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Antioxidant Properties of Ergosterol and Its Role in Yeast Resistance to Oxidation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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A procedure to measure the antiradical efficiency of polyphenols
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Oxidative stress responses of the yeast Saccharomyces cerevisiae
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Gabedit—A graphical user interface for computational chemistry softwares
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tert‐Butyl hydroperoxide‐induced differing plasma membrane and oxidative stress processes in yeast strains BY4741 and erg5Δ
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Mechanism and kinetics of the oxidative damage to ergosterol induced by peroxyl radicals in lipid media: a theoretical quantum chemistry study
inferredcites →https://doi.org/10.1007/bf02817672openalex-snapshot
Viability and formation of conjugated dienes in plasma membrane lipids ofSaccharomyces cerevisiae, schizosaccharomyces pombe, rhodotorula glutinis andCandida albicans exposed to hydrophilic, amphiphilic and hydrophobic pro-oxidants
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Survival kit of Saccharomyces cerevisiae for anhydrobiosis
inferredcites →https://doi.org/10.1007/s12551-013-0128-9openalex-snapshot
Membrane changes under oxidative stress: the impact of oxidized lipids
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Trehalose lowers membrane phase transitions in dry yeast cells
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Vitamin D is a membrane antioxidant Ability to inhibit iron‐dependent lipid peroxidation in liposomes compared to cholesterol, ergosterol and tamoxifen and relevance to anticancer action
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Inhibitors of sterol biosynthesis and their applications
inferredcites →https://doi.org/10.1016/0308-8146(83)90030-4openalex-snapshot
The effect of sterols on the oxidation of edible oils
inferredcites →https://doi.org/10.1016/0891-5849(91)90187-8openalex-snapshot
Another cholesterol hypothesis: Cholesterol as antioxidant
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Alterations in mitochondrial membrane fluidity by lipid peroxidation products
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New trends in photobiology
inferredcites →https://doi.org/10.1016/j.bbamem.2008.12.002openalex-snapshot
Mechanistic role of ergosterol in membrane rigidity and cycloheximide resistance in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1016/j.bbamem.2010.01.015openalex-snapshot
Lateral reorganization of plasma membrane is involved in the yeast resistance to severe dehydration
inferredcites →https://doi.org/10.1016/j.bbamem.2010.11.012openalex-snapshot
Nature of sterols affects plasma membrane behavior and yeast survival during dehydration
inferredcites →https://doi.org/10.1016/j.bbamem.2011.04.016openalex-snapshot
Cholesterol attenuates and prevents bilayer damage and breakdown in lipoperoxidized model membranes. A spin labeling EPR study
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Influence of cholesterol and ergosterol on membrane dynamics using different fluorescent reporter probes
inferredcites →https://doi.org/10.1016/j.biotechadv.2018.11.003openalex-snapshot
Anhydrobiosis: Inside yeast cells
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Physical Damage on Giant Vesicles Membrane as a Result of Methylene Blue Photoirradiation
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Decreased cellular permeability to H 2 O 2 protects Saccharomyces cerevisiae cells in stationary phase against oxidative stress
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Special relationship between sterols and oxygen: Were sterols an adaptation to aerobic life?
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2009.10.018openalex-snapshot
Oxidative stress responses and lipid peroxidation damage are induced during dehydration in the production of dry active wine yeasts
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Reaction time and DPPH concentration influence antioxidant activity and kinetic parameters of bioactive molecules and plant extracts in the reaction with the DPPH radical
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Diffusion of univalent ions across the lamellae of swollen phospholipids
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C11-BODIPY581/591, an oxidation-sensitive fluorescent lipid peroxidation probe: (micro)spectroscopic characterization and validation of methodology
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Effect of Oxidative Stress on Membrane Structure: Small-Angle X-Ray Diffraction Analysis
inferredcites →https://doi.org/10.1021/cr200021mopenalex-snapshot
Biosynthesis of Cholesterol and Other Sterols
inferredcites →https://doi.org/10.1021/cr9904009openalex-snapshot
Quantum Mechanical Continuum Solvation Models
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Estimation of inner shell Marcus terms for amino nitrogen compounds by molecular orbital calculations
inferredcites →https://doi.org/10.1021/jf102285bopenalex-snapshot
Ergosterol Profiles, Fatty Acid Composition, and Antioxidant Activities of Button Mushrooms as Affected by Tissue Part and Developmental Stage
inferredcites →https://doi.org/10.1021/jf500180uopenalex-snapshot
Re-evaluation of the 2,2-Diphenyl-1-picrylhydrazyl Free Radical (DPPH) Assay for Antioxidant Activity
inferredcites →https://doi.org/10.1021/jp509125bopenalex-snapshot
Kinetics and Thermodynamics of 1-Hydroxyethyl Radical Reaction with Unsaturated Lipids and Prenylflavonoids
inferredcites →https://doi.org/10.1038/nrm2330openalex-snapshot
Membrane lipids: where they are and how they behave
inferredcites →https://doi.org/10.1038/sj.emboj.7601466openalex-snapshot
Membrane potential governs lateral segregation of plasma membrane proteins and lipids in yeast
inferredcites →https://doi.org/10.1039/c5sc02311dopenalex-snapshot
Effect of lipid peroxidation on membrane permeability of cancer and normal cells subjected to oxidative stress
inferredcites →https://doi.org/10.1039/c6fo01600fopenalex-snapshot
Development of dairy beverages functionalized with pure ergosterol and mycosterol extracts: an alternative to phytosterol-based beverages
inferredcites →https://doi.org/10.1046/j.1432-1327.2000.01179.xopenalex-snapshot
Effects of singlet oxygen on membrane sterols in the yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1073/pnas.1117280109openalex-snapshot
Amphotericin primarily kills yeast by simply binding ergosterol
inferredcites →https://doi.org/10.1074/jbc.m110.154435openalex-snapshot
Gel Domains in the Plasma Membrane of Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1091/mbc.10.11.3943openalex-snapshot
Specific Sterols Required for the Internalization Step of Endocytosis in Yeast
inferredcites →https://doi.org/10.1091/mbc.e02-04-0186openalex-snapshot
Multiple Functions of Sterols in Yeast Endocytosis
inferredcites →https://doi.org/10.1103/revmodphys.65.599openalex-snapshot
Electron transfer reactions in chemistry. Theory and experiment
inferredcites →https://doi.org/10.1110/ps.8.6.1191openalex-snapshot
The 2.1 Å structure of an elicitin‐ergosterol complex: A recent addition to the Sterol Carrier Protein family
inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01011.xopenalex-snapshot
CHOLESTEROL AS AN EVOLUTIONARY RESPONSE TO LIVING WITH OXYGEN
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01667.xopenalex-snapshot
ERGOSTEROL BIOSYNTHESIS: A FUNGAL PATHWAY FOR LIFE ON LAND?
inferredcites →https://doi.org/10.1111/j.1751-1097.1989.tb05563.xopenalex-snapshot
A ROLE FOR STEROLS IN THE PORPHYRIN MEDIATED PHOTOSENSITIZATION OF YEAST
inferredcites →https://doi.org/10.1128/aac.47.8.2404-2412.2003openalex-snapshot
Candida albicans Mutations in the Ergosterol Biosynthetic Pathway and Resistance to Several Antifungal Agents
inferredcites →https://doi.org/10.1134/s0026261706030015openalex-snapshot
Tolerance of the yeast Yarrowia lipolytica to oxidative stress
inferredcites →https://doi.org/10.1146/annurev-pharmtox-010715-103233openalex-snapshot
Oxysterols: Old Tale, New Twists
inferredcites →https://doi.org/10.1146/annurev.mi.49.100195.000523openalex-snapshot
PHYSIOLOGICAL IMPLICATIONS OF STEROL BIOSYNTHESIS IN YEAST
inferredcites →https://doi.org/10.1371/journal.pone.0010899openalex-snapshot
Phylogenetic Distribution of Fungal Sterols
inferredcites →https://doi.org/10.1379/1466-1268(2003)008<0120:paoddo>2.0.co;2openalex-snapshot
Protection against oxidation during dehydration of yeast
inferredcites →https://doi.org/10.3389/fcell.2020.00337openalex-snapshot
Liquid-Ordered Phase Formation by Mammalian and Yeast Sterols: A Common Feature With Organizational Differences
inferredcites →https://doi.org/10.3390/genes11070795openalex-snapshot
Regulation of Ergosterol Biosynthesis in Saccharomyces cerevisiae
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inferred← citeshttps://doi.org/10.4103/japtr.japtr_525_23openalex-snapshot
Potential antioxidant and antiradical agents from Allium ascalonicum: Superoxide dismutase and density functional theory in silico studies
inferred← citeshttps://doi.org/10.5530/pj.2024.16.207openalex-snapshot
Phytochemical and Pharmacological Studies of Different Extracts of Stem Bark and Leaf of Flueggea leucopyrus Willd.
inferred← citeshttps://doi.org/10.58837/chula.the.2022.82openalex-snapshot
Anti-neuroinflammatory effects of auricularia polytricha extracts on bisphenol a (BPA)-induced microglial cell activation and reduction of hippocampal cell damage
inferred← citeshttps://doi.org/10.6084/m9.figshare.26656048openalex-snapshot
Additional file 1 of Four ways of implementing robustness quantification in strain characterisation
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
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and goes through ORCID: icsacinstitute.org/submit.