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Oxidative damage and phospholipid fatty acyl composition in skeletal muscle mitochondria from mice underexpressing or overexpressing uncoupling protein 3
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/bbrc.2001.4577openalex-snapshot
Uncoupling Protein-2 Participates in Cellular Defense against Oxidative Stress in Clonal β-Cells
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/bf01963830openalex-snapshot
Biogenesis of mitochondria 20 the effects of altered membrane lipid composition on mitochondrial oxidative phosphorylation inSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1007/s00360-002-0264-1openalex-snapshot
Proton leak in hepatocytes and liver mitochondria from archosaurs (crocodiles) and allometric relationships for ectotherms
inferredcites →https://doi.org/10.1016/0014-5793(71)80459-3openalex-snapshot
Respiratory chain linked H2O2 production in pigeon heart mitochondria
inferredcites →https://doi.org/10.1016/0163-7827(88)90013-6openalex-snapshot
Lipids and thyroid hormones
inferredcites →https://doi.org/10.1016/0304-4157(92)90035-9openalex-snapshot
Cardiolipins and biomembrane function
inferredcites →https://doi.org/10.1016/s0005-2728(00)00243-7openalex-snapshot
Mitochondrial proton leak and the uncoupling protein 1 homologues
inferredcites →https://doi.org/10.1016/s0005-2728(99)00041-9openalex-snapshot
Thyroid hormone status and membrane n-3 fatty acid content influence mitochondrial proton leak
inferredcites →https://doi.org/10.1016/s0005-2736(97)00160-0openalex-snapshot
The proton permeability of liposomes made from mitochondria) inner membrane phospholipids: No effect of fatty acid composition
inferredcites →https://doi.org/10.1016/s0005-2736(98)00232-6openalex-snapshot
Structure and function of the uncoupling protein from brown adipose tissue
inferredcites →https://doi.org/10.1016/s0014-5793(97)01159-9openalex-snapshot
High protonic potential actuates a mechanism of production of reactive oxygen species in mitochondria
inferredcites →https://doi.org/10.1016/s0014-5793(98)01073-4openalex-snapshot
Fatty acids as natural uncouplers preventing generation of O⋅−2 and H2O2 by mitochondria in the resting state
inferredcites →https://doi.org/10.1016/s0014-5793(99)01540-9openalex-snapshot
UCP2 and UCP3 rise in starved rat skeletal muscle but mitochondrial proton conductance is unchanged
inferredcites →https://doi.org/10.1016/s0022-2275(20)32497-4openalex-snapshot
Mitochondrial membrane peroxidizability index is inversely related to maximum life span in mammals
inferredcites →https://doi.org/10.1016/s0047-6374(98)00121-3openalex-snapshot
A low degree of fatty acid unsaturation leads to lower lipid peroxidation and lipoxidation-derived protein modification in heart mitochondria of the longevous pigeon than in the short-lived rat
inferredcites →https://doi.org/10.1016/s0305-0491(97)00357-xopenalex-snapshot
The Proton Permeability of the Inner Membrane of Liver Mitochondria from Ectothermic and Endothermic Vertebrates and from Obese Rats: Correlations with Standard Metabolic Rate and Phospholipid Fatty Acid Composition
inferredcites →https://doi.org/10.1017/s146479310000556xopenalex-snapshot
Thyroid hormones and their effects: a new perspective
inferredcites →https://doi.org/10.1023/a:1020576315771openalex-snapshot
Minireview: Cardiolipins and Mitochondrial Proton-Selective Leakage
inferredcites →https://doi.org/10.1023/a:1027328510931openalex-snapshot
Generating, Partitioning, Targeting and Functioning of Superoxide in Mitochondria
inferredcites →https://doi.org/10.1038/35019082openalex-snapshot
Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean
inferredcites →https://doi.org/10.1038/415096aopenalex-snapshot
Superoxide activates mitochondrial uncoupling proteins
inferredcites →https://doi.org/10.1038/82565openalex-snapshot
Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production
inferredcites →https://doi.org/10.1038/sj.ijo.0800936openalex-snapshot
The significance and mechanism of mitochondrial proton conductance
inferredcites →https://doi.org/10.1042/0264-6021:3610049openalex-snapshot
Artifactual uncoupling by uncoupling protein 3 in yeast mitochondria at the concentrations found in mouse and rat skeletal-muscle mitochondria
inferredcites →https://doi.org/10.1042/bj1280617openalex-snapshot
The cellular production of hydrogen peroxide
inferredcites →https://doi.org/10.1042/bj1340707openalex-snapshot
The mitochondrial generation of hydrogen peroxide. General properties and effect of hyperbaric oxygen
inferredcites →https://doi.org/10.1042/bj20021077openalex-snapshot
Oxidative damage and phospholipid fatty acyl composition in skeletal muscle mitochondria from mice underexpressing or overexpressing uncoupling protein 3
inferredcites →https://doi.org/10.1042/bj2750081openalex-snapshot
Evolution of energy metabolism. Proton permeability of the inner membrane of liver mitochondria is greater in a mammal than in a reptile
inferredcites →https://doi.org/10.1042/bj3220317openalex-snapshot
Quantification of malondialdehyde and 4-hydroxynonenal adducts to lysine residues in native and oxidized human low-density lipoprotein
inferredcites →https://doi.org/10.1042/bj3240565openalex-snapshot
N ε-(Carboxyethyl)lysine, a product of the chemical modification of proteins by methylglyoxal, increases with age in human lens proteins
inferredcites →https://doi.org/10.1042/bj3610049openalex-snapshot
Artifactual uncoupling by uncoupling protein 3 in yeast mitochondria at the concentrations found in mouse and rat skeletal-muscle mitochondria
inferredcites →https://doi.org/10.1073/pnas.011526698openalex-snapshot
Glutamic and aminoadipic semialdehydes are the main carbonyl products of metal-catalyzed oxidation of proteins
inferredcites →https://doi.org/10.1073/pnas.98.1.69openalex-snapshot
Glutamic and aminoadipic semialdehydes are the main carbonyl products of metal-catalyzed oxidation of proteins
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.m109736200openalex-snapshot
The Basal Proton Conductance of Skeletal Muscle Mitochondria from Transgenic Mice Overexpressing or Lacking Uncoupling Protein-3
inferredcites →https://doi.org/10.1074/jbc.m910177199openalex-snapshot
Lack of Obesity and Normal Response to Fasting and Thyroid Hormone in Mice Lacking Uncoupling Protein-3
inferredcites →https://doi.org/10.1074/jbc.m910179199openalex-snapshot
Energy Metabolism in Uncoupling Protein 3 Gene Knockout Mice
inferredcites →https://doi.org/10.1093/gerona/55.6.b286openalex-snapshot
Low Fatty Acid Unsaturation: A Mechanism for Lowered Lipoperoxidative Modification of Tissue Proteins in Mammalian Species With Long Life Spans
inferredcites →https://doi.org/10.1093/jn/82.1.19openalex-snapshot
Effect of Degree of Fatty Acid Unsaturation in Tocopherol Deficiency-induced Creatinuria
inferredcites →https://doi.org/10.1111/j.1432-1033.1988.tb14477.xopenalex-snapshot
Altered relationship between protonmotive force and respiration rate in non‐phosphorylating liver mitochondria isolated from rats of different thyroid hormone status
inferredcites →https://doi.org/10.1152/ajpcell.1999.276.3.c692openalex-snapshot
Contribution of mitochondrial proton leak to respiration rate in working skeletal muscle and liver and to SMR
inferredcites →https://doi.org/10.1152/ajpendo.2001.281.5.e975openalex-snapshot
Effects of fasting on muscle mitochondrial energetics and fatty acid metabolism in Ucp3(−/−) and wild-type mice
inferredcites →https://doi.org/10.1152/ajpregu.1996.271.6.r1550openalex-snapshot
Allometry of mitochondrial proton leak: influence of membrane surface area and fatty acid composition
inferredcites →https://doi.org/10.2337/diab.40.2.190openalex-snapshot
Effect of Diabetes and Aging on Carboxymethyllysine Levels in Human Urine
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4603445openalex-extracted
Protective Role of Citric Acid Against Arsenic, Mercury, Lead, Iron and Sodium Nitroprusside Induced Phospholipids Degradation
inferred← citeshttps://doi.org/10.1002/biof.54openalex-snapshot
Uncoupling proteins: A complex journey to function discovery
inferred← citeshttps://doi.org/10.1002/biof.5520240114openalex-snapshot
Hydroxynonenal and uncoupling proteins: A model for protection against oxidative damage
inferred← citeshttps://doi.org/10.1002/jcb.26758openalex-snapshot
Neonatal treatment with fluoxetine improves mitochondrial respiration and reduces oxidative stress in liver of adult rats
inferred← citeshttps://doi.org/10.1002/jcp.20048openalex-snapshot
Uncoupling protein‐3 sensitizes cells to mitochondrial‐dependent stimulus of apoptosis
inferred← citeshttps://doi.org/10.1007/978-94-007-2869-1_6openalex-snapshot
Uncoupling Proteins: Molecular, Functional, Regulatory, Physiological and Pathological Aspects
inferred← citeshttps://doi.org/10.1007/s00018-019-03148-8openalex-snapshot
Proinflammatory NFkB signalling promotes mitochondrial dysfunction in skeletal muscle in response to cellular fuel overloading
inferred← citeshttps://doi.org/10.1007/s00125-007-0765-2openalex-snapshot
Resistance to high-fat-diet-induced obesity and sexual dimorphism in the metabolic responses of transgenic mice with moderate uncoupling protein 3 overexpression in glycolytic skeletal muscles
inferred← citeshttps://doi.org/10.1007/s00204-015-1520-yopenalex-snapshot
Interactions between mitochondrial reactive oxygen species and cellular glucose metabolism
inferred← citeshttps://doi.org/10.1007/s00232-010-9247-4openalex-snapshot
Skeletal Muscle Type Comparison of Subsarcolemmal Mitochondrial Membrane Phospholipid Fatty Acid Composition in Rat
inferred← citeshttps://doi.org/10.1007/s00360-007-0219-7openalex-snapshot
Brown adipose tissue specific lack of uncoupling protein 3 is associated with impaired cold tolerance and reduced transcript levels of metabolic genes
inferred← citeshttps://doi.org/10.1007/s00395-014-0447-4openalex-snapshot
Lack of UCP3 does not affect skeletal muscle mitochondrial function under lipid-challenged conditions, but leads to sudden cardiac death
inferred← citeshttps://doi.org/10.1007/s00424-009-0724-5openalex-snapshot
Mitochondrial function as a determinant of life span
inferred← citeshttps://doi.org/10.1007/s00438-015-1126-3openalex-snapshot
Comparison of skeletal muscle miRNA and mRNA profiles among three pig breeds
inferred← citeshttps://doi.org/10.1007/s00726-003-0036-6openalex-snapshot
Analysis of 6-hydroxy-2-aminocaproic acid (HACA) as a specific marker of protein oxidation: The use of N(O,S)-ethoxycarbonyl trifluoroethyl ester derivatives and gas chromatography/mass spectrometry
inferred← citeshttps://doi.org/10.1007/s11010-014-2087-2openalex-snapshot
Oxidation of cardiolipin is involved in functional impairment and disintegration of liver mitochondria by hypoxia/reoxygenation in the presence of increased Ca2+ concentrations
inferred← citeshttps://doi.org/10.1007/s11357-008-9054-3openalex-snapshot
Energetics and longevity in birds
inferred← citeshttps://doi.org/10.1007/s13105-022-00882-9openalex-snapshot
Oxidative damage and mitochondrial functionality in hearts from KO UCP3 mice housed at thermoneutrality
inferred← citeshttps://doi.org/10.1007/s43630-023-00506-1openalex-snapshot
Antioxidant effects of LEDT in dystrophic muscle cells: involvement of PGC-1α and UCP-3 pathways
inferred← citeshttps://doi.org/10.1016/j.abb.2019.01.036openalex-snapshot
Energy-dissipating hub in muscle mitochondria: Potassium channels and uncoupling proteins
inferred← citeshttps://doi.org/10.1016/j.arr.2009.09.006openalex-snapshot
Compromised respiratory adaptation and thermoregulation in aging and age-related diseases
inferred← citeshttps://doi.org/10.1016/j.bbabio.2005.07.001openalex-snapshot
Uncoupling protein 3 protects aconitase against inactivation in isolated skeletal muscle mitochondria
inferred← citeshttps://doi.org/10.1016/j.bbabio.2006.05.016openalex-snapshot
Uncoupling proteins: A role in protection against reactive oxygen species—or not?
inferred← citeshttps://doi.org/10.1016/j.bbabio.2006.06.002openalex-snapshot
UCP2, UCP3, avUCP, what do they do when proton transport is not stimulated? Possible relevance to pyruvate and glutamine metabolism
inferred← citeshttps://doi.org/10.1016/j.bbabio.2008.07.003openalex-snapshot
Membrane phospholipids, lipoxidative damage and molecular integrity: A causal role in aging and longevity
inferred← citeshttps://doi.org/10.1016/j.bbabio.2009.01.003openalex-snapshot
UCP2, not a physiologically relevant uncoupler but a glucose sparing switch impacting ROS production and glucose sensing
inferred← citeshttps://doi.org/10.1016/j.bbabio.2010.01.004openalex-snapshot
Mitochondrial energy metabolism and ageing
inferred← citeshttps://doi.org/10.1016/j.bbabio.2010.02.033openalex-snapshot
Cold tolerance of UCP1-ablated mice: A skeletal muscle mitochondria switch toward lipid oxidation with marked UCP3 up-regulation not associated with increased basal, fatty acid- or ROS-induced uncoupling or enhanced GDP effects
inferred← citeshttps://doi.org/10.1016/j.bbabio.2010.02.035openalex-snapshot
The regulation and turnover of mitochondrial uncoupling proteins
inferred← citeshttps://doi.org/10.1016/j.bbabio.2011.04.003openalex-snapshot
Uncoupled respiration, ROS production, acute lipotoxicity and oxidative damage in isolated skeletal muscle mitochondria from UCP3-ablated mice
inferred← citeshttps://doi.org/10.1016/j.bbabio.2018.05.019openalex-snapshot
Mitochondrial uncoupling, ROS generation and cardioprotection
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2011.01.029openalex-snapshot
Mitochondrial longevity pathways
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.11.148openalex-snapshot
UCP2 mRNA expression is dependent on glucose metabolism in pancreatic islets
inferred← citeshttps://doi.org/10.1016/j.biocel.2006.07.009openalex-snapshot
Activation of mitochondrial-driven apoptosis in skeletal muscle cells is not mediated by reactive oxygen species production
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2012.09.005openalex-snapshot
Mitochondria-targeted antioxidants and metabolic modulators as pharmacological interventions to slow ageing
inferred← citeshttps://doi.org/10.1016/j.bpj.2013.11.3281openalex-snapshot
UCP2 Overexpression Worsens Mitochondrial Dysfunction and Accelerates Disease Progression in a Mouse Model of Amyotrophic Lateral Sclerosis
inferred← citeshttps://doi.org/10.1016/j.cbpa.2005.11.002openalex-snapshot
Energy, quiescence and the cellular basis of animal life spans
inferred← citeshttps://doi.org/10.1016/j.ceca.2020.102344openalex-snapshot
Mitochondrial reactive oxygen species in physiology and disease
inferred← citeshttps://doi.org/10.1016/j.chroma.2006.11.066openalex-snapshot
Evaluation of a gas chromatography/mass spectrometry method for the quantification of carboxymethyllysine in food samples
inferred← citeshttps://doi.org/10.1016/j.cmet.2005.06.002openalex-snapshot
Physiological functions of the mitochondrial uncoupling proteins UCP2 and UCP3
inferred← citeshttps://doi.org/10.1016/j.domaniend.2005.02.007openalex-snapshot
Potential involvement of mammalian and avian uncoupling proteins in the thermogenic effect of thyroid hormones
inferred← citeshttps://doi.org/10.1016/j.exger.2006.02.005openalex-snapshot
Involvement of UCP3 in mild uncoupling and lipotoxicity
inferred← citeshttps://doi.org/10.1016/j.exger.2008.09.011openalex-snapshot
Characterization of survival and phenotype throughout the life span in UCP2/UCP3 genetically altered mice
inferred← citeshttps://doi.org/10.1016/j.exger.2009.02.001openalex-snapshot
Expression of human uncoupling protein-3 in Drosophila insulin-producing cells increases insulin-like peptide (DILP) levels and shortens lifespan
inferred← citeshttps://doi.org/10.1016/j.febslet.2005.04.084openalex-snapshot
Hyperoxia‐mediated oxidative stress increases expression of UCP3 mRNA and protein in skeletal muscle
inferred← citeshttps://doi.org/10.1016/j.febslet.2006.01.059openalex-snapshot
The effect of high‐fat feeding on intramuscular lipid and lipid peroxidation levels in UCP3‐ablated mice
inferred← citeshttps://doi.org/10.1016/j.febslet.2007.01.085openalex-snapshot
Overexpression of mitochondrial uncoupling protein‐3 does not decrease production of the reactive oxygen species, elevated by palmitate in skeletal muscle cells
inferred← citeshttps://doi.org/10.1016/j.febslet.2008.11.016openalex-snapshot
The effect of UCP3 overexpression on mitochondrial ROS production in skeletal muscle of young versus aged mice
inferred← citeshttps://doi.org/10.1016/j.febslet.2008.12.023openalex-snapshot
UCP3 overexpression neutralizes oxidative stress rather than nitrosative stress in mouse myotubes
inferred← citeshttps://doi.org/10.1016/j.febslet.2011.11.012openalex-snapshot
Significance of uncoupling protein 3 in mitochondrial function upon mid- and long-term dietary high-fat exposure
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2004.05.034openalex-snapshot
Mitochondrial superoxide: production, biological effects, and activation of uncoupling proteins
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2004.10.016openalex-snapshot
Mitochondrial H+ leak and ROS generation: An odd couple
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2007.08.011openalex-snapshot
Mitochondrial uncoupling proteins—What is their physiological role?
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2008.09.026openalex-snapshot
Upregulation of uncoupling protein-3 in skeletal muscle during exercise: a potential antioxidant function
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2010.05.010openalex-snapshot
Uncoupling protein-3 lowers reactive oxygen species production in isolated mitochondria
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2013.04.007openalex-snapshot
The transcription factor Nrf2 promotes survival by enhancing the expression of uncoupling protein 3 under conditions of oxidative stress
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2015.03.032openalex-snapshot
4-Hydroxynonenal induces Nrf2-mediated UCP3 upregulation in mouse cardiomyocytes
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.05.014openalex-snapshot
Energy substrate metabolism, mitochondrial structure and oxidative stress after cardiac ischemia-reperfusion in mice lacking UCP3
inferred← citeshttps://doi.org/10.1016/j.gene.2013.04.048openalex-snapshot
Uncoupling protein 2 − 866G/A and uncoupling protein 3 − 55C/T polymorphisms in young South African Indian coronary artery disease patients
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2011.08.006openalex-snapshot
Fish oil and 3-thia fatty acid have additive effects on lipid metabolism but antagonistic effects on oxidative damage when fed to rats for 50 weeks
inferred← citeshttps://doi.org/10.1016/j.jshs.2013.03.006openalex-snapshot
Mitochondrial redox metabolism in aging: Effect of exercise interventions
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2016.04.003openalex-snapshot
Food restriction attenuates oxidative stress in brown adipose tissue of striped hamsters acclimated to a warm temperature
inferred← citeshttps://doi.org/10.1016/j.mad.2010.02.005openalex-snapshot
Mitochondrial redox metabolism: Aging, longevity and dietary effects
inferred← citeshttps://doi.org/10.1016/j.mad.2010.03.010openalex-snapshot
Mitochondrial uncoupling and lifespan
inferred← citeshttps://doi.org/10.1016/j.mcn.2013.10.002openalex-snapshot
UCP2 overexpression worsens mitochondrial dysfunction and accelerates disease progression in a mouse model of amyotrophic lateral sclerosis
inferred← citeshttps://doi.org/10.1016/j.metabol.2005.02.012openalex-snapshot
Effect of elevated lipid concentrations on human skeletal muscle gene expression
inferred← citeshttps://doi.org/10.1016/j.metabol.2009.07.009openalex-snapshot
Skeletal muscle insulin resistance: the interplay of local lipid excess and mitochondrial dysfunction
inferred← citeshttps://doi.org/10.1016/j.mito.2017.03.005openalex-snapshot
Uncoupling protein 2 and metabolic diseases
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2005.06.056openalex-snapshot
Regulation of mitochondrial uncoupling proteins in mouse inner ear ganglion cells in response to systemic kanamycin challenge
inferred← citeshttps://doi.org/10.1016/j.physbeh.2004.07.028openalex-snapshot
Adaptive thermogenesis and uncoupling proteins: a reappraisal of their roles in fat metabolism and energy balance
inferred← citeshttps://doi.org/10.1016/j.physbeh.2007.11.039openalex-snapshot
Mitochondrial uncoupling protein 3 and its role in cardiac- and skeletal muscle metabolism
inferred← citeshttps://doi.org/10.1016/j.plipres.2005.11.001openalex-snapshot
Putative function and physiological relevance of the mitochondrial uncoupling protein-3: Involvement in fatty acid metabolism?
inferred← citeshttps://doi.org/10.1016/j.regg.2010.02.001openalex-snapshot
Glicación de proteínas mitocondriales, estrés oxidativo y envejecimiento
inferred← citeshttps://doi.org/10.1016/j.tet.2010.01.103openalex-snapshot
Caged mitochondrial uncouplers that are released in response to hydrogen peroxide
inferred← citeshttps://doi.org/10.1016/s0014-5793(03)01386-3openalex-snapshot
Production of endogenous matrix superoxide from mitochondrial complex I leads to activation of uncoupling protein 3
inferred← citeshttps://doi.org/10.1016/s1566-3124(03)14003-5openalex-snapshot
Oxidative phosphorylation, mitochondrial proton cycling, free-radical production and aging
inferred← citeshttps://doi.org/10.1016/s1671-2927(08)60156-xopenalex-snapshot
Diet-Induced Thermogenesis
inferred← citeshttps://doi.org/10.1017/s0029665107005277openalex-snapshot
High-fat diet, muscular lipotoxicity and insulin resistance
inferred← citeshttps://doi.org/10.1021/jf063024jopenalex-snapshot
Kinetics of Formation of Three Indicators of the Maillard Reaction in Model Cookies: Influence of Baking Temperature and Type of Sugar
inferred← citeshttps://doi.org/10.1021/pr101048qopenalex-snapshot
Changes in Expression of Skeletal Muscle Proteins between Obesity-Prone and Obesity-Resistant Rats Induced by a High-Fat Diet
inferred← citeshttps://doi.org/10.1038/nm903openalex-snapshot
Uncoupling protein-2 prevents neuronal death and diminishes brain dysfunction after stroke and brain trauma
inferred← citeshttps://doi.org/10.1038/nrm1592openalex-snapshot
The mitochondrial uncoupling-protein homologues
inferred← citeshttps://doi.org/10.1038/sj.emboj.7600866openalex-snapshot
SOD2 overexpression: enhanced mitochondrial tolerance but absence of effect on UCP activity
inferred← citeshttps://doi.org/10.1038/srep22854openalex-snapshot
A genistein-enriched diet neither improves skeletal muscle oxidative capacity nor prevents the transition towards advanced insulin resistance in ZDF rats
inferred← citeshttps://doi.org/10.1042/bj20050494openalex-snapshot
Expression of UCP3 in CHO cells does not cause uncoupling, but controls mitochondrial activity in the presence of glucose
inferred← citeshttps://doi.org/10.1042/bj20110571openalex-snapshot
Hexokinase II acts through UCP3 to suppress mitochondrial reactive oxygen species production and maintain aerobic respiration
inferred← citeshttps://doi.org/10.1042/bss0710203openalex-snapshot
Mitochondrial superoxide and aging: uncoupling-protein activity and superoxide production
inferred← citeshttps://doi.org/10.1055/s-2005-870421openalex-snapshot
Towards Comprehension of the Physiological Role of UCP3
inferred← citeshttps://doi.org/10.1073/pnas.2318771121openalex-snapshot
Mitochondrial uncoupling proteins protect human airway epithelial ciliated cells from oxidative damage
inferred← citeshttps://doi.org/10.1074/jbc.m110.102699openalex-snapshot
UCP3 Translocates Lipid Hydroperoxide and Mediates Lipid Hydroperoxide-dependent Mitochondrial Uncoupling
inferred← citeshttps://doi.org/10.1074/jbc.m208262200openalex-snapshot
Superoxide Activates Mitochondrial Uncoupling Protein 2 from the Matrix Side
inferred← citeshttps://doi.org/10.1074/jbc.m308529200openalex-snapshot
Superoxide Activates Uncoupling Proteins by Generating Carbon-centered Radicals and Initiating Lipid Peroxidation
inferred← citeshttps://doi.org/10.1074/jbc.m408920200openalex-snapshot
Activation and Function of Mitochondrial Uncoupling Protein in Plants
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1079/pns2003336openalex-snapshot
The role of uncoupling protein 3 in fatty acid metabolism: protection against lipotoxicity?
inferred← citeshttps://doi.org/10.1080/17482970601066132openalex-snapshot
Lipid-induced cell stress and insulin resistance
inferred← citeshttps://doi.org/10.1080/1828051x.2021.2025161openalex-snapshot
Effects of a yeast cell wall product on the performance of broiler chickens and PGC-1α, TLR4, IL-10 and PPARγ genes expression
inferred← citeshttps://doi.org/10.1086/381464openalex-snapshot
Absence of UCP3 in Brown Adipose Tissue Does Not Impair Nonshivering Thermogenesis
inferred← citeshttps://doi.org/10.1089/ars.2006.8.582openalex-snapshot
Is the Mitochondrial Free Radical Theory of Aging Intact?
inferred← citeshttps://doi.org/10.1089/ars.2009.2427openalex-snapshot
Superoxide Anion Regulates the Mitochondrial Free Ca 2+ Through Uncoupling Proteins
inferred← citeshttps://doi.org/10.1089/ars.2009.2484openalex-snapshot
Hyperglycemia and Glycation in Diabetic Complications
inferred← citeshttps://doi.org/10.1093/cvr/cvq256openalex-snapshot
Mitochondrial reprogramming through cardiac oxygen sensors in ischaemic heart disease
inferred← citeshttps://doi.org/10.1093/emboj/cdg412openalex-snapshot
A signalling role for 4‐hydroxy‐2‐nonenal in regulation of mitochondrial uncoupling
inferred← citeshttps://doi.org/10.1093/ps/85.7.1259openalex-snapshot
Acute heat stress stimulates mitochondrial superoxide production in broiler skeletal muscle, possibly via downregulation of uncoupling protein content
inferred← citeshttps://doi.org/10.1093/ps/86.2.364openalex-snapshot
Acute Heat Stress Induces Oxidative Stress and Decreases Adaptation in Young White Leghorn Cockerels by Downregulation of Avian Uncoupling Protein
inferred← citeshttps://doi.org/10.1093/ps/86.2.372openalex-snapshot
Gene Expression in Breast Muscle and Duodenum from Low and High Feed Efficient Broilers
inferred← citeshttps://doi.org/10.1096/fj.03-0159hypopenalex-snapshot
A function for novel uncoupling proteins: antioxidant defense of mitochondrial matrix by translocating fatty acid peroxides from the inner to the outer membrane leaflet
inferred← citeshttps://doi.org/10.1096/fj.03-0515fjeopenalex-snapshot
Uncoupling protein 3 as a mitochondrial fatty acid anion exporter
inferred← citeshttps://doi.org/10.1096/fj.06-6966revopenalex-snapshot
Uncoupling protein‐3: clues in an ongoing mitochondrial mystery
inferred← citeshttps://doi.org/10.1096/fj.11-197772openalex-snapshot
Acclimatization of skeletal muscle mitochondria to high‐altitude hypoxia during an ascent of Everest
inferred← citeshttps://doi.org/10.1098/rspb.2007.1761openalex-snapshot
Novel reptilian uncoupling proteins: molecular evolution and gene expression during cold acclimation
inferred← citeshttps://doi.org/10.1111/j.1474-9726.2005.00157.xopenalex-snapshot
UCP1 deficiency increases susceptibility to diet‐induced obesity with age
inferred← citeshttps://doi.org/10.1113/expphysiol.2012.069468openalex-snapshot
Skeletal muscle mitochondrial dysfunction during chronic obstructive pulmonary disease: central actor and therapeutic target
inferred← citeshttps://doi.org/10.1126/sageke.2004.9.pe9openalex-snapshot
Regulation of Transcriptional Coactivator PGC-1α
inferred← citeshttps://doi.org/10.1136/ard.2009.111211openalex-snapshot
Oxidative damage in synovial tissue is associated with in vivo hypoxic status in the arthritic joint
inferred← citeshttps://doi.org/10.1139/h05-145openalex-snapshot
Regulation of Fatty Acid Transport Across the Mitochondrial Membranes in Human and Rodent Skeletal Muscle
inferred← citeshttps://doi.org/10.1152/ajpcell.00031.2005openalex-snapshot
Differential susceptibility of subsarcolemmal and intermyofibrillar mitochondria to apoptotic stimuli
inferred← citeshttps://doi.org/10.1152/ajpendo.00234.2003openalex-snapshot
Differential transcriptional activation of select metabolic genes in response to variations in exercise intensity and duration
inferred← citeshttps://doi.org/10.1152/ajpendo.00241.2009openalex-snapshot
Role of lipid-derived mediators in skeletal muscle insulin resistance
inferred← citeshttps://doi.org/10.1152/ajpendo.00336.2005openalex-snapshot
Exercise training restores uncoupling protein-3 content in limb muscles of patients with chronic obstructive pulmonary disease
inferred← citeshttps://doi.org/10.1152/ajpendo.00518.2012openalex-snapshot
Skeletal muscle uncoupling-induced longevity in mice is linked to increased substrate metabolism and induction of the endogenous antioxidant defense system
inferred← citeshttps://doi.org/10.1152/ajpheart.00595.2012openalex-snapshot
Macrophage migration inhibitory factor antagonizes pressure overload-induced cardiac hypertrophy
inferred← citeshttps://doi.org/10.1152/ajpregu.00421.2004openalex-snapshot
Chronic low-frequency stimulation upregulates uncoupling protein-3 in transforming rat fast-twitch skeletal muscle
inferred← citeshttps://doi.org/10.1152/ajpregu.90974.2008openalex-snapshot
Olive oil-supplemented diet alleviates acute heat stress-induced mitochondrial ROS production in chicken skeletal muscle
inferred← citeshttps://doi.org/10.1152/japplphysiol.00336.2004openalex-snapshot
Role of UCP3 in state 4 respiration during contractile activity-induced mitochondrial biogenesis
inferred← citeshttps://doi.org/10.1152/physiol.00046.2010openalex-snapshot
The Regulation and Physiology of Mitochondrial Proton Leak
inferred← citeshttps://doi.org/10.1155/2016/9340654openalex-snapshot
Cell Death and Heart Failure in Obesity: Role of Uncoupling Proteins
inferred← citeshttps://doi.org/10.1161/01.cir.0000051722.66074.60openalex-snapshot
Protective Role of Uncoupling Protein 2 in Atherosclerosis
inferred← citeshttps://doi.org/10.1161/circresaha.107.165472openalex-snapshot
Role of Mitochondrial Dysfunction in Insulin Resistance
inferred← citeshttps://doi.org/10.1172/jci.insight.86612openalex-snapshot
Maternal obesity reduces oxidative capacity in fetal skeletal muscle of Japanese macaques
inferred← citeshttps://doi.org/10.1172/jci19774openalex-snapshot
Superoxide-mediated activation of uncoupling protein 2 causes pancreatic β cell dysfunction
inferred← citeshttps://doi.org/10.1179/135100007x162158openalex-snapshot
4-Hydroxy-2-nonenal and uncoupling proteins: an approach for regulation of mitochondrial ROS production
inferred← citeshttps://doi.org/10.1186/1472-6793-10-5openalex-snapshot
Up-regulation of avian uncoupling protein in cold-acclimated and hyperthyroid ducklings prevents reactive oxygen species production by skeletal muscle mitochondria
inferred← citeshttps://doi.org/10.1186/1476-511x-11-22openalex-snapshot
Effect of conjugated linoleic acid on inhibition of prolyl hydroxylase 1 in hearts of mice
inferred← citeshttps://doi.org/10.1186/s12986-017-0191-5openalex-snapshot
Supramolecular structure of dietary fat in early life modulates expression of markers for mitochondrial content and capacity in adipose tissue of adult mice
inferred← citeshttps://doi.org/10.1210/en.2012-1390openalex-snapshot
Angiotensin Receptor Blockade Recovers Hepatic UCP2 Expression and Aconitase and SDH Activities and Ameliorates Hepatic Oxidative Damage in Insulin Resistant Rats
inferred← citeshttps://doi.org/10.1210/jc.2005-1572openalex-snapshot
Reduced Skeletal Muscle Uncoupling Protein-3 Content in Prediabetic Subjects and Type 2 Diabetic Patients: Restoration by Rosiglitazone Treatment
inferred← citeshttps://doi.org/10.1371/journal.pone.0029650openalex-snapshot
Further Support to the Uncoupling-to-Survive Theory: The Genetic Variation of Human UCP Genes Is Associated with Longevity
inferred← citeshttps://doi.org/10.1530/joe-14-0008openalex-snapshot
Estradiol stimulates mitochondrial biogenesis and adiponectin expression in skeletal muscle
inferred← citeshttps://doi.org/10.1590/s0100-879x2004001000003openalex-snapshot
Respiration, oxidative phosphorylation, and uncoupling protein in Candida albicans
inferred← citeshttps://doi.org/10.1677/joe-08-0210openalex-snapshot
Developmental programming of adult hyperinsulinemia, increased proinflammatory cytokine production, and altered skeletal muscle expression of SLC2A4 (GLUT4) and uncoupling protein 3
inferred← citeshttps://doi.org/10.18174/644648openalex-snapshot
Nutritional programming of white adipose tissue and mitochondrial function : Fat quality matters
inferred← citeshttps://doi.org/10.20870/productions-animales.2006.19.4.3497openalex-snapshot
Quel est le rôle des protéines découplantes mitochondriales chez les mammifères et les oiseaux ?
inferred← citeshttps://doi.org/10.2141/jpsa.44.439openalex-snapshot
Mitochondrial Oxidative Damage in Chicken Skeletal Muscle Induced by Acute Heat Stress
inferred← citeshttps://doi.org/10.2165/00007256-200838090-00003openalex-snapshot
Beneficial Effects of Exercise on Muscle Mitochondrial Function in Diabetes Mellitus
inferred← citeshttps://doi.org/10.2174/1389450043490451openalex-snapshot
Treating Obesity: Pharmacology of Energy Expenditure
inferred← citeshttps://doi.org/10.2337/diabetes.53.6.1412openalex-snapshot
Oxidative Capacity, Lipotoxicity, and Mitochondrial Damage in Type 2 Diabetes
inferred← citeshttps://doi.org/10.2353/ajpath.2009.080654openalex-snapshot
Alterations in Fatty Acid Utilization and an Impaired Antioxidant Defense Mechanism Are Early Events in Podocyte Injury
inferred← citeshttps://doi.org/10.2527/2004.82123493xopenalex-snapshot
Effect of heat exposure on uncoupling protein-3 mRNA abundance in porcine skeletal muscle
inferred← citeshttps://doi.org/10.26481/dis.20141017bbopenalex-snapshot
Mitochondria, lipotoxicity and skeletal muscle metabolism : implications for type 2 diabetes mellitus
inferred← citeshttps://doi.org/10.26512/2016.06.d.21746openalex-snapshot
Alterações da taxa metabólica por provimento de oxigênio advindo de alterações do sistema circulatório e respiratório e por substratos da cadeia de transporte de elétrons mitocondrial
inferred← citeshttps://doi.org/10.2741/2431openalex-snapshot
Response and adaptation of skeletal muscle to exercise - the role of reactive oxygen species
inferred← citeshttps://doi.org/10.2741/s161openalex-snapshot
Cold defence responses the role of oxidative stress
inferred← citeshttps://doi.org/10.3109/10715760903352841openalex-snapshot
Degradation of phospholipids by oxidative stress—Exceptional significance of cardiolipin
inferred← citeshttps://doi.org/10.3109/10715762.2010.498478openalex-snapshot
Pathological aspects of lipid peroxidation
inferred← citeshttps://doi.org/10.3109/15376516.2010.515081openalex-snapshot
Chromatographic determination of fatty acids in biological material
inferred← citeshttps://doi.org/10.3389/fcell.2019.00003openalex-snapshot
Emerging Roles in the Biogenesis of Cytochrome c Oxidase for Members of the Mitochondrial Carrier Family
inferred← citeshttps://doi.org/10.3390/antiox10111746openalex-snapshot
Mitochondrial Uncoupling Proteins (UCPs) as Key Modulators of ROS Homeostasis: A Crosstalk between Diabesity and Male Infertility?
inferred← citeshttps://doi.org/10.3390/antiox12020409openalex-snapshot
Inhibition of Mitochondrial Uncoupling Proteins Arrests Human Spermatozoa Motility without Compromising Viability
inferred← citeshttps://doi.org/10.3390/antiox9111132openalex-snapshot
The Advanced Lipoxidation End-Product Malondialdehyde-Lysine in Aging and Longevity
inferred← citeshttps://doi.org/10.3390/cells12172183openalex-snapshot
Mitochondrial Properties in Skeletal Muscle Fiber
inferred← citeshttps://doi.org/10.3390/cells9010012openalex-snapshot
Genetic Associations with Aging Muscle: A Systematic Review
inferred← citeshttps://doi.org/10.3390/genes13091612openalex-snapshot
Relationships between Uncoupling Protein Genes UCP1, UCP2 and UCP3 and Irisin Levels in Residents of the Coldest Region of Siberia
inferred← citeshttps://doi.org/10.3390/ijms23136892openalex-snapshot
Construction and Analysis of Disuse Atrophy Model of the Gastrocnemius Muscle in Chicken
inferred← citeshttps://doi.org/10.3402/fnr.v50i0.1578openalex-snapshot
Lipid-induced cell stress and insulin resistance
inferred← citeshttps://doi.org/10.3410/f.1448967.926071openalex-snapshot
Faculty Opinions recommendation of Mitochondrial function as a determinant of life span.
inferred← citeshttps://doi.org/10.3410/f.737118390.793580273openalex-snapshot
Faculty Opinions recommendation of Genetic Associations with Aging Muscle: A Systematic Review.
inferred← citeshttps://doi.org/10.37871/jels1127openalex-snapshot
A Review on the Possible Leakage of Electrons through the Electron Transport Chain within Mitochondria
inferred← citeshttps://doi.org/10.3892/ijmm.2019.4188openalex-snapshot
Mitochondrial electron transport chain, ROS generation and uncoupling (Review)
inferred← citeshttps://doi.org/10.70675/a7b15e3fz84e7z4915z9447zc112181e06e4openalex-snapshot
L'analyse du métabolisme des muscles squelettiques est crucial pour la conception d'exercices de précision dans le diabète de type 2 : les leçons tirées de modèles souris de fond génétique, de sexe et d'étiologie différents
inferred← citeshttps://doi.org/10.70675/c935051fz547ez47d9zbc6ez7fce6932ff15openalex-snapshot
Fonction mitochondriale et espèces réactives dérivées de l'oxygène : effets du genre et de l'entraînement en endurance chez le rat Wistar et l'anguille européenne
inferred← citeshttps://doi.org/10.70675/e05002c4z4806z4363z90b1z0e406b6c0e4copenalex-snapshot
Role of PGC-1β and TIF2 co-regulators in mouse skeletal muscle function
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