Exercise metabolism and adaptation in skeletal muscle
暂无分享,去创建一个
[1] R. Sum,et al. Associations of timing of physical activity with all-cause and cause-specific mortality in a prospective cohort study , 2023, Nature Communications.
[2] J. Alcazar,et al. Ten‐year longitudinal changes in muscle power, force, and velocity in young, middle‐aged, and older adults , 2023, Journal of cachexia, sarcopenia and muscle.
[3] Ruirui Liu,et al. Spatial metabolomics reveals skeletal myofiber subtypes , 2023, Science advances.
[4] J. C. McDermott,et al. Re-organization of nucleolar architecture in myogenic differentiation. , 2023, Journal of cell science.
[5] K. Esser,et al. Metabolism and exercise: the skeletal muscle clock takes centre stage , 2023, Nature Reviews Endocrinology.
[6] Longfei Ding,et al. Rab8a as a mitochondrial receptor for lipid droplets in skeletal muscle. , 2023, Developmental cell.
[7] C. S. Shaw,et al. Intramuscular lipid utilisation during exercise: A systematic review, meta-analysis and meta-regression. , 2023, Journal of applied physiology.
[8] A. Dopazo,et al. Senescence atlas reveals an aged-like inflamed niche that blunts muscle regeneration , 2022, Nature.
[9] J. Nie,et al. Acute effect of high-intensity interval training versus moderate-intensity continuous training on appetite perception: A systematic review and meta-analysis , 2022, Appetite.
[10] N. LeBrasseur,et al. p21 induces a senescence program and skeletal muscle dysfunction , 2022, Molecular metabolism.
[11] S. Paluska,et al. Sex based comparisons of muscle cellular adaptations after 10-weeks of progressive resistance training in middle-aged adults. , 2022, Journal of applied physiology.
[12] L. Grevendonk,et al. Skeletal muscle mitochondrial inertia is associated with carnitine acetyltransferase activity and physical function in humans , 2022, JCI Insight.
[13] K. Højlund,et al. Altered intramuscular network of lipid droplets and mitochondria in type 2 diabetes. , 2022, American journal of physiology. Cell physiology.
[14] H. Kanehisa,et al. Heavy Resistance Training Versus Plyometric Training for Improving Running Economy and Running Time Trial Performance: A Systematic Review and Meta-analysis , 2022, Sports Medicine - Open.
[15] E. Trexler,et al. Influence of Resistance Training Proximity-to-Failure on Skeletal Muscle Hypertrophy: A Systematic Review with Meta-analysis , 2022, Sports Medicine.
[16] H. Lamb,et al. Timing of physical activity in relation to liver fat content and insulin resistance , 2022, Diabetologia.
[17] J. McCarthy,et al. Skeletal Muscle Nuclei in Mice are not Post-mitotic , 2022, bioRxiv.
[18] A. Kavazis,et al. Skeletal Muscle DNA Methylation and mRNA Responses to a Bout of Higher versus Lower Load Resistance Exercise in Previously Trained Men , 2022, bioRxiv.
[19] Yuanyuan Lv,et al. A systematic review and meta-analysis on effects of aerobic exercise in people with Parkinson’s disease , 2022, npj Parkinson's Disease.
[20] J. Helgerud,et al. Aerobic high‐intensity intervals are superior to improve V̇O2max compared with sprint intervals in well‐trained men , 2022, Scandinavian journal of medicine & science in sports.
[21] Qian Yu,et al. Comparative Effectiveness of Multiple Exercise Interventions in the Treatment of Mental Health Disorders: A Systematic Review and Network Meta-Analysis , 2022, Sports Medicine - Open.
[22] Jonathan P. Davis,et al. Sarcomere dynamics revealed by a myofilament integrated FRET-based biosensor in live skeletal muscle fibers , 2022, Scientific Reports.
[23] M. Murgia,et al. Genes Whose Gain or Loss of Function Changes Type 1, 2A, 2X, or 2B Muscle Fibre Proportions in Mice—A Systematic Review , 2022, International journal of molecular sciences.
[24] Ferdinand von Meyenn,et al. H3K18 lactylation marks tissue-specific active enhancers , 2022, Genome Biology.
[25] J. Loscalzo,et al. Ultrasensitive sensors reveal the spatiotemporal landscape of lactate metabolism in physiology and disease. , 2022, Cell metabolism.
[26] G. D’Hulst,et al. Resistance exercise enhances long-term mTORC1 sensitivity to leucine , 2022, Molecular metabolism.
[27] B. Schoenfeld,et al. Progressive overload without progressing load? The effects of load or repetition progression on muscular adaptations , 2022, PeerJ.
[28] Piero Carninci,et al. Distinctive exercise-induced inflammatory response and exerkine induction in skeletal muscle of people with type 2 diabetes , 2022, Science advances.
[29] H. Sakurai,et al. Skeletal muscle releases extracellular vesicles with distinct protein and microRNA signatures that function in the muscle microenvironment , 2022, PNAS nexus.
[30] S. Forbes,et al. Effects of creatine supplementation on memory in healthy individuals: a systematic review and meta-analysis of randomized controlled trials , 2022, Nutrition reviews.
[31] J. Halling,et al. Impact of Aging and Lifelong Exercise Training on Mitochondrial Function and Network Connectivity in Human Skeletal Muscle. , 2022, The journals of gerontology. Series A, Biological sciences and medical sciences.
[32] C. Pope,et al. Dose–response association of aerobic and muscle-strengthening physical activity with mortality: a national cohort study of 416 420 US adults , 2022, British Journal of Sports Medicine.
[33] G. Patti,et al. Saturation of the mitochondrial NADH shuttles drives aerobic glycolysis in proliferating cells. , 2022, Molecular cell.
[34] Dorte B. Bekker-Jensen,et al. ZAKβ is activated by cellular compression and mediates contraction‐induced MAP kinase signaling in skeletal muscle , 2022, The EMBO journal.
[35] F. Kolpakov,et al. Alternative transcription start sites contribute to acute-stress-induced transcriptome response in human skeletal muscle , 2022, Human Genomics.
[36] Yu Lin,et al. Identification of enhancers responsible for the coordinated expression of myosin heavy chain isoforms in skeletal muscle , 2022, BMC Genomics.
[37] D. Plews,et al. Factors Influencing Substrate Oxidation During Submaximal Cycling: A Modelling Analysis , 2022, Sports Medicine.
[38] C. Zinn,et al. The Ergogenic Effects of Acute Carbohydrate Feeding on Resistance Exercise Performance: A Systematic Review and Meta-analysis , 2022, Sports Medicine.
[39] Pengyi Yang,et al. Phosphoproteomics of three exercise modalities identifies canonical signaling and C18ORF25 as an AMPK substrate regulating skeletal muscle function. , 2022, Cell metabolism.
[40] Ian R. Lanza,et al. Characterization of cellular senescence in aging skeletal muscle , 2022, Nature Aging.
[41] Ludger J. E. Goeminne,et al. Evidence for a neuromuscular circuit involving hypothalamic interleukin-6 in the control of skeletal muscle metabolism , 2022, Science advances.
[42] K. Y. Loh,et al. An exercise-inducible metabolite that suppresses feeding and obesity , 2022, Nature.
[43] B. Deplancke,et al. A Tead1-Apelin axis directs paracrine communication from myogenic to endothelial cells in skeletal muscle , 2022, iScience.
[44] Simon J. Vogrin,et al. Progressive Resistance Training for Concomitant Increases in Muscle Strength and Bone Mineral Density in Older Adults: A Systematic Review and Meta-Analysis , 2022, Sports Medicine.
[45] B. Schoenfeld,et al. Comparison of Power Training vs Traditional Strength Training on Physical Function in Older Adults , 2022, JAMA network open.
[46] K. Nair,et al. Enhancement of anaerobic glycolysis – a role of PGC-1α4 in resistance exercise , 2022, Nature Communications.
[47] C. G. Perry,et al. A HIF-1 signature dominates the attenuation in the human skeletal muscle transcriptional response to high-intensity interval training. , 2022, Journal of applied physiology.
[48] T. Lundberg,et al. The Effects of Concurrent Aerobic and Strength Training on Muscle Fiber Hypertrophy: A Systematic Review and Meta-Analysis , 2022, Sports Medicine.
[49] M. D. de Angelis,et al. Does a Hypertrophying Muscle Fibre Reprogramme its Metabolism Similar to a Cancer Cell? , 2022, Sports Medicine.
[50] C. Sette,et al. Spatially resolved transcriptomics reveals innervation-responsive functional clusters in skeletal muscle , 2022, bioRxiv.
[51] Saptarsi M. Haldar,et al. Transcription factors KLF15 and PPARδ cooperatively orchestrate genome-wide regulation of lipid metabolism in skeletal muscle , 2022, The Journal of biological chemistry.
[52] A. Katz. A century of exercise physiology: key concepts in regulation of glycogen metabolism in skeletal muscle , 2022, European Journal of Applied Physiology.
[53] Kevin A. Murach,et al. Senolytic treatment rescues blunted muscle hypertrophy in old mice , 2022, GeroScience.
[54] Ian R. Lanza,et al. Exerkines in health, resilience and disease , 2022, Nature Reviews Endocrinology.
[55] W. Bredie,et al. Maltodextrin-Based Carbohydrate Oral Rinsing and Exercise Performance: Systematic Review and Meta-Analysis , 2022, Sports Medicine.
[56] J. Concordet,et al. A fast Myosin super enhancer dictates muscle fiber phenotype through competitive interactions with Myosin genes , 2022, Nature communications.
[57] D. Fitzpatrick-Lewis,et al. Systematic review and meta‐analysis of protein intake to support muscle mass and function in healthy adults , 2022, Journal of cachexia, sarcopenia and muscle.
[58] X. Zhuang,et al. Spatially resolved epigenomic profiling of single cells in complex tissues , 2022, Cell.
[59] D. Lieberman,et al. Interleukin 6 as an energy allocator in muscle tissue , 2022, Nature Metabolism.
[60] L. Ferrucci,et al. Muscle mitochondrial energetics predicts mobility decline in well‐functioning older adults: The baltimore longitudinal study of aging , 2022, Aging cell.
[61] Prasanna Katti,et al. Mitochondrial network configuration influences sarcomere and myosin filament structure in striated muscles , 2022, bioRxiv.
[62] R. Barroso,et al. Muscle hypertrophy and strength gains after resistance training with different volume matched loads: a systematic review and meta-analysis. , 2022, Applied physiology, nutrition, and metabolism = Physiologie appliquee, nutrition et metabolisme.
[63] J. Santos-Concejero,et al. A Systematic Review of The Effects of Different Resistance Training Volumes on Muscle Hypertrophy , 2022, Journal of human kinetics.
[64] Kevin A. Murach,et al. Deletion of SA β‐Gal+ cells using senolytics improves muscle regeneration in old mice , 2021, Aging cell.
[65] J. Auwerx,et al. The exercise-induced long noncoding RNA CYTOR promotes fast-twitch myogenesis in aging , 2021, Science Translational Medicine.
[66] Sean J. Humphrey,et al. Personalized phosphoproteomics identifies functional signaling , 2021, Nature Biotechnology.
[67] J. Sadoshima,et al. Skeletal muscle NOX4 is required for adaptive responses that prevent insulin resistance , 2021, Science advances.
[68] P. Meikle,et al. High-intensity training induces non-stoichiometric changes in the mitochondrial proteome of human skeletal muscle without reorganisation of respiratory chain content , 2021, Nature Communications.
[69] N. Hodson,et al. RPS6 phosphorylation occurs to a greater extent in the periphery of human skeletal muscle fibers, near focal adhesions, after anabolic stimuli. , 2021, American journal of physiology. Cell physiology.
[70] W. Hammerschmidt,et al. MicroRNAs are minor constituents of extracellular vesicles that are rarely delivered to target cells , 2021, PLoS genetics.
[71] J. Adamski,et al. Effects of Acute and Chronic Resistance Exercise on the Skeletal Muscle Metabolome , 2021, Metabolites.
[72] M. Zavolan,et al. Dual roles of mTORC1-dependent activation of the ubiquitin-proteasome system in muscle proteostasis , 2021, bioRxiv.
[73] K. Doma,et al. Compatibility of Concurrent Aerobic and Strength Training for Skeletal Muscle Size and Function: An Updated Systematic Review and Meta-Analysis , 2021, Sports Medicine.
[74] M. Murgia,et al. Protein profile of fiber types in human skeletal muscle: a single-fiber proteomics study , 2021, Skeletal Muscle.
[75] N. Ørtenblad,et al. Specific ATPases drive compartmentalized glycogen utilization in rat skeletal muscle , 2021, bioRxiv.
[76] D. Bishop,et al. Impacts of high‐intensity exercise on the metabolomics profile of human skeletal muscle tissue , 2021, Scandinavian journal of medicine & science in sports.
[77] D. O'Gorman,et al. Endurance exercise training-responsive miR-19b-3p improves skeletal muscle glucose metabolism , 2021, Nature Communications.
[78] Ye Sun,et al. Regulation of the evolutionarily conserved muscle myofibrillar matrix by cell type dependent and independent mechanisms , 2021, Nature Communications.
[79] Sandra Kleiner,et al. Muscle-secreted neurturin couples myofiber oxidative metabolism and slow motor neuron identity. , 2021, Cell metabolism.
[80] Yaqian Qu,et al. The Role of cAMP-PKA Pathway in Lactate-Induced Intramuscular Triglyceride Accumulation and Mitochondria Content Increase in Mice , 2021, Frontiers in Physiology.
[81] Clint L. Miller,et al. Mitochondria-localized AMPK responds to local energetics and contributes to exercise and energetic stress-induced mitophagy , 2021, Proceedings of the National Academy of Sciences.
[82] D. Carslake,et al. Association of physical activity intensity and bout length with mortality: An observational study of 79,503 UK Biobank participants , 2021, PLoS medicine.
[83] H. Ellingsgaard,et al. Blocking endogenous IL-6 impairs mobilization of free fatty acids during rest and exercise in lean and obese men , 2021, Cell reports. Medicine.
[84] S. Malitsky,et al. Clock proteins and training modify exercise capacity in a daytime-dependent manner , 2021, Proceedings of the National Academy of Sciences.
[85] Kevin A. Murach,et al. Myonuclear transcriptional dynamics in response to exercise following satellite cell depletion , 2021, iScience.
[86] W. Roman,et al. mRNA distribution in skeletal muscle is associated with mRNA size. , 2021, Journal of cell science.
[87] M. Rivas,et al. Time trajectories in the transcriptomic response to exercise - a meta-analysis , 2021, Nature Communications.
[88] L. S. Churchman,et al. Balanced mitochondrial and cytosolic translatomes underlie the biogenesis of human respiratory complexes , 2021, bioRxiv.
[89] Franck P. Martial,et al. Bright daytime light enhances circadian amplitude in a diurnal mammal , 2021, Proceedings of the National Academy of Sciences.
[90] S. Preibisch,et al. Cap-dependent translation initiation monitored in living cells , 2021, bioRxiv.
[91] B. Ekblom,et al. Variablity in vastus lateralis fiber type distribution, fiber size and myonuclear content along and the between legs. , 2021, Journal of applied physiology.
[92] J. Oppert,et al. Effect of exercise on cardiometabolic health of adults with overweight or obesity: Focus on blood pressure, insulin resistance, and intrahepatic fat—A systematic review and meta‐analysis , 2021, Obesity reviews : an official journal of the International Association for the Study of Obesity.
[93] J. Werneck-de-Castro,et al. Exercise-Stimulated ROS Sensitive Signaling Pathways in Skeletal Muscle , 2021, Antioxidants.
[94] J. Coon,et al. Mapping of the contraction-induced phosphoproteome identifies TRIM28 as a significant regulator of skeletal muscle size and function , 2021, Cell reports.
[95] Eric T. Wang,et al. Microtubule-based transport is essential to distribute RNA and nascent protein in skeletal muscle , 2021, Nature Communications.
[96] B. Drust,et al. The Comparative Methylome and Transcriptome After Change of Direction Compared to Straight Line Running Exercise in Human Skeletal Muscle , 2021, Frontiers in Physiology.
[97] Emily A. Scarborough,et al. Microtubules orchestrate local translation to enable cardiac growth , 2021, Nature Communications.
[98] M. Mann,et al. Deep muscle-proteomic analysis of freeze-dried human muscle biopsies reveals fiber type-specific adaptations to exercise training , 2021, Nature communications.
[99] T. Moritz,et al. Plasma Metabolome Profiling of Resistance Exercise and Endurance Exercise in Humans. , 2020, Cell reports.
[100] P. Schrauwen,et al. Exercise training elicits superior metabolic effects when performed in the afternoon compared to morning in metabolically compromised humans , 2020, Physiological reports.
[101] D. Bishop,et al. Exercise mitigates sleep-loss-induced changes in glucose tolerance, mitochondrial function, sarcoplasmic protein synthesis, and diurnal rhythms , 2020, Molecular Metabolism.
[102] P. Baldi,et al. Atlas of exercise metabolism reveals time-dependent signatures of metabolic homeostasis. , 2020, Cell metabolism.
[103] P. Maire,et al. Single-nucleus RNA-seq and FISH identify coordinated transcriptional activity in mammalian myofibers , 2020, Nature Communications.
[104] David D. Thomas,et al. Super-relaxed state of myosin in human skeletal muscle is fiber-type dependent. , 2020, American journal of physiology. Cell physiology.
[105] C. Henríquez-Olguín,et al. RNA-bound PGC-1α controls gene expression in liquid-like nuclear condensates , 2020, Proceedings of the National Academy of Sciences.
[106] P. Aagaard,et al. Subcellular localization‐ and fibre type‐dependent utilization of muscle glycogen during heavy resistance exercise in elite power and Olympic weightlifters , 2020, Acta physiologica.
[107] Omar K. Yaghi,et al. pH-Gated Succinate Secretion Regulates Muscle Remodeling in Response to Exercise , 2020, Cell.
[108] B. Dallagiovanna,et al. Long Non-coding RNAs Are Differentially Expressed After Different Exercise Training Programs , 2020, Frontiers in Physiology.
[109] C. Wahlestedt,et al. Molecular Transducers of Human Skeletal Muscle Remodeling under Different Loading States , 2020, Cell reports.
[110] D. Bishop,et al. An Examination and Critique of Current Methods to Determine Exercise Intensity , 2020, Sports Medicine.
[111] B. Glancy,et al. The unified myofibrillar matrix for force generation in muscle , 2020, Nature Communications.
[112] M. Lindholm,et al. Skeletal Muscle Transcriptomic Comparison between Long-Term Trained and Untrained Men and Women. , 2020, Cell reports.
[113] K. Vissing,et al. Exercise‐dependent increases in protein synthesis are accompanied by chromatin modifications and increased MRTF‐SRF signalling , 2020, Acta physiologica.
[114] A. Akalin,et al. Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells , 2020, Nature Communications.
[115] Ferdinand von Meyenn,et al. Exercise promotes satellite cell contribution to myofibers in a load-dependent manner , 2020, bioRxiv.
[116] K. Meijer,et al. One-leg inactivity induces a reduction in mitochondrial oxidative capacity, intramyocellular lipid accumulation and reduced insulin signalling upon lipid infusion: a human study with unilateral limb suspension , 2020, Diabetologia.
[117] M. Stevens,et al. Modeling the transport of nuclear proteins along single skeletal muscle cells , 2020, Proceedings of the National Academy of Sciences.
[118] David A. Knowles,et al. Molecular Choreography of Acute Exercise , 2020, Cell.
[119] P. Carmeliet,et al. PHD1 controls muscle mTORC1 in a hydroxylation-independent manner by stabilizing leucyl tRNA synthetase , 2020, Nature Communications.
[120] H. Bush,et al. Circadian rhythm phase shifts caused by timed exercise vary with chronotype. , 2020, JCI insight.
[121] Kevin A. Murach,et al. Fusion-Independent Satellite Cell Communication to Muscle Fibers During Load-Induced Hypertrophy , 2020, Function.
[122] E. Stevenson,et al. The effects of vitamin C and E on exercise-induced physiological adaptations: a systematic review and Meta-analysis of randomized controlled trials , 2019, Critical reviews in food science and nutrition.
[123] D. Bishop,et al. Forty high-intensity interval training sessions blunt exercise-induced changes in the nuclear protein content of PGC-1α and p53 in human skeletal muscle. , 2019, American journal of physiology. Endocrinology and metabolism.
[124] S. Medler. Mixing it up: the biological significance of hybrid skeletal muscle fibers , 2019, Journal of Experimental Biology.
[125] Kevin A. Murach,et al. Cores of Reproducibility in Physiology (CORP): Fiber Typing Human Skeletal Muscle with Fluorescent Immunohistochemistry. , 2019, Journal of applied physiology.
[126] A. Pertille,et al. Effects of Creatine Supplementation on Renal Function: A Systematic Review and Meta-Analysis. , 2019, Journal of renal nutrition : the official journal of the Council on Renal Nutrition of the National Kidney Foundation.
[127] D. Bishop,et al. Transcriptomic profiling of skeletal muscle adaptations to exercise and inactivity , 2019, Nature Communications.
[128] J. Kao,et al. Voltage-energized Calcium-sensitive ATP Production by Mitochondria , 2019, Nature Metabolism.
[129] Nolan J. Hoffman,et al. Phosphoproteomics reveals conserved exercise‐stimulated signaling and AMPK regulation of store‐operated calcium entry , 2019, The EMBO journal.
[130] Pierre Baldi,et al. Time of Exercise Specifies the Impact on Muscle Metabolic Pathways and Systemic Energy Homeostasis. , 2019, Cell metabolism.
[131] Luigi Ferrucci,et al. Semi-automated 3D segmentation of human skeletal muscle using Focused Ion Beam-Scanning Electron Microscopic images. , 2019, Journal of structural biology.
[132] J. Grgic,et al. How many times per week should a muscle be trained to maximize muscle hypertrophy? A systematic review and meta-analysis of studies examining the effects of resistance training frequency , 2019, Journal of sports sciences.
[133] P. Puigserver,et al. ER and Nutrient Stress Promote Assembly of Respiratory Chain Supercomplexes through the PERK-eIF2α Axis. , 2019, Molecular cell.
[134] B. Viollet,et al. AMPK and TBC1D1 Regulate Muscle Glucose Uptake After, but Not During, Exercise and Contraction , 2019, Diabetes.
[135] Sudha Seshadri,et al. Physical inactivity, cardiometabolic disease, and risk of dementia: an individual-participant meta-analysis , 2019, BMJ.
[136] M. Snyder,et al. Lifelong physical activity is associated with promoter hypomethylation of genes involved in metabolism, myogenesis, contractile properties and oxidative stress resistance in aged human skeletal muscle , 2019, Scientific Reports.
[137] A. Goldberg,et al. 26S Proteasomes are rapidly activated by diverse hormones and physiological states that raise cAMP and cause Rpn6 phosphorylation , 2019, Proceedings of the National Academy of Sciences.
[138] J. Zierath,et al. Circadian rhythms and exercise — re-setting the clock in metabolic disease , 2019, Nature Reviews Endocrinology.
[139] C. Henríquez-Olguín,et al. Cytosolic ROS production by NADPH oxidase 2 regulates muscle glucose uptake during exercise , 2019, Nature Communications.
[140] Robert W. Taylor,et al. Quantitative 3D Mapping of the Human Skeletal Muscle Mitochondrial Network , 2019, Cell reports.
[141] C. Kahn,et al. TGF-β2 is an exercise-induced adipokine that regulates glucose and fatty acid metabolism , 2018, Nature Metabolism.
[142] B. Glancy,et al. Subcellular connectomic analyses of energy networks in striated muscle , 2018, Nature Communications.
[143] J. Zierath,et al. Afternoon exercise is more efficacious than morning exercise at improving blood glucose levels in individuals with type 2 diabetes: a randomised crossover trial , 2018, Diabetologia.
[144] D. Hood,et al. The Role of p53 in Determining Mitochondrial Adaptations to Endurance Training in Skeletal Muscle , 2018, Scientific Reports.
[145] Duck-chul Lee,et al. Muscular Strength as a Predictor of All-Cause Mortality in an Apparently Healthy Population: A Systematic Review and Meta-Analysis of Data From Approximately 2 Million Men and Women. , 2018, Archives of physical medicine and rehabilitation.
[146] Peter R. Huntjens,et al. Distinct lipid droplet characteristics and distribution unmask the apparent contradiction of the athlete's paradox , 2018, Molecular metabolism.
[147] D. Rivas,et al. JNK regulates muscle remodeling via myostatin/SMAD inhibition , 2018, Nature Communications.
[148] V. Pertegato,et al. Transcriptional programming of lipid and amino acid metabolism by the skeletal muscle circadian clock , 2018, PLoS biology.
[149] M. Cesari,et al. The exerkine apelin reverses age-associated sarcopenia , 2018, Nature Medicine.
[150] S B Heymsfield,et al. Human energy expenditure: advances in organ‐tissue prediction models , 2018, Obesity reviews : an official journal of the International Association for the Study of Obesity.
[151] R. Talmadge,et al. Muscle health and performance in monozygotic twins with 30 years of discordant exercise habits , 2018, European Journal of Applied Physiology.
[152] F. Scheer,et al. Circadian misalignment induces fatty acid metabolism gene profiles and compromises insulin sensitivity in human skeletal muscle , 2018, Proceedings of the National Academy of Sciences.
[153] D. Bishop,et al. Training-Induced Changes in Mitochondrial Content and Respiratory Function in Human Skeletal Muscle , 2018, Sports Medicine.
[154] W. Hopkins,et al. Skeletal Muscle Glycogen Content at Rest and During Endurance Exercise in Humans: A Meta-Analysis , 2018, Sports Medicine.
[155] Wei Xu,et al. A DGKζ-FoxO-ubiquitin proteolytic axis controls fiber size during skeletal muscle remodeling , 2018, Science Signaling.
[156] K. Häkkinen,et al. Autophagy is induced by resistance exercise in young men, but unfolded protein response is induced regardless of age , 2018, Acta physiologica.
[157] J. Louis,et al. Fuel for the Work Required: A Theoretical Framework for Carbohydrate Periodization and the Glycogen Threshold Hypothesis , 2018, Sports Medicine.
[158] T. Pereira,et al. Kynurenic Acid and Gpr35 Regulate Adipose Tissue Energy Homeostasis and Inflammation. , 2018, Cell metabolism.
[159] H. Westerblad,et al. Molecular Basis for Exercise-Induced Fatigue: The Importance of Strictly Controlled Cellular Ca2+ Handling. , 2018, Cold Spring Harbor perspectives in medicine.
[160] S. Shepherd,et al. Human Skeletal Muscle Possesses an Epigenetic Memory of Hypertrophy , 2018, Scientific Reports.
[161] L. Gladden,et al. Lactate metabolism: historical context, prior misinterpretations, and current understanding , 2018, European Journal of Applied Physiology.
[162] Ming Zhang,et al. Leisure-time physical activity and incident metabolic syndrome: a systematic review and dose-response meta-analysis of cohort studies. , 2017, Metabolism: clinical and experimental.
[163] J. Saucerman,et al. Ampk phosphorylation of Ulk1 is required for targeting of mitochondria to lysosomes in exercise-induced mitophagy , 2017, Nature Communications.
[164] R. Voituriez,et al. Myofibril contraction and cross-linking drive nuclear movement to the periphery of skeletal muscle , 2017, Nature Cell Biology.
[165] G. Heigenhauser,et al. Resistance exercise initiates mechanistic target of rapamycin (mTOR) translocation and protein complex co-localisation in human skeletal muscle , 2017, Scientific Reports.
[166] Helen R Marucci-Wellman,et al. Chronotypes in the US – Influence of age and sex , 2017, PloS one.
[167] M. Mann,et al. Single Muscle Fiber Proteomics Reveals Fiber-Type-Specific Features of Human Muscle Aging. , 2017, Cell reports.
[168] B. Schoenfeld,et al. Dose-response relationship between weekly resistance training volume and increases in muscle mass: A systematic review and meta-analysis , 2017, Journal of sports sciences.
[169] D. Schübeler,et al. Impact of cytosine methylation on DNA binding specificities of human transcription factors , 2017, Science.
[170] J. Auwerx,et al. PPARδ Promotes Running Endurance by Preserving Glucose. , 2017, Cell metabolism.
[171] Sriram Subramaniam,et al. Power Grid Protection of the Muscle Mitochondrial Reticulum. , 2017, Cell reports.
[172] P. Schjerling,et al. Rac1 and AMPK Account for the Majority of Muscle Glucose Uptake Stimulated by Ex Vivo Contraction but Not In Vivo Exercise , 2017, Diabetes.
[173] C. S. Shaw,et al. Exercise Increases Human Skeletal Muscle Insulin Sensitivity via Coordinated Increases in Microvascular Perfusion and Molecular Signaling , 2017, Diabetes.
[174] Rickey E Carter,et al. Enhanced Protein Translation Underlies Improved Metabolic and Physical Adaptations to Different Exercise Training Modes in Young and Old Humans. , 2017, Cell metabolism.
[175] Maximilian Kleinert,et al. Exercise-stimulated glucose uptake — regulation and implications for glycaemic control , 2017, Nature Reviews Endocrinology.
[176] J. Auwerx,et al. Enhanced Respiratory Chain Supercomplex Formation in Response to Exercise in Human Skeletal Muscle. , 2017, Cell metabolism.
[177] J. McCarthy,et al. Myogenic Progenitor Cells Control Extracellular Matrix Production by Fibroblasts during Skeletal Muscle Hypertrophy. , 2017, Cell stem cell.
[178] C. Ballmann,et al. Adult expression of PGC-1α and -1β in skeletal muscle is not required for endurance exercise-induced enhancement of exercise capacity. , 2016, American journal of physiology. Endocrinology and metabolism.
[179] B. Viollet,et al. Enhanced Muscle Insulin Sensitivity After Contraction/Exercise Is Mediated by AMPK , 2016, Diabetes.
[180] J. McCarthy,et al. Expression of Muscle‐Specific Ribosomal Protein L3‐Like Impairs Myotube Growth , 2016, Journal of cellular physiology.
[181] R. Rauramaa,et al. Long-term Change in Cardiorespiratory Fitness and All-Cause Mortality: A Population-Based Follow-up Study. , 2016, Mayo Clinic proceedings.
[182] G. Muscat,et al. The Nuclear Receptor, Nor-1, Induces the Physiological Responses Associated With Exercise. , 2016, Molecular endocrinology.
[183] K. Esser,et al. Muscle-specific loss of Bmal1 leads to disrupted tissue glucose metabolism and systemic glucose homeostasis , 2016, Skeletal Muscle.
[184] F. Scheer,et al. Circadian misalignment increases cardiovascular disease risk factors in humans , 2016, Proceedings of the National Academy of Sciences.
[185] Stephen C. Cannon,et al. A peptide encoded by a transcript annotated as long noncoding RNA enhances SERCA activity in muscle , 2016, Science.
[186] F. Polleux,et al. AMP-activated protein kinase mediates mitochondrial fission in response to energy stress , 2016, Science.
[187] Roy Taylor,et al. Ingestion of glucose or sucrose prevents liver but not muscle glycogen depletion during prolonged endurance-type exercise in trained cyclists. , 2015, American journal of physiology. Endocrinology and metabolism.
[188] B. Viollet,et al. AMPKα is essential for acute exercise-induced gene responses but not for exercise training-induced adaptations in mouse skeletal muscle. , 2015, American journal of physiology. Endocrinology and metabolism.
[189] G. Piazzesi,et al. Force generation by skeletal muscle is controlled by mechanosensing in myosin filaments , 2015, Nature.
[190] Nolan J Hoffman,et al. Global Phosphoproteomic Analysis of Human Skeletal Muscle Reveals a Network of Exercise-Regulated Kinases and AMPK Substrates. , 2015, Cell metabolism.
[191] R. Ross,et al. Separate Effects of Intensity and Amount of Exercise on Interindividual Cardiorespiratory Fitness Response. , 2015, Mayo Clinic proceedings.
[192] S. Bicciato,et al. The calcineurin-NFAT pathway controls activity-dependent circadian gene expression in slow skeletal muscle , 2015, Molecular metabolism.
[193] G. Sporiš,et al. Effectiveness of High-Intensity Interval Training (HIT) and Continuous Endurance Training for VO2max Improvements: A Systematic Review and Meta-Analysis of Controlled Trials , 2015, Sports Medicine.
[194] S. Seiler,et al. Rethinking the role of fat oxidation: substrate utilisation during high-intensity interval training in well-trained and recreationally trained runners , 2015, BMJ Open Sport & Exercise Medicine.
[195] Sriram Subramaniam,et al. Mitochondrial reticulum for cellular energy distribution in muscle , 2015, Nature.
[196] Jessica R Gooding,et al. Carnitine Acetyltransferase Mitigates Metabolic Inertia and Muscle Fatigue during Exercise. , 2015, Cell metabolism.
[197] D. Ferreira,et al. Intercellular: local and systemic actions of skeletal muscle PGC-1s , 2015, Trends in Endocrinology & Metabolism.
[198] K. Esser,et al. The endogenous molecular clock orchestrates the temporal separation of substrate metabolism in skeletal muscle , 2015, Skeletal Muscle.
[199] G. Naughton,et al. Creatine Supplementation and Lower Limb Strength Performance: A Systematic Review and Meta-Analyses , 2015, Sports Medicine.
[200] J. Gill,et al. Moderate Exercise Increases Affinity of Large Very Low-Density Lipoproteins for Hydrolysis by Lipoprotein Lipase. , 2015, The Journal of clinical endocrinology and metabolism.
[201] J. Dubé,et al. Adipose triglyceride lipase (ATGL) deletion from adipocytes, but not skeletal myocytes, impairs acute exercise performance in mice , 2015, American journal of physiology. Endocrinology and metabolism.
[202] A. Arampatzis,et al. Human tendon adaptation in response to mechanical loading: a systematic review and meta-analysis of exercise intervention studies on healthy adults , 2015, Sports Medicine - Open.
[203] G. Lanfranchi,et al. The mitochondrial calcium uniporter controls skeletal muscle trophism in vivo. , 2015, Cell reports.
[204] L. Bruce Gladden,et al. Lactate is always the end product of glycolysis , 2015, Front. Neurosci..
[205] John M. Shelton,et al. A Micropeptide Encoded by a Putative Long Noncoding RNA Regulates Muscle Performance , 2015, Cell.
[206] J. Tegnér,et al. An integrative analysis reveals coordinated reprogramming of the epigenome and the transcriptome in human skeletal muscle after training , 2014, Epigenetics.
[207] Ina Schuppe-Koistinen,et al. Skeletal Muscle PGC-1α1 Modulates Kynurenine Metabolism and Mediates Resilience to Stress-Induced Depression , 2014, Cell.
[208] David S. Paul,et al. Compartmentalized Acyl-CoA Metabolism in Skeletal Muscle Regulates Systemic Glucose Homeostasis , 2014, Diabetes.
[209] V. Hakim,et al. Six Homeoproteins and a linc-RNA at the Fast MYH Locus Lock Fast Myofiber Terminal Phenotype , 2014, PLoS genetics.
[210] Pierre Baldi,et al. Muscle insulin sensitivity and glucose metabolism are controlled by the intrinsic muscle clock , 2013, Molecular metabolism.
[211] R. Zimmermann,et al. Contraction‐induced lipolysis is not impaired by inhibition of hormone‐sensitive lipase in skeletal muscle , 2013, The Journal of physiology.
[212] Sara Cipolat,et al. Mitochondrial Cristae Shape Determines Respiratory Chain Supercomplexes Assembly and Respiratory Efficiency , 2013, Cell.
[213] K. Baar,et al. Inhibition of Myostatin Signaling through Notch Activation following Acute Resistance Exercise , 2013, PloS one.
[214] D. Hood,et al. Acute exercise induces tumour suppressor protein p53 translocation to the mitochondria and promotes a p53–Tfam–mitochondrial DNA complex in skeletal muscle , 2013, The Journal of physiology.
[215] M. Jackson,et al. Studies of mitochondrial and nonmitochondrial sources implicate nicotinamide adenine dinucleotide phosphate oxidase(s) in the increased skeletal muscle superoxide generation that occurs during contractile activity. , 2013, Antioxidants & redox signaling.
[216] D. Schoeller,et al. Effect of contrasted levels of habitual physical activity on metabolic flexibility. , 2013, Journal of applied physiology.
[217] T. Abe,et al. Resistance training induced increase in VO2max in young and older subjects , 2013, European Review of Aging and Physical Activity.
[218] B. Spiegelman,et al. A PGC-1α Isoform Induced by Resistance Training Regulates Skeletal Muscle Hypertrophy , 2012, Cell.
[219] P. Neufer,et al. Mitochondrial creatine kinase activity and phosphate shuttling are acutely regulated by exercise in human skeletal muscle , 2012, The Journal of physiology.
[220] J. Quadrilatero,et al. Rapid Determination of Myosin Heavy Chain Expression in Rat, Mouse, and Human Skeletal Muscle Using Multicolor Immunofluorescence Analysis , 2012, PloS one.
[221] D. O'Gorman,et al. Acute exercise remodels promoter methylation in human skeletal muscle. , 2012, Cell metabolism.
[222] G. Muscat,et al. The nuclear receptor, Nor-1, markedly increases type II oxidative muscle fibers and resistance to fatigue. , 2012, Molecular endocrinology.
[223] J. Stamler,et al. Oxygen-coupled redox regulation of the skeletal muscle ryanodine receptor-Ca2+ release channel by NADPH oxidase 4 , 2011, Proceedings of the National Academy of Sciences.
[224] R. Enoka,et al. Human motor unit recordings: Origins and insight into the integrated motor system , 2011, Brain Research.
[225] R. A. Howlett,et al. Kinetic control of oxygen consumption during contractions in self‐perfused skeletal muscle , 2011, The Journal of physiology.
[226] R. Rizzuto,et al. A forty-kilodalton protein of the inner membrane is the mitochondrial calcium uniporter , 2011, Nature.
[227] V. Mootha,et al. Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter , 2011, Nature.
[228] B. Saltin,et al. Human skeletal muscle glycogen utilization in exhaustive exercise: role of subcellular localization and fibre type , 2011, The Journal of physiology.
[229] M. Rennie,et al. Enhanced amino acid sensitivity of myofibrillar protein synthesis persists for up to 24 h after resistance exercise in young men. , 2011, The Journal of nutrition.
[230] P. Aagaard,et al. Subcellular localization-dependent decrements in skeletal muscle glycogen and mitochondria content following short-term disuse in young and old men. , 2010, American journal of physiology. Endocrinology and metabolism.
[231] Nicholas Gant,et al. Carbohydrate in the mouth immediately facilitates motor output , 2010, Brain Research.
[232] K. Sahlin,et al. Increased subsarcolemmal lipids in type 2 diabetes: effect of training on localization of lipids, mitochondria, and glycogen in sedentary human skeletal muscle. , 2010, American journal of physiology. Endocrinology and metabolism.
[233] A. Garnham,et al. Exercise‐induced histone modifications in human skeletal muscle , 2009, The Journal of physiology.
[234] A. Edelman,et al. CaMKK is an upstream signal of AMP-activated protein kinase in regulation of substrate metabolism in contracting skeletal muscle. , 2009, American journal of physiology. Regulatory, integrative and comparative physiology.
[235] R. Schwenk,et al. Additive effects of insulin and muscle contraction on fatty acid transport and fatty acid transporters, FAT/CD36, FABPpm, FATP1, 4 and 6 , 2009, FEBS letters.
[236] Michael Stumvoll,et al. Antioxidants prevent health-promoting effects of physical exercise in humans , 2009, Proceedings of the National Academy of Sciences.
[237] N. Vollaard,et al. Systematic analysis of adaptations in aerobic capacity and submaximal energy metabolism provides a unique insight into determinants of human aerobic performance. , 2009, Journal of applied physiology.
[238] B. Spiegelman,et al. HIF-independent regulation of VEGF and angiogenesis by the transcriptional coactivator PGC-1α , 2008, Nature.
[239] B. Spiegelman,et al. AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1α , 2007, Proceedings of the National Academy of Sciences.
[240] J. Callés-Escandon,et al. Fatty acid binding protein facilitates sarcolemmal fatty acid transport but not mitochondrial oxidation in rat and human skeletal muscle , 2007, The Journal of physiology.
[241] M. Tarnopolsky,et al. Influence of endurance exercise training and sex on intramyocellular lipid and mitochondrial ultrastructure, substrate use, and mitochondrial enzyme activity. , 2007, American journal of physiology. Regulatory, integrative and comparative physiology.
[242] B. Spiegelman,et al. Transducer of regulated CREB-binding proteins (TORCs) induce PGC-1α transcription and mitochondrial biogenesis in muscle cells , 2006, Proceedings of the National Academy of Sciences.
[243] P. Gallagher,et al. Single muscle fiber adaptations with marathon training. , 2006, Journal of applied physiology.
[244] Jonathan R Lindner,et al. Mixed meal and light exercise each recruit muscle capillaries in healthy humans. , 2006, American journal of physiology. Endocrinology and metabolism.
[245] Laurent Malisoux,et al. Stretch-shortening cycle exercises: an effective training paradigm to enhance power output of human single muscle fibers. , 2006, Journal of applied physiology.
[246] M. Febbraio,et al. Regulation of HSL serine phosphorylation in skeletal muscle and adipose tissue. , 2006, American journal of physiology. Endocrinology and metabolism.
[247] E. Hoffman,et al. Genotype Associations With Increases In Blood Creatine Kinase And Myoglobin Following Intense Eccentric Exercise: 883 Board #105 9:00 AM ??? 10:30 AM , 2005 .
[248] T. Roche,et al. Formation of a complex of the catalytic subunit of pyruvate dehydrogenase phosphatase isoform 1 (PDP1c) and the L2 domain forms a Ca2+ binding site and captures PDP1c as a monomer. , 2004, Biochemistry.
[249] H. Galbo,et al. Contractions induce phosphorylation of the AMPK site Ser565 in hormone-sensitive lipase in muscle. , 2004, Biochemical and biophysical research communications.
[250] Peter Krustrup,et al. ATP and heat production in human skeletal muscle during dynamic exercise: higher efficiency of anaerobic than aerobic ATP resynthesis , 2003, The Journal of physiology.
[251] C. Reggiani,et al. Orthologous myosin isoforms and scaling of shortening velocity with body size in mouse, rat, rabbit and human muscles , 2003, The Journal of physiology.
[252] L. Spriet,et al. Effects of dynamic exercise intensity on the activation of hormone‐sensitive lipase in human skeletal muscle , 2003, The Journal of physiology.
[253] B. Roman,et al. Phosphocreatine kinetics at the onset of contractions in skeletal muscle of MM creatine kinase knockout mice. , 2002, American journal of physiology. Cell physiology.
[254] Jiandie D. Lin,et al. Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres , 2002, Nature.
[255] B. Saltin,et al. Intramuscular fatty acid metabolism in contracting and non‐contracting human skeletal muscle , 2002, The Journal of physiology.
[256] Simon C Watkins,et al. Skeletal muscle lipid content and insulin resistance: evidence for a paradox in endurance-trained athletes. , 2001, The Journal of clinical endocrinology and metabolism.
[257] K. Sahlin,et al. The role of phosphorylcreatine and creatine in the regulation of mitochondrial respiration in human skeletal muscle , 2001, The Journal of physiology.
[258] P. Gallagher,et al. Reduction in hybrid single muscle fiber proportions with resistance training in humans. , 2001, Journal of applied physiology.
[259] W. Saris,et al. The effects of increasing exercise intensity on muscle fuel utilisation in humans , 2001, The Journal of physiology.
[260] B. Saltin,et al. Production of interleukin‐6 in contracting human skeletal muscles can account for the exercise‐induced increase in plasma interleukin‐6 , 2000, The Journal of physiology.
[261] R. Ross,et al. Skeletal muscle mass and distribution in 468 men and women aged 18-88 yr. , 2000, Journal of applied physiology.
[262] J. Zierath,et al. Postexercise glucose uptake and glycogen synthesis in skeletal muscle from GLUT4‐deficient mice , 1999, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[263] M. McKenna,et al. Creatine supplementation increases muscle total creatine but not maximal intermittent exercise performance. , 1999, Journal of applied physiology.
[264] J Bangsbo,et al. Muscle interstitial glucose and lactate levels during dynamic exercise in humans determined by microdialysis. , 1999, Journal of applied physiology.
[265] C. Bouchard,et al. Familial aggregation of VO(2max) response to exercise training: results from the HERITAGE Family Study. , 1999, Journal of applied physiology.
[266] G Cederblad,et al. Muscle creatine loading in men. , 1996, Journal of applied physiology.
[267] C. Reggiani,et al. Myofibrillar ATPase activity in skinned human skeletal muscle fibres: fibre type and temperature dependence. , 1996, The Journal of physiology.
[268] D. Constantin-Teodosiu,et al. Carnitine metabolism in human muscle fiber types during submaximal dynamic exercise. , 1996, Journal of applied physiology.
[269] C. Willíams,et al. The metabolic responses of human type I and II muscle fibres during maximal treadmill sprinting. , 1994, The Journal of physiology.
[270] G. Brooks,et al. Balance of carbohydrate and lipid utilization during exercise: the "crossover" concept. , 1994, Journal of applied physiology.
[271] C. Willíams,et al. Human muscle metabolism during intermittent maximal exercise. , 1993, Journal of applied physiology.
[272] M. Johnston,et al. Identification of the DNA binding site for NGFI-B by genetic selection in yeast. , 1991, Science.
[273] G. Rutter,et al. The binding of Ca2+ ions to pig heart NAD+-isocitrate dehydrogenase and the 2-oxoglutarate dehydrogenase complex. , 1989, The Biochemical journal.
[274] J. J. Quintinskie,et al. Calcium uptake in mitochondria from different skeletal muscle types. , 1985, Journal of applied physiology.
[275] S. Street,et al. Lateral transmission of tension in frog myofibers: A myofibrillar network and transverse cytoskeletal connections are possible transmitters , 1983, Journal of cellular physiology.
[276] N. J. Edgell,et al. Role of calcium ions in the regulation of intramitochondrial metabolism. Effects of Na+, Mg2+ and ruthenium red on the Ca2+-stimulated oxidation of oxoglutarate and on pyruvate dehydrogenase activity in intact rat heart mitochondria. , 1980, The Biochemical journal.
[277] OUP accepted manuscript , 2021, Nucleic Acids Research.
[278] E. Horton,et al. Skeletal muscle plasma membrane glucose transport and glucose transporters after exercise. , 1990, Journal of applied physiology.