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Glutathione dysregulation and the etiology and progression of human diseases
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Cu/Zn SOD deficiency potentiates hearing loss and cochlear pathology in aged 129,CD-1 mice
inferredcites →https://doi.org/10.1002/1529-0131(199805)41:5<838::aid-art10>3.0.co;2-sopenalex-snapshot
Decreased production of interleukin-12 and other Th1-type cytokines in patients with recent-onset systemic lupus erythematosus
inferredcites →https://doi.org/10.1002/1529-0131(199908)42:8<1644::aid-anr12>3.0.co;2-lopenalex-snapshot
Th1/Th2 balance of peripheral T helper cells in systemic lupus erythematosus
inferredcites →https://doi.org/10.1002/ana.10483openalex-snapshot
Oxidative stress in Parkinson's disease
inferredcites →https://doi.org/10.1002/ana.20687openalex-snapshot
A patient with neurological symptoms and abnormal leukotriene metabolism: A new defect in leukotriene biosynthesis
inferredcites →https://doi.org/10.1002/ana.410210403openalex-snapshot
Amino acids, glutathione, and glutathione transferase activity in the brains of patients with Alzheimer's disease
inferredcites →https://doi.org/10.1002/ana.410260606openalex-snapshot
Abnormalities of the electron transport chain in idiopathic parkinson's disease
inferredcites →https://doi.org/10.1002/ana.410360305openalex-snapshot
Alterations in glutathione levels in Parkinson's disease and other neurodegenerative disorders affecting basal ganglia
inferredcites →https://doi.org/10.1002/biof.5520170104openalex-snapshot
Glutathione transport in the endo/sarcoplasmic reticulum
inferredcites →https://doi.org/10.1002/hep.1840040402openalex-snapshot
Hepatic Glutathione Homeostasis in the Rat: Efflux Accounts for Glutathione Turnover
inferredcites →https://doi.org/10.1002/hep.1840040431openalex-snapshot
New Developments in Glutathione Metabolism and Their Potential Application in Therapy
inferredcites →https://doi.org/10.1002/hep.1840220521openalex-snapshot
Impaired biliary excretion and whole body elimination of methylmercury in rats with a congenital defect in biliary glutathione excretion
inferredcites →https://doi.org/10.1002/jat.736openalex-snapshot
The glutathione defense system in the pathogenesis of rheumatoid arthritis
inferredcites →https://doi.org/10.1002/jcb.21508openalex-snapshot
N ‐acetylcysteine stimulates osteoblastic differentiation of mouse calvarial cells
inferredcites →https://doi.org/10.1002/jcp.1041290210openalex-snapshot
Elevation of intracellular glutathione content associated with mitogenic stimulation of quiescent fibroblasts
inferredcites →https://doi.org/10.1002/jnr.10308openalex-snapshot
Glutathione release from cultured brain cells: Multidrug resistance protein 1 mediates the release of GSH from rat astroglial cells
inferredcites →https://doi.org/10.1002/jnr.20424openalex-snapshot
Gender differences in glutathione metabolism in Alzheimer's disease
inferredcites →https://doi.org/10.1006/bbrc.1998.8998openalex-snapshot
Expression of Bcl-2 Increases Intracellular Glutathione by Inhibiting Methionine-Dependent GSH Efflux
inferredcites →https://doi.org/10.1006/bbrc.1999.1888openalex-snapshot
Apoptosis in Human Disease: A New Skin for the Old Ceremony?
inferredcites →https://doi.org/10.1006/bbrc.2000.3930openalex-snapshot
Knockout of the Mouse Glutamate Cysteine Ligase Catalytic Subunit (Gclc) Gene: Embryonic Lethal When Homozygous, and Proposed Model for Moderate Glutathione Deficiency When Heterozygous
inferredcites →https://doi.org/10.1006/bbrc.2001.4274openalex-snapshot
GSH Role on Platelet-Derived Growth Factor Receptor Tyrosine Phosphorylation Induced by H2O2
inferredcites →https://doi.org/10.1006/bbrc.2001.4935openalex-snapshot
S-Nitrosoglutathione Increases Cystic Fibrosis Transmembrane Regulator Maturation
inferredcites →https://doi.org/10.1007/bf00400095openalex-snapshot
Weakened cellular scavenging activity against oxidative stress in diabetes mellitus: regulation of glutathione synthesis and efflux
inferredcites →https://doi.org/10.1007/bf01271295openalex-snapshot
Glutathione depletion in rat brain does not cause nigrostriatal pathway degeneration
inferredcites →https://doi.org/10.1007/bf01291884openalex-snapshot
Alterations in the distribution of glutathione in the substantia nigra in Parkinson's disease
inferredcites →https://doi.org/10.1007/bf02152299openalex-snapshot
Der Glutathiongehalt der Linse bei verschiedenen Kataraktformen
inferredcites →https://doi.org/10.1007/bf03159937openalex-snapshot
Alzheimer’s and Parkinson’s disease
inferredcites →https://doi.org/10.1007/s00430-003-0212-zopenalex-snapshot
Effects of S-acetylglutathione in cell and animal model of herpes simplex virus type 1 infection
inferredcites →https://doi.org/10.1007/s101620010043openalex-snapshot
Targeted Mutation of the Gene for Cellular Glutathione Peroxidase (Gpx1) Increases Noise-Induced Hearing Loss in Mice
inferredcites →https://doi.org/10.1007/s10555-007-9039-1openalex-snapshot
Physiological and pharmacological functions of Mrp2, Mrp3 and Mrp4 as determined from recent studies on gene-disrupted mice
inferredcites →https://doi.org/10.1007/s11010-006-9270-zopenalex-snapshot
Role of antioxidant systems, lipid peroxidation, and nitric oxide in postmenopausal osteoporosis
inferredcites →https://doi.org/10.1007/s11064-007-9315-zopenalex-snapshot
Modulation of [3H]Dopamine Release by Glutathione in Mouse Striatal Slices
inferredcites →https://doi.org/10.1016/0006-2952(90)90503-dopenalex-snapshot
Glutathione-degrading capacities of liver and kidney in different species
inferredcites →https://doi.org/10.1016/0006-2952(91)90359-dopenalex-snapshot
Polarity of hepatic glutathione and glutathione S-conjugate efflux, and intraorgan mercapturic acid formation in the skate
inferredcites →https://doi.org/10.1016/0014-4835(91)90023-8openalex-snapshot
Effect of pigmentation on glutathione redox cycle antioxidant defense in whole as well as different regions of human cataractous lens
inferredcites →https://doi.org/10.1016/0024-3205(92)90509-nopenalex-snapshot
The physiological consequences of glutathione variations
inferredcites →https://doi.org/10.1016/0039-6257(87)90115-9openalex-snapshot
Pathophysiology of age-related macular degeneration
inferredcites →https://doi.org/10.1016/0039-6257(88)90174-9openalex-snapshot
Solar radiation and age-related macular degeneration
inferredcites →https://doi.org/10.1016/0041-008x(84)90276-xopenalex-snapshot
State of sulfhydryl in selenite cataract
inferredcites →https://doi.org/10.1016/0092-8674(93)80065-mopenalex-snapshot
Bcl-2-deficient mice demonstrate fulminant lymphoid apoptosis, polycystic kidneys, and hypopigmented hair
inferredcites →https://doi.org/10.1016/0092-8674(93)80066-nopenalex-snapshot
Bcl-2 functions in an antioxidant pathway to prevent apoptosis
inferredcites →https://doi.org/10.1016/0162-3109(89)90020-9openalex-snapshot
Lymphocyte proliferation in glutathione-depleted lymphocytes: direct relationship between glutathione availability and the proliferative response
inferredcites →https://doi.org/10.1016/0166-3542(95)00008-aopenalex-snapshot
Evidence for antiviral activity of glutathione: in vitro inhibition of herpes simplex virus type 1 replication
inferredcites →https://doi.org/10.1016/0304-4165(77)90152-0openalex-snapshot
Glutathione dependent control of protein disulfide-sulfhydryl content by subcellular fractions of hepatic tissue
inferredcites →https://doi.org/10.1016/0304-4165(78)90037-5openalex-snapshot
The fate of extracellular glutathione in the rat☆
inferredcites →https://doi.org/10.1016/0306-4522(92)90524-6openalex-snapshot
Glutathione: New candidate neuropeptide in the central nervous system
inferredcites →https://doi.org/10.1016/0921-8734(92)90029-oopenalex-snapshot
Reactive oxygen and DNA damage in mitochondria
inferredcites →https://doi.org/10.1016/0959-8049(96)00051-2openalex-snapshot
Glutathione and related enzymes in multidrug resistance
inferredcites →https://doi.org/10.1016/j.ajo.2005.06.043openalex-snapshot
Antioxidant Supplements Prevent Oxidation of Cysteine/Cystine Redox in Patients With Age-Related Macular Degeneration
inferredcites →https://doi.org/10.1016/j.arcmed.2006.09.010openalex-snapshot
Effects of Calcitonin, Risedronate, and Raloxifene on Erythrocyte Antioxidant Enzyme Activity, Lipid Peroxidation, and Nitric Oxide in Postmenopausal Osteoporosis
inferredcites →https://doi.org/10.1016/j.atherosclerosis.2007.05.012openalex-snapshot
Anti-oxidant and anti-atherogenic properties of liposomal glutathione: Studies in vitro, and in the atherosclerotic apolipoprotein E-deficient mice
inferredcites →https://doi.org/10.1016/j.bbrc.2003.09.086openalex-snapshot
Transcription factor Nrf2 is required for the constitutive and inducible expression of multidrug resistance-associated protein1 in mouse embryo fibroblasts
inferredcites →https://doi.org/10.1016/j.bbrc.2004.09.220openalex-snapshot
Intracellular glutathione status regulates mouse bone marrow monocyte-derived macrophage differentiation and phagocytic activity
inferredcites →https://doi.org/10.1016/j.biocel.2006.07.001openalex-snapshot
Free radicals and antioxidants in normal physiological functions and human disease
inferredcites →https://doi.org/10.1016/j.biopha.2004.02.005openalex-snapshot
Allergic contact dermatitis is accompanied by severe abnormal changes in antioxidativity of blood
inferredcites →https://doi.org/10.1016/j.biopha.2008.01.017openalex-snapshot
Glutathione and Parkinson's disease: Is this the elephant in the room?
inferredcites →https://doi.org/10.1016/j.cbi.2006.03.001openalex-snapshot
Mitochondrial glutathione transport: Physiological, pathological and toxicological implications
inferredcites →https://doi.org/10.1016/j.cell.2007.09.037openalex-snapshot
Spatiotemporal Coupling of cAMP Transporter to CFTR Chloride Channel Function in the Gut Epithelia
inferredcites →https://doi.org/10.1016/j.coph.2007.04.005openalex-snapshot
N-Acetylcysteine—a safe antidote for cysteine/glutathione deficiency
inferredcites →https://doi.org/10.1016/j.coph.2007.04.006openalex-snapshot
Glutathionylation pathways in drug response
inferredcites →https://doi.org/10.1016/j.expneurol.2006.09.004openalex-snapshot
Characterization of intracellular elevation of glutathione (GSH) with glutathione monoethyl ester and GSH in brain and neuronal cultures: Relevance to Parkinson's disease
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.02.074openalex-snapshot
Nrf2 signaling in coordinated activation of antioxidant gene expression
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.06.001openalex-snapshot
Retinal Oxidative Stress Induced by High Intraocular Pressure
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.06.011openalex-snapshot
Human glutamate cysteine ligase gene regulation through the electrophile response element
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.06.040openalex-snapshot
Genetically altered mice to evaluate glutathione homeostasis in health and disease
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.11.029openalex-snapshot
Age-associated oxidative damage leads to absence of γ-cystathionase in over 50% of rat lenses: Relevance in cataractogenesis
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2006.01.035openalex-snapshot
Sphingolipid signaling and redox regulation
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2006.09.022openalex-snapshot
Antioxidants in cystic fibrosis
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2007.06.014openalex-snapshot
S-glutathionylation in protein redox regulation
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2007.11.008openalex-snapshot
Nonequilibrium thermodynamics of thiol/disulfide redox systems: A perspective on redox systems biology
inferredcites →https://doi.org/10.1016/j.it.2004.05.001openalex-snapshot
Mitochondrial hyperpolarization: a checkpoint of T-cell life, death and autoimmunity
inferredcites →https://doi.org/10.1016/j.jnutbio.2005.05.013openalex-snapshot
Novel mechanisms of natural antioxidant compounds in biological systems: involvement of glutathione and glutathione-related enzymes
inferredcites →https://doi.org/10.1016/j.jnutbio.2006.12.003openalex-snapshot
Oxidative stress and antioxidants: a link to disease and prevention?
inferredcites →https://doi.org/10.1016/j.mam.2004.02.013openalex-snapshot
Molecular bases of the treatment of Alzheimer's disease with antioxidants: prevention of oxidative stress
inferredcites →https://doi.org/10.1016/j.mam.2008.08.004openalex-snapshot
Plasma membrane glutathione transporters and their roles in cell physiology and pathophysiology
inferredcites →https://doi.org/10.1016/j.metabol.2006.01.003openalex-snapshot
Insulin decreases intracellular oxidative stress in patients with type 2 diabetes mellitus
inferredcites →https://doi.org/10.1016/j.molmed.2004.09.003openalex-snapshot
Nrf2–Keap1 defines a physiologically important stress response mechanism
inferredcites →https://doi.org/10.1016/j.mrfmmm.2005.02.025openalex-snapshot
Regulation of glutathione in inflammation and chronic lung diseases
inferredcites →https://doi.org/10.1016/j.neulet.2006.08.033openalex-snapshot
Relationship between the clinical scoring and demyelination in central nervous system with total antioxidant capacity of plasma during experimental autoimmune encephalomyelitis development in mice
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2006.06.025openalex-snapshot
Oxidative imbalance in the aging inner ear
inferredcites →https://doi.org/10.1016/j.neuroscience.2005.01.059openalex-snapshot
Monoaminergic dysregulation in glutathione-deficient mice: Possible relevance to schizophrenia?
inferredcites →https://doi.org/10.1016/j.neuroscience.2007.08.028openalex-snapshot
Integrating glutathione metabolism and mitochondrial dysfunction with implications for Parkinson’s disease: A dynamic model
inferredcites →https://doi.org/10.1016/j.taap.2003.10.008openalex-snapshot
Activation of plasma membrane reduced glutathione transport in death receptor apoptosis of HepG2 cells
inferredcites →https://doi.org/10.1016/j.taap.2004.09.008openalex-snapshot
Molecular mechanisms of reduced glutathione transport: role of the MRP/CFTR/ABCC and OATP/SLC21A families of membrane proteins
inferredcites →https://doi.org/10.1016/j.taap.2004.10.012openalex-snapshot
Multidrug resistance proteins: role of P-glycoprotein, MRP1, MRP2, and BCRP (ABCG2) in tissue defense
inferredcites →https://doi.org/10.1016/j.tox.2003.12.006openalex-snapshot
Bone metabolism and oxidative stress in postmenopausal rats with iron overload
inferredcites →https://doi.org/10.1016/j.trsl.2007.03.012openalex-snapshot
Potential role of the antioxidant N-acetylcysteine in slowing bone resorption in early post-menopausal women: a pilot study
inferredcites →https://doi.org/10.1016/s0005-2736(01)00454-0openalex-snapshot
Inhibition of Mrp2- and Ycf1p-mediated transport by reducing agents: evidence for GSH transport on rat Mrp2
inferredcites →https://doi.org/10.1016/s0006-291x(02)02245-3openalex-snapshot
S-Nitrosoglutathione induces functional ΔF508-CFTR in airway epithelial cells
inferredcites →https://doi.org/10.1016/s0009-2797(00)00286-6openalex-snapshot
Modulation of aldose reductase activity through S-thiolation by physiological thiols
inferredcites →https://doi.org/10.1016/s0009-2797(98)00008-8openalex-snapshot
Clinical studies of reversal of drug resistance based on glutathione
inferredcites →https://doi.org/10.1016/s0009-8981(01)00766-5openalex-snapshot
A duality in the roles of reactive oxygen species with respect to bone metabolism
inferredcites →https://doi.org/10.1016/s0009-8981(03)00200-6openalex-snapshot
Analysis of glutathione: implication in redox and detoxification
inferredcites →https://doi.org/10.1016/s0009-8981(99)00150-3openalex-snapshot
Antioxidants and lipid peroxidation status in the blood of patients with psoriasis
inferredcites →https://doi.org/10.1016/s0014-5793(97)00263-9openalex-snapshot
Erythrocyte thiol status regulates band 3 phosphotyrosine level via oxidation/reduction of band 3‐associated phosphotyrosine phosphatase
inferredcites →https://doi.org/10.1016/s0021-9258(18)54551-8openalex-snapshot
Intrahepatic conversion of a glutathione conjugate to its mercapturic acid. Metabolism of 1-chloro-2,4-dinitrobenzene in isolated perfused rat and guinea pig livers.
inferredcites →https://doi.org/10.1016/s0021-9258(19)57482-8openalex-snapshot
Intrabiliary glutathione hydrolysis. A source of glutamate in bile.
inferredcites →https://doi.org/10.1016/s0021-9258(19)84550-7openalex-snapshot
Sodium gradient-dependent L-glutamate transport is localized to the canalicular domain of liver plasma membranes. Studies in rat liver sinusoidal and canalicular membrane vesicles.
inferredcites →https://doi.org/10.1016/s0022-3476(99)70101-0openalex-snapshot
Decreased levels of nitrosothiols in the lower airways of patients with cystic fibrosis and normal pulmonary function
inferredcites →https://doi.org/10.1016/s0022-3565(25)10916-6openalex-snapshot
L-cysteine and S-(1,2-dichlorovinyl)-L-cysteine transport in rat liver canalicular membrane vesicles: potential reabsorption mechanisms for biliary metabolites of glutathione and its S-conjugates.
inferredcites →https://doi.org/10.1016/s0022-510x(98)00095-1openalex-snapshot
Mitochondrial function, GSH and iron in neurodegeneration and Lewy body diseases
inferredcites →https://doi.org/10.1016/s0026-0495(98)90357-2openalex-snapshot
Influence of reduced glutathione infusion on glucose metabolism in patients with non—insulin-dependent diabetes mellitus
inferredcites →https://doi.org/10.1016/s0026-895x(25)08878-9openalex-snapshot
Stimulation of N-methyl-D-aspartate receptor-mediated calcium entry into dissociated neurons by reduced and oxidized glutathione.
inferredcites →https://doi.org/10.1016/s0026-895x(25)10239-3openalex-snapshot
Hormonal and cell density regulation of hepatic gamma-glutamylcysteine synthetase gene expression.
inferredcites →https://doi.org/10.1016/s0026-895x(25)14926-2openalex-snapshot
Structural and conformational properties of peptides interacting with the glutathione receptor of hydra.
inferredcites →https://doi.org/10.1016/s0031-6997(24)01370-xopenalex-snapshot
Endogenous Glutathione Conjugates: Occurrence and Biological Functions
inferredcites →https://doi.org/10.1016/s0065-2423(01)35014-xopenalex-snapshot
The biochemistry of aging
inferredcites →https://doi.org/10.1016/s0074-7742(07)82016-2openalex-snapshot
Oxidative Stress and the Pathogenesis of Neurodegenerative Disorders
inferredcites →https://doi.org/10.1016/s0076-6879(05)01025-6openalex-snapshot
Gene Expression of γ‐Glutamyltranspeptidase
inferredcites →https://doi.org/10.1016/s0140-6736(89)91909-0openalex-snapshot
SYSTEMIC GLUTATHIONE DEFICIENCY IN SYMPTOM-FREE HIV-SEROPOSITIVE INDIVIDUALS
inferredcites →https://doi.org/10.1016/s0140-6736(89)92366-0openalex-snapshot
MITOCHONDRIAL COMPLEX I DEFICIENCY IN PARKINSON'S DISEASE
inferredcites →https://doi.org/10.1016/s0168-8278(01)00037-xopenalex-snapshot
Novel roles for glutathione in gene expression, cell death, and membrane transport of organic solutes
inferredcites →https://doi.org/10.1016/s0197-0186(00)00031-0openalex-snapshot
Modulation of glutamate receptor functions by glutathione
inferredcites →https://doi.org/10.1016/s0197-4580(99)00018-4openalex-snapshot
Age-related cochlear hair cell loss is enhanced in mice lacking copper/zinc superoxide dismutase
inferredcites →https://doi.org/10.1016/s0304-4165(02)00525-1openalex-snapshot
Covalent coupling of reduced glutathione with ribose: loss of cosubstrate ability to glutathione peroxidase
inferredcites →https://doi.org/10.1016/s0306-4522(97)00347-3openalex-snapshot
Differential compartmentalization of brain ascorbate and glutathione between neurons and glia
inferredcites →https://doi.org/10.1016/s0306-4522(99)00442-xopenalex-snapshot
Specific glutathione binding sites in pig cerebral cortical synaptic membranes
inferredcites →https://doi.org/10.1016/s0378-4347(94)80050-2openalex-snapshot
Determination of extracellular glutathione in rat brain by microdialysis and high-performance liquid chromatography with fluorescence detection
inferredcites →https://doi.org/10.1016/s0753-3322(03)00043-xopenalex-snapshot
The importance of glutathione in human disease
inferredcites →https://doi.org/10.1016/s0891-5849(01)00480-4openalex-snapshot
Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple
inferredcites →https://doi.org/10.1016/s0891-5849(01)00530-5openalex-snapshot
Rethinking cystic fibrosis pathology: the critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation
inferredcites →https://doi.org/10.1016/s0891-5849(01)00751-1openalex-snapshot
Altered differentiation in rat and rabbit limb bud micromass cultures by glutathione modulating agents
inferredcites →https://doi.org/10.1016/s0891-5849(02)00780-3openalex-snapshot
Oxidatively modified proteins in aging and disease1,2 1Guest Editor: Earl Stadtman 2This article is part of a series of reviews on “Oxidatively Modified Proteins in Aging and Disease.” The full list of papers may be found on the homepage of the journal.
inferredcites →https://doi.org/10.1016/s0891-5849(03)00023-6openalex-snapshot
Inhibition of influenza infection by glutathione
inferredcites →https://doi.org/10.1016/s0891-5849(97)00286-4openalex-snapshot
Glutathione in Human Plasma: Decline in Association with Aging, Age-Related Macular Degeneration, and Diabetes
inferredcites →https://doi.org/10.1016/s0891-5849(99)00177-xopenalex-snapshot
Glutathione and its role in cellular functions
inferredcites →https://doi.org/10.1016/s0925-4439(97)00067-7openalex-snapshot
Lipid peroxidation, antioxidant protection and aging
inferredcites →https://doi.org/10.1021/jm070037vopenalex-snapshot
Synthesis and Study of l -Dopa−Glutathione Codrugs as New Anti-Parkinson Agents with Free Radical Scavenging Properties
inferredcites →https://doi.org/10.1024/0300-9831.74.5.329openalex-snapshot
Changes in rat lens proteins and glutathione reductase activity with advancing age
inferredcites →https://doi.org/10.1038/414813aopenalex-snapshot
Biochemistry and molecular cell biology of diabetic complications
inferredcites →https://doi.org/10.1038/nri1530openalex-snapshot
Protein tyrosine phosphatases and the immune response
inferredcites →https://doi.org/10.1038/sj.cdd.4401793openalex-snapshot
Regulation of osteoclast differentiation by the redox-dependent modulation of nuclear import of transcription factors
inferredcites →https://doi.org/10.1038/sj.eye.6701853openalex-snapshot
Plasma homocysteine and total thiol content in patients with exudative age-related macular degeneration
inferredcites →https://doi.org/10.1038/sj.npp.1301624openalex-snapshot
Glutathione Precursor, N-Acetyl-Cysteine, Improves Mismatch Negativity in Schizophrenia Patients
inferredcites →https://doi.org/10.1038/sj.onc.1203324openalex-snapshot
Cell line dependence of Bcl-2-induced alteration of glutathione handling
inferredcites →https://doi.org/10.1042/bj1170957openalex-snapshot
Free and protein-bound glutathione in normal and cataractous human lenses
inferredcites →https://doi.org/10.1042/bj20051435openalex-snapshot
Direct evidence for S-nitrosation of mitochondrial complex I
inferredcites →https://doi.org/10.1042/bj3010649openalex-snapshot
Inhibition of the differentiation of human myeloid cell lines by redox changes induced through glutathione depletion
inferredcites →https://doi.org/10.1042/bj3250315openalex-snapshot
Bcl-xL overexpression attenuates glutathione depletion in FL5.12 cells following interleukin-3 withdrawal
inferredcites →https://doi.org/10.1042/bj3260167openalex-snapshot
Differential regulation of γ-glutamylcysteine synthetase heavy and light subunit gene expression
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GSH extrusion and the mitochondrial pathway of apoptotic signalling
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CD4+ lymphocytes from HIV-infected patients display impaired CD45-associated tyrosine phosphatase activity which is enhanced by anti-oxidants
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Schizophrenia: glutathione deficit in cerebrospinal fluid and prefrontal cortex in vivo
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A Possible Role of Glutathione as an Endogenous Agonist at the N‐Methyl‐ d ‐Aspartate Recognition Domain in Rat Brain
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Effect of Peroxynitrite on the Mitochondrial Respiratory Chain: Differential Susceptibility of Neurones and Astrocytes in Primary Culture
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Shift of the Cellular Oxidation‐Reduction Potential in Neural Cells Expressing Bcl‐2
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Enhanced Oxidative Stress and Altered Antioxidants in Brains of Bcl‐2‐Deficient Mice
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Role of Endogenous Glutathione in the Oxidation of Dopamine
inferredcites →https://doi.org/10.1046/j.1471-4159.1998.71052112.xopenalex-snapshot
Conjugates of Catecholamines with Cysteine and GSH in Parkinson's Disease: Possible Mechanisms of Formation Involving Reactive Oxygen Species
inferredcites →https://doi.org/10.1046/j.1471-4159.1999.0730889.xopenalex-snapshot
Glutathione and Signal Transduction in the Mammalian CNS
inferredcites →https://doi.org/10.1046/j.1471-4159.1999.731683.xopenalex-snapshot
Inhibitors of Mitochondrial Respiration, Iron (II), and Hydroxyl Radical Evoke Release and Extracellular Hydrolysis of Glutathione in Rat Striatum and Substantia Nigra
inferredcites →https://doi.org/10.1046/j.1471-4159.2002.01013.xopenalex-snapshot
Effects of dopamine on the glutathione metabolism of cultured astroglial cells: implications for Parkinson's disease
inferredcites →https://doi.org/10.1046/j.1471-4159.2002.01082.xopenalex-snapshot
Expression of mRNAs of multidrug resistance proteins (Mrps) in cultured rat astrocytes, oligodendrocytes, microglial cells and neurones
inferredcites →https://doi.org/10.1046/j.1471-4159.2003.01821.xopenalex-snapshot
Differential effect of nitric oxide on glutathione metabolism and mitochondrial function in astrocytes and neurones: implications for neuroprotection/neurodegeneration?
inferredcites →https://doi.org/10.1046/j.1523-1747.2003.12510.xopenalex-snapshot
Thiol Antioxidants Block the Activation of Antigen-Presenting Cells by Contact Sensitizers
inferredcites →https://doi.org/10.1046/j.1523-1755.2002.00168.xopenalex-snapshot
Glucose-induced oxidative stress in mesangial cells
inferredcites →https://doi.org/10.1055/s-2008-1040481openalex-snapshot
Importance and Regulation of Hepatic Glutathione
inferredcites →https://doi.org/10.1067/mhn.2002.127627openalex-snapshot
Influence of Lecithin on Mitochondrial DNA and Age‐Related Hearing Loss
inferredcites →https://doi.org/10.1067/mlc.2000.105977openalex-snapshot
Blood glutathione decreases in chronic diseases
inferredcites →https://doi.org/10.1073/pnas.0501078102openalex-snapshot
Increased glutathione S -transferase activity rescues dopaminergic neuron loss in a Drosophila model of Parkinson's disease
inferredcites →https://doi.org/10.1073/pnas.0511304103openalex-snapshot
High-dose oral N -acetylcysteine, a glutathione prodrug, modulates inflammation in cystic fibrosis
inferredcites →https://doi.org/10.1073/pnas.192445199openalex-snapshot
A role for glutathione peroxidase in protecting pancreatic β cells against oxidative stress in a model of glucose toxicity
inferredcites →https://doi.org/10.1073/pnas.86.15.5974openalex-snapshot
Tumor necrosis factor alpha activates human immunodeficiency virus type 1 through induction of nuclear factor binding to the NF-kappa B sites in the long terminal repeat.
inferredcites →https://doi.org/10.1073/pnas.87.11.4063openalex-snapshot
Augmentation of glutathione in the fluid lining the epithelium of the lower respiratory tract by directly administering glutathione aerosol.
inferredcites →https://doi.org/10.1073/pnas.87.24.9943openalex-snapshot
Intracellular thiols regulate activation of nuclear factor kappa B and transcription of human immunodeficiency virus.
inferredcites →https://doi.org/10.1073/pnas.87.9.3343openalex-snapshot
Glutathione regulates activation-dependent DNA synthesis in highly purified normal human T lymphocytes stimulated via the CD2 and CD3 antigens.
inferredcites →https://doi.org/10.1073/pnas.93.15.7923openalex-snapshot
Growth retardation and cysteine deficiency in gamma-glutamyl transpeptidase-deficient mice.
inferredcites →https://doi.org/10.1073/pnas.94.10.5361openalex-snapshot
Functional antioxidant responsive elements
inferredcites →https://doi.org/10.1073/pnas.94.5.1967openalex-snapshot
Glutathione deficiency is associated with impaired survival in HIV disease
inferredcites →https://doi.org/10.1073/pnas.95.6.3071openalex-snapshot
Glutathione levels in antigen-presenting cells modulate Th1 versus Th2 response patterns
inferredcites →https://doi.org/10.1073/pnas.96.19.10857openalex-snapshot
Prevention of glucose toxicity in HIT-T15 cells and Zucker diabetic fatty rats by antioxidants
inferredcites →https://doi.org/10.1073/pnas.97.10.5101openalex-snapshot
Glutathione synthesis is essential for mouse development but not for cell growth in culture
inferredcites →https://doi.org/10.1074/jbc.271.25.15146openalex-snapshot
Long Exposure to High Glucose Concentration Impairs the Responsive Expression of γ-Glutamylcysteine Synthetase by Interleukin-1β and Tumor Necrosis Factor-α in Mouse Endothelial Cells
inferredcites →https://doi.org/10.1074/jbc.271.26.15420openalex-snapshot
Rapid and Specific Efflux of Reduced Glutathione during Apoptosis Induced by Anti-Fas/APO-1 Antibody
inferredcites →https://doi.org/10.1074/jbc.271.49.31243openalex-snapshot
The Upstream Regulatory Region of the Carbamoyl-phosphate Synthetase I Gene Controls Its Tissue-specific, Developmental, and Hormonal Regulation in Vivo
inferredcites →https://doi.org/10.1074/jbc.273.26.16184openalex-snapshot
Identification of Glutathione as a Driving Force and Leukotriene C4 as a Substrate for oatp1, the Hepatic Sinusoidal Organic Solute Transporter
inferredcites →https://doi.org/10.1074/jbc.273.50.33449openalex-snapshot
ATP-dependent Transport of Reduced Glutathione on YCF1, the Yeast Orthologue of Mammalian Multidrug Resistance Associated Proteins
inferredcites →https://doi.org/10.1074/jbc.m010403200openalex-snapshot
Perturbation of the Pore of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Inhibits Its ATPase Activity
inferredcites →https://doi.org/10.1074/jbc.m209372200openalex-snapshot
Initial Characterization of the Glutamate-Cysteine Ligase Modifier Subunit Gclm(−/−) Knockout Mouse
inferredcites →https://doi.org/10.1074/jbc.m301924200openalex-snapshot
Mammalian Osmolytes and S-Nitrosoglutathione Promote ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Protein Maturation and Function
inferredcites →https://doi.org/10.1074/jbc.m303753200openalex-snapshot
Down-regulation of Glutathione and Bcl-2 Synthesis in Mouse B16 Melanoma Cells Avoids Their Survival during Interaction with the Vascular Endothelium
inferredcites →https://doi.org/10.1074/jbc.m406371200openalex-snapshot
Bcl-2 Attenuation of Oxidative Cell Death Is Associated with Up-regulation of γ-Glutamylcysteine Ligase via Constitutive NF-κB Activation
inferredcites →https://doi.org/10.1074/jbc.m408531200openalex-snapshot
Acceleration of Glutathione Efflux and Inhibition of γ-Glutamyltranspeptidase Sensitize Metastatic B16 Melanoma Cells to Endothelium-induced Cytotoxicity
inferredcites →https://doi.org/10.1074/jbc.m513231200openalex-snapshot
Mechanisms of Cystic Fibrosis Transmembrane Conductance Regulator Activation by S-Nitrosoglutathione
inferredcites →https://doi.org/10.1074/jbc.m611019200openalex-snapshot
Glutathione Export during Apoptosis Requires Functional Multidrug Resistance-associated Proteins
inferredcites →https://doi.org/10.1080/009841098159097openalex-snapshot
GLUTATHIONE S-CONJUGATE FORMATION AND METABOLISM IN HepG2 CELLS: A CELL MODEL OF MERCAPTURIC ACID BIOSYNTHESIS
inferredcites →https://doi.org/10.1080/08035250410025285openalex-snapshot
Physiological and pathological aspects of GSH metabolism
inferredcites →https://doi.org/10.1080/10408360500523878openalex-snapshot
Glutathione in Cancer Biology and Therapy
inferredcites →https://doi.org/10.1080/10715760000300291openalex-snapshot
Regulation ofγ-glutamylcysteine synthetase subunit gene expression: Insights into transcriptional control of antioxidant defenses
inferredcites →https://doi.org/10.1080/13813450701661198openalex-snapshot
The central role of glutathione in the pathophysiology of human diseases
inferredcites →https://doi.org/10.1080/1521654032000114320openalex-snapshot
Nitric Oxide and Reactive Oxygen Species in Parkinson's Disease
inferredcites →https://doi.org/10.1080/15287399409531852openalex-snapshot
Glutathione conjugation and conversion to mercapturic acids can occur as an intrahepatic process
inferredcites →https://doi.org/10.1084/jem.188.5.797openalex-snapshot
Multidrug Resistance Protein 1 Protects the Oropharyngeal Mucosal Layer and the Testicular Tubules against Drug-induced Damage
inferredcites →https://doi.org/10.1089/ars.2005.7.508openalex-snapshot
Redox Mechanisms of Cytoprotection by Bcl-2
inferredcites →https://doi.org/10.1089/ars.2006.1465openalex-snapshot
Involvement of Oxidative Stress in the Pathogenesis of Diabetes
inferredcites →https://doi.org/10.1089/ars.2008.2089openalex-snapshot
Molecular Mechanisms and Clinical Implications of Reversible Protein S -Glutathionylation
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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C-subfamily ATP binding cassette transporters extrude the calcium fluorescent probe fluo-4 from a cone photoreceptor cell line
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Iron N-(2-hydroxy acetophenone) glycinate (FeNG), a non-toxic glutathione depletor circumvents doxorubicin resistance in Ehrlich ascites carcinoma cells in vivo
inferred← citeshttps://doi.org/10.1007/s10534-023-00537-2openalex-snapshot
Translational toxicology of metal(loid) species: linking their bioinorganic chemistry in the bloodstream to organ damage onset
inferred← citeshttps://doi.org/10.1007/s10545-013-9605-3openalex-snapshot
Glutathione metabolism in cobalamin deficiency type C (cblC)
inferred← citeshttps://doi.org/10.1007/s10735-024-10329-8openalex-snapshot
Protective effects of ghrelin on pancreas in fructose diet and streptozotocin-induced diabetic rats
inferred← citeshttps://doi.org/10.1007/s10787-025-01870-3openalex-snapshot
Traumatic Brian Injury (TBI) unraveled: molecular disruptions and therapeutic avenues
inferred← citeshttps://doi.org/10.1007/s10854-021-06808-3openalex-snapshot
Fabrication of polyethyleneimine surface-functionalized fluorescent carbon dots and its applications towards highly sensitive and selective detection of glutathione in aqueous medium and in vitro cell imaging of HeLa cells
inferred← citeshttps://doi.org/10.1007/s10863-018-9748-xopenalex-snapshot
Aberrant GSH reductase and NOX activities concur with defective CFTR to pro-oxidative imbalance in cystic fibrosis airways
inferred← citeshttps://doi.org/10.1007/s10930-011-9385-2openalex-snapshot
Glutathione and Vitamin B12 Cooperate in Stabilization of a B12 Trafficking Chaperone Protein
inferred← citeshttps://doi.org/10.1007/s10930-019-09834-7openalex-snapshot
The Relevance of Glutathione Reductase Inhibition by Fluoxetine to Human Health and Disease: Insights Derived from a Combined Kinetic and Docking Study
inferred← citeshttps://doi.org/10.1007/s11011-019-00511-3openalex-snapshot
Evidence of hippocampal astrogliosis and antioxidant imbalance after L-tyrosine chronic administration in rats
inferred← citeshttps://doi.org/10.1007/s11011-021-00676-wopenalex-snapshot
Oxidative stress in phenylketonuria—evidence from human studies and animal models, and possible implications for redox signaling
inferred← citeshttps://doi.org/10.1007/s11033-019-04931-3openalex-snapshot
Salvia lachnostachys Benth has antitumor and chemopreventive effects against solid Ehrlich carcinoma
inferred← citeshttps://doi.org/10.1007/s11033-022-08048-yopenalex-snapshot
The role of ferroptosis in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1007/s11033-022-08191-6openalex-snapshot
Characterization of a glutamate-cysteine ligase in Bombyx mori
inferred← citeshttps://doi.org/10.1007/s11033-024-09595-2openalex-snapshot
Vitamin C alleviates hyperglycemic stress in retinal pigment epithelial cells
inferred← citeshttps://doi.org/10.1007/s11051-026-06670-6openalex-snapshot
Sulfonated viologen cavitand nanocarriers enable glutathione-triggered doxorubicin release and enhanced nuclear delivery in cancer cells
inferred← citeshttps://doi.org/10.1007/s11062-021-09887-4openalex-snapshot
Hydrogen Sulfide and Pathophysiology of the CNS
inferred← citeshttps://doi.org/10.1007/s11064-012-0775-4openalex-snapshot
Brain Region-Specific Glutathione Redox Imbalance in Autism
inferred← citeshttps://doi.org/10.1007/s11064-013-1199-5openalex-snapshot
A Guide to the Metabolic Pathways and Function of Metabolites Observed in Human Brain 1H Magnetic Resonance Spectra
inferred← citeshttps://doi.org/10.1007/s11064-014-1481-1openalex-snapshot
Glutathione-Dependent Detoxification Processes in Astrocytes
inferred← citeshttps://doi.org/10.1007/s11064-022-03735-5openalex-snapshot
1α,25-Dihydroxyvitamin D3 (VD3) Shows a Neuroprotective Action Against Rotenone Toxicity on PC12 Cells: An In Vitro Model of Parkinson’s Disease
inferred← citeshttps://doi.org/10.1007/s11064-024-04152-6openalex-snapshot
Physical Exercise-Induced Activation of NRF2 and BDNF as a Promising Strategy for Ferroptosis Regulation in Parkinson’s Disease
inferred← citeshttps://doi.org/10.1007/s11095-011-0528-0openalex-snapshot
Mitochondrial Antioxidants Alleviate Oxidative and Nitrosative Stress in a Cellular Model of Sepsis
inferred← citeshttps://doi.org/10.1007/s11095-025-04004-0openalex-snapshot
Pharmaceutical Roots to Mitochondrial Routes: Targeting Neurodegeneration
inferred← citeshttps://doi.org/10.1007/s11244-025-02133-9openalex-snapshot
State-of-the-Art Oxidation Mechanisms of Sulfur-Containing Amino Acids: Insights into Redox Chemistry, Metal-Ion Catalysis, and Biomedical Implications
inferred← citeshttps://doi.org/10.1007/s11244-025-02141-9openalex-snapshot
Glutathione Production from Spent Yeast of Bioethanol Manufacture: Impact of Extraction Techniques with Commercial Applicability of Biotechnological Significance
inferred← citeshttps://doi.org/10.1007/s11306-010-0250-7openalex-snapshot
Trend analysis of metabonomics and systematic review of metabonomics-derived cancer marker metabolites
inferred← citeshttps://doi.org/10.1007/s11306-012-0430-8openalex-snapshot
Metabonomic investigation of rat tissues following intravenous administration of cyanidin 3-glucoside at a physiologically relevant dose
inferred← citeshttps://doi.org/10.1007/s11306-019-1473-xopenalex-snapshot
UHPLC-QTOF/MS-based metabolomics investigation for the protective mechanism of Danshen in Alzheimer’s disease cell model induced by Aβ1–42
inferred← citeshttps://doi.org/10.1007/s11307-020-01570-0openalex-snapshot
Tumor Microenvironment Biosensors for Hyperpolarized Carbon-13 Magnetic Resonance Spectroscopy
inferred← citeshttps://doi.org/10.1007/s11356-015-5037-yopenalex-snapshot
Induction of reactive oxygen species in marine phytoplankton under crude oil exposure
inferred← citeshttps://doi.org/10.1007/s11356-020-08959-yopenalex-snapshot
Bisphenol-A induced antioxidants imbalance and cytokines alteration leading to immune suppression during larval development of Labeo rohita
inferred← citeshttps://doi.org/10.1007/s11356-021-16693-2openalex-snapshot
Free radical biology in neurological manifestations: mechanisms to therapeutics interventions
inferred← citeshttps://doi.org/10.1007/s11356-022-19499-yopenalex-snapshot
Exploring the multifaceted role of TGF-β signaling in diabetic complications
inferred← citeshttps://doi.org/10.1007/s11427-017-9271-1openalex-snapshot
Magnetic nanoparticles based cancer therapy: current status and applications
inferred← citeshttps://doi.org/10.1007/s11481-011-9300-9openalex-snapshot
Effects of Obovatol on GSH Depleted Glia-Mediated Neurotoxicity and Oxidative Damage
inferred← citeshttps://doi.org/10.1007/s12010-022-04107-zopenalex-snapshot
Synthesis and Anticancer Potential of New Hydroxamic Acid Derivatives as Chemotherapeutic Agents
inferred← citeshttps://doi.org/10.1007/s12012-010-9083-xopenalex-snapshot
Glycolaldehyde Induces Oxidative Stress in the Heart: A Clue to Diabetic Cardiomyopathy?
inferred← citeshttps://doi.org/10.1007/s12035-012-8320-7openalex-snapshot
Infectious Agents and Neurodegeneration
inferred← citeshttps://doi.org/10.1007/s12035-016-9779-4openalex-snapshot
Human Glutathione S-Transferase Enzyme Gene Polymorphisms and Their Association With Neurocysticercosis
inferred← citeshttps://doi.org/10.1007/s12094-022-02891-yopenalex-snapshot
Role of papillary thyroid carcinoma patients with Hashimoto thyroiditis: evaluation of oxidative stress and inflammatory markers
inferred← citeshttps://doi.org/10.1007/s12192-013-0424-0openalex-snapshot
Comparative cytoprotective effects of carbocysteine and fluticasone propionate in cigarette smoke extract-stimulated bronchial epithelial cells
inferred← citeshttps://doi.org/10.1007/s12263-009-0142-5openalex-snapshot
Modulation of multiple pathways involved in the maintenance of neuronal function during aging by fisetin
inferred← citeshttps://doi.org/10.1007/s12272-019-01183-4openalex-snapshot
Allyl isothiocyanate may reverse the expression of MRP1 in COPD rats via the Notch1 signaling pathway
inferred← citeshttps://doi.org/10.1007/s12291-023-01167-8openalex-snapshot
Effects of Dietary Zinc Deficiency and Supplementation on Prepubertal Rat Testes: Sulfhydryl and Antioxidant Status
inferred← citeshttps://doi.org/10.1007/s12640-014-9473-0openalex-snapshot
Neurodegenerative Aspects in Vulnerability to Schizophrenia Spectrum Disorders
inferred← citeshttps://doi.org/10.1007/s12640-019-00142-7openalex-snapshot
Synthesis of Quercetin-Metal Complexes, In Vitro and In Silico Anticholinesterase and Antioxidant Evaluation, and In Vivo Toxicological and Anxiolitic Activities
inferred← citeshttps://doi.org/10.1007/s12640-020-00254-5openalex-snapshot
Glutathione in Chlorpyrifos-and Chlorpyrifos-Oxon-Induced Toxicity: a Comparative Study Focused on Non-cholinergic Toxicity in HT22 Cells
inferred← citeshttps://doi.org/10.1007/s12672-025-03251-2openalex-snapshot
Alterations in GSH/GSSG and CyS/CySS redox status in small cell lung cancer patients undergoing chemotherapy
inferred← citeshttps://doi.org/10.1007/s13105-013-0270-7openalex-snapshot
Positive influence of a natural product as propolis on antioxidant status and lipid peroxidation in senescent rats
inferred← citeshttps://doi.org/10.1007/s13204-022-02713-1openalex-snapshot
Fabrication of polyaspartic acid surface-modified highly fluorescent carbon quantum dot nanoprobe for sensing of reduced glutathione in real sample
inferred← citeshttps://doi.org/10.1007/s13577-023-00905-7openalex-snapshot
Neutrophil (dys)function due to altered immuno-metabolic axis in type 2 diabetes: implications in combating infections
inferred← citeshttps://doi.org/10.1007/s40257-014-0069-5openalex-snapshot
Bilirubin Levels and Their Association with Carotid Intima Media Thickness and High-Sensitivity C-reactive Protein in Patients with Psoriasis Vulgaris
inferred← citeshttps://doi.org/10.1016/b978-0-12-394309-5.00004-3openalex-snapshot
Mechanisms for Countering Oxidative Stress and Damage in Retinal Pigment Epithelium
inferred← citeshttps://doi.org/10.1016/b978-0-12-804598-5.00001-5openalex-snapshot
The Medical Applications of Nanomaterials in the Central Nervous System
inferred← citeshttps://doi.org/10.1016/b978-0-12-810422-4.00020-8openalex-snapshot
Sulfur Amino Acids and Skeletal Muscle
inferred← citeshttps://doi.org/10.1016/b978-0-12-818462-2.00015-2openalex-snapshot
Saffron—Immunity System
inferred← citeshttps://doi.org/10.1016/b978-0-12-821185-4.00012-9openalex-snapshot
Smart Drug Delivery Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-822819-7.00007-7openalex-snapshot
Application of magnetic nanoparticles as drug delivery in cancer
inferred← citeshttps://doi.org/10.1016/b978-0-323-43044-9.00097-2openalex-snapshot
Naturally Occurring Antioxidants
inferred← citeshttps://doi.org/10.1016/b978-0-323-90219-9.00005-4openalex-snapshot
Therapeutic applications of low-molecular-weight thiols and selenocompounds
inferred← citeshttps://doi.org/10.1016/b978-0-323-90219-9.00006-6openalex-snapshot
A thiol chemistry perspective on redox medicine
inferred← citeshttps://doi.org/10.1016/b978-0-323-98808-7.00009-6openalex-snapshot
Functional nutrigenomics: A personalized shift in treating inflammation
inferred← citeshttps://doi.org/10.1016/b978-0-443-22049-4.00016-3openalex-snapshot
Cellulose-based hydrogels for biosensing applications
inferred← citeshttps://doi.org/10.1016/b978-1-4377-2333-5.00108-5openalex-snapshot
Naturally Occurring Antioxidants
inferred← citeshttps://doi.org/10.1016/j.ab.2011.04.013openalex-snapshot
Detection of glutathione in whole blood after stabilization with N-ethylmaleimide
inferred← citeshttps://doi.org/10.1016/j.abb.2009.08.008openalex-snapshot
Aggravation of ischemia–reperfusion-triggered acute renal failure in xCT-deficient mice
inferred← citeshttps://doi.org/10.1016/j.aca.2020.04.006openalex-snapshot
L-cystine-linked BODIPY-adsorbed monolayer MoS2 quantum dots for ratiometric fluorescent sensing of biothiols based on the inner filter effect
inferred← citeshttps://doi.org/10.1016/j.actbio.2013.09.029openalex-snapshot
Thiolated hyaluronan-based hydrogels crosslinked using oxidized glutathione: An injectable matrix designed for ophthalmic applications
inferred← citeshttps://doi.org/10.1016/j.addr.2016.05.015openalex-snapshot
Stimuli responsive drug delivery systems based on nano-graphene for cancer therapy
inferred← citeshttps://doi.org/10.1016/j.afres.2026.102325openalex-snapshot
Ethanolic extract from giant red shrimp (Aristaeomorpha foliacea) cephalothorax: A waste-derived sustainable ingredient with antioxidant and anti-lipotoxic activity
inferred← citeshttps://doi.org/10.1016/j.animal.2021.100173openalex-snapshot
Effects of free and dipeptide forms of methionine supplementation on oxidative metabolism of broilers under high temperature
inferred← citeshttps://doi.org/10.1016/j.apr.2019.11.023openalex-snapshot
Aqueous particulate matter (PM2.5) from Brazil alters antioxidant profile responses and causes oxidative stress
inferred← citeshttps://doi.org/10.1016/j.apsusc.2017.12.058openalex-snapshot
Synthesis and characterization of diselenide linked poly(ethylene glycol) nanogel as multi-responsive drug carrier
inferred← citeshttps://doi.org/10.1016/j.arabjc.2018.06.019openalex-snapshot
Highly selective and sensitive optosensing of glutathione based on fluorescence resonance energy transfer of upconversion nanoparticles coated with a Rhodamine B derivative
inferred← citeshttps://doi.org/10.1016/j.arr.2023.102066openalex-snapshot
Glutathione and glutathione-dependent enzymes: From biochemistry to gerontology and successful aging
inferred← citeshttps://doi.org/10.1016/j.arres.2022.100043openalex-snapshot
Alterations in thiol redox state and lipid peroxidation in the brain areas of male mice during aging
inferred← citeshttps://doi.org/10.1016/j.arres.2025.100131openalex-snapshot
Glutathione deficiency and heart failure: a systematic review of human and animal evidence
inferred← citeshttps://doi.org/10.1016/j.autrev.2012.12.007openalex-snapshot
Interaction between glutathione and apoptosis in systemic lupus erythematosus
inferred← citeshttps://doi.org/10.1016/j.bbacli.2016.05.006openalex-snapshot
Analysis of glutathione levels in the brain tissue samples from HIV-1-positive individuals and subject with Alzheimer's disease and its implication in the pathophysiology of the disease process
inferred← citeshttps://doi.org/10.1016/j.bbadis.2011.12.012openalex-snapshot
Oxidative stress and antioxidant therapy in cystic fibrosis
inferred← citeshttps://doi.org/10.1016/j.bbadis.2013.05.008openalex-snapshot
Increased proton leak and SOD2 expression in myotubes from obese non-diabetic subjects with a family history of type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.bbadis.2018.03.014openalex-snapshot
New therapeutic activity of metabolic enhancer piracetam in treatment of neurodegenerative disease: Participation of caspase independent death factors, oxidative stress, inflammatory responses and apoptosis
inferred← citeshttps://doi.org/10.1016/j.bbagen.2016.05.017openalex-snapshot
Live-cell imaging approaches for the investigation of xenobiotic-induced oxidant stress
inferred← citeshttps://doi.org/10.1016/j.bbagen.2019.01.007openalex-snapshot
Glutathione antioxidant system and methylmercury-induced neurotoxicity: An intriguing interplay
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2010.07.007openalex-snapshot
Oxidative stress and alterations in actin cytoskeleton trigger glutathione efflux in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/j.bbamem.2013.11.002openalex-snapshot
Differential functional rescue of Lys513 and Lys516 processing mutants of MRP1 (ABCC1) by chemical chaperones reveals different domain–domain interactions of the transporter
inferred← citeshttps://doi.org/10.1016/j.bbr.2014.05.066openalex-snapshot
Sensory-motor performance after acute glutathione depletion by l-buthionine sulfoximine injection into substantia nigra pars compacta
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.04.087openalex-snapshot
Glutathione is a physiologic reservoir of neuronal glutamate
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.07.103openalex-snapshot
Glutathione increases the binding affinity of a bovine B12 trafficking chaperone bCblC for vitamin B12
inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.03.031openalex-snapshot
Destabilization of a bovine B12 trafficking chaperone protein by oxidized form of glutathione
inferred← citeshttps://doi.org/10.1016/j.bbrc.2012.03.120openalex-snapshot
Selective death of cancer cells by preferential induction of reactive oxygen species in response to (-)-epigallocatechin-3-gallate
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.08.081openalex-snapshot
Oxidative stress potentially enhances FcεRI-mediated leukotriene C4 release dependent on the late-phase increase of intracellular glutathione in mast cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.11.075openalex-snapshot
Processing of glutathionylcobalamin by a bovine B12 trafficking chaperone bCblC involved in intracellular B12 metabolism
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.07.088openalex-snapshot
The role of nuclear factor E2-Related factor 2 and uncoupling protein 2 in glutathione metabolism: Evidence from an in vivo gene knockout study
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.07.095openalex-snapshot
Redox imbalance in a model of rat mimicking Hutchinson-Gilford progeria syndrome
inferred← citeshttps://doi.org/10.1016/j.bbrc.2026.153284openalex-snapshot
Ferroptosis regulation and acute leukemia: Mechanisms and therapeutic perspectives
inferred← citeshttps://doi.org/10.1016/j.bcp.2013.02.013openalex-snapshot
Modulation of mitochondrial glutathione status and cellular energetics in primary cultures of proximal tubular cells from remnant kidney of uninephrectomized rats
inferred← citeshttps://doi.org/10.1016/j.bcp.2013.04.010openalex-snapshot
Concurrent regulation of the transcription factors Nrf2 and ATF4 mediates the enhancement of glutathione levels by the flavonoid fisetin
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