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Mitochondrial proton and electron leaks

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What this work says

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

inferredcites →https://doi.org/10.1002/j.1460-2075.1985.tb04049.xopenalex-snapshot

The reconstituted isolated uncoupling protein is a membrane potential driven H+ translocator.

inferredcites →https://doi.org/10.1007/978-1-4615-6111-8_47openalex-snapshot

Reactive oxygen species, mitochondria, apoptosis and aging

inferredcites →https://doi.org/10.1007/s10863-009-9232-8openalex-snapshot

Uncoupling protein-1 (UCP1) contributes to the basal proton conductance of brown adipose tissue mitochondria

inferredcites →https://doi.org/10.1016/j.bbabio.2003.11.001openalex-snapshot

Alkylsulfonates activate the uncoupling protein UCP1: implications for the transport mechanism

inferredcites →https://doi.org/10.1016/j.bbabio.2005.08.003openalex-snapshot

The topology of superoxide production by complex III and glycerol 3-phosphate dehydrogenase in Drosophila mitochondria

inferredcites →https://doi.org/10.1016/j.bbabio.2006.04.024openalex-snapshot

Participation of ATP/ADP antiporter in oleate- and oleate hydroperoxide-induced uncoupling suppressed by GDP and carboxyatractylate

inferredcites →https://doi.org/10.1016/j.bbabio.2008.04.020openalex-snapshot

Mitochondrial uncoupling protein 1 expression in thymocytes

inferredcites →https://doi.org/10.1016/j.bbabio.2009.01.012openalex-snapshot

Architecture of complex I and its implications for electron transfer and proton pumping

inferredcites →https://doi.org/10.1016/j.cmet.2007.10.010openalex-snapshot

Respiratory Uncoupling in Skeletal Muscle Delays Death and Diminishes Age-Related Disease

inferredcites →https://doi.org/10.1016/j.cmet.2008.12.014openalex-snapshot

UCP1 Ablation Induces Obesity and Abolishes Diet-Induced Thermogenesis in Mice Exempt from Thermal Stress by Living at Thermoneutrality

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2004.05.034openalex-snapshot

Mitochondrial superoxide: production, biological effects, and activation of uncoupling proteins

inferredcites →https://doi.org/10.1016/j.freeradbiomed.2009.01.010openalex-snapshot

Reactive oxygen species regulation by AIF- and complex I-depleted brain mitochondria

inferredcites →https://doi.org/10.1016/s0005-2728(03)00027-6openalex-snapshot

Intrinsic and extrinsic uncoupling of oxidative phosphorylation

inferredcites →https://doi.org/10.1016/s0005-2728(89)80063-5openalex-snapshot

Slip and leak in mitochondrial oxidative phosphorylation

inferredcites →https://doi.org/10.1016/s0021-9258(17)30658-0openalex-snapshot

New substrates and competitive inhibitors of the Cl- translocating pathway of the uncoupling protein of brown adipose tissue mitochondria.

inferredcites →https://doi.org/10.1016/s0021-9258(19)38245-6openalex-snapshot

Non-ohmic proton conductance of the mitochondrial inner membrane in hepatocytes.

inferredcites →https://doi.org/10.1016/s0076-6879(09)05023-xopenalex-snapshot

Chapter 23 Measuring Mitochondrial Bioenergetics in INS-1E Insulinoma Cells

inferredcites →https://doi.org/10.1016/s0092-8674(01)00378-6openalex-snapshot

Uncoupling Protein-2 Negatively Regulates Insulin Secretion and Is a Major Link between Obesity, β Cell Dysfunction, and Type 2 Diabetes

inferredcites →https://doi.org/10.1021/bi0342160openalex-snapshot

Architecture of the QoSite of the Cytochromebc1Complex Probed by Superoxide Production

inferredcites →https://doi.org/10.1023/a:1006873518427openalex-snapshot

Reactive oxygen species, mitochondria, apoptosis and aging

inferredcites →https://doi.org/10.1023/a:1016027302232openalex-snapshot

Does Any Yeast Mitochondrial Carrier Have a Native Uncoupling Protein Function?

inferredcites →https://doi.org/10.1038/191144a0openalex-snapshot

Coupling of Phosphorylation to Electron and Hydrogen Transfer by a Chemi-Osmotic type of Mechanism

inferredcites →https://doi.org/10.1038/80450openalex-snapshot

Skeletal muscle respiratory uncoupling prevents diet-induced obesity and insulin resistance in mice

inferredcites →https://doi.org/10.1038/nprot.2008.56openalex-snapshot

The selective detection of mitochondrial superoxide by live cell imaging

inferredcites →https://doi.org/10.1038/sj.ijo.0800936openalex-snapshot

The significance and mechanism of mitochondrial proton conductance

inferredcites →https://doi.org/10.1042/bj20040485openalex-snapshot

Superoxide production by NADH:ubiquinone oxidoreductase (complex I) depends on the pH gradient across the mitochondrial inner membrane

inferredcites →https://doi.org/10.1042/bj20050890openalex-snapshot

The basal proton conductance of mitochondria depends on adenine nucleotide translocase content

inferredcites →https://doi.org/10.1042/bj20081386openalex-snapshot

How mitochondria produce reactive oxygen species

inferredcites →https://doi.org/10.1042/bj2750075openalex-snapshot

Effect of protonmotive force on the relative proton stoichiometries of the mitochondrial proton pumps

inferredcites →https://doi.org/10.1042/bsr20080002openalex-snapshot

Stimulation of mitochondrial proton conductance by hydroxynonenal requires a high membrane potential

inferredcites →https://doi.org/10.1042/bst0360976openalex-snapshot

The production of reactive oxygen species by complex I

inferredcites →https://doi.org/10.1046/j.1467-789x.2001.00043.xopenalex-snapshot

Mitochondrial uncoupling as a target for drug development for the treatment of obesity

inferredcites →https://doi.org/10.1056/nejmoa0808718openalex-snapshot

Cold-Activated Brown Adipose Tissue in Healthy Men

inferredcites →https://doi.org/10.1056/nejmoa0808949openalex-snapshot

Functional Brown Adipose Tissue in Healthy Adults

inferredcites →https://doi.org/10.1056/nejmoa0810780openalex-snapshot

Identification and Importance of Brown Adipose Tissue in Adult Humans

inferredcites →https://doi.org/10.1073/pnas.0510977103openalex-snapshot

The mechanism of superoxide production by NADH:ubiquinone oxidoreductase (complex I) from bovine heart mitochondria

inferredcites →https://doi.org/10.1073/pnas.0809580105openalex-snapshot

The mechanism of transport by mitochondrial carriers based on analysis of symmetry

inferredcites →https://doi.org/10.1074/jbc.271.5.2615openalex-snapshot

On the Mechanism of Fatty Acid-induced Proton Transport by Mitochondrial Uncoupling Protein

inferredcites →https://doi.org/10.1074/jbc.m207217200openalex-snapshot

Topology of Superoxide Production from Different Sites in the Mitochondrial Electron Transport Chain

inferredcites →https://doi.org/10.1074/jbc.m402375200openalex-snapshot

Native UCP1 Displays Simple Competitive Kinetics between the Regulators Purine Nucleotides and Fatty Acids

inferredcites →https://doi.org/10.1074/jbc.m406576200openalex-snapshot

Inhibitors of the Quinone-binding Site Allow Rapid Superoxide Production from Mitochondrial NADH:Ubiquinone Oxidoreductase (Complex I)

inferredcites →https://doi.org/10.1074/jbc.m407715200openalex-snapshot

Complex III Releases Superoxide to Both Sides of the Inner Mitochondrial Membrane

inferredcites →https://doi.org/10.1074/jbc.m803871200openalex-snapshot

Essential Role for Uncoupling Protein-3 in Mitochondrial Adaptation to Fasting but Not in Fatty Acid Oxidation or Fatty Acid Anion Export

inferredcites →https://doi.org/10.1111/j.1471-4159.2006.04223.xopenalex-snapshot

Characteristics of α‐glycerophosphate‐evoked H2O2 generation in brain mitochondria

inferredcites →https://doi.org/10.1113/expphysiol.2006.034330openalex-snapshot

Mitochondrial function, fibre types and ageing: new insights from human muscle in vivo

inferredcites →https://doi.org/10.1146/annurev.physiol.66.032102.150251openalex-snapshot

The Cytochrome bc1 Complex: Function in the Context of Structure

inferredcites →https://doi.org/10.1152/ajpcell.1996.271.4.c1380openalex-snapshot

Contribution of mitochondrial proton leak to skeletal muscle respiration and to standard metabolic rate

inferredcites →https://doi.org/10.1152/physiolgenomics.00070.2005openalex-snapshot

Uncoupling protein 1 in fish uncovers an ancient evolutionary history of mammalian nonshivering thermogenesis

inferredcites →https://doi.org/10.1152/physiolgenomics.00183.2007openalex-snapshot

Marsupial uncoupling protein 1 sheds light on the evolution of mammalian nonshivering thermogenesis

inferredcites →https://doi.org/10.1152/physrev.00015.2003openalex-snapshot

Brown Adipose Tissue: Function and Physiological Significance

inferredcites →https://doi.org/10.1210/en.2008-1642openalex-snapshot

Persistent Oxidative Stress Due to Absence of Uncoupling Protein 2 Associated with Impaired Pancreatic β-Cell Function

inferredcites →https://doi.org/10.1523/jneurosci.1899-04.2004openalex-snapshot

Mitochondrial α-Ketoglutarate Dehydrogenase Complex Generates Reactive Oxygen Species

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Curcumin for protecting mitochondria and downregulating inflammation

inferred← citeshttps://doi.org/10.1016/b978-0-443-18858-9.00024-xopenalex-snapshot

Mitochondrial transfer in the immune compartment

inferred← citeshttps://doi.org/10.1016/b978-0-443-34069-7.00008-2openalex-snapshot

Epigenetics and the kidney

inferred← citeshttps://doi.org/10.1016/b978-0-444-64056-7.00009-xopenalex-snapshot

Quercetin: Prooxidant Effect and Apoptosis in Cancer

inferred← citeshttps://doi.org/10.1016/bs.adgen.2025.02.002openalex-snapshot

FAcTs on fire: Exploring thermogenesis

inferred← citeshttps://doi.org/10.1016/bs.ircmb.2022.10.002openalex-snapshot

Role of mitochondrial outer membrane permeabilization during bacterial infection

inferred← citeshttps://doi.org/10.1016/bs.mie.2019.02.039openalex-snapshot

REX technologies for profiling and decoding the electrophile signaling axes mediated by Rosetta Stone proteins

inferred← citeshttps://doi.org/10.1016/bs.pmbts.2020.04.018openalex-snapshot

Oxidative stress, metabolic and mitochondrial abnormalities associated with autism spectrum disorder

inferred← citeshttps://doi.org/10.1016/j.abb.2015.03.025openalex-snapshot

Functional characterization of CYP107W1 from Streptomyces avermitilis and biosynthesis of macrolide oligomycin A

inferred← citeshttps://doi.org/10.1016/j.abb.2020.108416openalex-snapshot

Mechanisms involved in the unbalanced redox homeostasis in osteoblastic cellular model of Alkaptonuria

inferred← citeshttps://doi.org/10.1016/j.abb.2023.109690openalex-snapshot

Effects of ROS pathway inhibitors and NADH and FADH2 linked substrates on mitochondrial bioenergetics and ROS emission in the heart and kidney cortex and outer medulla

inferred← citeshttps://doi.org/10.1016/j.actbio.2019.08.007openalex-snapshot

Matrix-guided control of mitochondrial function in cardiac myocytes

inferred← citeshttps://doi.org/10.1016/j.ajog.2020.11.005openalex-snapshot

Placental energy metabolism in health and disease—significance of development and implications for preeclampsia

inferred← citeshttps://doi.org/10.1016/j.anireprosci.2021.106779openalex-snapshot

Effect of glucose concentration and cryopreservation on mitochondrial functions of bull spermatozoa and relationship with sire conception rate

inferred← citeshttps://doi.org/10.1016/j.apsb.2021.08.007openalex-snapshot

Anti-aging effects of chlorpropamide depend on mitochondrial complex-II and the production of mitochondrial reactive oxygen species

inferred← citeshttps://doi.org/10.1016/j.aquaculture.2018.12.041openalex-snapshot

Acute but not chronic hyperoxia increases metabolic rate without altering the cardiorespiratory response in Atlantic salmon alevins

inferred← citeshttps://doi.org/10.1016/j.aquatox.2014.11.005openalex-snapshot

Modulation of cadmium-induced mitochondrial dysfunction and volume changes by temperature in rainbow trout (Oncorhynchus mykiss)

inferred← citeshttps://doi.org/10.1016/j.aquatox.2015.10.006openalex-snapshot

Effects of copper, hypoxia and acute temperature shifts on mitochondrial oxidation in rainbow trout (Oncorhynchus mykiss) acclimated to warm temperature

inferred← citeshttps://doi.org/10.1016/j.aquatox.2017.06.011openalex-snapshot

Effect of contaminants of emerging concern on liver mitochondrial function in Chinook salmon

inferred← citeshttps://doi.org/10.1016/j.aquatox.2018.03.031openalex-snapshot

High-throughput assessment of oxidative respiration in fish embryos: Advancing adverse outcome pathways for mitochondrial dysfunction

inferred← citeshttps://doi.org/10.1016/j.aquatox.2019.105264openalex-snapshot

Effects of bioenergetics, temperature and cadmium on liver mitochondria reactive oxygen species production and consumption

inferred← citeshttps://doi.org/10.1016/j.aquatox.2023.106658openalex-snapshot

Mitochondrial dysfunction and oxidative stress contribute to cross-generational toxicity of benzo(a)pyrene in Danio rerio

inferred← citeshttps://doi.org/10.1016/j.aquatox.2026.108044openalex-snapshot

Roundup® induces oxidative stress in zebrafish liver cell line (ZF-L): Role of the Nrf pathway and uncoupling proteins

inferred← citeshttps://doi.org/10.1016/j.arr.2014.09.002openalex-snapshot

Proteome analysis in the assessment of ageing

inferred← citeshttps://doi.org/10.1016/j.arr.2025.102938openalex-snapshot

Metabolic reprogramming of pancreatic beta cells in type 2 diabetes and its therapeutic strategy

inferred← citeshttps://doi.org/10.1016/j.arres.2024.100108openalex-snapshot

Mitochondria-targeted antioxidant, mitoQ protects hepatic tissue from N-nitrosodiethylamine-induced damage by modulating mitochondrial function and redox status

inferred← citeshttps://doi.org/10.1016/j.bbabio.2012.05.014openalex-snapshot

Functional characterization of UCP1 in mammalian HEK293 cells excludes mitochondrial uncoupling artefacts and reveals no contribution to basal proton leak

inferred← citeshttps://doi.org/10.1016/j.bbabio.2013.03.001openalex-snapshot

Molecular mechanisms for generating transmembrane proton gradients

inferred← citeshttps://doi.org/10.1016/j.bbabio.2014.02.008openalex-snapshot

Brite/beige fat and UCP1 — is it thermogenesis?

inferred← citeshttps://doi.org/10.1016/j.bbabio.2014.05.230openalex-snapshot

Mitochondrial dysfunctions in brain of bulbectomized mice — Model of sporadic Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/j.bbabio.2016.10.003openalex-snapshot

The conserved regulation of mitochondrial uncoupling proteins: From unicellular eukaryotes to mammals

inferred← citeshttps://doi.org/10.1016/j.bbabio.2018.11.007openalex-snapshot

Uncoupling mechanism and redox regulation of mitochondrial uncoupling protein 1 (UCP1)

inferred← citeshttps://doi.org/10.1016/j.bbabio.2018.11.017openalex-snapshot

Fasting promotes functional changes in liver mitochondria

inferred← citeshttps://doi.org/10.1016/j.bbabio.2019.03.001openalex-snapshot

Proton leakage across lipid bilayers: Oxygen atoms of phospholipid ester linkers align water molecules into transmembrane water wires

inferred← citeshttps://doi.org/10.1016/j.bbabio.2022.148582openalex-snapshot

Naked mole-rat and Damaraland mole-rat exhibit lower respiration in mitochondria, cellular and organismal levels

inferred← citeshttps://doi.org/10.1016/j.bbabio.2025.149561openalex-snapshot

Mitochondrial Reactive Oxygen Species Production in Lungs of Rats with Different Susceptibilities to Hyperoxia-Induced Acute Lung Injury

inferred← citeshttps://doi.org/10.1016/j.bbabio.2026.149605openalex-snapshot

Effects of increases in temperature and genipin on mitochondrial function in primary fibroblast cells of dogs of different sizes and ages

inferred← citeshttps://doi.org/10.1016/j.bbadis.2018.10.011openalex-snapshot

The role of mitochondria in sepsis-induced cardiomyopathy

inferred← citeshttps://doi.org/10.1016/j.bbadis.2020.165967openalex-snapshot

Placental mitochondrial dysfunction with metabolic diseases: Therapeutic approaches

inferred← citeshttps://doi.org/10.1016/j.bbagen.2017.05.020openalex-snapshot

2102Ep embryonal carcinoma cells have compromised respiration and shifted bioenergetic profile distinct from H9 human embryonic stem cells

inferred← citeshttps://doi.org/10.1016/j.bbagen.2020.129523openalex-snapshot

Adaptation of striated muscles to Wolframin deficiency in mice: Alterations in cellular bioenergetics

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2024.119886openalex-snapshot

Vasoactive intestinal peptide induces metabolic rewiring of human-derived cytotrophoblast cells to promote cell migration

inferred← citeshttps://doi.org/10.1016/j.bbcan.2021.188534openalex-snapshot

Mitochondria: The metabolic switch of cellular oncogenic transformation

inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.03.098openalex-snapshot

Inhibition by purine nucleotides of the release of reactive oxygen species from muscle mitochondria: Indication for a function of uncoupling proteins as superoxide anion transporters

inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.06.029openalex-snapshot

Neuronal mitochondrial dysfunction in a cellular model of circadian rhythm disruption is rescued by donepezil

inferred← citeshttps://doi.org/10.1016/j.bcp.2022.115337openalex-snapshot

Adipose tissue mitochondrial dysfunction and cardiometabolic diseases: On the search for novel molecular targets

inferred← citeshttps://doi.org/10.1016/j.biocel.2012.08.024openalex-snapshot

Energy-converting respiratory Complex I: On the way to the molecular mechanism of the proton pump

inferred← citeshttps://doi.org/10.1016/j.biochi.2016.11.013openalex-snapshot

Targeted mitochondrial uncoupling beyond UCP1 – The fine line between death and metabolic health

inferred← citeshttps://doi.org/10.1016/j.biochi.2016.12.005openalex-snapshot

Meaningful respirometric measurements of UCP1-mediated thermogenesis

inferred← citeshttps://doi.org/10.1016/j.biochi.2023.06.008openalex-snapshot

Proton leak through the UCPs and ANT carriers and beyond: A breath for the electron transport chain

inferred← citeshttps://doi.org/10.1016/j.biopha.2024.116545openalex-snapshot

Mechanical stress induced mitochondrial dysfunction in cardiovascular diseases: Novel mechanisms and therapeutic targets

inferred← citeshttps://doi.org/10.1016/j.biosystems.2025.105544openalex-snapshot

Coupling of the energetic and purinergic activities of ATP in ischemic and hypoxic disease states

inferred← citeshttps://doi.org/10.1016/j.bmc.2012.11.051openalex-snapshot

Effects of cytoprotective antioxidants on lymphocytes from representative mitochondrial neurodegenerative diseases

inferred← citeshttps://doi.org/10.1016/j.bpj.2012.11.3808openalex-snapshot

Integrating Mitochondrial Energetics, Redox and ROS Metabolic Networks: A Two-Compartment Model

inferred← citeshttps://doi.org/10.1016/j.brainres.2016.02.007openalex-snapshot

Mitochondrial specific therapeutic targets following brain injury

inferred← citeshttps://doi.org/10.1016/j.brainres.2025.149493openalex-snapshot

Arsenic-induced mice model of Parkinson’s disease: Revealing the neurotoxicity of arsenic through mitochondrial complexes inhibition and dopaminergic neurodegeneration in the substantia nigra region of brain

inferred← citeshttps://doi.org/10.1016/j.canlet.2019.03.020openalex-snapshot

Reactive oxygen species and cancer: A complex interaction

inferred← citeshttps://doi.org/10.1016/j.canlet.2021.11.022openalex-snapshot

The aryl-ureido fatty acid CTU activates endoplasmic reticulum stress and PERK/NOXA-mediated apoptosis in tumor cells by a dual mitochondrial-targeting mechanism

inferred← citeshttps://doi.org/10.1016/j.carbpol.2018.01.079openalex-snapshot

Hydroxyethyl methacrylate grafted carboxy methyl tamarind (CMT-g-HEMA) polysaccharide based matrix as a suitable scaffold for skin tissue engineering

inferred← citeshttps://doi.org/10.1016/j.carbpol.2021.117992openalex-snapshot

Octanoyl glycol chitosan enhances the proliferation and differentiation of tonsil-derived mesenchymal stem cells

inferred← citeshttps://doi.org/10.1016/j.cbi.2010.12.002openalex-snapshot

Bioenergetic function in cardiovascular cells: The importance of the reserve capacity and its biological regulation

inferred← citeshttps://doi.org/10.1016/j.cbpa.2013.01.008openalex-snapshot

Depression of mitochondrial respiration during daily torpor of the Djungarian hamster, Phodopus sungorus, is specific for liver and correlates with body temperature

inferred← citeshttps://doi.org/10.1016/j.cbpa.2013.09.002openalex-snapshot

Metabolic depression during warm torpor in the Golden spiny mouse (Acomys russatus) does not affect mitochondrial respiration and hydrogen peroxide release

inferred← citeshttps://doi.org/10.1016/j.cbpa.2014.07.009openalex-snapshot

Cellular metabolic rates from primary dermal fibroblast cells isolated from birds of different body masses

inferred← citeshttps://doi.org/10.1016/j.cbpa.2021.111082openalex-snapshot

Invited review: Thermal effects on oxidative stress in vertebrate ectotherms

inferred← citeshttps://doi.org/10.1016/j.cbpb.2015.03.005openalex-snapshot

Molecular cloning and tissue expression of uncoupling protein 1, 2 and 3 genes in Chinese perch (Siniperca chuatsi)

inferred← citeshttps://doi.org/10.1016/j.cbpb.2019.110375openalex-snapshot

Heart mitochondria from naked mole-rats (Heterocephalus glaber) are more coupled, but similarly susceptible to anoxia-reoxygenation stress than in laboratory mice (Mus musculus)

inferred← citeshttps://doi.org/10.1016/j.cbpb.2021.110613openalex-snapshot

Comparative functional analyses of UCP1 to unravel evolution, ecophysiology and mechanisms of mammalian thermogenesis

inferred← citeshttps://doi.org/10.1016/j.cbpc.2026.110618openalex-snapshot

Evaluating the use of the extracellular flux analyzer assay to determine mitochondrial effects of pesticides with zebrafish (Danio rerio)

inferred← citeshttps://doi.org/10.1016/j.cej.2024.150036openalex-snapshot

Triggering triboelectric nanogenerator antibacterial Activities: Effect of charge polarity and host material correlation

inferred← citeshttps://doi.org/10.1016/j.cell.2018.08.042openalex-snapshot

Atlas of Circadian Metabolism Reveals System-wide Coordination and Communication between Clocks

inferred← citeshttps://doi.org/10.1016/j.cmet.2012.10.016openalex-snapshot

Adipose-Specific Deletion of TFAM Increases Mitochondrial Oxidation and Protects Mice against Obesity and Insulin Resistance

inferred← citeshttps://doi.org/10.1016/j.cmet.2018.06.009openalex-snapshot

Serine Synthesis via PHGDH Is Essential for Heme Production in Endothelial Cells

inferred← citeshttps://doi.org/10.1016/j.cmet.2018.11.002openalex-snapshot

New Advances in Adaptive Thermogenesis: UCP1 and Beyond

inferred← citeshttps://doi.org/10.1016/j.cophys.2022.100491openalex-snapshot

A theoretical argument to support the biological benefits for insulin stimulating mitochondrial oxidative phosphorylation

inferred← citeshttps://doi.org/10.1016/j.cryobiol.2018.02.010openalex-snapshot

Role of superoxide ion formation in hypothermia/rewarming induced contractile dysfunction in cardiomyocytes

inferred← citeshttps://doi.org/10.1016/j.cryobiol.2025.105231openalex-snapshot

Ellagic acid maintains post-thaw goat sperm quality via protecting mitochondrial function from ROS damage

inferred← citeshttps://doi.org/10.1016/j.device.2023.100001openalex-snapshot

A light-driven nanopipette ion pump for probing subcellular oxygen levels

inferred← citeshttps://doi.org/10.1016/j.diff.2015.01.001openalex-snapshot

The cellular and molecular progression of mitochondrial dysfunction induced by 2,4-dinitrophenol in developing zebrafish embryos

inferred← citeshttps://doi.org/10.1016/j.drup.2018.11.001openalex-snapshot

Modulating ROS to overcome multidrug resistance in cancer

inferred← citeshttps://doi.org/10.1016/j.ejcb.2020.151073openalex-snapshot

ROS and oncogenesis with special reference to EMT and stemness

inferred← citeshttps://doi.org/10.1016/j.ejcb.2025.151488openalex-snapshot

Galectin-8 drives ERK-dependent mitochondrial fragmentation, perinuclear relocation and mitophagy, with metabolic adaptations for cell proliferation

inferred← citeshttps://doi.org/10.1016/j.ejphar.2013.12.006openalex-snapshot

Mildronate, the inhibitor of l-carnitine transport, induces brain mitochondrial uncoupling and protects against anoxia-reoxygenation

inferred← citeshttps://doi.org/10.1016/j.ejphar.2014.12.020openalex-snapshot

Aspirin may influence cellular energy status

inferred← citeshttps://doi.org/10.1016/j.ejphar.2022.175470openalex-snapshot

Inclusion of the in-chain sulfur in 3-thiaCTU increases the efficiency of mitochondrial targeting and cell killing by anticancer aryl-urea fatty acids

inferred← citeshttps://doi.org/10.1016/j.ekir.2024.05.005openalex-snapshot

The Role of Mitochondrial Dysfunction in CKD-Related Vascular Calcification: From Mechanisms to Therapeutics

inferred← citeshttps://doi.org/10.1016/j.exger.2017.10.015openalex-snapshot

Mechanisms driving the ageing heart

inferred← citeshttps://doi.org/10.1016/j.exger.2019.110712openalex-snapshot

The effect of short-term methionine restriction on glutathione synthetic capacity and antioxidant responses at the whole tissue and mitochondrial level in the rat liver

inferred← citeshttps://doi.org/10.1016/j.expneurol.2020.113307openalex-snapshot

Mitochondrial damage & lipid signaling in traumatic brain injury

inferred← citeshttps://doi.org/10.1016/j.fct.2019.110672openalex-snapshot

Phenolic compounds from coffee by-products modulate adipogenesis-related inflammation, mitochondrial dysfunction, and insulin resistance in adipocytes, via insulin/PI3K/AKT signaling pathways

inferred← citeshttps://doi.org/10.1016/j.fct.2022.112819openalex-snapshot

Beauvericin (BEA) and enniatin B (ENNB)-induced impairment of mitochondria and lysosomes - Potential sources of intracellular reactive iron triggering ferroptosis in Atlantic salmon primary hepatocytes

inferred← citeshttps://doi.org/10.1016/j.febslet.2013.04.035openalex-snapshot

The pH sensitivity of H2O2 metabolism in skeletal muscle mitochondria

inferred← citeshttps://doi.org/10.1016/j.fm.2026.105276openalex-snapshot

Electrochemical identification of riboflavin-mediated redox adaptation in Escherichia coli under mild heat stress

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2012.04.033openalex-snapshot

Ionizing radiation induces mitochondrial reactive oxygen species production accompanied by upregulation of mitochondrial electron transport chain function and mitochondrial content under control of the cell cycle checkpoint

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2014.09.004openalex-snapshot

Antioxidant properties of UCP1 are evolutionarily conserved in mammals and buffer mitochondrial reactive oxygen species

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2015.03.017openalex-snapshot

Zinc and calcium modulate mitochondrial redox state and morphofunctional integrity

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.02.004openalex-snapshot

The circadian gene Rev-erbα improves cellular bioenergetics and provides preconditioning for protection against oxidative stress

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2016.04.001openalex-snapshot

Mitochondrial generation of superoxide and hydrogen peroxide as the source of mitochondrial redox signaling

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2017.01.022openalex-snapshot

Carbon monoxide reverses the metabolic adaptation of microglia cells to an inflammatory stimulus

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2019.09.031openalex-snapshot

Oxidative stress mediates ethanol-induced skeletal muscle mitochondrial dysfunction and dysregulated protein synthesis and autophagy

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2020.09.009openalex-snapshot

4-Hydroxy-7-oxo-5-heptenoic acid lactone can induce mitochondrial dysfunction in retinal pigmented epithelial cells

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2022.11.036openalex-snapshot

WITHDRAWN: Mitochondria need their sleep: Sleep-wake cycling and the role of redox, bioenergetics, and temperature regulation, involving cysteine-mediated redox signaling, uncoupling proteins, and substrate cycles

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2024.02.005openalex-snapshot

Coenzyme Q deficiency in endothelial mitochondria caused by hypoxia; remodeling of the respiratory chain and sensitivity to anoxia/reoxygenation

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2026.06.013openalex-snapshot

Mitochondrial disease: mechanisms, signalling, and therapeutic opportunities

inferred← citeshttps://doi.org/10.1016/j.gene.2018.06.082openalex-snapshot

Emerging role of nutrition and the non-coding landscape in type 2 diabetes mellitus: A review of literature

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