deposition and Toxicity in Alzheimer Disease
inferredcites →https://doi.org/10.1002/ana.410360510openalex-snapshot
Oxidative damage to mitochondrial DNA is increased in Alzheimer's disease
inferredcites →https://doi.org/10.1002/ana.410370609openalex-snapshot
Expression of heme oxygenase‐1 in the senescent and alzheimer‐diseased brain
inferredcites →https://doi.org/10.1002/ddr.10099openalex-snapshot
Metals and oxidative homeostasis in Alzheimer's disease
inferredcites →https://doi.org/10.1006/abbi.1998.0772openalex-snapshot
Myeloperoxidase and Horseradish Peroxidase Catalyze Tyrosine Nitration in Proteins from Nitrite and Hydrogen Peroxide
inferredcites →https://doi.org/10.1007/bf00688828openalex-snapshot
Fine structural localization of acid phosphatase in senile plaques in Alzheimer's presenile dementia
inferredcites →https://doi.org/10.1007/bf02815160openalex-snapshot
Mitochondrial membrane fluidity and oxidative damage to mitochondrial DNA in aged and AD human brain
inferredcites →https://doi.org/10.1007/s004010050420openalex-snapshot
Filament heterogeneity within the dystrophic neurites of senile plaques suggests blockage of fast axonal transport in Alzheimer's disease
inferredcites →https://doi.org/10.1016/b978-1-898563-87-7.50013-6openalex-snapshot
Prion and Alzheimer Diseases: The Road to Pathogenesis is Paved with Copper
inferredcites →https://doi.org/10.1016/s0002-9440(10)64296-4openalex-snapshot
Microtubule Reduction in Alzheimer's Disease and Aging Is Independent of τ Filament Formation
inferredcites →https://doi.org/10.1016/s0006-8993(96)00782-2openalex-snapshot
Increased regional brain concentrations of ceruloplasmin in neurodegenerative disorders
inferredcites →https://doi.org/10.1016/s0021-9258(17)31849-5openalex-snapshot
Analysis of microtubule-associated protein tau glycation in paired helical filaments.
inferredcites →https://doi.org/10.1016/s0042-6989(96)00210-6openalex-snapshot
Cytochrome oxidase in Alzheimer's disease: Biochemical, histochemical, and immunohistochemical analyses of the visual and other systems
inferredcites →https://doi.org/10.1016/s0076-6879(99)09012-6openalex-snapshot
[10] In situ methods for detection and localization of markers of oxidative stress: Application in neurodegenerative disorders
inferredcites →https://doi.org/10.1016/s0140-6736(05)72173-5openalex-snapshot
Amyloid-β junkies
inferredcites →https://doi.org/10.1016/s0196-9781(02)00069-4openalex-snapshot
The state versus amyloid-β: the trial of the most wanted criminal in Alzheimer disease
inferredcites →https://doi.org/10.1016/s0197-4580(00)00211-6openalex-snapshot
Copernicus revisited: amyloid beta in Alzheimer's disease
inferredcites →https://doi.org/10.1016/s0197-4580(00)00250-5openalex-snapshot
Life span and synapses: will there be a primary senile dementia?
inferredcites →https://doi.org/10.1016/s0891-5849(00)00494-9openalex-snapshot
Redox-active iron mediates amyloid-β toxicity
inferredcites →https://doi.org/10.1016/s0891-5849(99)00016-7openalex-snapshot
Is increased redox-active iron in Alzheimer disease a failure of the copper-binding protein ceruloplasmin?
inferredcites →https://doi.org/10.1021/ja01594a086openalex-snapshot
Methods of Enzymology.
inferredcites →https://doi.org/10.1023/a:1020731021276openalex-snapshot
Adventiously-bound redox active iron and copper are at the center of oxidative damage in Alzheimer disease
inferredcites →https://doi.org/10.1038/373481a0openalex-snapshot
A tombstone in Alzheimer's?
inferredcites →https://doi.org/10.1038/374316b0openalex-snapshot
Early AGEing and Alzheimer's
inferredcites →https://doi.org/10.1038/382120b0openalex-snapshot
Oxidative damage in Alzheimer's
inferredcites →https://doi.org/10.1038/ng0996-55openalex-snapshot
Apolipoprotein E allele–specific antioxidant activity and effects on cytotoxicity by oxidative insults and β–amyloid peptides
inferredcites →https://doi.org/10.1046/j.1471-4159.1995.65031399.xopenalex-snapshot
Induction of Heme Oxygenase‐1 mRNA and Protein in Neocortex and Cerebral Vessels in Alzheimer's Disease
inferredcites →https://doi.org/10.1046/j.1471-4159.1997.68052092.xopenalex-snapshot
4‐Hydroxynonenal‐Derived Advanced Lipid Peroxidation End Products Are Increased in Alzheimer's Disease
inferredcites →https://doi.org/10.1046/j.1471-4159.2000.0740270.xopenalex-snapshot
In Situ Oxidative Catalysis by Neurofibrillary Tangles and Senile Plaques in Alzheimer’s Disease
inferredcites →https://doi.org/10.1073/pnas.86.1.99openalex-snapshot
Heme oxygenase is the major 32-kDa stress protein induced in human skin fibroblasts by UVA radiation, hydrogen peroxide, and sodium arsenite.
inferredcites →https://doi.org/10.1073/pnas.91.12.5710openalex-snapshot
Advanced Maillard reaction end products are associated with Alzheimer disease pathology.
inferredcites →https://doi.org/10.1074/jbc.274.33.23223openalex-snapshot
Aqueous Dissolution of Alzheimer's Disease Aβ Amyloid Deposits by Biometal Depletion
inferredcites →https://doi.org/10.1074/jbc.c000165200openalex-snapshot
Evidence that the β-Amyloid Plaques of Alzheimer's Disease Represent the Redox-silencing and Entombment of Aβ by Zinc
inferredcites →https://doi.org/10.1074/jbc.m100175200openalex-snapshot
Alzheimer's Disease Amyloid-β Binds Copper and Zinc to Generate an Allosterically Ordered Membrane-penetrating Structure Containing Superoxide Dismutase-like Subunits
inferredcites →https://doi.org/10.1074/jbc.m110913200openalex-snapshot
High Molecular Weight Neurofilament Proteins Are Physiological Substrates of Adduction by the Lipid Peroxidation Product Hydroxynonenal
inferredcites →https://doi.org/10.1093/jnen/59.11.1011openalex-snapshot
Neuronal Oxidative Stress Precedes Amyloid-β Deposition in Down Syndrome
inferredcites →https://doi.org/10.1093/jnen/59.12.1118openalex-snapshot
Cell Death or Synaptic Loss in Alzheimer Disease
inferredcites →https://doi.org/10.1093/jnen/60.8.759openalex-snapshot
Oxidative Damage Is the Earliest Event in Alzheimer Disease
inferredcites →https://doi.org/10.1097/00002093-200307000-00005openalex-snapshot
Copper, Zinc, and the Metallobiology of Alzheimer Disease
inferredcites →https://doi.org/10.1097/00005072-199610000-00001openalex-snapshot
The Pathogenesis of Alzheimer Disease: An Alternative to the Amyloid Hypothesis
inferredcites →https://doi.org/10.1111/j.1749-6632.2000.tb05557.xopenalex-snapshot
Arson: Tracking the Culprit in Alzheimer's Disease
inferredcites →https://doi.org/10.1212/wnl.59.8.1153openalex-snapshot
Elevation of serum copper levels in Alzheimer’s disease
inferredcites →https://doi.org/10.1515/bchm3.1994.375.2.81openalex-snapshot
Extensive Nitration of Protein Tyrosines in Human Atherosclerosis Detected by Immunohistochemistry
inferredcites →https://doi.org/10.1523/jneurosci.17-08-02653.1997openalex-snapshot
Widespread Peroxynitrite-Mediated Damage in Alzheimer’s Disease
inferredcites →https://doi.org/10.1523/jneurosci.19-06-01959.1999openalex-snapshot
RNA Oxidation Is a Prominent Feature of Vulnerable Neurons in Alzheimer’s Disease
inferredcites →https://doi.org/10.1523/jneurosci.21-09-03017.2001openalex-snapshot
Mitochondrial Abnormalities in Alzheimer's Disease
inferredcites →https://doi.org/10.1523/jneurosci.21-17-06577.2001openalex-snapshot
Axonal Tau mRNA Localization Coincides with Tau Protein in Living Neuronal Cells and Depends on Axonal Targeting Signal
inferredcites →https://doi.org/10.2165/00023210-200216050-00006openalex-snapshot
The Role of Iron and Copper in the Aetiology of Neurodegenerative Disorders
inferredcites →https://doi.org/10.3233/jad-1998-1103openalex-snapshot
Reactive Oxygen Species Mediate Cellular Damage in Alzheimer Disease

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.4750682openalex-extracted
Interactive Effects of Ammonia-N and Salinity Levels on Oxidative Stress Factors, Liver Enzymes, and Acid Phosphatase Activity in Nile Tilapia (Oreochromis Niloticus)
inferred← citeshttps://doi.org/10.1002/14651858.cd008782openalex-snapshot
Plasma and Cerebro Spinal Fluid Amyloid Beta 42, 40 and the 42:40 ratio for diagnosis of incipient Dementia in a population with objective cognitive decline.
inferred← citeshttps://doi.org/10.1002/14651858.cd008782.pub2openalex-snapshot
Plasma and Cerebro Spinal Fluid Amyloid Beta 42, 40 and the 42:40 ratio for diagnosis of incipient Dementia in a population with objective cognitive decline.
inferred← citeshttps://doi.org/10.1002/14651858.cd008782.pub3openalex-snapshot
Plasma and CSF Abeta for the longitudinal prediction of Alzheimer's disease dementia and other dementias in people with cognitive decline but no dementia
inferred← citeshttps://doi.org/10.1002/14651858.cd008782.pub4openalex-snapshot
Plasma and cerebrospinal fluid amyloid beta for the diagnosis of Alzheimer's disease dementia and other dementias in people with mild cognitive impairment (MCI)
inferred← citeshttps://doi.org/10.1002/9780470929278.ch20openalex-snapshot
Mass Spectrometry in the Analysis of DNA, Protein, Peptide, and Lipid Biomarkers of Oxidative Stress
inferred← citeshttps://doi.org/10.1002/9780813814438.ch9openalex-snapshot
Oxidative Modification of Proteins: An Overview
inferred← citeshttps://doi.org/10.1002/ajp.22956openalex-snapshot
Loss of ferritin‐positive microglia relates to increased iron, RNA oxidation, and dystrophic microglia in the brains of aged male marmosets
inferred← citeshttps://doi.org/10.1002/cbic.200900597openalex-snapshot
A Prochelator Activated by Hydrogen Peroxide Prevents Metal‐Induced Amyloid β Aggregation
inferred← citeshttps://doi.org/10.1002/cjoc.200690066openalex-snapshot
Effect of Cu2+ on K+ Current in Acutely Isolated Rat Hippocampal Neurons by Whole Cell Patch Clamp Technique
inferred← citeshttps://doi.org/10.1002/cjoc.202100426openalex-snapshot
New Strategies for Nitrogen Fixation and Pollution Control
inferred← citeshttps://doi.org/10.1002/glia.23804openalex-snapshot
Increased oxidative stress, hyperphosphorylation of tau, and dystrophic microglia in the hippocampus of aged Tupaia belangeri
inferred← citeshttps://doi.org/10.1002/jps.20834openalex-snapshot
Selective oxidation of Zn2+—insulin catalyzed by Cu2+
inferred← citeshttps://doi.org/10.1002/nbm.922openalex-snapshot
High‐field magnetic resonance imaging of brain iron: birth of a biomarker?
inferred← citeshttps://doi.org/10.1002/rcm.2395openalex-snapshot
Liquid chromatography/tandem mass spectrometry characterization of oxidized amyloid beta peptides as potential biomarkers of Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/xrs.898openalex-snapshot
Characterization of Fe, Cu and Zn in organs of PDAPP transgenic mice by XRF spectrometry
inferred← citeshttps://doi.org/10.1007/0-387-36802-7_8openalex-snapshot
Mechanisms of DNA Damage and Repair in Alzheimer Disease
inferred← citeshttps://doi.org/10.1007/978-0-387-72974-9_10openalex-snapshot
The Role of Oxidative Damage to Nucleic Acids in the Pathogenesis of Neurological Disease
inferred← citeshttps://doi.org/10.1007/978-1-4419-7104-3_18openalex-snapshot
Oxidative Stress and Alzheimer Disease: Mechanisms and Therapeutic Opportunities
inferred← citeshttps://doi.org/10.1007/978-1-60761-898-0_34openalex-snapshot
Animal Models of Metallic Dementia
inferred← citeshttps://doi.org/10.1007/978-1-60761-956-7_9openalex-snapshot
Oxidative Stress in Alzheimer’s Disease: A Critical Appraisal of the Causes and the Consequences
inferred← citeshttps://doi.org/10.1007/s00702-011-0597-6openalex-snapshot
Iron-chelating backbone coupled with monoamine oxidase inhibitory moiety as novel pluripotential therapeutic agents for Alzheimer’s disease: a tribute to Moussa Youdim
inferred← citeshttps://doi.org/10.1007/s12011-014-0093-6openalex-snapshot
Anatomical Region Differences and Age-Related Changes in Copper, Zinc, and Manganese Levels in the Human Brain
inferred← citeshttps://doi.org/10.1007/s12161-021-02024-1openalex-snapshot
Application of Phenolic Extraction Strategies and Evaluation of the Antioxidant Activity of Peanut Skins as an Agricultural By-product for Food Industry
inferred← citeshttps://doi.org/10.1016/j.bbrep.2016.12.010openalex-snapshot
Protease activity of legumain is inhibited by an increase of cystatin E/M in the DJ-1-knockout mouse spleen, cerebrum and heart
inferred← citeshttps://doi.org/10.1016/j.bcp.2014.01.002openalex-snapshot
Alzheimer disease therapeutics: Focus on the disease and not just plaques and tangles
inferred← citeshttps://doi.org/10.1016/j.biochi.2015.09.022openalex-snapshot
Structure and function of legumain in health and disease
inferred← citeshttps://doi.org/10.1016/j.biopha.2006.11.001openalex-snapshot
Implication of the transcription factor E2F-1 in the modulation of neuronal apoptosis
inferred← citeshttps://doi.org/10.1016/j.bmc.2022.117088openalex-snapshot
Phenolic furanochromene hydrazone derivatives: Synthesis, antioxidant activity, ferroptosis inhibition, DNA cleavage and DNA molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.ccr.2011.07.004openalex-snapshot
Structural characterization of Cu2+, Ni2+ and Zn2+ binding sites of model peptides associated with neurodegenerative diseases
inferred← citeshttps://doi.org/10.1016/j.disamonth.2010.06.001openalex-snapshot
Alzheimer Disease
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.126710openalex-snapshot
Lead induced intracellular copper redox imbalance with aggravated cellular dysfunction
inferred← citeshttps://doi.org/10.1016/j.exger.2007.09.007openalex-snapshot
Age-dependent oxidation and aggregation of ZnT-1: A role for metal catalyzed oxidation?
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.07.028openalex-snapshot
Roles of dioxins and heavy metals in cancer and neurological diseases using ROS-mediated mechanisms
inferred← citeshttps://doi.org/10.1016/j.jconrel.2018.05.011openalex-snapshot
Nose-to-brain drug delivery: An update on clinical challenges and progress towards approval of anti-Alzheimer drugs
inferred← citeshttps://doi.org/10.1016/j.neuint.2007.04.021openalex-snapshot
Geniposide, a novel agonist for GLP-1 receptor, prevents PC12 cells from oxidative damage via MAP kinase pathway
inferred← citeshttps://doi.org/10.1016/j.neulet.2006.07.070openalex-snapshot
Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2012.05.009openalex-snapshot
Intranasal deferoxamine reverses iron-induced memory deficits and inhibits amyloidogenic APP processing in a transgenic mouse model of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.pathophys.2006.05.004openalex-snapshot
Oxidative stress in Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2007.06.001openalex-snapshot
Iron dysregulation in Alzheimer's disease: Multimodal brain permeable iron chelating drugs, possessing neuroprotective-neurorescue and amyloid precursor protein-processing regulatory activities as therapeutic agents
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2007.07.009openalex-snapshot
Brain iron metabolism: Neurobiology and neurochemistry
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.8b00094openalex-snapshot
Quinone-Based Antitumor Agent Sepantronium Bromide (YM155) Causes Oxygen-Independent Redox-Activated Oxidative DNA Damage
inferred← citeshttps://doi.org/10.1021/acs.jproteome.4c00688openalex-snapshot
Multiplatform Lipid Analysis of the Brain of Aging Mice by Mass Spectrometry
inferred← citeshttps://doi.org/10.1021/acsomega.5c11345openalex-snapshot
Selective Reversal of Cu-Amyloid Aggregation Monitored in Real Time by Fluorescence Anisotropy: Ni-Bme-Dach vs EDTA Benchmarks
inferred← citeshttps://doi.org/10.1021/cn300060vopenalex-snapshot
An N-Heterocyclic Amine Chelate Capable of Antioxidant Capacity and Amyloid Disaggregation
inferred← citeshttps://doi.org/10.1021/cr040410wopenalex-snapshot
Copper Homeostasis and Neurodegenerative Disorders (Alzheimer's, Prion, and Parkinson's Diseases and Amyotrophic Lateral Sclerosis)
inferred← citeshttps://doi.org/10.1021/tx700210jopenalex-snapshot
Oxidative Stress and Neurotoxicity
inferred← citeshttps://doi.org/10.1038/s41598-020-67117-zopenalex-snapshot
Iron stored in ferritin is chemically reduced in the presence of aggregating Aβ(1-42)
inferred← citeshttps://doi.org/10.1038/s41598-024-84136-2openalex-snapshot
The influence of ammonia-N and salinity levels on oxidative stress markers, hepatic enzymes, and acid phosphatase activity in Nile tilapia (Oreochromis niloticus)
inferred← citeshttps://doi.org/10.1039/b919237aopenalex-snapshot
Minding metals: Tailoring multifunctional chelating agents for neurodegenerative disease
inferred← citeshttps://doi.org/10.1039/c2mt20164jopenalex-snapshot
Metallobiology of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine neurotoxicity
inferred← citeshttps://doi.org/10.1039/c4ra09193kopenalex-snapshot
Drug-like chelating agents: a potential lead for Alzheimer's disease
inferred← citeshttps://doi.org/10.1039/c5dt02130hopenalex-snapshot
Computer-assisted designed “selenoxy–chinolin”: a new catalytic mechanism of the GPx-like cycle and inhibition of metal-free and metal-associated Aβ aggregation
inferred← citeshttps://doi.org/10.1074/jbc.m112.446070openalex-snapshot
Activation of Asparaginyl Endopeptidase Leads to Tau Hyperphosphorylation in Alzheimer Disease
inferred← citeshttps://doi.org/10.1074/jbc.m113.511345openalex-snapshot
Capturing a Reactive State of Amyloid Aggregates
inferred← citeshttps://doi.org/10.1080/08977190500361788openalex-snapshot
Insulin-like growth factor-1 prevents Aβ[25–35]/(H2O2)- induced apoptosis in lymphocytes by reciprocal NF-κB activation and p53 inhibition via PI3K-dependent pathway
inferred← citeshttps://doi.org/10.1080/19390211.2017.1350248openalex-snapshot
Altered Potassium Ion Channel Function as a Possible Mechanism of Increased Blood Pressure in Rats Fed Thermally Oxidized Palm Oil Diets
inferred← citeshttps://doi.org/10.1089/ars.2008.2263openalex-snapshot
Oxidative Stress and Autophagy in the Regulation of Lysosome-Dependent Neuron Death
inferred← citeshttps://doi.org/10.1089/ars.2009.2929openalex-snapshot
Neuroprotective Multifunctional Iron Chelators: From Redox-Sensitive Process to Novel Therapeutic Opportunities
inferred← citeshttps://doi.org/10.1089/ars.2011.4082openalex-snapshot
Alzheimer's Disease: Redox Dysregulation As a Common Denominator for Diverse Pathogenic Mechanisms
inferred← citeshttps://doi.org/10.1111/bph.13318openalex-snapshot
Neuroprotective effects of multifaceted hybrid agents targeting MAO, cholinesterase, iron and β‐amyloid in ageing and Alzheimer's disease
inferred← citeshttps://doi.org/10.1111/cns.13050openalex-snapshot
Early compensatory responses against neuronal injury: A new therapeutic window of opportunity for Alzheimer's Disease?
inferred← citeshttps://doi.org/10.1111/cns.70634openalex-snapshot
Integrated Multi‐Omics Analysis and Cross‐Model Validation Reveal Mitochondrial Signatures in Alzheimer's Disease
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17β‐Oestradiol Stimulation of G‐Proteins in Aged and Alzheimer’s Human Brain: Comparison with Phytoestrogens
inferred← citeshttps://doi.org/10.1111/j.1440-1789.2008.00901.xopenalex-snapshot
Redox active iron accumulation in aceruloplasminemia
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Genetic basis of Alzheimer's dementia: role of mtDNA mutations
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Simultaneous Manipulation of Multiple Brain Targets by Green Tea Catechins: A Potential Neuroprotective Strategy for Alzheimer and Parkinson Diseases
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Pharmacological and Clinical Aspects of Heme Oxygenase
inferred← citeshttps://doi.org/10.1152/ajpcell.00193.2006openalex-snapshot
Building the power house: recent advances in mitochondrial studies through proteomics and systems biology
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/10.1159/000129365openalex-snapshot
Metal Concentrations in Plasma and Cerebrospinal Fluid in Patients with Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1177/1073858408325269openalex-snapshot
Neurotrophic Support and Oxidative Stress: Converging Effects in the Normal and Diseased Nervous System
inferred← citeshttps://doi.org/10.1186/1471-2202-9-s2-s2openalex-snapshot
Physiological and pathological aspects of Aβ in iron homeostasis via 5'UTR in the APP mRNA and the therapeutic use of iron-chelators
inferred← citeshttps://doi.org/10.1186/1750-1326-4-32openalex-snapshot
Ectopic localization of FOXO3a protein in Lewy bodies in Lewy body dementia and Parkinson's disease
inferred← citeshttps://doi.org/10.1371/journal.pone.0114174openalex-snapshot
β-Amyloid Precursor Protein Does Not Possess Ferroxidase Activity but Does Stabilize the Cell Surface Ferrous Iron Exporter Ferroportin
inferred← citeshttps://doi.org/10.21474/ijar01/6024openalex-snapshot
A REVIEW ARTICLE ON THE FORMATION, MECHANISM AND BIOCHEMISTRY OF MDA AND MDA AS A BIOMARKER OF OXIDATIVE STRESS.
inferred← citeshttps://doi.org/10.2174/15672050113106660179openalex-snapshot
The Effects of Different Antioxidants on the Activity of Cerebrocortical MnSOD and Na,K-ATPase from post mortem Alzheimer’s Disease and Age-matched Normal Brains
inferred← citeshttps://doi.org/10.2174/156720506778249399openalex-snapshot
Role of Metals in Neuronal Apoptosis: Challenges Associated with Neurodegeneration
inferred← citeshttps://doi.org/10.2217/14796708.2.3.265openalex-snapshot
Nanoparticles: A Step Forward for Iron Chelation in the Brain
inferred← citeshttps://doi.org/10.2298/mpns1208301jopenalex-snapshot
Mechanisms of neurodegeneration in Alzheimer’s disease
inferred← citeshttps://doi.org/10.2310/7290.2009.00017openalex-snapshot
Impact of Magnetic Labeling on Human and Mouse Stem Cells and Their Long-Term Magnetic Resonance Tracking in a Rat Model of Parkinson Disease
inferred← citeshttps://doi.org/10.2741/2132openalex-snapshot
Mitochondrial dysfunction in human pathologies
inferred← citeshttps://doi.org/10.31032/ijbpas/2019/8.4.4696openalex-snapshot
DIFFERENTIAL EXPRESSION AND SPECIFICITY OF MMP-9, MDA AND 8-OHdG IN NEWLY DIAGNOSED SCHIZOPHRENICS
inferred← citeshttps://doi.org/10.31032/ijbpas/2019/8.6.4728openalex-snapshot
ADAPTED HEIGHTS OF MARKERS FOR OXIDATIVE TRAUMA CAUSED BY LEAD TOXICITY ARE IMPERATIVE IN VERDICT AND FORECAST OF ANEMIA
inferred← citeshttps://doi.org/10.3233/jad-179927openalex-snapshot
Dementia Research: Populations, Progress, Problems, and Predictions
inferred← citeshttps://doi.org/10.3233/jad-2012-121528openalex-snapshot
Oxidative Stress in Alzheimer's Disease and Mild Cognitive Impairment with High Sensitivity and Specificity
inferred← citeshttps://doi.org/10.3389/ebm.2024.10185openalex-snapshot
Reversal of atherosclerosis by restoration of vascular copper homeostasis
inferred← citeshttps://doi.org/10.3389/fnmol.2019.00007openalex-snapshot
Noradrenaline Acting on Alpha1 Adrenoceptor as well as by Chelating Iron Reduces Oxidative Burden on the Brain: Implications With Rapid Eye Movement Sleep
inferred← citeshttps://doi.org/10.3390/antiox10091483openalex-snapshot
Melatonin: Regulation of Biomolecular Condensates in Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.3390/cells12050763openalex-snapshot
The Neuroprotective Activities of the Novel Multi-Target Iron-Chelators in Models of Alzheimer’s Disease, Amyotrophic Lateral Sclerosis and Aging
inferred← citeshttps://doi.org/10.3390/met5042070openalex-snapshot
Iron, Aging, and Neurodegeneration
inferred← citeshttps://doi.org/10.5812/archneurosci.20078openalex-snapshot
Oxidative Stress Gated by Fenton and Haber Weiss Reactions and Its Association With Alzheimer’s Disease
inferred← citeshttps://doi.org/10.70675/449f1d52z9b40z487cza9cczb4edaf3b75f1openalex-snapshot
Development of copper ligands for therepeutic applications
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