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Oxidative Stress and Neurotoxicity
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inferredcites →https://doi.org/10.1002/(sici)1097-4547(19981201)54:5<691::aid-jnr14>3.0.co;2-fopenalex-snapshot
Dopamine, in the presence of tyrosinase, covalently modifies and inactivates tyrosine hydroxylase
inferredcites →https://doi.org/10.1002/ana.10483openalex-snapshot
Oxidative stress in Parkinson's disease
inferredcites →https://doi.org/10.1002/ana.10512openalex-snapshot
Proteolytic stress: A unifying concept for the etiopathogenesis of Parkinson's disease
inferredcites →https://doi.org/10.1002/ana.410310310openalex-snapshot
Selective accumulation of aluminum and iron in the neurofibrillary tangles of Alzheimer's disease: A laser microprobe (LAMMA) study
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/ana.410440518openalex-snapshot
Protein modification by the lipid peroxidation product 4‐hydroxynonenal in the spinal cords of amyotrophic lateral sclerosis patients
inferredcites →https://doi.org/10.1002/cne.21160openalex-snapshot
Motor neuron degeneration in amyotrophic lateral sclerosis mutant superoxide dismutase‐1 transgenic mice: Mechanisms of mitochondriopathy and cell death
inferredcites →https://doi.org/10.1002/humu.20336openalex-snapshot
Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40
inferredcites →https://doi.org/10.1002/jcb.21110openalex-snapshot
Differential regulation of cyclooxygenase‐2 and inducible nitric oxide synthase by 4‐hydroxynonenal in human osteoarthritic chondrocytes through ATF‐2/CREB‐1 transactivation and concomitant inhibition of NF‐κB signaling cascade
inferredcites →https://doi.org/10.1002/jnr.20587openalex-snapshot
Elevated protein carbonylation in the brain white matter and gray matter of patients with multiple sclerosis
inferredcites →https://doi.org/10.1002/mas.20006openalex-snapshot
Proteins as biomarkers of oxidative/nitrosative stress in diseases: The contribution of redox proteomics
inferredcites →https://doi.org/10.1002/mds.21013openalex-snapshot
Ubiquitin–proteasome system and Parkinson's disease
inferredcites →https://doi.org/10.1002/psc.626openalex-snapshot
Methionine regulates copper/hydrogen peroxide oxidation products of Aβ
inferredcites →https://doi.org/10.1006/abbi.1999.1404openalex-snapshot
Increased Neuronal Glucose-6-phosphate Dehydrogenase and Sulfhydryl Levels Indicate Reductive Compensation to Oxidative Stress in Alzheimer Disease
inferredcites →https://doi.org/10.1006/exnr.1997.6750openalex-snapshot
Increased Peroxidation and Reduced Antioxidant Enzyme Activity in Alzheimer's Disease
inferredcites →https://doi.org/10.1006/exnr.2002.8050openalex-snapshot
Altered Proteasomal Function in Sporadic Parkinson's Disease
inferredcites →https://doi.org/10.1006/nbdi.2002.0466openalex-snapshot
Systemic Increase of Oxidative Nucleic Acid Damage in Parkinson's Disease and Multiple System Atrophy
inferredcites →https://doi.org/10.1007/0-387-23226-5_3openalex-snapshot
Oxidative stress in Alzheimer’s Disease: Implications for Prevention and Therapy
inferredcites →https://doi.org/10.1007/978-3-211-33328-0_22openalex-snapshot
Iron dyshomeostasis in Parkinson’s disease
inferredcites →https://doi.org/10.1007/978-3-211-45295-0_32openalex-snapshot
Parkin and defective ubiquitination in Parkinson’s disease
inferredcites →https://doi.org/10.1007/978-3-211-45295-0_42openalex-snapshot
Controversies on new animal models of Parkinson’s disease Pro and Con: the rotenone model of Parkinson’s disease (PD)
inferredcites →https://doi.org/10.1007/978-3-7091-6301-6_27openalex-snapshot
Glutamate excitotoxicity — a mechanism for axonal damage and oligodendrocyte death in Multiple Sclerosis?
inferredcites →https://doi.org/10.1007/bf00309621openalex-snapshot
Extracellular neurofibrillary tangles reflect neuronal loss and provide further evidence of extensive protein cross-linking in Alzheimer disease
inferredcites →https://doi.org/10.1007/bf01289410openalex-snapshot
How superoxide radical damages the cell
inferredcites →https://doi.org/10.1007/bf02854904openalex-snapshot
Causes and consequences of methamphetamine and MDMA toxicity
inferredcites →https://doi.org/10.1007/s000110050480openalex-snapshot
The activation of protein kinase C induces higher production of reactive oxygen species by mononuclear cells in patients with multiple sclerosis than in controls
inferredcites →https://doi.org/10.1007/s00415-004-0348-9openalex-snapshot
The role of oxidative stress in the pathogenesis of multiple sclerosis: The need for effective antioxidant therapy
inferredcites →https://doi.org/10.1007/s00415-005-0037-3openalex-snapshot
Oxidative stress in serum and peripheral blood leukocytes in patients with different disease courses of multiple sclerosis
inferredcites →https://doi.org/10.1007/s004150050399openalex-snapshot
Nonenzymatic antioxidants of blood in multiple sclerosis
inferredcites →https://doi.org/10.1007/s00702-001-0683-2openalex-snapshot
Dopamine efflux by MPTP and hydroxyl radical generation
inferredcites →https://doi.org/10.1007/s00702-004-0201-4openalex-snapshot
Huntington?s disease: pathomechanism and therapeutic perspectives
inferredcites →https://doi.org/10.1007/s00702-006-0492-8openalex-snapshot
Carboxyl-terminal fragment of amyloid precursor protein and hydrogen peroxide induce neuronal cell death through different pathways
inferredcites →https://doi.org/10.1007/s00726-003-0011-2openalex-snapshot
Free radical-mediated oxidation of free amino acids and amino acid residues in proteins
inferredcites →https://doi.org/10.1007/s00726-003-0018-8openalex-snapshot
Peroxynitrite reactivity with amino acids and proteins
inferredcites →https://doi.org/10.1007/s11064-005-2449-yopenalex-snapshot
Role of ERK in Hydrogen Peroxide-Induced Cell Death of Human Glioma Cells
inferredcites →https://doi.org/10.1007/s11064-006-9110-2openalex-snapshot
Oxidative Stress in Skin Fibroblasts Cultures of Patients with Huntington’s Disease
inferredcites →https://doi.org/10.1007/s11064-006-9239-zopenalex-snapshot
Enzyme-Catalyzed Side Reactions with Molecular Oxygen may Contribute to Cell Signaling and Neurodegenerative Diseases
inferredcites →https://doi.org/10.1016/0006-8993(96)00729-9openalex-snapshot
Glycoxidation and oxidative stress in Parkinson disease and diffuse Lewy body disease
inferredcites →https://doi.org/10.1016/0014-5793(94)00650-4openalex-snapshot
Alzheimer paired helical filaments Restoration of the biological activity by dephosphorylation
inferredcites →https://doi.org/10.1016/0166-2236(95)93897-7openalex-snapshot
Radical AGEing in Alzheimer's disease
inferredcites →https://doi.org/10.1016/0378-4274(89)90168-9openalex-snapshot
Biochemical mechanism of action of the dopaminergic neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)
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.arr.2004.01.002openalex-snapshot
Contribution of redox-active iron and copper to oxidative damage in Alzheimer disease
inferredcites →https://doi.org/10.1016/j.arr.2004.01.003openalex-snapshot
Does cellular iron dysregulation play a causative role in Parkinson’s disease?
inferredcites →https://doi.org/10.1016/j.arr.2004.02.001openalex-snapshot
Brain iron deposition and the free radical-mitochondrial theory of ageing
inferredcites →https://doi.org/10.1016/j.bbadis.2004.06.017openalex-snapshot
Tau phosphorylation: physiological and pathological consequences
inferredcites →https://doi.org/10.1016/j.bbadis.2004.06.019openalex-snapshot
Can tau filaments be both physiologically beneficial and toxic?
inferredcites →https://doi.org/10.1016/j.bbadis.2004.09.008openalex-snapshot
Tau pathology in Alzheimer disease and other tauopathies
inferredcites →https://doi.org/10.1016/j.bbadis.2006.03.008openalex-snapshot
Oxidative stress in ALS: A mechanism of neurodegeneration and a therapeutic target
inferredcites →https://doi.org/10.1016/j.bbadis.2006.05.004openalex-snapshot
Structure, folding, and misfolding of Cu,Zn superoxide dismutase in amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1016/j.bbadis.2006.06.006openalex-snapshot
Failure of protein quality control in amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1016/j.bbadis.2006.10.014openalex-snapshot
Alzheimer disease, the two-hit hypothesis: An update
inferredcites →https://doi.org/10.1016/j.bbapap.2004.08.007openalex-snapshot
The oxidative environment and protein damage
inferredcites →https://doi.org/10.1016/j.bbapap.2004.08.010openalex-snapshot
Methionine oxidation and aging
inferredcites →https://doi.org/10.1016/j.bbapap.2004.10.008openalex-snapshot
Methionine oxidation, α-synuclein and Parkinson's disease
inferredcites →https://doi.org/10.1016/j.bbrc.2006.01.136openalex-snapshot
Oxidative stress promotes mutant huntingtin aggregation and mutant huntingtin-dependent cell death by mimicking proteasomal malfunction
inferredcites →https://doi.org/10.1016/j.bcp.2005.08.022openalex-snapshot
Mitochondria-targeted peptide prevents mitochondrial depolarization and apoptosis induced by tert-butyl hydroperoxide in neuronal cell lines
inferredcites →https://doi.org/10.1016/j.brainres.2004.01.012openalex-snapshot
Oxidative stress signalling in Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.brainresbull.2003.08.011openalex-snapshot
Hydrogen peroxide induces apoptosis in cerebral vascular smooth muscle cells: possible relation to neurodegenerative diseases and strokes
inferredcites →https://doi.org/10.1016/j.cbpa.2006.02.034openalex-snapshot
Pathogenic superoxide dismutase structure, folding, aggregation and turnover
inferredcites →https://doi.org/10.1016/j.cbpa.2007.01.678openalex-snapshot
Copper and Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.chemphyslip.2003.10.010openalex-snapshot
Isoprostanes and related products of lipid peroxidation in neurodegenerative diseases
inferredcites →https://doi.org/10.1016/j.ejphar.2006.06.026openalex-snapshot
Oxidative stress in Alzheimer's disease brain: New insights from redox proteomics
inferredcites →https://doi.org/10.1016/j.expneurol.2006.04.024openalex-snapshot
Emerging evidence for the neuroprotective role of α-synuclein
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.06.012openalex-snapshot
Reactions of 4-hydroxynonenal with proteins and cellular targets
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.2004.11.005openalex-snapshot
Alzheimer-specific epitopes of tau represent lipid peroxidation-induced conformations
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2005.07.021openalex-snapshot
Biliverdin reductase, a major physiologic cytoprotectant, suppresses experimental autoimmune encephalomyelitis
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2006.12.004openalex-snapshot
Molecular mechanisms of 6-hydroxydopamine-induced cytotoxicity in PC12 cells: Involvement of hydrogen peroxide-dependent and -independent action
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2007.01.003openalex-snapshot
The oxidative stress mediator 4-hydroxynonenal is an intracellular agonist of the nuclear receptor peroxisome proliferator-activated receptor-β/δ (PPARβ/δ)
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2007.02.004openalex-snapshot
Increased affinity for copper mediated by cysteine 111 in forms of mutant superoxide dismutase 1 linked to amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1016/j.ijdevneu.2004.07.013openalex-snapshot
Amyloid‐induced neurofibrillary tangle formation in Alzheimer's disease: insight from transgenic mouse and tissue‐culture models
inferredcites →https://doi.org/10.1016/j.jmb.2006.12.041openalex-snapshot
Structural Studies of the Alzheimer’s Amyloid Precursor Protein Copper-binding Domain Reveal How it Binds Copper Ions
inferredcites →https://doi.org/10.1016/j.jneuroim.2003.11.021openalex-snapshot
α-Lipoic acid is effective in prevention and treatment of experimental autoimmune encephalomyelitis
inferredcites →https://doi.org/10.1016/j.lfs.2005.04.043openalex-snapshot
Blockade of 5-HT3 receptor with MDL7222 and Y25130 reduces hydrogen peroxide-induced neurotoxicity in cultured rat cortical cells
inferredcites →https://doi.org/10.1016/j.molcel.2007.03.016openalex-snapshot
Hydrogen Peroxide Sensing and Signaling
inferredcites →https://doi.org/10.1016/j.molmed.2006.09.007openalex-snapshot
Understanding the molecular causes of Parkinson's disease
inferredcites →https://doi.org/10.1016/j.nbd.2004.03.014openalex-snapshot
On the neurotoxicity mechanism of leukoaminochrome o-semiquinone radical derived from dopamine oxidation: mitochondria damage, necrosis, and hydroxyl radical formation
inferredcites →https://doi.org/10.1016/j.nbd.2005.06.017openalex-snapshot
Increased expression and function of glutamate transporters in multiple sclerosis
inferredcites →https://doi.org/10.1016/j.neuint.2005.12.018openalex-snapshot
Lipid peroxidation associated cardiolipin loss and membrane depolarization in rat brain mitochondria
inferredcites →https://doi.org/10.1016/j.neulet.2006.12.044openalex-snapshot
Elevated cerebrospinal fluid F2-isoprostane levels indicating oxidative stress in healthy siblings of multiple sclerosis patients
inferredcites →https://doi.org/10.1016/j.neuro.2006.05.006openalex-snapshot
Effects of inhaled manganese on biomarkers of oxidative stress in the rat brain
inferredcites →https://doi.org/10.1016/j.neuro.2007.02.013openalex-snapshot
Gene expression profiling of MPP+-treated MN9D cells: A mechanism of toxicity study
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.02.019openalex-snapshot
Free radical-mediated neurotoxicity may be caused by inhibition of mitochondrial dehydrogenases in vitro and in vivo
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.10.056openalex-snapshot
Oxidative stress and mitochondrial dysfunction in neurodegenerative diseases
inferredcites →https://doi.org/10.1016/j.pbb.2003.10.016openalex-snapshot
Behavioral effects of manganese injected in the rat substantia nigra are potentiated by dicumarol, a DT-diaphorase inhibitor
inferredcites →https://doi.org/10.1016/j.pnpbp.2004.12.007openalex-snapshot
Mitochondrial aging and dysfunction in Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.tins.2004.01.007openalex-snapshot
More than just two peas in a pod: common amyloidogenic properties of tau and α-synuclein in neurodegenerative diseases
inferredcites →https://doi.org/10.1016/s0002-9440(10)65396-5openalex-snapshot
Parkinson's Disease Is Associated with Oxidative Damage to Cytoplasmic DNA and RNA in Substantia Nigra Neurons
inferredcites →https://doi.org/10.1016/s0005-2728(98)00165-0openalex-snapshot
Mitochondrial involvement in Alzheimer’s disease
inferredcites →https://doi.org/10.1016/s0006-291x(87)80183-3openalex-snapshot
Model study on the bioreduction of paraquat, MPP+, and analogs. Evidence against a “redox cycling” mechanism in MPTP neurotoxicity
inferredcites →https://doi.org/10.1016/s0006-2952(97)00062-2openalex-snapshot
Reactive oxygen species and Alzheimer's disease
inferredcites →https://doi.org/10.1016/s0006-8993(00)02215-0openalex-snapshot
Overexpression of human α-synuclein causes dopamine neuron death in rat primary culture and immortalized mesencephalon-derived cells
inferredcites →https://doi.org/10.1016/s0006-8993(98)00002-xopenalex-snapshot
Abnormal localization of iron regulatory protein in Alzheimer's disease
inferredcites →https://doi.org/10.1016/s0006-8993(99)01415-8openalex-snapshot
An immunochemical study on tau glycation in paired helical filaments
inferredcites →https://doi.org/10.1016/s0014-5793(00)02323-1openalex-snapshot
Phosphorylated, but not native, tau protein assembles following reaction with the lipid peroxidation product, 4‐hydroxy‐2‐nonenal
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/s0021-9258(19)84109-1openalex-snapshot
Mitochondrial Protein Nitration Primes Neurodegeneration in Experimental Autoimmune Encephalomyelitis
inferredcites →https://doi.org/10.1016/s0022-510x(00)00343-9openalex-snapshot
Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis
inferredcites →https://doi.org/10.1016/s0022-510x(98)00042-2openalex-snapshot
Histochemical detection of 4-hydroxynonenal protein in Alzheimer amyloid
inferredcites →https://doi.org/10.1016/s0022-510x(98)00092-6openalex-snapshot
Copper, iron and zinc in Alzheimer's disease senile plaques
inferredcites →https://doi.org/10.1016/s0076-6879(99)00117-2openalex-snapshot
Modification of proteins and lipids by myeloperoxidase
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/s0092-8674(00)81107-1openalex-snapshot
Multiple Sclerosis: A Coordinated Immunological Attack against Myelin in the Central Nervous System
inferredcites →https://doi.org/10.1016/s0098-2997(03)00009-8openalex-snapshot
Basic aspects of the biochemical reactivity of 4-hydroxynonenal
inferredcites →https://doi.org/10.1016/s0140-6736(04)16901-8openalex-snapshot
Pathogenetic mechanisms of parkin in Parkinson's disease
inferredcites →https://doi.org/10.1016/s0163-7827(03)00014-6openalex-snapshot
4-Hydroxy-2-nonenal: a product and mediator of oxidative stress
inferredcites →https://doi.org/10.1016/s0165-5728(98)00175-1openalex-snapshot
Reactive oxygen species are required for the phagocytosis of myelin by macrophages
inferredcites →https://doi.org/10.1016/s0301-0082(01)00003-xopenalex-snapshot
Molecular pathways involved in the neurotoxicity of 6-OHDA, dopamine and MPTP: contribution to the apoptotic theory in Parkinson's disease
inferredcites →https://doi.org/10.1016/s0304-3940(01)02514-9openalex-snapshot
Hydroxynonenal adducts indicate a role for lipid peroxidation in neocortical and brainstem Lewy bodies in humans
inferredcites →https://doi.org/10.1016/s0304-3940(98)00469-8openalex-snapshot
Oxidative stress and overexpression of manganese superoxide dismutase in patients with Alzheimer's disease
inferredcites →https://doi.org/10.1016/s0304-3940(99)00178-0openalex-snapshot
Frequent coexistence of Lewy bodies and neurofibrillary tangles in the same neurons of patients with diffuse Lewy body disease
inferredcites →https://doi.org/10.1016/s0378-4274(02)00076-0openalex-snapshot
Role of hydroxyl radical formation in neurotoxicity as revealed by in vivo free radical trapping
inferredcites →https://doi.org/10.1016/s0891-5849(00)00158-1openalex-snapshot
How important is oxidative damage? Lessons from Alzheimer’s disease
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(01)00570-6openalex-snapshot
Active glycation in neurofibrillary pathology of Alzheimer disease: Nε-(Carboxymethyl) lysine and hexitol-lysine
inferredcites →https://doi.org/10.1016/s0891-5849(03)00042-xopenalex-snapshot
Reduction of inclusion body pathology in ApoE-deficient mice fed a combination of antioxidants
inferredcites →https://doi.org/10.1016/s0891-5849(98)00293-7openalex-snapshot
Neuroinflammatory processes are important in neurodegenerative diseases: an hypothesis to explain the increased formation of reactive oxygen and nitrogen species as major factors involved in neurodegenerative disease development
inferredcites →https://doi.org/10.1016/s0925-4439(00)00041-7openalex-snapshot
Cellular cofactors potentiating induction of stress and cytotoxicity by amyloid β-peptide
inferredcites →https://doi.org/10.1016/s1050-1738(01)00094-9openalex-snapshot
Oxidative DNA Damage and Cardiovascular Disease
inferredcites →https://doi.org/10.1016/s1367-5931(99)80035-0openalex-snapshot
Redox metals and neu rodegenerative disease
inferredcites →https://doi.org/10.1016/s1388-1981(01)00100-7openalex-snapshot
Aldehydic lipid peroxidation products derived from linoleic acid
inferredcites →https://doi.org/10.1021/ar0500766openalex-snapshot
Small Molecule Oxidation Products Trigger Disease-Associated Protein Misfolding
inferredcites →https://doi.org/10.1021/bi0272151openalex-snapshot
Metal Binding and Oxidation of Amyloid-β within Isolated Senile Plaque Cores: Raman Microscopic Evidence
inferredcites →https://doi.org/10.1021/bi7000246openalex-snapshot
The Impact of the E46K Mutation on the Properties of α-Synuclein in Its Monomeric and Oligomeric States
inferredcites →https://doi.org/10.1021/bi980022mopenalex-snapshot
Copper-Binding Amyloid Precursor Protein Undergoes a Site-Specific Fragmentation in the Reduction of Hydrogen Peroxide
inferredcites →https://doi.org/10.1021/bi990438fopenalex-snapshot
The Aβ Peptide of Alzheimer's Disease Directly Produces Hydrogen Peroxide through Metal Ion Reduction
inferredcites →https://doi.org/10.1021/ja0288800openalex-snapshot
Site-Specific Synthesis and Reactivity of Oligonucleotides Containing Stereochemically Defined 1,N2-Deoxyguanosine Adducts of the Lipid Peroxidation Product trans-4-Hydroxynonenal
inferredcites →https://doi.org/10.1021/ja036733bopenalex-snapshot
Free Radical Reactions of Methionine in Peptides: Mechanisms Relevant to β-Amyloid Oxidation and Alzheimer's Disease
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/10.1021/jm00006a010openalex-snapshot
Generation of the Neurotoxin 6-Hydroxydopamine by Peroxidase/H2O2 Oxidation of Dopamine
inferredcites →https://doi.org/10.1021/jm970099topenalex-snapshot
Iron-Mediated Generation of the Neurotoxin 6-Hydroxydopamine Quinone by Reaction of Fatty Acid Hydroperoxides with Dopamine: A Possible Contributory Mechanism for Neuronal Degeneration in Parkinson's Disease
inferredcites →https://doi.org/10.1021/ol034729zopenalex-snapshot
Total Syntheses of Bioactive Oxidized Ethanolamine Phospholipids
inferredcites →https://doi.org/10.1021/tx000101aopenalex-snapshot
Characterization of 4-Oxo-2-nonenal as a Novel Product of Lipid Peroxidation
inferredcites →https://doi.org/10.1021/tx0101550openalex-snapshot
Redox Properties of Met35in Neurotoxic β-Amyloid Peptide. A Molecular Modeling Study
inferredcites →https://doi.org/10.1021/tx034248oopenalex-snapshot
Induction of Apoptosis in Colorectal Carcinoma Cells Treated with 4-Hydroxy-2-nonenal and Structurally Related Aldehydic Products of Lipid Peroxidation
inferredcites →https://doi.org/10.1021/tx0497144openalex-snapshot
Dopamine-Dependent Iron Toxicity in Cells Derived from Rat Hypothalamus
inferredcites →https://doi.org/10.1021/tx050080qopenalex-snapshot
4-Oxo-2-nonenal Is Both More Neurotoxic and More Protein Reactive than 4-Hydroxy-2-nonenal
inferredcites →https://doi.org/10.1021/tx050211nopenalex-snapshot
Alterations in Gene Expression Induced by the Lipid Peroxidation Product, 4-Hydroxy-2-nonenal
inferredcites →https://doi.org/10.1021/tx0502903openalex-snapshot
Detection and Quantification of Endogenous Cyclic DNA Adducts Derived from trans-4-Hydroxy-2-nonenal in Human Brain Tissue by Isotope Dilution Capillary Liquid Chromatography Nanoelectrospray Tandem Mass Spectrometry
inferredcites →https://doi.org/10.1021/tx050321uopenalex-snapshot
Endogenous Reactive Intermediates as Modulators of Cell Signaling and Cell Death
inferredcites →https://doi.org/10.1021/tx0600503openalex-snapshot
Translesion DNA Synthesis across the Heptanone−Etheno-2‘-Deoxycytidine Adduct in Cells
inferredcites →https://doi.org/10.1021/tx600270fopenalex-snapshot
Chemical Nature of Stochastic Generation of Protein-based Carbonyls: Metal-catalyzed Oxidation versus Modification by Products of Lipid Oxidation
inferredcites →https://doi.org/10.1021/tx9501445openalex-snapshot
Oxidative Damage and Tyrosine Nitration from Peroxynitrite
inferredcites →https://doi.org/10.1021/tx970100ropenalex-snapshot
Synthesis and 32P-Postlabeling/High-Performance Liquid Chromatography Separation of Diastereomeric 1,N2-(1,3-Propano)-2‘-deoxyguanosine 3‘-Phosphate Adducts Formed from 4-Hydroxy-2-nonenal
inferredcites →https://doi.org/10.1023/a:1007604414773openalex-snapshot
NO Synthase and NO-Dependent Signal Pathways in Brain Aging and Neurodegenerative Disorders: The Role of Oxidant/Antioxidant Balance
inferredcites →https://doi.org/10.1023/a:1007608615682openalex-snapshot
Isoprostanes, Novel Markers of Oxidative Injury, Help Understanding the Pathogenesis of Neurodegenerative Diseases
inferredcites →https://doi.org/10.1023/b:jobb.0000041772.74810.92openalex-snapshot
Mitochondrial Dysfunction and Oxidative Damage in Alzheimer's and Parkinson's Diseases and Coenzyme Q10 as a Potential Treatment
inferredcites →https://doi.org/10.1038/399a040openalex-snapshot
Progress in determining the causes and treatment of multiple sclerosis
inferredcites →https://doi.org/10.1038/71555openalex-snapshot
Glutamate excitotoxicity in a model of multiple sclerosis
inferredcites →https://doi.org/10.1038/nature05292openalex-snapshot
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
inferredcites →https://doi.org/10.1038/nm1314openalex-snapshot
Dopamine covalently modifies and functionally inactivates parkin
inferredcites →https://doi.org/10.1038/nn823openalex-snapshot
Mutant SOD1 causes motor neuron disease independent of copper chaperone–mediated copper loading
inferredcites →https://doi.org/10.1038/nrn1434openalex-snapshot
Oxidative stress in neurodegeneration: cause or consequence?
inferredcites →https://doi.org/10.1038/sj.jcbfm.9600119openalex-snapshot
SOD1 Overexpression and Female Sex Exhibit Region-Specific Neuroprotection after Global Cerebral Ischemia Due to Cardiac Arrest
inferredcites →https://doi.org/10.1042/bj3400821openalex-snapshot
Copper(II)-induced self-oligomerization of α-synuclein
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.1471-4159.1997.69031326.xopenalex-snapshot
A Generalised Increase in Protein Carbonyls in the Brain in Parkinson's but Not Incidental Lewy Body Disease
inferredcites →https://doi.org/10.1046/j.1471-4159.1997.69052064.xopenalex-snapshot
Evidence of Increased Oxidative Damage in Both Sporadic and Familial Amyotrophic Lateral Sclerosis
inferredcites →https://doi.org/10.1046/j.1471-4159.1998.70010268.xopenalex-snapshot
Increased Protein Oxidation in Human Substantia Nigra Pars Compacta in Comparison with Basal Ganglia and Prefrontal Cortex Measured with an Improved Dinitrophenylhydrazine Assay
inferredcites →https://doi.org/10.1046/j.1471-4159.1998.71052034.xopenalex-snapshot
Increased Nuclear DNA Oxidation in the Brain in Alzheimer's Disease
inferredcites →https://doi.org/10.1046/j.1471-4159.1998.71062465.xopenalex-snapshot
New Phosphorylation Sites Identified in Hyperphosphorylated Tau (Paired Helical Filament‐Tau) from Alzheimer's Disease Brain Using Nanoelectrospray Mass Spectrometry
inferredcites →https://doi.org/10.1046/j.1471-4159.1999.0720751.xopenalex-snapshot
Protein‐Bound Acrolein
inferredcites →https://doi.org/10.1046/j.1471-4159.1999.0720771.xopenalex-snapshot
Increased DNA Oxidation and Decreased Levels of Repair Products in Alzheimer's Disease Ventricular CSF
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/10.1046/j.1471-4159.2000.0742296.xopenalex-snapshot
Dopamine‐Induced Apoptosis Is Mediated by Oxidative Stress and Is Enhanced by Cyanide in Differentiated PC12 Cells
inferredcites →https://doi.org/10.1046/j.1471-4159.2000.0751219.xopenalex-snapshot
Characterization of Copper Interactions with Alzheimer Amyloid β Peptides
inferredcites →https://doi.org/10.1046/j.1471-4159.2001.00125.xopenalex-snapshot
Reaction of oxidized dopamine with endogenous cysteine residues in the human dopamine transporter
inferredcites →https://doi.org/10.1046/j.1471-4159.2001.00149.xopenalex-snapshot
Effect of the overexpression of wild‐type or mutant α‐synuclein on cell susceptibility to insult
inferredcites →https://doi.org/10.1046/j.1471-4159.2001.00243.xopenalex-snapshot
Copper neurotoxicity is dependent on dopamine‐mediated copper uptake and one‐electron reduction of aminochrome in a rat substantia nigra neuronal cell line
inferredcites →https://doi.org/10.1046/j.1471-4159.2003.01642.xopenalex-snapshot
Proteasome inhibition by paired helical filament‐tau in brains of patients with Alzheimer's disease
inferredcites →https://doi.org/10.1073/pnas.0601696103openalex-snapshot
Folding of Cu/Zn superoxide dismutase suggests structural hotspots for gain of neurotoxic function in ALS: Parallels to precursors in amyloid disease
inferredcites →https://doi.org/10.1073/pnas.0610923104openalex-snapshot
Overexpression of CCS in G93A-SOD1 mice leads to accelerated neurological deficits with severe mitochondrial pathology
inferredcites →https://doi.org/10.1073/pnas.0730423100openalex-snapshot
Misfolded CuZnSOD and amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1073/pnas.91.11.4766openalex-snapshot
Advanced glycation end products contribute to amyloidosis in Alzheimer disease.
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/10.1073/pnas.91.16.7787openalex-snapshot
Glycated tau protein in Alzheimer disease: a mechanism for induction of oxidant stress.
inferredcites →https://doi.org/10.1073/pnas.93.7.2696openalex-snapshot
Immunohistochemical detection of 4-hydroxynonenal protein adducts in Parkinson disease.
inferredcites →https://doi.org/10.1073/pnas.94.18.9866openalex-snapshot
Iron accumulation in Alzheimer disease is a source of redox-generated free radicals
inferredcites →https://doi.org/10.1074/jbc.272.21.13597openalex-snapshot
Structural Identification by Mass Spectrometry of Oxidized Phospholipids in Minimally Oxidized Low Density Lipoprotein That Induce Monocyte/Endothelial Interactions and Evidence for Their Presence in Vivo
inferredcites →https://doi.org/10.1074/jbc.272.33.20313openalex-snapshot
Protein Oxidation in Aging, Disease, and Oxidative Stress
inferredcites →https://doi.org/10.1074/jbc.273.21.12817openalex-snapshot
Dramatic Aggregation of Alzheimer Aβ by Cu(II) Is Induced by Conditions Representing Physiological Acidosis
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.274.41.28849openalex-snapshot
Role of Cytochrome c as a Stimulator of α-Synuclein Aggregation in Lewy Body Disease
inferredcites →https://doi.org/10.1074/jbc.274.52.37111openalex-snapshot
Cu(II) Potentiation of Alzheimer Aβ Neurotoxicity
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/10.1074/jbc.m206428200openalex-snapshot
Metalloenzyme-like Activity of Alzheimer's Disease β-Amyloid
inferredcites →https://doi.org/10.1074/jbc.m300629200openalex-snapshot
Structure of the Alzheimer's Disease Amyloid Precursor Protein Copper Binding Domain
inferredcites →https://doi.org/10.1074/jbc.m405146200openalex-snapshot
α-Synuclein Is Required for the Fibrillar Nature of Ubiquitinated Inclusions Induced by Proteasomal Inhibition in Primary Neurons
inferredcites →https://doi.org/10.1074/jbc.m407410200openalex-snapshot
Clioquinol Mediates Copper Uptake and Counteracts Copper Efflux Activities of the Amyloid Precursor Protein of Alzheimer's Disease
inferredcites →https://doi.org/10.1074/jbc.m408906200openalex-snapshot
Functional Consequences of α-Synuclein Tyrosine Nitration
inferredcites →https://doi.org/10.1074/jbc.m411936200openalex-snapshot
Trolox and 17β-Estradiol Protect against Amyloid β-Peptide Neurotoxicity by a Mechanism That Involves Modulation of the Wnt Signaling Pathway
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inferred← citeshttps://doi.org/10.1007/s00702-022-02462-zopenalex-snapshot
Site-activated multi target iron chelators with acetylcholinesterase (AChE) and monoamine oxidase (MAO) inhibitory activities for Alzheimer’s disease therapy
inferred← citeshttps://doi.org/10.1007/s00706-011-0475-9openalex-snapshot
Iron, cysteine and Parkinson’s disease
inferred← citeshttps://doi.org/10.1007/s00775-009-0600-yopenalex-snapshot
Copper in the brain and Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s00775-016-1376-5openalex-snapshot
Role of N-terminal methionine residues in the redox activity of copper bound to alpha-synuclein
inferred← citeshttps://doi.org/10.1007/s00894-026-06666-yopenalex-snapshot
Theoretical exploration of iseluxine as a promising natural antioxidant
inferred← citeshttps://doi.org/10.1007/s10068-015-0245-2openalex-snapshot
Neuroprotective effect of α-tocopherolhydroquinone against glutamate-induced cytotoxicity in N18-RE-105 cells
inferred← citeshttps://doi.org/10.1007/s10545-015-9863-3openalex-snapshot
Disturbance of redox homeostasis as a contributing underlying pathomechanism of brain and liver alterations in 3‐hydroxy‐3‐methylglutaryl‐CoA lyase deficiency
inferred← citeshttps://doi.org/10.1007/s10571-010-9502-3openalex-snapshot
Neuroprotective Effect of Rosmarinus officinalis Extract on Human Dopaminergic Cell line, SH-SY5Y
inferred← citeshttps://doi.org/10.1007/s10571-011-9713-2openalex-snapshot
Neuroprotective Effects of 2-Cyclopropylimino-3-Methyl-1,3-Thiazoline Hydrochloride Against Oxidative Stress
inferred← citeshttps://doi.org/10.1007/s10895-022-03082-2openalex-snapshot
Connecting the Dots: Macromolecular Crowding and Protein Aggregation
inferred← citeshttps://doi.org/10.1007/s11011-014-9510-yopenalex-snapshot
Serum uric acid level is associated with the prevalence but not with survival of amyotrophic lateral sclerosis in a Chinese population
inferred← citeshttps://doi.org/10.1007/s11011-017-0012-6openalex-snapshot
Multidirectional inhibition of cortico-hippocampal neurodegeneration by kolaviron treatment in rats
inferred← citeshttps://doi.org/10.1007/s11011-017-0028-yopenalex-snapshot
Acute and chronic treatment with quetiapine induces antidepressant-like behavior and exerts antioxidant effects in the rat brain
inferred← citeshttps://doi.org/10.1007/s11011-018-0379-zopenalex-snapshot
Pretreatment with crocin along with treadmill exercise ameliorates motor and memory deficits in hemiparkinsonian rats by anti-inflammatory and antioxidant mechanisms
inferred← citeshttps://doi.org/10.1007/s11011-019-00456-7openalex-snapshot
Disability in multiple sclerosis is associated with age and inflammatory, metabolic and oxidative/nitrosative stress biomarkers: results of multivariate and machine learning procedures
inferred← citeshttps://doi.org/10.1007/s11011-022-00998-3openalex-snapshot
Asiatic acid attenuates aluminium chloride-induced behavioral changes, neuronal loss and astrocyte activation in rats
inferred← citeshttps://doi.org/10.1007/s11033-024-09905-8openalex-snapshot
Exploring the neuroprotective potential of KC14 peptide from Cyprinus carpio against oxidative stress-induced neurodegeneration by regulating antioxidant mechanism
inferred← citeshttps://doi.org/10.1007/s11064-008-9730-9openalex-snapshot
Effects of Acrylamide on the Nervous Tissue Antioxidant System and Sciatic Nerve Electrophysiology in the Rat
inferred← citeshttps://doi.org/10.1007/s11064-009-0035-4openalex-snapshot
Effects of Hydroxysafflor Yellow A in the Attenuation of MPTP Neurotoxicity in Mice
inferred← citeshttps://doi.org/10.1007/s11064-010-0185-4openalex-snapshot
Antioxidant Activity and Protective Effects of Tripterygium regelii Extract on Hydrogen Peroxide-Induced Injury in Human Dopaminergic Cells, SH-SY5Y
inferred← citeshttps://doi.org/10.1007/s11064-010-0293-1openalex-snapshot
Site-Activated Chelators Derived from Anti-Parkinson Drug Rasagiline as a Potential Safer and More Effective Approach to the Treatment of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/s11064-011-0449-7openalex-snapshot
Role of Quercetin on PCBs (Aroclor-1254) Induced Impairment of Dopaminergic Receptor mRNA Expression in Cerebral Cortex of Adult Male Rats
inferred← citeshttps://doi.org/10.1007/s11064-023-03992-yopenalex-snapshot
An Overview of Chemistry, Kinetics, Toxicity and Therapeutic Potential of Boldine in Neurological Disorders
inferred← citeshttps://doi.org/10.1007/s11064-025-04461-4openalex-snapshot
Aluminum Disrupts Motor Function, Cholinergic System, Redox Balance, Pro-Apoptotic and Pro-Inflammatory Pathways in Nauphoeta cinerea Model
inferred← citeshttps://doi.org/10.1007/s11144-017-1286-8openalex-snapshot
Hydrogen atom transfer versus proton coupled electron transfer mechanism of gallic acid with different peroxy radicals
inferred← citeshttps://doi.org/10.1007/s11356-016-8050-xopenalex-snapshot
Possible antioxidant effect of Lycium barbarum polysaccharides on hepatic cadmium-induced oxidative stress in rats
inferred← citeshttps://doi.org/10.1007/s11356-018-3430-zopenalex-snapshot
Acute and chronic toxicity effects of acrylonitrile to the juvenile marine flounder Paralichthys olivaceus
inferred← citeshttps://doi.org/10.1007/s11356-019-06112-yopenalex-snapshot
Manganese attenuates the effects of arsenic on neurobehavioral and biochemical changes in mice co-exposed to arsenic and manganese
inferred← citeshttps://doi.org/10.1007/s11481-012-9358-zopenalex-snapshot
Anti-Inflammatory Effects of Ladostigil and Its Metabolites in Aged Rat Brain and in Microglial Cells
inferred← citeshttps://doi.org/10.1007/s11481-013-9433-0openalex-snapshot
Dose-dependent Effects of Ladostigil on Microglial Activation and Cognition in Aged Rats
inferred← citeshttps://doi.org/10.1007/s12011-026-05320-1openalex-snapshot
Molecular Basis of Ferroptosis and Pyroptosis in Lead-Induced Neurotoxicity: A Narrative Review of Current Evidence and Therapeutic Implications
inferred← citeshttps://doi.org/10.1007/s12031-009-9182-yopenalex-snapshot
Rosmarinic Acid Inhibits 6-OHDA-induced Neurotoxicity by Anti-oxidation in MES23.5 Cells
inferred← citeshttps://doi.org/10.1007/s12031-010-9457-3openalex-snapshot
Inhibition of Axonal Transport Caused by tert-Butyl Hydroperoxide in Cultured Mouse Dorsal Root Ganglion Neurons
inferred← citeshttps://doi.org/10.1007/s12031-011-9693-1openalex-snapshot
Neurorescue Effect of Rosmarinic Acid on 6-Hydroxydopamine-Lesioned Nigral Dopamine Neurons in Rat Model of Parkinson's Disease
inferred← citeshttps://doi.org/10.1007/s12031-021-01829-3openalex-snapshot
Gut Microbiota Composition and Epigenetic Molecular Changes Connected to the Pathogenesis of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1007/s12031-025-02465-xopenalex-snapshot
Subacute Iron Exposure in Rats Induces Behavioral Impairments, Oxidative Stress, and Histopathological Alterations
inferred← citeshttps://doi.org/10.1007/s12035-013-8409-7openalex-snapshot
DNA Repair Mechanisms in Huntington’s Disease
inferred← citeshttps://doi.org/10.1007/s12035-015-9648-6openalex-snapshot
Genetic, Immune-Inflammatory, and Oxidative Stress Biomarkers as Predictors for Disability and Disease Progression in Multiple Sclerosis
inferred← citeshttps://doi.org/10.1007/s12035-016-0277-5openalex-snapshot
Glucocorticoid-Induced Leucine Zipper in Central Nervous System Health and Disease
inferred← citeshttps://doi.org/10.1007/s12035-024-03915-0openalex-snapshot
Significance of Melatonin in the Regulation of Circadian Rhythms and Disease Management
inferred← citeshttps://doi.org/10.1007/s12035-025-05524-xopenalex-snapshot
Modulating NLRP3 Inflammasome Activity and Enhancing Cortical Synaptic Plasticity: Nanoparticulate Hydrogen’s Role in Relief of Post-traumatic Anxiety-like Behaviors in Rats
inferred← citeshttps://doi.org/10.1007/s12192-014-0502-yopenalex-snapshot
Silica nanoparticles induce oxidative stress and inflammation of human peripheral blood mononuclear cells
inferred← citeshttps://doi.org/10.1007/s12640-012-9313-zopenalex-snapshot
Cholinergic Dysfunctions and Enhanced Oxidative Stress in the Neurobehavioral Toxicity of Lambda-Cyhalothrin in Developing Rats
inferred← citeshttps://doi.org/10.1007/s12640-013-9402-7openalex-snapshot
1-Methyl-1,2,3,4-Tetrahydroisoquinoline, an Endogenous Amine with Unexpected Mechanism of Action: New Vistas of Therapeutic Application
inferred← citeshttps://doi.org/10.1007/s12640-015-9528-xopenalex-snapshot
“Boomerang Neuropathology” of Late-Onset Alzheimer’s Disease is Shrouded in Harmful “BDDS”: Breathing, Diet, Drinking, and Sleep During Aging
inferred← citeshttps://doi.org/10.1007/s12640-016-9596-6openalex-snapshot
Enriched Flavonoid Fraction from Cecropia pachystachya Trécul Leaves Exerts Antidepressant-like Behavior and Protects Brain Against Oxidative Stress in Rats Subjected to Chronic Mild Stress
inferred← citeshttps://doi.org/10.1007/s12640-018-9988-xopenalex-snapshot
Hinokitiol Offers Neuroprotection Against 6-OHDA-Induced Toxicity in SH-SY5Y Neuroblastoma Cells by Downregulating mRNA Expression of MAO/α-Synuclein/LRRK2/PARK7/PINK1/PTEN Genes
inferred← citeshttps://doi.org/10.1007/s12640-019-00095-xopenalex-snapshot
Protective Role of Epigallocatechin Gallate in a Rat Model of Cisplatin-Induced Cerebral Inflammation and Oxidative Damage: Impact of Modulating NF-κB and Nrf2
inferred← citeshttps://doi.org/10.1007/s12640-023-00667-yopenalex-snapshot
Neuroprotective Potential of Tannic Acid Against Neurotoxic Outputs of Monosodium Glutamate in Rat Cerebral Cortex
inferred← citeshttps://doi.org/10.1007/s12668-021-00845-2openalex-snapshot
Current Updates On the In vivo Assessment of Zinc Oxide Nanoparticles Toxicity Using Animal Models
inferred← citeshttps://doi.org/10.1007/s13738-012-0111-6openalex-snapshot
Non-specific peroxidase activity and catalase-inhibitory behavior of fibrillar aggregates after interaction with heme: relevance to the etiology of amyloid-related neurodegenerative disorders using the experimental-based evidences
inferred← citeshttps://doi.org/10.1007/s13738-014-0538-zopenalex-snapshot
Direct evidence for non-specific peroxidase activity of ‘‘ferritin–heme” complex: possible role in the development of neurodegenerative diseases
inferred← citeshttps://doi.org/10.1007/s40473-025-00304-2openalex-snapshot
Pathophysiology of Alzheimer’s Disease: Herbal Neurogenesis and Synthetic Molecular Interventions
inferred← citeshttps://doi.org/10.1007/s44187-025-00612-2openalex-snapshot
Dietary raw and roasted pumpkin seed supplementation exerts neuroprotective effects in healthy rats as demonstrated by biochemical and histopathological analysis
inferred← citeshttps://doi.org/10.1007/s44337-024-00074-yopenalex-snapshot
Trans-cinnamaldehyde attenuates neuronal cytotoxicity and memory impairment in comorbid exposure to sleep-deprivation and formalin inhalation in rat model
inferred← citeshttps://doi.org/10.1007/s44446-025-00007-5openalex-snapshot
Neurobehavioral and molecular changes in rats exposed to either captagon or counterfeit captagon
inferred← citeshttps://doi.org/10.1016/b978-0-12-380860-8.00001-xopenalex-snapshot
Drosophila Models of Parkinson's Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-386467-3.00006-6openalex-snapshot
Multimodal drugs and their future for Alzheimer's and Parkinson's disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-398314-5.00001-5openalex-snapshot
Inflammation in Anxiety
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.12620-4openalex-snapshot
Fluorescent Probes for Reactive Oxygen Species
inferred← citeshttps://doi.org/10.1016/b978-0-12-800254-4.00005-2openalex-snapshot
Nitric Oxide in the Nervous System
inferred← citeshttps://doi.org/10.1016/b978-0-12-803951-9.00016-1openalex-snapshot
Citric Acid an Antioxidant in Liver
inferred← citeshttps://doi.org/10.1016/b978-0-12-815249-2.00021-xopenalex-snapshot
The Myth and Therapeutic Potentials of Postbiotics
inferred← citeshttps://doi.org/10.1016/b978-0-12-817780-8.00021-9openalex-snapshot
Nigella sativa L. and thymoquinone as neuroprotective antioxidants
inferred← citeshttps://doi.org/10.1016/b978-0-323-85544-0.00009-5openalex-snapshot
Role of nanoparticles in neurotoxicity
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.00233-3openalex-snapshot
Biomarkers of Neurotoxicity and Disease
inferred← citeshttps://doi.org/10.1016/b978-0-323-95735-9.00025-5openalex-snapshot
Stress-associated neurodegenerative disorders: A mechanistic exploration
inferred← citeshttps://doi.org/10.1016/b978-0-444-64199-1.00007-5openalex-snapshot
Zebrafish Early Life Stages for Toxicological Screening: Insights From Molecular and Biochemical Markers
inferred← citeshttps://doi.org/10.1016/b978-1-63067-044-3.50014-5openalex-snapshot
Autoxidation of Plasma Lipids, Generation of Bioactive Products, and Their Biological Relevance
inferred← citeshttps://doi.org/10.1016/bs.ant.2020.11.003openalex-snapshot
Neurotoxicity mechanisms of manganese in the central nervous system
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2016.07.005openalex-snapshot
Mechanisms of Parkinson's Disease
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2015.10.001openalex-snapshot
S-Glutathionylation and Redox Protein Signaling in Drug Addiction
inferred← citeshttps://doi.org/10.1016/j.ab.2015.12.014openalex-snapshot
An improved Bathocuproine assay for accurate valence identification and quantification of copper bound by biomolecules
inferred← citeshttps://doi.org/10.1016/j.abb.2017.04.005openalex-snapshot
Ascorbic acid inhibits human insulin aggregation and protects against amyloid induced cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.aca.2021.338205openalex-snapshot
Organoselenium-based BOPHY as a sensor for detection of hypochlorous acid in mammalian cells
inferred← citeshttps://doi.org/10.1016/j.addr.2021.03.008openalex-snapshot
Responsive optical probes for deep-tissue imaging: Photoacoustics and second near-infrared fluorescence
inferred← citeshttps://doi.org/10.1016/j.ajp.2012.02.023openalex-snapshot
A preliminary study on the influence of glutathione S transferase T1 (GSTT1) as a risk factor for late onset Alzheimer's disease in North Indian population
inferred← citeshttps://doi.org/10.1016/j.ajp.2012.05.007openalex-snapshot
Psychiatric genetics research in Asia
inferred← citeshttps://doi.org/10.1016/j.apsb.2024.10.004openalex-snapshot
Oxidative stress and inflammation in the pathogenesis of neurological disorders: Mechanisms and implications
inferred← citeshttps://doi.org/10.1016/j.aquatox.2020.105673openalex-snapshot
Can ocean warming alter sub-lethal effects of antiepileptic and antihistaminic pharmaceuticals in marine bivalves?
inferred← citeshttps://doi.org/10.1016/j.aquatox.2026.107799openalex-snapshot
Acute triclosan exposure induces multidimensional toxicity in zebrafish larvae: Disruption of development, behavior, immune function, and cell death mechanisms
inferred← citeshttps://doi.org/10.1016/j.arr.2009.04.002openalex-snapshot
Biomarkers of oxidative and nitrosative damage in Alzheimer's disease and mild cognitive impairment
inferred← citeshttps://doi.org/10.1016/j.arr.2022.101639openalex-snapshot
Oxidative stress and antioxidant defenses in mild cognitive impairment: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.arr.2024.102357openalex-snapshot
Neurodegenerative disorders: Mechanisms of degeneration and therapeutic approaches with their clinical relevance
inferred← citeshttps://doi.org/10.1016/j.bbadis.2008.11.004openalex-snapshot
Methionine does not reduce Cu(II)–β-amyloid!—Rectification of the roles of methionine-35 and reducing agents in metal-centered oxidation chemistry of Cu(II)–β-amyloid
inferred← citeshttps://doi.org/10.1016/j.bbadis.2009.05.005openalex-snapshot
Activation of PKCδ and ERK1/2 in the sensitivity to UV-induced apoptosis of human cells harboring 4977 bp deletion of mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/j.bbadis.2009.07.002openalex-snapshot
Is multiple sclerosis a mitochondrial disease?
inferred← citeshttps://doi.org/10.1016/j.bbadis.2009.09.011openalex-snapshot
Reversible and irreversible modifications of skeletal muscle proteins in a rat model of acute oxidative stress
inferred← citeshttps://doi.org/10.1016/j.bbagen.2017.06.016openalex-snapshot
Radical-trapping and preventive antioxidant effects of 2-hydroxymelatonin and 4-hydroxymelatonin: Contributions to the melatonin protection against oxidative stress
inferred← citeshttps://doi.org/10.1016/j.bbalip.2013.01.020openalex-snapshot
Anti-inflammatory mechanism of exogenous C2 ceramide in lipopolysaccharide-stimulated microglia
inferred← citeshttps://doi.org/10.1016/j.bbi.2012.11.001openalex-snapshot
Increased resistance of immobilized-stressed mice to infection: Correlation with behavioral alterations
inferred← citeshttps://doi.org/10.1016/j.bbr.2021.113226openalex-snapshot
Behavior and oxidative stress parameters in rats subjected to the animal's models induced by chronic mild stress and 6-hydroxydopamine
inferred← citeshttps://doi.org/10.1016/j.bbr.2022.113750openalex-snapshot
Nitric oxide impairs spatial learning and memory in a rat model of Alzheimer’s disease via disturbance of glutamate response in the hippocampal dentate gyrus during spatial learning
inferred← citeshttps://doi.org/10.1016/j.bcp.2012.04.021openalex-snapshot
Inhibition of ROS-induced apoptosis in endothelial cells by nitrone spin traps via induction of phase II enzymes and suppression of mitochondria-dependent pro-apoptotic signaling
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