Circadian Rhythms, Skeletal Muscle Molecular Clocks, and Exercise

Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus

Damiola, F., Le Minh, N., Preitner, N., Kornmann, B., Fleury-Olela, F., & Schibler, U. (2000) · Genes & Development · doi:10.1101/gad.183500 · Cited by 2,394 · see citing works

Coordinated Transcription of Key Pathways in the Mouse by the Circadian Clock

Panda, S., Antoch, M. P., Miller, B. H., Su, A. I., Schook, A. C., Straume, M., Schultz, P. G., Kay, S. A., Takahashi, J. S., & Hogenesch, J. B. (2002) · Cell · doi:10.1016/s0092-8674(02)00722-5 · Cited by 2,272 · see citing works

Central and Peripheral Circadian Clocks in Mammals

Mohawk, J. A., Green, C. B., & Takahashi, J. S. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153128 · Cited by 2,265 · see citing works

The Orphan Nuclear Receptor REV-ERBα Controls Circadian Transcription within the Positive Limb of the Mammalian Circadian Oscillator

Preitner, N., Damiola, F., Luis-Lopez-Molina, Zakany, J., Duboule, D., Albrecht, U., & Schibler, U. (2002) · Cell · doi:10.1016/s0092-8674(02)00825-5 · Cited by 2,198 · see citing works

Circadian Rhythms in Drinking Behavior and Locomotor Activity of Rats Are Eliminated by Hypothalamic Lesions

Stephan, F. K., & Zucker, I. (1972) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.69.6.1583 · Cited by 2,039 · see citing works

A Serum Shock Induces Circadian Gene Expression in Mammalian Tissue Culture Cells

Balsalobre, A., Damiola, F., & Schibler, U. (1998) · Cell · doi:10.1016/s0092-8674(00)81199-x · Cited by 2,001 · see citing works

The NAD+-dependent deacetylase SIRT1 modulates CLOCK-mediated chromatin remodeling and circadian control

Nakahata, Y., Kaluzova, M., Grimaldi, B., Sahar, S., Hirayama, J., Chen, D., Guarente, L. P., & Sassone-Corsi, P. (2008) · Cell · doi:10.1016/j.cell.2008.07.002 · Cited by 1,427 · see citing works

A Functional Genomics Strategy Reveals Rora as a Component of the Mammalian Circadian Clock

Sato, T. K., Panda, S., Miraglia, L. J., Reyes, T. M., Rudic, R. D., McNamara, P., Naik, K. A., FitzGerald, G. A., Kay, S. A., & Hogenesch, J. B. (2004) · Neuron · doi:10.1016/j.neuron.2004.07.018 · Cited by 1,115 · see citing works

Mammalian circadian biology: elucidating genome-wide levels of temporal organization

Lowrey, P. L., & Takahashi, J. S. (2004) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.5.061903.175925 · Cited by 976 · see citing works

Positional Syntenic Cloning and Functional Characterization of the Mammalian Circadian Mutation tau

Lowrey, P. L., Shimomura, K., Antoch, M. P., Yamazaki, S., Zemenides, P. D., Ralph, M. R., Menaker, M., & Takahashi, J. S. (2000) · Science · doi:10.1126/science.288.5465.483 · Cited by 860 · see citing works

A Mutation of the Circadian System in Golden Hamsters

Ralph, M. R., & Menaker, M. (1988) · Science · doi:10.1126/science.3413487 · Cited by 700 · see citing works

Rhythmic histone acetylation underlies transcription in the mammalian circadian clock

Etchegaray, J.-P., Lee, C., Wade, P. A., & Reppert, S. M. (2003) · Nature · doi:10.1038/nature01314 · Cited by 679 · see citing works

Functional Identification of the Mouse Circadian Clock Gene by Transgenic BAC Rescue

Antoch, M. P., Song, E.-J., Chang, A., Vitaterna, M. H., Zhao, Y., Wilsbacher, L. D., Sangoram, A. M., King, D. P., Pinto, L. H., & Takahashi, J. S. (1997) · Cell · doi:10.1016/s0092-8674(00)80246-9 · Cited by 665 · see citing works

Spectral sensitivity of a novel photoreceptive system mediating entrainment of mammalian circadian rhythms

Takahashi, J. S., DeCoursey, P. J., Bauman, L., & Menaker, M. (1984) · Nature · doi:10.1038/308186a0 · Cited by 528 · see citing works

Circadian and CLOCK-controlled regulation of the mouse transcriptome and cell proliferation

Miller, B. H., McDearmon, E. L., Panda, S., Hayes, K. R., Zhang, J., Andrews, J. L., Antoch, M. P., Walker, J. R., Esser, K. A., Hogenesch, J. B., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611724104 · Cited by 509 · see citing works

Intrinsic circadian clock of the mammalian retina: importance for retinal processing of visual information

Storch, K.-F., Paz, C., Signorovitch, J., Raviola, E., Pawlyk, B., Li, T., & Weitz, C. J. (2007) · Cell · doi:10.1016/j.cell.2007.06.045 · Cited by 460 · see citing works

CLOCK and BMAL1 regulate <i>MyoD</i> and are necessary for maintenance of skeletal muscle phenotype and function

Andrews, J. L., Zhang, X., McCarthy, J. J., McDearmon, E. L., Hornberger, T. A., Russell, B., Campbell, K. S., Arbogast, S., Reid, M. B., Walker, J. R., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1014523107 · Cited by 389 · cited 4× · see citing works

Differential effects of PER2 phosphorylation: molecular basis for the human familial advanced sleep phase syndrome (FASPS)Preprint

Vanselow, K., Vanselow, J. T., Westermark, P. O., Reischl, S., Maier, B., Korte, T., Herrmann, A., Herzel, H., Schlösser, A., & Kramer, A. (2006) · Genes & Development · doi:10.1101/gad.397006 · Cited by 383 · see citing works

CircaDB: a database of mammalian circadian gene expression profiles

Pizarro, A., Hayer, K. E., Lahens, N. F., & Hogenesch, J. B. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks1161 · Cited by 367 · see citing works

Identification of the circadian transcriptome in adult mouse skeletal muscle

McCarthy, J. J., Andrews, J. L., McDearmon, E. L., Campbell, K. S., Barber, B. K., Miller, B. H., Walker, J. R., Hogenesch, J. B., Takahashi, J. S., & Esser, K. A. (2007) · Physiological Genomics · doi:10.1152/physiolgenomics.00066.2007 · Cited by 363 · see citing works

Competing E3 Ubiquitin Ligases Govern Circadian Periodicity by Degradation of CRY in Nucleus and Cytoplasm

Yoo, S. H., Mohawk, J. A., Siepka, S. M., Shan, Y., Huh, S. K., Hong, H., Kornblum, I., Kumar, V., Koike, N., Xu, M., et al. (2013) · Cell · doi:10.1016/j.cell.2013.01.055 · Cited by 341 · see citing works

A noncanonical E-box enhancer drives mouse Period2 circadian oscillations in vivo

Yoo, S. H., Ko, C. H., Lowrey, P. L., Buhr, E. D., Song, E.-J., Chang, S., Yoo, O. J., Yamazaki, S., Lee, C., & Takahashi, J. S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409763102 · Cited by 299 · see citing works

Scheduled exercise phase shifts the circadian clock in skeletal muscle

WOLFF, G., & ESSER, K. A. (2012) · Medicine &amp; Science in Sports &amp; Exercise · doi:10.1249/mss.0b013e318255cf4c · Cited by 291 · see citing works

Time- and exercise-dependent gene regulation in human skeletal muscle

Zambon, A. C., McDearmon, E. L., Salomonis, N., Vranizan, K. M., Johansen, K. L., Adey, D., Takahashi, J. S., Schambelan, M., & Conklin, B. R. (2003) · Genome Biology · doi:10.1186/gb-2003-4-10-r61 · Cited by 254 · see citing works

Rapid down-regulation of mammalian Period genes during behavioral resetting of the circadian clock

Maywood, E. S., Mrosovsky, N., Field, M. D., & Hastings, M. H. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.26.15211 · Cited by 248 · see citing works

Regularly scheduled voluntary exercise synchronizes the mouse circadian clock

Edgar, D. M., & Dement, W. C. (1991) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1991.261.4.r928 · Cited by 219 · see citing works

Voluntary scheduled exercise alters diurnal rhythms of behaviour, physiology and gene expression in wild‐type and vasoactive intestinal peptide‐deficient mice

Schroeder, A., Truong, D. A., Loh, D. H., Jordan, M. C., Roos, K. P., & Colwell, C. S. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.233676 · Cited by 135 · see citing works

Circadian Biology: A 2.5 Billion Year Old Clock

Loudon, A. S. I. (2012) · Current Biology · doi:10.1016/j.cub.2012.06.023 · Cited by 107 · see citing works

Circadian clocks

Idda, M. L., Bertolucci, C., Vallone, D., Gothilf, Y., Sánchez‐Vázquez, F. J., & Foulkes, N. S. (2012) · Progress in brain research · doi:10.1016/b978-0-444-59427-3.00003-4 · Cited by 89 · see citing works

Stoichiometric Relationship among Clock Proteins Determines Robustness of Circadian Rhythms

Lee, Y., Chen, R., Lee, C., & Lee, C. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.207217 · Cited by 82 · see citing works

Endurance training ameliorates the metabolic and performance characteristics of circadian<i>Clock</i>mutant mice

Pastore, S., & Hood, D. A. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01505.2012 · Cited by 66 · see citing works

A non-canonical E-box within the MyoD core enhancer is necessary for circadian expression in skeletal muscle

Zhang, X., Patel, S. P., McCarthy, J. J., Rabchevsky, A. G., Goldhamer, D. J., & Esser, K. A. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr1297 · Cited by 62 · see citing works

Age-Associated Disruption of Molecular Clock Expression in Skeletal Muscle of the Spontaneously Hypertensive Rat

Miyazaki, M., Schroder, E. A., Edelmann, S. E., Hughes, M. E., Kornacker, K., Balke, C. W., & Esser, K. A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027168 · Cited by 58 · see citing works

Restoration of circadian behavior by anterior hypothalamic heterografts

Sollars, P. J., Kimble, D. P., & Pickard, G. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-02109.1995 · Cited by 45 · see citing works

The circadian protein Clock localizes to the sarcomeric Z-disk and is a sensor of myofilament cross-bridge activity in cardiac myocytes

Qi, L., & Boateng, S. Y. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.10.168 · Cited by 24 · see citing works

Human circadian phase–response curves for exercise

Youngstedt, S. D., Elliott, J. A., & Kripke, D. F. (2019) · The Journal of Physiology · doi:10.1113/jp276943 · Cited by 263 · see citing works

Effects of metformin on weight loss: potential mechanisms

Malin, S. K., & Kashyap, S. R. (2014) · Current Opinion in Endocrinology, Diabetes &amp; Obesity · doi:10.1097/med.0000000000000095 · Cited by 223 · see citing works

The impact of sleep on age-related sarcopenia: Possible connections and clinical implications

Piovezan, R. D., Abucham, J., dos Santos, R. V. T., de Mello, M. T., Tufik, S., & Poyares, D. R. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2015.07.003 · Cited by 215 · see citing works

Circadian metabolism in the light of evolution

Gerhart-Hines, Z., & Lazar, M. A. (2015) · Endocrine Reviews · doi:10.1210/er.2015-1007 · Cited by 178 · see citing works

The endogenous molecular clock orchestrates the temporal separation of substrate metabolism in skeletal muscle

Hodge, B. A., Wen, Y., Riley, L. A., Zhang, X., England, J. H., Harfmann, B. D., Schroder, E. A., & Esser, K. A. (2015) · Skeletal Muscle · doi:10.1186/s13395-015-0039-5 · Cited by 175 · see citing works

Bmal1 function in skeletal muscle regulates sleep

Ehlen, J. C., Brager, A. J., Baggs, J. E., Pinckney, L., Gray, C. L., DeBruyne, J. P., Esser, K. A., Takahashi, J. S., & Paul, K. N. (2017) · eLife · doi:10.7554/elife.26557 · Cited by 144 · see citing works

Understanding the variation in exercise responses to guide personalized physical activity prescriptions

Noone, J., Mucinski, J. M., DeLany, J. P., Sparks, L. M., & Goodpaster, B. H. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2023.12.025 · Cited by 128 · see citing works

Sleep, circadian biology and skeletal muscle interactions: Implications for metabolic health

Morrison, M., Halson, S. L., Weakley, J., & Hawley, J. A. (2022) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2022.101700 · Cited by 118 · see citing works

An epigenetic clock for human skeletal muscle

Voisin, S. A. C., Harvey, N. R., Haupt, L. M., Griffiths, L. R., Ashton, K. J., Coffey, V. G., Doering, T. M., Thompson, J. M., Benedict, C., Cedernaes, J., et al. (2020) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12556 · Cited by 111 · see citing works

The Effect of Exercise Timing on Glycemic Control: A Randomized Clinical Trial

Teo, S. Y. M., Kanaley, J. A., Guelfi, K. J., Marston, K. J., & Fairchild, T. J. (2019) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002139 · Cited by 94 · see citing works

Single-nucleus RNA-seq of differentiating human myoblasts reveals the extent of fate heterogeneity

Zeng, W., Jiang, S., Kong, X., El-Ali, N. C., Ball, A. R., I-Hsing, C., Hashimoto, N., Yokomori, K., & Mortazavi, A. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw739 · Cited by 91 · see citing works

The effects of time of day-specific resistance training on adaptations in skeletal muscle hypertrophy and muscle strength: a systematic review and meta-analysis.

Grgic, J., Lazinica, B., Garofolini, A., Schoenfeld, B. J., Saner, N. J., & Mikulic, P. (2019) · Chronobiology International · doi:10.1080/07420528.2019.1567524 · Cited by 83 · see citing works

Circadian and photic modulation of daily rhythms in diurnal mammals

Yan, L., Smale, L., & Núñez, A. A. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14172 · Cited by 75 · see citing works

Clock-Enhancing Small Molecules and Potential Applications in Chronic Diseases and Aging

Gloston, G. F., Yoo, S. H., & Chen, Z. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00100 · Cited by 73 · see citing works

Time-restricted feeding influences immune responses without compromising muscle performance in older men

Gasmi, M., Sellami, M., Denham, J., Padulo, J., Kuvačić, G., Selmi, W., & Khalıfa, R. (2018) · Nutrition · doi:10.1016/j.nut.2017.12.014 · Cited by 68 · see citing works

Glucose Homeostasis: Regulation by Peripheral Circadian Clocks in Rodents and Humans

Gachon, F., Loizides‐Mangold, U., Petrenko, V., & Dibner, C. (2017) · Endocrinology · doi:10.1210/en.2017-00218 · Cited by 63 · see citing works

The effects of sleep disruption on metabolism, hunger, and satiety, and the influence of psychosocial stress and exercise: A narrative review

Rogers, E. M., Banks, N. F., & Jenkins, N. D. M. (2024) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.3667 · Cited by 62 · see citing works

Three months of bed rest induce a residual transcriptomic signature resilient to resistance exercise countermeasures

Fernandez‐Gonzalo, R., Tesch, P. A., Lundberg, T. R., Alkner, B. A., Rullman, E., & Gustafsson, T. P. (2020) · The FASEB Journal · doi:10.1096/fj.201902976r · Cited by 59 · see citing works

Ticking for Metabolic Health: The Skeletal‐Muscle Clocks

Gutierrez‐Monreal, M. A., Harmsen, J., Schrauwen, P., & Esser, K. A. (2020) · Obesity · doi:10.1002/oby.22826 · Cited by 62 · see citing works

Inferring dynamic topology for decoding spatiotemporal structures in complex heterogeneous networks

Wang, S., Herzog, E. D., Kiss, I. Z., Schwartz, W. J., Bloch, G., Sebek, M., Granados‐Fuentes, D., Wang, L. Y., & Li, J.-S. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1721286115 · Cited by 57 · see citing works

Interplay between diet, exercise and the molecular circadian clock in orchestrating metabolic adaptations of adipose tissue

Dollet, L., & Zierath, J. R. (2019) · The Journal of Physiology · doi:10.1113/jp276488 · Cited by 55 · see citing works

The myonuclear DNA methylome in response to an acute hypertrophic stimulus

von Walden, F., Rea, M., Mobley, C. B., Fondufe‐Mittendorf, Y. N., McCarthy, J. J., Peterson, C. A., & Murach, K. A. (2020) · Epigenetics · doi:10.1080/15592294.2020.1755581 · Cited by 53 · see citing works

Atypical expression of circadian clock genes in denervated mouse skeletal muscle

Nakao, R., Yamamoto, S., Horikawa, K., Yasumoto, Y., Nikawa, T., Mukai, C. N., & Oishi, K. (2015) · Chronobiology International · doi:10.3109/07420528.2014.1003350 · Cited by 44 · see citing works

Ageing in relation to skeletal muscle dysfunction: redox homoeostasis to regulation of gene expression

Goljanek‐Whysall, K., Iwanejko, L., Vasilaki, A., Pekovic‐Vaughan, V., & McDonagh, B. (2016) · Mammalian Genome · doi:10.1007/s00335-016-9643-x · Cited by 31 · see citing works

Cryptochromes Suppress HIF1α in Muscles

Vaughan, M. E., Wallace, M., Handzlik, M. K., Chan, A. B., Metallo, C. M., & Lamia, K. A. (2020) · iScience · doi:10.1016/j.isci.2020.101338 · Cited by 33 · see citing works

Impact of time-of-day and chronotype on neuromuscular performance in semi-professional female volleyball players

Martín-López, J., Sedliak, M., Valadés, D., Muñoz, A., Buffet‐García, J., García-Oviedo, R., Rodríguez-Aragón, M., Pérez‐López, A., & López‐Samanes, Á. (2022) · Chronobiology International · doi:10.1080/07420528.2022.2057322 · Cited by 31 · see citing works

Irisin/BDNF signaling in the muscle-brain axis and circadian system: A review

Inyushkin, A. N., Полетаев, В., Михайловна, И. Е., Сергеевич, К. И., & Inyushkin, A. A. (2023) · Journal of Biomedical Research · doi:10.7555/jbr.37.20230133 · Cited by 30 · see citing works

Effects of diurnal exercise timing on appetite, energy intake and body composition: A parallel randomized trial

Teo, S. Y. M., Kanaley, J. A., Guelfi, K. J., Dimmock, J. A., Jackson, B., & Fairchild, T. J. (2021) · Appetite · doi:10.1016/j.appet.2021.105600 · Cited by 30 · see citing works

Positive association between physical activity and PER3 expression in older adults

Takahashi, M., Haraguchi, A., Tahara, Y., Aoki, N., Fukazawa, M., Tanisawa, K., Ito, T., Nakaoka, T., Higuchi, M., & Shibata, S. (2017) · Scientific Reports · doi:10.1038/srep39771 · Cited by 26 · see citing works

Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy

Scotton, C., Bovolenta, M., Schwartz, E., Falzarano, M. S., Martoni, E., Passarelli, C., Armaroli, A., Osman, H., Rodolico, C., Messina, S., et al. (2016) · Journal of Cell Science · doi:10.1242/jcs.175927 · Cited by 25 · see citing works

Cachexia Disrupts Diurnal Regulation of Activity, Feeding, and Muscle Mechanistic Target of Rapamycin Complex 1 in Mice

Counts, B. R., Hardee, J. P., Fix, D. K., VanderVeen, B. N., Montalvo, R. N., & Carson, J. A. (2019) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002166 · Cited by 23 · see citing works

Transcriptomic and epigenomic landscapes of muscle growth during the postnatal period of broilers

Gu, S., Huang, Q., Jie, Y., Sun, C., Wen, C., & Yang, N. (2024) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-024-01049-w · Cited by 22 · see citing works

Circadian secretion rhythm of GLP-1 and its influencing factors

Liu, C., Liu, Y., Xin, Y., & Wang, Y. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.991397 · Cited by 22 · see citing works

A high-resolution view of the heterogeneous aging endothelium

Dobner, S., Tóth, F., & de Rooij, L. P. M. H. (2024) · Angiogenesis · doi:10.1007/s10456-023-09904-6 · Cited by 21 · see citing works

Time to Reset: The Interplay Between Circadian Rhythms and Redox Homeostasis in Skeletal Muscle Ageing and Systemic Health

Sutton, E. R., & Pekovic‐Vaughan, V. (2025) · Antioxidants · doi:10.3390/antiox14091132 · Cited by 17 · see citing works

iMS‐Bmal1−/− mice show evident signs of sarcopenia that are counteracted by exercise and melatonin therapies

Fernández‐Martínez, J., Ramírez‐Casas, Y., Aranda‐Martínez, P., López‐Rodríguez, A., Sayed, R. K. A., Escames, G., & Acuña-Castroviejo, D. (2023) · Journal of Pineal Research · doi:10.1111/jpi.12912 · Cited by 17 · see citing works

Anabolic Heterogeneity Following Resistance Training: A Role for Circadian Rhythm?

CAMERA, D. M. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00569 · Cited by 17 · see citing works

Sleep Hygiene Practices: Where to Now?

Chow, C. M. (2022) · Hygiene · doi:10.3390/hygiene2030013 · Cited by 16 · see citing works

Effect of Aerobic Exercise and Time‐Restricted Feeding on Metabolic Markers and Circadian Rhythm in Mice Fed with the High‐Fat Diet

Raza, G. S., Kaya, Y., Stenbäck, V., Sharma, R., Sodum, N., Mutt, S. J., Gagnon, D. D., Tulppo, M. P., Järvelin, M., Herzig, K., et al. (2024) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202300465 · Cited by 15 · see citing works

Single-cell RNA transcriptome uncovers distinct developmental trajectories in the embryonic skeletal muscle of Daheng broiler and Tibetan chicken

Li, J., Yang, D., Chen, C., Wang, J., Wang, Z., Yang, C., Yu, C., & Li, Z. (2025) · BMC Genomics · doi:10.1186/s12864-025-11363-w · Cited by 15 · see citing works

Mechanosensors control skeletal muscle mass, molecular clocks, and metabolism

Vanmunster, M., Rojo‐García, A. V., Pacolet, A., Dalle, S., Koppo, K., Jonkers, I., Lories, R. J. U., & Suhr, F. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04346-7 · Cited by 14 · see citing works

GCKR rs780094 Polymorphism as A Genetic Variant Involved in Physical Exercise

Espinosa‐Salinas, I., de la Iglesia, R., Colmenarejo, G., Molina, S., Reglero, G., Martínez, J. A., Loria‐Kohen, V., & de Molina, A. R. (2019) · Genes · doi:10.3390/genes10080570 · Cited by 14 · see citing works

Changes in Northern Elephant Seal Skeletal Muscle Following Thirty Days of Fasting and Reduced Activity

Wright, T. J., Davis, R. W., Holser, R. R., Hückstädt, L. A., Danesi, C. P., Porter, C. C., Widen, S. G., Williams, T. M., da Costa, D. P., & Sheffield‐Moore, M. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.564555 · Cited by 14 · see citing works

Growing up strong: The importance of physical, mental, and emotional strength during childhood and adolescence with focus on dietary factors

Leidy, H. J., & Gwin, J. A. (2020) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2020-0058 · Cited by 12 · see citing works

Resetting Time: The Role of Exercise Timing in Circadian Reprogramming for Metabolic Health

Hesketh, S. J. (2025) · Obesities · doi:10.3390/obesities5030059 · Cited by 13 · see citing works

Ageing of human myofibres in the Vastus Lateralis muscle: A narrative review

Granic, A., Simoes, D. C. M., Bowen, T. S., Almaghtuf, N., Richardson, G. D., & Sayer, A. A. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103022 · Cited by 8 · see citing works

Diurnal gait fluctuations in single- and dual- task conditions

Bessot, N., Polyte, R., Quesney, M., Bulla, J., & Gauthier, A. (2020) · Chronobiology International · doi:10.1080/07420528.2020.1773493 · Cited by 8 · see citing works

Circadian rhythm mediates the relationship between physical activity and quality of life in younger and older cancer survivors

Su, C. C., Su, P., Wang, S., & Lin, C. (2015) · Chronobiology International · doi:10.3109/07420528.2015.1102150 · Cited by 7 · see citing works

Commentaries on Viewpoint: The rigorous study of exercise adaptations: Why mRNA might not be enough

Hornberger, T. A., Carter, H. N., Hood, D. A., Figueiredo, V. C., Dupont‐Versteegden, E. E., Peterson, C. A., McCarthy, J. J., CAMERA, D. M., Hawley, J. A., Chaillou, T., et al. (2016) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00509.2016 · Cited by 7 · see citing works

Acute Effects of Global Postural Re-Education on Non-Specific Low Back Pain. Does Time-of-Day Play a Role?

Merinero, D., Rodríguez-Aragón, M., Álvarez-González, J., López‐Samanes, Á., & Pascual, J. L. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18020713 · Cited by 6 · see citing works

Chronobioethics: Symphony of biological clocks observed by 7-day/24-h ambulatory blood pressure monitoring and cardiovascular health

Otsuka, K., Beaty, L. A., Sato, M., Shitakura, K., Kikuchi, T., Okajima, K., Terada, S., & Cornélissen, G. (2024) · Biomedical Journal · doi:10.1016/j.bj.2024.100753 · Cited by 5 · see citing works

Synergy between time-restricted feeding and time-restricted running is necessary to shift the muscle clock in male wistar rats

Shiba, A., de Goede, P., Tandari, R., Foppen, E., Korpel, N. L., Coopmans, T. V., Hellings, T. P., Jansen, M. W., Ruitenberg, A., Ritsema, W. I. G. R., et al. (2024) · Neurobiology of Sleep and Circadian Rhythms · doi:10.1016/j.nbscr.2024.100106 · Cited by 5 · see citing works

An epigenetic clock for human skeletal musclePreprint

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Rutin as a Circadian Modulator Preserves Skeletal Muscle Mitochondrial Function and Reduces Oxidative Stress to Protect Against D-Galactose-Induced Aging In Vitro and In Vivo

Choi, Y., Lee, S., & Kim, E. (2025) · Nutrients · doi:10.3390/nu17223571 · Cited by 4 · see citing works

Blood Clock Correlation Distance (BloodCCD) as a novel marker to detect circadian rhythm disruption in cancer survivors with insomnia

Altman, B. J., Lin, P., Mattick, L. J., Outland, E. H., Bautista, J., Li, C., Gada, U., Morris, K. M., Knudsen-Clark, A. M., Mwangi, D., et al. (2025) · BJC Reports · doi:10.1038/s44276-025-00176-9 · Cited by 4 · see citing works

Time of day of exercise does not affect the beneficial effect of exercise on bone structure in older female rats

Cao, J., & Gregoire, B. R. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1142057 · Cited by 4 · see citing works

The impact of aerobic exercise timing on BMAL1 protein expression and antioxidant responses in skeletal muscle of mice

Xu, L., Jia, J., Yu, J., Miao, S., & Zhang, Y. (2024) · Free Radical Research · doi:10.1080/10715762.2024.2348789 · Cited by 4 · see citing works

Aging of the Suprachiasmatic Nucleus, CIRCLONSA Syndrome , Implications for Regenerative Medicine and Restoration of the Master Body Clock

Björk, V. (2021) · Rejuvenation Research · doi:10.1089/rej.2020.2388 · Cited by 3 · see citing works

Skeletal muscle clock and metabolism

Li, Y., & Chen, W. (2020) · Biological Rhythm Research · doi:10.1080/09291016.2020.1816037 · Cited by 3 · see citing works

Temporal tuning of daily rhythms helps advanced cancer patients and cancer survivors feel better, live better, and live longer

Hrushesky, W. J. M., Grutsch, J. F., Huff, D. F. Q., Kazlausky, T., & Tavolacci, L. (2016) · ChronoPhysiology and Therapy · doi:10.2147/cpt.s74070 · Cited by 3 · see citing works

Muscular strength and power and endurance performance at loads exceeding 25% of one-repetition maximum are unaffected by time-of-day in resistance-trained male participants

del Val‐Manzano, M., Montalvo‐Alonso, J. J., Valadés, D., Ferragut, C., Martín-López, J., López‐Samanes, Á., & Pérez-López, A. (2025) · Chronobiology International · doi:10.1080/07420528.2025.2524520 · Cited by 2 · see citing works

Chrono-Exercise Medicine: Why Biological Timing Matters for Human Health

Hesketh, S. J. (2026) · Biomedicines · doi:10.3390/biomedicines14071601 · Cited by 2 · see citing works

Sleep and exercise

Kline, C. E. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-815373-4.00020-4 · Cited by 2 · see citing works

Physical activity in older adults

Valenti, G. (2016) · doi:10.26481/dis.20160610gv · Cited by 3 · see citing works

Melatonin supplementation to sows in mid to late gestation affects offspring circadian, myogenic, and growth factor transcript abundance in pre and postnatal skeletal muscle

Dobbins, T. W., Swanson, R. M., Dennis, A. A., Rivera, J., Dinh, T. T., Lemley, C. O., & Burnett, D. D. (2024) · Journal of Animal Science · doi:10.1093/jas/skae377 · Cited by 1 · see citing works

Identifying Chronotype for the Preservation of Muscle Mass, Quality and Strength

Barrientos-Salinas, R., Dahdah, N., Alvarez-Luis, J., Vilarrasa, N., & García-Rovés, P. M. (2026) · Nutrients · doi:10.3390/nu18020221 · Cited by 1 · see citing works

The Role of Exercise in Cardiovascular Metabolism and Its Importance for Adolescent Metabolic Health

Susanto, H., Firdaus, S. R. A., Sholeh, M., Sugiharto, S., & Pranoto, A. (2026) · Advances in experimental medicine and biology · doi:10.1007/978-981-95-7000-3_18 · Cited by 1 · see citing works

Circadian rhythms, NRF2 signalling and redox homeostasis: A holy grail for a healthy life course?

Sutton, E., & Pekovic‐Vaughan, V. (2026) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2026.05.318 · Cited by 1 · see citing works

Self selected music during warm up improves anaerobic performance in female handball players across time of day

Bougrine, H., Gandouzi, I., Dergaa, I., Maitre, J., Alaizari, A. A., Aljuhani, O. E., Paillard, T., & Souissi, N. (2025) · Scientific Reports · doi:10.1038/s41598-025-21414-7

Developing Circadian Therapeutics Against Age-Related Metabolic Decline

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Time of Exercise, As a New Identified Zeitgeber for Modulating the Molecular Clocks in Skeletal Muscle

Arazi, H. (2016) · Journal of Molecular and Genetic Medicine · doi:10.4172/1747-0862.1000224

Circadian Rhythm and Health : Influence of Food Intake Timing and Regular Exercise

Lee, K., & Kim, S. K. (2023) · Korean Journal of Sport Science · doi:10.24985/kjss.2023.34.2.187

A 24-hour perspective on insulin resistance

Harmsen, J. (2023) · doi:10.26481/dis.20231213jh

The Circadian Clock as a Drug Target for Anti-Ageing Strategies

Rizvi, S. I., & Majumdar, G. (2024) · Springer eBooks · doi:10.1007/978-981-97-6695-6_8

Sleep and exercise

Kline, C. E. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-13954-3.00031-0

Circadian rhythm changes in space

Otsuka, K., Cornélissen, G., Beaty, L. A., & Mukai, C. N. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-32904-3.00021-2

Additional file 2 of Transcriptomic and epigenomic landscapes of muscle growth during the postnatal period of broilers

Gu, S., Huang, Q., Jie, Y., Sun, C., Wen, C., & Yang, N. (2024) · Figshare · doi:10.6084/m9.figshare.26734011

Additional file 1 of Transcriptomic and epigenomic landscapes of muscle growth during the postnatal period of broilers

Gu, S., Huang, Q., Jie, Y., Sun, C., Wen, C., & Yang, N. (2024) · Figshare · doi:10.6084/m9.figshare.26734008

Caractérisation moléculaire et pharmacologique de l'horloge circadienne située dans l'habénula

Salaberry, N. L. (2018) · doi:10.70675/8d54db3cz09e1z4999zbcb5za35dc04505ca

FBXL21 regulates diurnal proteostasis and stress response by targeting DNAJB6 and client proteinsPreprint

Lim, J. Y., Wi, J., Wirianto, M., Han, C., Kim, S. Y., Nguyen, J., Jung, S., Eckel‐Mahan, K. L., Jung, S. Y., Esser, K. A., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.20.726545

Stephanoside B modulates metabolic gene expression and lengthens the circadian bmal1 oscillation period in differentiated myotubes revealed by real-time bioluminescence

Saiki, R., Tomita, T., Yamamoto, S., & Luebaeteh, F. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-12382-w

Type 1 diabetes differentially disrupts right and left ventricular daily rhythms

Bettadapura, S. S., Torres, S. J., Schmitt, M. P., Roberts, B. L., & Bruns, D. R. (2026) · Function · doi:10.1152/function.041.2026

FBXL21 regulates diurnal proteostasis in skeletal muscle by targeting DNAJB6 and client proteins

Lim, J. Y., Wi, J., Wirianto, M., Han, C., Kim, S. Y., Nguyen, J., Jung, S., Eckel‐Mahan, K. L., Jung, S. Y., Esser, K. A., et al. (2026) · EMBO Reports · doi:10.1038/s44319-026-00922-1

Rev‐erb‐α in Skeletal Muscle Adaptation: Integrating Circadian Control Mechanisms and Exercise Dynamic Responses

Neto, I. V. D. S., da Rocha, A. L., Pinto, A. P., Ramos, E. L. P., Ropelle, E. R., Pauli, J. R., de Freitas, E. C., & da Silva, A. S. R. (2026) · Journal of Cellular Physiology · doi:10.1002/jcp.70239

Timing the effort: Chronobiological drivers of skeletal muscle adaptation and metabolic health

Aykora, E., Erbil, G., & Aykora, D. (2026) · Chronobiology International · doi:10.1080/07420528.2026.2750361

Exercise timing and circadian rhythms

Wolff, C. A., & Esser, K. A. (2019) · Current Opinion in Physiology · doi:10.1016/j.cophys.2019.04.020 · Cited by 69 · see citing works

Foreword

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Time to Train: The Involvement of the Molecular Clock in Exercise Adaptation of Skeletal Muscle

Mansingh, S., & Handschin, C. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.902031 · Cited by 28 · see citing works

Time of Exercise, As a New Identified Zeitgeber for Modulating the Molecular Clocks in Skeletal Muscle

Arazi, H. (2016) · Journal of Molecular and Genetic Medicine · doi:10.4172/1747-0862.1000224

Circadian Rhythms, the Molecular Clock, and Skeletal Muscle

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