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Exercise induces transient transcriptional activation of the PGC‐1α gene in human skeletal muscle
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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/cphy.cp100119openalex-snapshot
Skeletal Muscle Adaptability: Significance for Metabolism and Performance
inferredcites →https://doi.org/10.1002/cphy.cp120124openalex-snapshot
Muscle Plasticity: Energy Demand and Supply Processes
inferredcites →https://doi.org/10.1002/cphy.cp120125openalex-snapshot
Regulation of Gene Expression in Skeletal Muscle by Contractile Activity
inferredcites →https://doi.org/10.1006/abio.1987.9999openalex-snapshot
Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction
inferredcites →https://doi.org/10.1016/0003-2697(87)90021-2openalex-snapshot
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
inferredcites →https://doi.org/10.1016/s0006-291x(02)00881-1openalex-snapshot
Effects of low-intensity prolonged exercise on PGC-1 mRNA expression in rat epitrochlearis muscle
inferredcites →https://doi.org/10.1016/s0092-8674(00)80611-xopenalex-snapshot
Mechanisms Controlling Mitochondrial Biogenesis and Respiration through the Thermogenic Coactivator PGC-1
inferredcites →https://doi.org/10.1016/s0092-8674(00)80880-6openalex-snapshot
Calcineurin Signaling and Muscle Remodeling
inferredcites →https://doi.org/10.1016/s0092-8674(00)81410-5openalex-snapshot
A Cold-Inducible Coactivator of Nuclear Receptors Linked to Adaptive Thermogenesis
inferredcites →https://doi.org/10.1016/s0167-4781(02)00343-3openalex-snapshot
Nuclear activators and coactivators in mammalian mitochondrial biogenesis
inferredcites →https://doi.org/10.1016/s0304-4165(98)00018-xopenalex-snapshot
Induction of nuclear respiratory factor-1 expression by an acute bout of exercise in rat muscle
inferredcites →https://doi.org/10.1016/s1043-2760(01)00457-xopenalex-snapshot
PGC-1, a versatile coactivator
inferredcites →https://doi.org/10.1038/35093050openalex-snapshot
Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1
inferredcites →https://doi.org/10.1038/nature00904openalex-snapshot
Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres
inferredcites →https://doi.org/10.1073/pnas.061035098openalex-snapshot
Restoration of insulin-sensitive glucose transporter (GLUT4) gene expression in muscle cells by the transcriptional coactivator PGC-1
inferredcites →https://doi.org/10.1113/jphysiol.2002.016832openalex-snapshot
Influence of pre‐exercise muscle glycogen content on exercise‐induced transcriptional regulation of metabolic genes
inferredcites →https://doi.org/10.1126/science.1071163openalex-snapshot
Regulation of Mitochondrial Biogenesis in Skeletal Muscle by CaMK
inferredcites →https://doi.org/10.1126/science.286.5443.1368openalex-snapshot
Activation of PPARγ Coactivator-1 Through Transcription Factor Docking
inferredcites →https://doi.org/10.1128/mcb.20.5.1868-1876.2000openalex-snapshot
The Coactivator PGC-1 Cooperates with Peroxisome Proliferator-Activated Receptor α in Transcriptional Control of Nuclear Genes Encoding Mitochondrial Fatty Acid Oxidation Enzymes
inferredcites →https://doi.org/10.1128/mcb.21.2.644-654.2001openalex-snapshot
Mitochondrial DNA Instability and Peri-Implantation Lethality Associated with Targeted Disruption of Nuclear Respiratory Factor 1 in Mice
inferredcites →https://doi.org/10.1152/ajpendo.00475.2001openalex-snapshot
Exercise training increases lipid metabolism gene expression in human skeletal muscle
inferredcites →https://doi.org/10.1152/ajpendo.2000.278.6.e1078openalex-snapshot
Exercise attenuates the fasting-induced transcriptional activation of metabolic genes in skeletal muscle
inferredcites →https://doi.org/10.1152/ajpendo.2000.279.4.e806openalex-snapshot
Transcriptional regulation of gene expression in human skeletal muscle during recovery from exercise
inferredcites →https://doi.org/10.1152/ajpendo.2001.281.6.e1340openalex-snapshot
Chronic activation of AMP kinase results in NRF-1 activation and mitochondrial biogenesis
inferredcites →https://doi.org/10.1152/jappl.1985.59.5.1647openalex-snapshot
Dynamic knee extension as model for study of isolated exercising muscle in humans
inferredcites →https://doi.org/10.1152/jappl.2001.90.3.1137openalex-snapshot
Invited Review: Contractile activity-induced mitochondrial biogenesis in skeletal muscle
inferredcites →https://doi.org/10.1152/jappl.2001.91.3.1017openalex-snapshot
Energy-sensing and signaling by AMP-activated protein kinase in skeletal muscle
inferredcites →https://doi.org/10.1172/jci10268openalex-snapshot
Peroxisome proliferator–activated receptor γ coactivator-1 promotes cardiac mitochondrial biogenesis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/1873-3468.70158openalex-snapshot
Purinergic signaling by ATP induces exercise‐like effects and ameliorates insulin resistance in HT22 mouse hippocampal cells
inferred← citeshttps://doi.org/10.1002/2211-5463.12898openalex-snapshot
FOXO1 suppresses PGC‐1β gene expression in skeletal muscles
inferred← citeshttps://doi.org/10.1002/9781118480045.ch12openalex-snapshot
Skeletal Muscle and Exercise
inferred← citeshttps://doi.org/10.1002/9781444303315openalex-snapshot
Olympic Textbook of Science in Sport
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Mitochondrial Changes in Aging with Particular Reference to Muscle, and Possible Clinical Consequences
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IRF4 in Skeletal Muscle Regulates Exercise Capacity via PTG/Glycogen Pathway
inferred← citeshttps://doi.org/10.1002/ajpa.23762openalex-snapshot
BDNF, endurance activity, and mechanisms underlying the evolution of hominin brains
inferred← citeshttps://doi.org/10.1002/cbf.2859openalex-snapshot
The impact of antioxidant supplements and endurance exercise on genes of the carbohydrate and lipid metabolism in skeletal muscle of mice
inferred← citeshttps://doi.org/10.1002/cphy.c100042openalex-snapshot
Molecular Mechanisms of Muscle Plasticity with Exercise
inferred← citeshttps://doi.org/10.1002/cphy.c100052openalex-snapshot
Regulation of Mitochondrial Biogenesis and GLUT4 Expression by Exercise
inferred← citeshttps://doi.org/10.1002/cphy.c100074openalex-snapshot
Mechanisms of Exercise‐Induced Mitochondrial Biogenesis in Skeletal Muscle: Implications for Health and Disease
inferred← citeshttps://doi.org/10.1002/cphy.c110065openalex-snapshot
Exercise Training and Peripheral Arterial Disease
inferred← citeshttps://doi.org/10.1002/cphy.c200033openalex-snapshot
State of Knowledge on Molecular Adaptations to Exercise in Humans: Historical Perspectives and Future Directions
inferred← citeshttps://doi.org/10.1002/dta.2198openalex-snapshot
Equine performance genes and the future of doping in horseracing
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2011.tb00346.xopenalex-snapshot
Regulation of Mitochondrial Biogenesis and GLUT4 Expression by Exercise
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2011.tb00363.xopenalex-snapshot
Molecular Mechanisms of Muscle Plasticity with Exercise
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2011.tb00370.xopenalex-snapshot
Mechanisms of Exercise‐Induced Mitochondrial Biogenesis in Skeletal Muscle: Implications for Health and Disease
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2012.tb00473.xopenalex-snapshot
Exercise Training and Peripheral Arterial Disease
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2022.tb00211.xopenalex-snapshot
State of Knowledge on Molecular Adaptations to Exercise in Humans: Historical Perspectives and Future Directions
inferred← citeshttps://doi.org/10.1002/jcp.30539openalex-snapshot
PGC‐1α regulates myonuclear accretion after moderate endurance training
inferred← citeshttps://doi.org/10.1002/jcsm.12007openalex-snapshot
Preserved muscle oxidative metabolic phenotype in newly diagnosed non‐small cell lung cancer cachexia
inferred← citeshttps://doi.org/10.1002/jcsm.12226openalex-snapshot
The mitochondrial metabolic reprogramming agent trimetazidine as an ‘exercise mimetic’ in cachectic C26‐bearing mice
inferred← citeshttps://doi.org/10.1002/jcsm.12313openalex-snapshot
Searching for a mitochondrial root to the decline in muscle function with ageing
inferred← citeshttps://doi.org/10.1002/mnfr.201701043openalex-snapshot
l ‐Citrulline Supplementation‐Increased Skeletal Muscle PGC‐1α Expression Is Associated with Exercise Performance and Increased Skeletal Muscle Weight
inferred← citeshttps://doi.org/10.1002/phy2.140openalex-snapshot
The truncated splice variants, NT -PGC -1α and PGC -1α4 , increase with both endurance and resistance exercise in human skeletal muscle
inferred← citeshttps://doi.org/10.1002/pmic.201500382openalex-snapshot
Uncovering the exercise‐related proteome signature in skeletal muscle
inferred← citeshttps://doi.org/10.1007/4735_2007_0256openalex-snapshot
Transcriptional regulation by the p38 MAPK signaling pathway in mammalian cells
inferred← citeshttps://doi.org/10.1007/978-0-387-69945-5_3openalex-snapshot
Regulation of Mitochondrial Fuel Handling by the Peroxisome Proliferator-Activated Receptors
inferred← citeshttps://doi.org/10.1007/978-1-4614-4493-0_5openalex-snapshot
Biological Pathways Impacting Cancer Survival: Exercise as a Countermeasure for the Development and Progression of Cachexia
inferred← citeshttps://doi.org/10.1007/978-1-4614-7318-3_10openalex-snapshot
Perspective and Direction for Future Research
inferred← citeshttps://doi.org/10.1007/978-1-59259-963-9_69openalex-snapshot
Skeletal Muscle Hypertrophy and Response to Training
inferred← citeshttps://doi.org/10.1007/978-1-60327-139-4_9openalex-snapshot
Interaction Between Physical Activity and Genetic Factors in Complex Metabolic Disease
inferred← citeshttps://doi.org/10.1007/978-1-60761-355-8_5openalex-snapshot
The Interaction Between Genetic Variation and Exercise and Physical Activity in the Determination of Body Composition and Obesity Status
inferred← citeshttps://doi.org/10.1007/978-3-030-04816-7_2openalex-snapshot
Exercise, Gene Regulation, and Cardiometabolic Disease
inferred← citeshttps://doi.org/10.1007/978-3-030-04816-7_3openalex-snapshot
Exercise and the Mitochondria
inferred← citeshttps://doi.org/10.1007/978-3-031-27192-2_7openalex-snapshot
Muscle Biopsy to Investigate Mitochondrial Turnover
inferred← citeshttps://doi.org/10.1007/978-3-031-88361-3_3openalex-snapshot
Mitochondrial Quality Control
inferred← citeshttps://doi.org/10.1007/978-3-319-61013-9_8openalex-snapshot
Mitochondria in Muscle and Exercise
inferred← citeshttps://doi.org/10.1007/978-3-662-53386-4_21-1openalex-snapshot
Sportmedizinische Grundlagen: Adaptation des Körpers an Bewegung
inferred← citeshttps://doi.org/10.1007/978-3-662-53410-6_21openalex-snapshot
Sportmedizinische Grundlagen: Adaptation des Körpers an Bewegung
inferred← citeshttps://doi.org/10.1007/978-88-470-0376-7_3openalex-snapshot
Exercise-Induced Mitochondrial Biogenesis in Skeletal Muscle
inferred← citeshttps://doi.org/10.1007/978-88-470-2418-2_8openalex-snapshot
Muscle Biopsy To Investigate Mitochondrial Turnover
inferred← citeshttps://doi.org/10.1007/978-94-007-2869-1_9openalex-snapshot
Role of Mitochondrial Function in Insulin Resistance
inferred← citeshttps://doi.org/10.1007/978-94-017-8742-0_24openalex-snapshot
Mitochondrial Biogenesis and Quality Control
inferred← citeshttps://doi.org/10.1007/978-981-10-3292-9_8openalex-snapshot
The Role and Regulation of PGC-1α and PGC-1β in Skeletal Muscle Adaptation
inferred← citeshttps://doi.org/10.1007/978-981-10-4304-8_17openalex-snapshot
Exercise-Induced Mitochondrial Adaptations in Addressing Heart Failure
inferred← citeshttps://doi.org/10.1007/978-981-13-1435-3_24openalex-snapshot
Physical Exercise for Muscle Atrophy
inferred← citeshttps://doi.org/10.1007/978-981-92-0631-5_1openalex-snapshot
Recovery as a Biological Process
inferred← citeshttps://doi.org/10.1007/bf03346630openalex-snapshot
Two weekly sessions of combined aerobic and resistance exercise are sufficient to provide beneficial effects in subjects with Type 2 diabetes mellitus and metabolic syndrome
inferred← citeshttps://doi.org/10.1007/s00018-009-0146-8openalex-snapshot
The response of human skeletal muscle tissue to hypoxia
inferred← citeshttps://doi.org/10.1007/s00109-026-02694-6openalex-snapshot
Molecular regulation of PGC-1α: from protein-protein interactions and post-translational modifications to pharmacological modulation
inferred← citeshttps://doi.org/10.1007/s00125-006-0268-6openalex-snapshot
PGC-1α: a potent transcriptional cofactor involved in the pathogenesis of type 2 diabetes
inferred← citeshttps://doi.org/10.1007/s00125-007-0594-3openalex-snapshot
Patients with type 2 diabetes have normal mitochondrial function in skeletal muscle
inferred← citeshttps://doi.org/10.1007/s00125-009-1420-xopenalex-snapshot
Novel pharmacological approaches to combat obesity and insulin resistance: targeting skeletal muscle with ‘exercise mimetics’
inferred← citeshttps://doi.org/10.1007/s00125-010-1666-3openalex-snapshot
Activation of the mitogen-activated protein kinase (MAPK) signalling pathway in the liver of mice is related to plasma glucose levels after acute exercise
inferred← citeshttps://doi.org/10.1007/s00213-018-5041-2openalex-snapshot
PGC-1α–FNDC5–BDNF signaling pathway in skeletal muscle confers resilience to stress in mice subjected to chronic social defeat
inferred← citeshttps://doi.org/10.1007/s00216-012-6533-2openalex-snapshot
Defining a molecular portrait of physical fitness
inferred← citeshttps://doi.org/10.1007/s00223-018-0459-4openalex-snapshot
Deletion of the Transcription Factor PGC-1α in Mice Negatively Regulates Bone Mass
inferred← citeshttps://doi.org/10.1007/s00232-011-9365-7openalex-snapshot
Na,K-ATPase Activity in Mouse Muscle is Regulated by AMPK and PGC-1α
inferred← citeshttps://doi.org/10.1007/s00281-013-0406-4openalex-snapshot
Functional crosstalk of PGC-1 coactivators and inflammation in skeletal muscle pathophysiology
inferred← citeshttps://doi.org/10.1007/s00360-009-0398-5openalex-snapshot
Temporal and spatial patterns of gene expression in skeletal muscles in response to swim training in adult zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1007/s00360-016-0977-1openalex-snapshot
Exercise quantity-dependent muscle hypertrophy in adult zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1007/s00421-005-0022-7openalex-snapshot
Gene expression in human skeletal muscle: alternative normalization method and effect of repeated biopsies
inferred← citeshttps://doi.org/10.1007/s00421-005-0082-8openalex-snapshot
Gene expression in skeletal muscle of coronary artery disease patients after concentric and eccentric endurance training
inferred← citeshttps://doi.org/10.1007/s00421-005-0085-5openalex-snapshot
Regular endurance training reduces the exercise induced HIF-1α and HIF-2α mRNA expression in human skeletal muscle in normoxic conditions
inferred← citeshttps://doi.org/10.1007/s00421-006-0238-1openalex-snapshot
New fundamental resistance exercise determinants of molecular and cellular muscle adaptations
inferred← citeshttps://doi.org/10.1007/s00421-006-0376-5openalex-snapshot
Reduced plasma free fatty acid availability during exercise: effect on gene expression
inferred← citeshttps://doi.org/10.1007/s00421-007-0479-7openalex-snapshot
Four weeks one-leg training and high fat diet does not alter PPARα protein or mRNA expression in human skeletal muscle
inferred← citeshttps://doi.org/10.1007/s00421-009-1143-1openalex-snapshot
Successive bouts of cycling stimulates genes associated with mitochondrial biogenesis
inferred← citeshttps://doi.org/10.1007/s00421-010-1544-1openalex-snapshot
Mitochondrial gene expression in elite cyclists: effects of high-intensity interval exercise
inferred← citeshttps://doi.org/10.1007/s00421-011-2129-3openalex-snapshot
Substrate use and biochemical response to a 3,211-km bicycle tour in trained cyclists
inferred← citeshttps://doi.org/10.1007/s00421-012-2504-8openalex-snapshot
Exercise with low glycogen increases PGC-1α gene expression in human skeletal muscle
inferred← citeshttps://doi.org/10.1007/s00421-012-2524-4openalex-snapshot
Combined whole-body vibration, resistance exercise, and sustained vascular occlusion increases PGC-1α and VEGF mRNA abundances
inferred← citeshttps://doi.org/10.1007/s00421-013-2783-8openalex-snapshot
Hypoxia refines plasticity of mitochondrial respiration to repeated muscle work
inferred← citeshttps://doi.org/10.1007/s00421-016-3402-2openalex-snapshot
Exercise duration-matched interval and continuous sprint cycling induce similar increases in AMPK phosphorylation, PGC-1α and VEGF mRNA expression in trained individuals
inferred← citeshttps://doi.org/10.1007/s00421-016-3405-zopenalex-snapshot
Concomitant application of sprint and high-intensity interval training on maximal oxygen uptake and work output in well-trained cyclists
inferred← citeshttps://doi.org/10.1007/s00421-017-3684-zopenalex-snapshot
Training and acute exercise modulates mitochondrial dynamics in football players’ blood mononuclear cells
inferred← citeshttps://doi.org/10.1007/s00421-022-05107-xopenalex-snapshot
Minimal adaptation of the molecular regulators of mitochondrial dynamics in response to unilateral limb immobilisation and retraining in middle-aged men
inferred← citeshttps://doi.org/10.1007/s00421-024-05549-5openalex-snapshot
Integrative effects of resistance training and endurance training on mitochondrial remodeling in skeletal muscle
inferred← citeshttps://doi.org/10.1007/s00424-005-0030-9openalex-snapshot
Interaction between signalling pathways involved in skeletal muscle responses to endurance exercise
inferred← citeshttps://doi.org/10.1007/s00424-005-1497-0openalex-snapshot
Endurance training modulates the muscular transcriptome response to acute exercise
inferred← citeshttps://doi.org/10.1007/s00424-010-0834-0openalex-snapshot
PGC-1α-mediated adaptations in skeletal muscle
inferred← citeshttps://doi.org/10.1007/s00424-019-02266-3openalex-snapshot
Cardiac adaptation to exercise training in health and disease
inferred← citeshttps://doi.org/10.1007/s00432-019-02911-5openalex-snapshot
Molecular and cellular adaptations to exercise training in skeletal muscle from cancer patients treated with chemotherapy
inferred← citeshttps://doi.org/10.1007/s00438-022-01878-2openalex-snapshot
PGC-1α affects skeletal muscle and adipose tissue development by regulating mitochondrial biogenesis
inferred← citeshttps://doi.org/10.1007/s00726-020-02934-0openalex-snapshot
Effects of long-term taurine supplementation on age-related changes in skeletal muscle function of Sprague–Dawley rats
inferred← citeshttps://doi.org/10.1007/s00774-020-01201-2openalex-snapshot
Role of irisin in effects of chronic exercise on muscle and bone in ovariectomized mice
inferred← citeshttps://doi.org/10.1007/s10519-008-9245-9openalex-snapshot
Genetic Influences on Change in BMI from Middle to Old Age: A 29-Year Follow-up Study of Twin Sisters
inferred← citeshttps://doi.org/10.1007/s10522-014-9546-8openalex-snapshot
Exercise improves mitochondrial and redox-regulated stress responses in the elderly: better late than never!
inferred← citeshttps://doi.org/10.1007/s11010-012-1486-5openalex-snapshot
Both short intense and prolonged moderate in vitro stimulation reduce the mRNA expression of calcium-regulatory proteins in rat skeletal muscle
inferred← citeshttps://doi.org/10.1007/s11010-015-2413-3openalex-snapshot
Transcriptional modulation of mitochondria biogenesis pathway at and above critical speed in mice
inferred← citeshttps://doi.org/10.1007/s11033-014-3453-6openalex-snapshot
PPAR-α and PPARGC1A gene variants have strong effects on aerobic performance of Turkish elite endurance athletes
inferred← citeshttps://doi.org/10.1007/s11033-020-06017-xopenalex-snapshot
Effect of different muscle contraction mode on the expression of Myostatin, IGF-1, and PGC-1 alpha family members in human Vastus Lateralis muscle
inferred← citeshttps://doi.org/10.1007/s11033-021-06224-0openalex-snapshot
The effects of different training modalities on monocarboxylate transporters MCT1 and MCT4, hypoxia inducible factor-1α (HIF-1α), and PGC-1α gene expression in rat skeletal muscles
inferred← citeshttps://doi.org/10.1007/s11154-010-9134-4openalex-snapshot
Endothelial dysfunction in diabetes mellitus: Molecular mechanisms and clinical implications
inferred← citeshttps://doi.org/10.1007/s11427-015-4833-4openalex-snapshot
Transcriptional regulatory circuits controlling muscle fiber type switching
inferred← citeshttps://doi.org/10.1007/s11892-004-0020-xopenalex-snapshot
Gene expression in the pathophysiology of type 2 diabetes mellitus
inferred← citeshttps://doi.org/10.1007/s12020-012-9676-1openalex-snapshot
Exercise and nutritional interventions for improving aging muscle health
inferred← citeshttps://doi.org/10.1007/s12170-008-0058-4openalex-snapshot
Interactions between genes and physical activity in cardiovascular disease
inferred← citeshttps://doi.org/10.1007/s12263-014-0415-5openalex-snapshot
Heritability and genetic etiology of habitual physical activity: a twin study with objective measures
inferred← citeshttps://doi.org/10.1007/s12265-016-9695-zopenalex-snapshot
Calcific Aortic Valve Disease: Part 2—Morphomechanical Abnormalities, Gene Reexpression, and Gender Effects on Ventricular Hypertrophy and Its Reversibility
inferred← citeshttps://doi.org/10.1007/s12576-013-0300-9openalex-snapshot
Vitamin C supplementation does not alter high-intensity endurance training-induced mitochondrial biogenesis in rat epitrochlearis muscle
inferred← citeshttps://doi.org/10.1007/s12576-014-0321-zopenalex-snapshot
Exercise-induced expression of peroxisome proliferator-activated receptor γ coactivator-1α isoforms in skeletal muscle of endurance-trained males
inferred← citeshttps://doi.org/10.1007/s12576-016-0491-yopenalex-snapshot
Peroxisome proliferator-activated receptor gamma co-activator 1 gene Gly482Ser polymorphism is associated with the response of low-density lipoprotein cholesterol concentrations to exercise training in elderly Japanese
inferred← citeshttps://doi.org/10.1007/s12603-015-0628-3openalex-snapshot
Consumption of chilies, but not sweet peppers, is positively related to handgrip strength in an adult population
inferred← citeshttps://doi.org/10.1007/s13105-012-0178-7openalex-snapshot
Three weeks of erythropoietin treatment hampers skeletal muscle mitochondrial biogenesis in rats
inferred← citeshttps://doi.org/10.1007/s13105-017-0576-yopenalex-snapshot
Multi-regulatory network of ROS: the interconnection of ROS, PGC-1 alpha, and AMPK-SIRT1 during exercise
inferred← citeshttps://doi.org/10.1007/s13105-023-00965-1openalex-snapshot
Effect of hypobaric hypoxia on the fiber type transition of skeletal muscle: a synergistic therapy of exercise preconditioning with a nanocurcumin formulation
inferred← citeshttps://doi.org/10.1007/s13105-025-01069-8openalex-snapshot
The impact of high altitude (hypobaric hypoxia) on insulin resistance in humans
inferred← citeshttps://doi.org/10.1007/s13577-024-01057-yopenalex-snapshot
The effects of exercise on epigenetic modifications: focus on DNA methylation, histone modifications and non-coding RNAs
inferred← citeshttps://doi.org/10.1007/s40279-013-0140-zopenalex-snapshot
Autophagic Cellular Responses to Physical Exercise in Skeletal Muscle
inferred← citeshttps://doi.org/10.1007/s40279-014-0162-1openalex-snapshot
Interference between Concurrent Resistance and Endurance Exercise: Molecular Bases and the Role of Individual Training Variables
inferred← citeshttps://doi.org/10.1007/s40279-018-0894-4openalex-snapshot
Principles of Exercise Prescription, and How They Influence Exercise-Induced Changes of Transcription Factors and Other Regulators of Mitochondrial Biogenesis
inferred← citeshttps://doi.org/10.1007/s40279-021-01620-9openalex-snapshot
The Effects of Dietary Protein Supplementation on Acute Changes in Muscle Protein Synthesis and Longer-Term Changes in Muscle Mass, Strength, and Aerobic Capacity in Response to Concurrent Resistance and Endurance Exercise in Healthy Adults: A Systematic Review
inferred← citeshttps://doi.org/10.1007/s40279-024-02039-8openalex-snapshot
Vertical Strength Transfer Phenomenon Between Upper Body and Lower Body Exercise: Systematic Scoping Review
inferred← citeshttps://doi.org/10.1007/s40279-026-02401-yopenalex-snapshot
Maximizing Adaptations in Concurrent Training: An Umbrella Review of Meta-analyses
inferred← citeshttps://doi.org/10.1007/s40519-018-0491-4openalex-snapshot
Metabolic cross-talk between skeletal muscle and adipose tissue in high-intensity interval training vs. moderate-intensity continuous training by regulation of PGC-1α
inferred← citeshttps://doi.org/10.1007/s42978-019-00041-5openalex-snapshot
Mitophagy Regulation in Skeletal Muscle: Effect of Endurance Exercise and Age
inferred← citeshttps://doi.org/10.1016/b978-0-12-381510-1.00016-8openalex-snapshot
Transcriptional Control of Striated Muscle Mitochondrial Biogenesis and Function
inferred← citeshttps://doi.org/10.1016/b978-0-12-381510-1.00064-8openalex-snapshot
Skeletal Muscle Adaptation to Exercise
inferred← citeshttps://doi.org/10.1016/b978-0-12-384878-9.00005-4openalex-snapshot
Drosophila Models of Cardiac Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.11413-8openalex-snapshot
Exercise and Physical Activity Recommendations for Optimizing Musculoskeletal Health in Older Adults
inferred← citeshttps://doi.org/10.1016/b978-0-12-811752-1.00016-xopenalex-snapshot
Impact of Lifestyle and Clinical Interventions on Mitochondrial Function in Obesity and Type 2 Diabetes
inferred← citeshttps://doi.org/10.1016/b978-0-12-816193-7.00010-5openalex-snapshot
Exercise and DNA methylation in skeletal muscle
inferred← citeshttps://doi.org/10.1016/b978-0-12-816193-7.00023-3openalex-snapshot
Proteomics and metabolomics research in exercise and sport
inferred← citeshttps://doi.org/10.1016/b978-0-12-821751-1.00007-5openalex-snapshot
Currently available therapies in mitochondrial disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-822146-4.00002-8openalex-snapshot
Molecular mechanisms of exercise providing therapeutic rationale to counter sarcopenia
inferred← citeshttps://doi.org/10.1016/b978-0-12-822498-4.00028-2openalex-snapshot
Mitochondrial biogenesis for the treatment of spinal cord injury
inferred← citeshttps://doi.org/10.1016/b978-0-12-822923-1.00027-3openalex-snapshot
Hesperidin and naringenin
inferred← citeshttps://doi.org/10.1016/b978-0-443-15260-3.00018-1openalex-snapshot
Molecular regulation of mitochondrial turnover by exercise: tissue adaptation through mitochondrial biogenesis and mitophagy
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2021.03.005openalex-snapshot
The mitochondrial calcium homeostasis orchestra plays its symphony: Skeletal muscle is the guest of honor
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2015.07.006openalex-snapshot
Exercise and Gene Expression
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2015.07.007openalex-snapshot
Exercise and the Regulation of Mitochondrial Turnover
inferred← citeshttps://doi.org/10.1016/j.abb.2019.03.019openalex-snapshot
The secret messages between mitochondria and nucleus in muscle cell biology
inferred← citeshttps://doi.org/10.1016/j.apsb.2019.11.017openalex-snapshot
Herbal drug discovery for the treatment of nonalcoholic fatty liver disease
inferred← citeshttps://doi.org/10.1016/j.arr.2009.03.003openalex-snapshot
The coordination of nuclear and mitochondrial communication during aging and calorie restriction
inferred← citeshttps://doi.org/10.1016/j.arr.2014.09.005openalex-snapshot
The measurement of protein synthesis for assessing proteostasis in studies of slowed aging
inferred← citeshttps://doi.org/10.1016/j.arr.2020.101175openalex-snapshot
Metabolic regulation of aging and age-related disease
inferred← citeshttps://doi.org/10.1016/j.arres.2023.100076openalex-snapshot
High–intensity exercise training induces the oxidative modification of malate dehydrogenase 2 in skeletal muscles
inferred← citeshttps://doi.org/10.1016/j.bbagen.2009.07.031openalex-snapshot
Transcriptional and post-transcriptional regulation of mitochondrial biogenesis in skeletal muscle: Effects of exercise and aging
inferred← citeshttps://doi.org/10.1016/j.bbagen.2013.12.004openalex-snapshot
Mitochondrial function in metabolic health: A genetic and environmental tug of war
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2006.06.010openalex-snapshot
The contraction induced increase in gene expression of peroxisome proliferator-activated receptor (PPAR)-γ coactivator 1α (PGC-1α), mitochondrial uncoupling protein 3 (UCP3) and hexokinase II (HKII) in primary rat skeletal muscle cells is dependent on reactive oxygen species
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2007.10.001openalex-snapshot
Regulation of mitochondrial oxidative phosphorylation through cell signaling
inferred← citeshttps://doi.org/10.1016/j.bbih.2025.101030openalex-snapshot
Physical exercise to rebalance kynurenine metabolism in borderline personality disorder – Preliminary findings
inferred← citeshttps://doi.org/10.1016/j.bbrc.2003.09.020openalex-snapshot
Role of calcineurin in striated muscle: development, adaptation, and disease
inferred← citeshttps://doi.org/10.1016/j.bbrc.2009.02.077openalex-snapshot
Identification and characterization of an alternative promoter of the human PGC-1α gene
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.07.074openalex-snapshot
Salicylates promote mitochondrial biogenesis by regulating the expression of PGC-1α in murine 3T3-L1 pre-adipocytes
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.10.101openalex-snapshot
Exercise training increases CISD family protein expression in murine skeletal muscle and white adipose tissue
inferred← citeshttps://doi.org/10.1016/j.bbrc.2025.151974openalex-snapshot
An updated and comprehensive review of the health benefits and pharmacological activities of hesperidin
inferred← citeshttps://doi.org/10.1016/j.bcp.2017.10.006openalex-snapshot
Pharmacological targeting of exercise adaptations in skeletal muscle: Benefits and pitfalls
inferred← citeshttps://doi.org/10.1016/j.bcp.2021.114640openalex-snapshot
Hypothalamus-skeletal muscle crosstalk during exercise and its role in metabolism modulation
inferred← citeshttps://doi.org/10.1016/j.biocel.2009.02.004openalex-snapshot
Role of mitochondrial dynamics proteins in the pathophysiology of obesity and type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.biochi.2025.12.011openalex-snapshot
Extracellular mitochondria: a potential player involved in exercise health benefits
inferred← citeshttps://doi.org/10.1016/j.bone.2015.02.008openalex-snapshot
Skeletal muscle as an endocrine organ: PGC-1α, myokines and exercise
inferred← citeshttps://doi.org/10.1016/j.brainres.2007.07.063openalex-snapshot
Quantitative immuno-electron microscopic analysis of depolarization-induced expression of PGC-1α in cultured rat visual cortical neurons
inferred← citeshttps://doi.org/10.1016/j.cbpc.2004.04.003openalex-snapshot
Using humans to study the physiological evolution of energy metabolism: a tribute to Peter Hochachka
inferred← citeshttps://doi.org/10.1016/j.cellsig.2011.07.013openalex-snapshot
Recent progress toward understanding the molecular mechanisms that regulate skeletal muscle mass
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.10.001openalex-snapshot
Phosphoproteomics of Acute Cell Stressors Targeting Exercise Signaling Networks Reveal Drug Interactions Regulating Protein Secretion
inferred← citeshttps://doi.org/10.1016/j.cmet.2010.11.008openalex-snapshot
Total Skeletal Muscle PGC-1 Deficiency Uncouples Mitochondrial Derangements from Fiber Type Determination and Insulin Sensitivity
inferred← citeshttps://doi.org/10.1016/j.cmet.2011.01.019openalex-snapshot
Exercise and PGC-1α-Independent Synchronization of Type I Muscle Metabolism and Vasculature by ERRγ
inferred← citeshttps://doi.org/10.1016/j.cmet.2012.01.001openalex-snapshot
Acute Exercise Remodels Promoter Methylation in Human Skeletal Muscle
inferred← citeshttps://doi.org/10.1016/j.cmet.2012.12.012openalex-snapshot
Exercise Metabolism and the Molecular Regulation of Skeletal Muscle Adaptation
inferred← citeshttps://doi.org/10.1016/j.cmet.2015.05.011openalex-snapshot
Understanding the Cellular and Molecular Mechanisms of Physical Activity-Induced Health Benefits
inferred← citeshttps://doi.org/10.1016/j.cmet.2015.06.016openalex-snapshot
Exercise Metabolism: Historical Perspective
inferred← citeshttps://doi.org/10.1016/j.cmet.2017.04.025openalex-snapshot
Molecular Mechanisms Underlying Cardiac Adaptation to Exercise
inferred← citeshttps://doi.org/10.1016/j.cmet.2017.04.029openalex-snapshot
PPARβ Is Essential for Maintaining Normal Levels of PGC-1α and Mitochondria and for the Increase in Muscle Mitochondria Induced by Exercise
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2019.08.007openalex-snapshot
Effects of exercise in a cold environment on gene expression for mitochondrial biogenesis and mitophagy
inferred← citeshttps://doi.org/10.1016/j.cub.2018.01.004openalex-snapshot
Mitophagy and Quality Control Mechanisms in Mitochondrial Maintenance
inferred← citeshttps://doi.org/10.1016/j.cyto.2021.155712openalex-snapshot
The effects of exercise training on inflammatory biomarkers in patients with breast cancer: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.ddmod.2012.12.002openalex-snapshot
New insights in the regulation of skeletal muscle PGC-1α by exercise and metabolic diseases
inferred← citeshttps://doi.org/10.1016/j.drudis.2014.03.006openalex-snapshot
Epigenetic adaptation to regular exercise in humans
inferred← citeshttps://doi.org/10.1016/j.ecl.2008.07.006openalex-snapshot
Exercise and the Treatment of Diabetes and Obesity
inferred← citeshttps://doi.org/10.1016/j.exger.2010.01.011openalex-snapshot
PGC-1α is required for training-induced prevention of age-associated decline in mitochondrial enzymes in mouse skeletal muscle
inferred← citeshttps://doi.org/10.1016/j.exger.2011.03.004openalex-snapshot
Mitochondrial biogenesis and angiogenesis in skeletal muscle of the elderly
inferred← citeshttps://doi.org/10.1016/j.exger.2013.07.015openalex-snapshot
Role of PGC-1α in exercise training- and resveratrol-induced prevention of age-associated inflammation
inferred← citeshttps://doi.org/10.1016/j.exger.2013.08.004openalex-snapshot
Exercise training attenuates aging-associated mitochondrial dysfunction in rat skeletal muscle: Role of PGC-1α
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.2026.113100openalex-snapshot
Exercise training improves mitochondrial oxidative energy metabolism through PGC-1α-dependent transcriptional pathway in the aged rat heart
inferred← citeshttps://doi.org/10.1016/j.expneurol.2019.113064openalex-snapshot
β2-adrenergic receptor-mediated mitochondrial biogenesis improves skeletal muscle recovery following spinal cord injury
inferred← citeshttps://doi.org/10.1016/j.foodres.2016.03.001openalex-snapshot
Functional effects of milk bioactive peptides on skeletal muscle of rats
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2007.02.029openalex-snapshot
Antioxidant supplementation enhances the exercise-induced increase in mitochondrial uncoupling protein 3 and endothelial nitric oxide synthase mRNA content in human skeletal muscle
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2015.10.412openalex-snapshot
Vitamin C and E supplementation prevents some of the cellular adaptations to endurance-training in humans
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2024.07.026openalex-snapshot
Molecular aspects of the exercise response and training adaptation in skeletal muscle
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2026.01.002openalex-snapshot
MOTS-c improves intrinsic muscle mitochondrial bioenergetic health and efficiency in a PGC-1α/AMPK-dependent manner
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2026.08.040openalex-snapshot
Exercise and phytochemicals as modulators of redox homeostasis in aging
inferred← citeshttps://doi.org/10.1016/j.hjc.2018.08.002openalex-snapshot
Inter-tissue expression patterns of the key metabolic biomarker PGC-1α in severely obese individuals: Implication in obesity-induced disease
inferred← citeshttps://doi.org/10.1016/j.imr.2014.09.004openalex-snapshot
Exercise-induced PGC-1α transcriptional factors in skeletal muscle
inferred← citeshttps://doi.org/10.1016/j.imr.2016.05.003openalex-snapshot
Function of specialized regulatory proteins and signaling pathways in exercise-induced muscle mitochondrial biogenesis
inferred← citeshttps://doi.org/10.1016/j.jff.2023.105542openalex-snapshot
Ensemble Machine learning model identified citrusinol as functional food candidate for improving myotube differentiation and controlling CT26-Induced myotube atrophy
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2025.110006openalex-snapshot
Ergothioneine as a functional nutraceutical: Mechanisms, bioavailability, and therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.jshs.2020.03.004openalex-snapshot
The roles of microRNA in redox metabolism and exercise-mediated adaptation
inferred← citeshttps://doi.org/10.1016/j.jshs.2024.05.001openalex-snapshot
Reactive oxygen species promote endurance exercise-induced adaptations in skeletal muscles
inferred← citeshttps://doi.org/10.1016/j.jshs.2025.101049openalex-snapshot
Adaptations in mitochondrial quality control and interactions with innate immune signaling within skeletal muscle: A narrative review
inferred← citeshttps://doi.org/10.1016/j.jstrokecerebrovasdis.2016.11.003openalex-snapshot
Resistive Training and Molecular Regulators of Vascular-Metabolic Risk in Chronic Stroke
inferred← citeshttps://doi.org/10.1016/j.jtemb.2026.127893openalex-snapshot
Voluntary wheel running combined with low-dose lithium supplementation improves novel object recognition in male DBA/2 J mdx mice
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2017.04.008openalex-snapshot
Local muscle cooling does not impact expression of mitochondrial-related genes
inferred← citeshttps://doi.org/10.1016/j.lfs.2016.11.016openalex-snapshot
Satellite cell activation induced by aerobic muscle adaptation in response to endurance exercise in humans and rodents
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