Exercise and inflammation

PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

Mootha, V. K., Lindgren, C. M., Eriksson, K.-F., Subramanian, A., Sihag, S., Lehar, J., Puigserver, P., Carlsson, E., Ridderstråle, M., Laurila, E., et al. (2003) · Nature Genetics · doi:10.1038/ng1180 · Cited by 10,197 · see citing works

Innate immune recognition

Janeway, C. A., & Medzhitov, R. (2002) · Annual Review of Immunology · doi:10.1146/annurev.immunol.20.083001.084359 · Cited by 8,394 · see citing works

The Danger Model: A Renewed Sense of Self

Matzinger, P. (2002) · Science · doi:10.1126/science.1071059 · Cited by 4,205 · see citing works

Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α

Lagouge, M., Argmann, C., Gerhart-Hines, Z., Meziane, H., Lerin, C., Daussin, F., Messadeq, N., Milne, J., Lambert, P., Elliott, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.11.013 · Cited by 4,057 · see citing works

NF-κB at the crossroads of life and death

Karin, M., & Lin, A. (2002) · Nature Immunology · doi:10.1038/ni0302-221 · Cited by 2,709 · see citing works

Local and systemic insulin resistance resulting from hepatic activation of IKK-β and NF-κB

Cai, D., Yuan, M., Frantz, D. F., Melendez, P. A., Hansen, L., Lee, J., & Shoelson, S. E. (2005) · Nature Medicine · doi:10.1038/nm1166 · Cited by 2,245 · see citing works

Sirtuin activators mimic caloric restriction and delay ageing in metazoans

Wood, J. G., Rogina, B., Lavu, S., Howitz, K., Helfand, S. L., Tatar, M., & Sinclair, D. (2004) · Nature · doi:10.1038/nature02789 · Cited by 1,868 · see citing works

Exercise and the immune system: regulation, integration, and adaptation

Pedersen, B. K., & Hoffman-Goetz, L. (2000) · Physiological Reviews · doi:10.1152/physrev.2000.80.3.1055 · Cited by 1,710 · see citing works

Novel Signal Transduction Pathway Utilized by Extracellular HSP70

Asea, A., Rehli, M., Kabingu, E., Boch, J. A., Baré, O., Auron, P. E., Stevenson, M. A., & Calderwood, S. K. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200497200 · Cited by 1,510 · see citing works

IKKβ/NF-κB Activation Causes Severe Muscle Wasting in Mice

Cai, D., Frantz, J. D., Tawa, N. E., Melendez, P. A., Oh, B.-C., Lidov, H. G. W., Hasselgren, P.-O., Frontera, W. R., Lee, J., Glass, D. J., et al. (2004) · Cell · doi:10.1016/j.cell.2004.09.027 · Cited by 1,367 · see citing works

Production of interleukin-6 in contracting human skeletal muscles can account for the exercise-induced increase in plasma interleukin-6

Steensberg, A., van Hall, G., Osada, T., Sacchetti, M., Saltin, B., & Pedersen, B. K. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00237.x · Cited by 1,095 · see citing works

Adipose Tissue

Scherer, P. E. (2006) · Diabetes · doi:10.2337/db06-0263 · Cited by 1,062 · see citing works

Immune function in sport and exercise

Gleeson, M. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00008.2007 · Cited by 1,016 · see citing works

PGC-1α protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophy-specific gene transcription

Sandri, M., Lin, J., Handschin, C., Yang, W., Arany, Z. P., Lecker, S. H., Goldberg, A. L., & Spiegelman, B. M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0607795103 · Cited by 974 · see citing works

Role of Myokines in Exercise and Metabolism

Pedersen, B. K., Åkerström, T. C. A., Nielsen, A. R., & Fischer, C. P. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00080.2007 · Cited by 841 · see citing works

Interleukin-6 Is a Novel Factor Mediating Glucose Homeostasis During Skeletal Muscle Contraction

Febbraio, M. A., Hiscock, N., Sacchetti, M., Fischer, C. P., & Pedersen, B. K. (2004) · Diabetes · doi:10.2337/diabetes.53.7.1643 · Cited by 455 · see citing works

Exercise, Infection, and Immunity

Nieman, D. C. (1994) · International Journal of Sports Medicine · doi:10.1055/s-2007-1021128 · Cited by 429 · see citing works

Skeletal myocytes are a source of interleukin‐6 mRNA expression and protein release during contraction: evidence of fiber type specificity

Hiscock, N. J., Chan, S. M. H., Bisucci, T., Darby, I. A., & Febbraio, M. A. (2004) · The FASEB Journal · doi:10.1096/fj.03-1259fje · Cited by 273 · see citing works

Protein kinase B/Akt: a nexus of growth factor and cytokine signaling in determining muscle mass

Frost, R. A., & Lang, C. H. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00089.2007 · Cited by 200 · see citing works

The physiological regulation of toll‐like receptor expression and function in humans

Lancaster, G. I., Khan, Q., Drysdale, P., Wallace, F., Jeukendrup, A. E., Drayson, M. T., & Gleeson, M. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2004.081224 · Cited by 176 · see citing works

Dangerous exercise: lessons learned from dysregulated inflammatory responses to physical activity

Cooper, D. M., Radom‐Aizik, S., Schwindt, C. D., & Zaldivar, F. P. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00225.2007 · Cited by 152 · see citing works

Suppression of plasma free fatty acids upregulates peroxisome proliferator-activated receptor (PPAR) α and δ and PPAR coactivator 1α in human skeletal muscle, but not lipid regulatory genes

Watt, M. J., Southgate, R. J., Holmes, A. G., & Febbraio, M. A. (2004) · Journal of Molecular Endocrinology · doi:10.1677/jme.1.01499 · Cited by 144 · see citing works

ERK1/2 inhibition prevents contraction‐induced increase in plasma membrane FAT/CD36 content and FA uptake in rodent muscle

Turcotte, L. P., Raney, M. A., & Todd, M. K. (2005) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.2005.01445.x · Cited by 80 · see citing works

Protein kinase inhibitors can suppress stress-induced dissociation of Hsp27

Kato, K., Ito, H., Iwamoto, I., Iida, K., & Inaguma, Y. (2001) · Cell Stress and Chaperones · doi:10.1379/1466-1268(2001)006 · Cited by 51 · see citing works

The role of exercise and PGC1α in inflammation and chronic disease

Handschin, C., & Spiegelman, B. M. (2008) · Nature · doi:10.1038/nature07206 · Cited by 1,083 · see citing works

Endometriosis: Epidemiology, Classification, Pathogenesis, Treatment and Genetics (Review of Literature)

Smolarz, B., Szyłło, K., & Romanowicz, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910554 · Cited by 560 · see citing works

An official European Respiratory Society statement on physical activity in COPD

Watz, H., Pitta, F., Rochester, C. L., Garcia-Aymerich, J., ZuWallack, R., Troosters, T., Vaes, A. W., Puhan, M. A., Jehn, M., Polkey, M. I., et al. (2014) · European Respiratory Journal · doi:10.1183/09031936.00046814 · Cited by 526 · see citing works

Insulin resistance induced by physical inactivity is associated with multiple transcriptional changes in skeletal muscle in young men

Alibegovic, A. C., Sonne, M. P., Højbjerre, L., Bork-Jensen, J., Jacobsen, S., Nilsson, E., Færch, K., Hiscock, N., Mortensen, B., Friedrichsen, M., et al. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00590.2009 · Cited by 247 · see citing works

Exercise-Induced Cognitive Plasticity, Implications for Mild Cognitive Impairment and Alzheimer’s Disease

Foster, P. P., Rosenblatt, K. P., & Kuljiš, R. O. (2011) · Frontiers in Neurology · doi:10.3389/fneur.2011.00028 · Cited by 204 · see citing works

Physical Exercise in MCI Elderly Promotes Reduction of Pro-Inflammatory Cytokines and Improvements on Cognition and BDNF Peripheral Levels

Nascimento, C. M. C., Pereira, J., de Andrade, L. P., Garuffi, M., Talib, L. L., Forlenza, O. V., Carral, J. M. C., Cominetti, M. R., & Stella, F. (2014) · Current Alzheimer Research · doi:10.2174/156720501108140910122849 · Cited by 195 · see citing works

Low Physical Activity and Risk of Cardiovascular and All-Cause Mortality in Renal Transplant Recipients

Zelle, D. M., Corpeleijn, E., Stolk, R. P., Greef, M. H. G. D., Gans, R. O. B., van der Heide, J. J. H., Navis, G. J., & Bakker, S. J. L. (2011) · Clinical Journal of the American Society of Nephrology · doi:10.2215/cjn.03340410 · Cited by 193 · see citing works

The effectiveness of self-care and lifestyle interventions in primary dysmenorrhea: a systematic review and meta-analysis

Armour, M., Smith, C. A., Steel, K. A., & MacMillan, F. (2019) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-019-2433-8 · Cited by 167 · see citing works

Exercise for dysmenorrhoea

Armour, M., Ee, C., Naidoo, D., Ayati, Z., Chalmers, J., Steel, K. A., de Manincor, M., & Delshad, E. (2019) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd004142.pub4 · Cited by 148 · see citing works

The many roles of PGC-1α in muscle — recent developments

Chan, M. C., & Arany, Z. P. (2014) · Metabolism · doi:10.1016/j.metabol.2014.01.006 · Cited by 125 · see citing works

Endometriosis and physical exercises: a systematic review

Bonocher, C. M., Montenegro, M. L., Rosa e Silva, J. C., Ferriani, R. A., & Meola, J. (2014) · Reproductive Biology and Endocrinology · doi:10.1186/1477-7827-12-4 · Cited by 115 · see citing works

Resistance exercise training influences skeletal muscle immune activation: a microarray analysis

Gordon, P. M., Liu, D., Sartor, M. A., IglayReger, H. B., Pistilli, E. E., Gutmann, L., Nader, G. A., & Hoffman, E. P. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00860.2011 · Cited by 98 · see citing works

Increased inflammatory cytokine expression in the vastus lateralis of patients with knee osteoarthritis

Levinger, I., Levinger, P., Caldow, M. K., Feller, J. A., Bartlett, J. R., Bergman, N. R., McKenna, M. J., & Cameron‐Smith, D. (2011) · Arthritis & Rheumatism · doi:10.1002/art.30287 · Cited by 99 · see citing works

Post-traumatic Stress Disorder and Cardiovascular Disease

Burg, M. M., & Soufer, R. (2016) · Current Cardiology Reports · doi:10.1007/s11886-016-0770-5 · Cited by 72 · see citing works

Inflammation, hepatic enzymes and resistance training in individuals with metabolic risk factors

Levinger, I., Goodman, C. A., Peake, J. M., GARNHAM, A. P., Hare, D. L., Jerums, G., & Selig, S. E. (2009) · Diabetic Medicine · doi:10.1111/j.1464-5491.2009.02679.x · Cited by 68 · see citing works

PGC-1α and Myokines in the Aging Muscle – A Mini-Review

Arnold, A.-S., Egger, A., & Handschin, C. (2011) · Gerontology · doi:10.1159/000281883 · Cited by 65 · see citing works

Efficacy of exercise on pelvic pain and posture associated with endometriosis: within subject design

Awad, E., Ahmed, H. A. H., Yousef, A., & Abbas, R. (2017) · Journal of Physical Therapy Science · doi:10.1589/jpts.29.2112 · Cited by 61 · see citing works

Dysmenorrhea, a Narrative Review of Therapeutic Options

Kirsch, E. P., Rahman, S., Kerolus, K., Hasan, R., Kowalska, D., Desai, A., & Bergese, S. D. (2024) · Journal of Pain Research · doi:10.2147/jpr.s459584 · Cited by 59 · see citing works

Factors influencing the post-exercise hepcidin-25 response in elite athletes

Peeling, P., McKay, A. K. A., Pyne, D. B., Guelfi, K. J., McCormick, R., Laarakkers, C. M., Swinkels, D. W., Garvican‐Lewis, L. A., ROSS, M. L. R., Sharma, A. P., et al. (2017) · European Journal of Applied Physiology · doi:10.1007/s00421-017-3611-3 · Cited by 57 · see citing works

Physiological Responses to Passive Exercise in Adults Receiving Mechanical Ventilation

Amidei, C., & Sole, M. L. (2013) · American Journal of Critical Care · doi:10.4037/ajcc2013284 · Cited by 47 · see citing works

Level and correlates of physical activity and sedentary behavior in patients with type 2 diabetes: A cross-sectional analysis of the Italian Diabetes and Exercise Study_2

Balducci, S., D’Errico, V., Haxhi, J., Sacchetti, M., Orlando, G., Cardelli, P., Di Biase, N., Bollanti, L., Conti, F., Zanuso, S., et al. (2017) · PLOS ONE · doi:10.1371/journal.pone.0173337 · Cited by 46 · see citing works

High-Intensity Interval Training Is Associated With Alterations in Blood Biomarkers Related to Brain Injury

Battista, A. P. D., Moes, K. A., Shiu, M. Y., Hutchison, M. G., Churchill, N. W., Thomas, S. G., & Rhind, S. G. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01367 · Cited by 46 · see citing works

Hepatoprotective Effect of Quercetin on Endoplasmic Reticulum Stress and Inflammation after Intense Exercise in Mice through Phosphoinositide 3‐Kinase and Nuclear Factor‐Kappa B

Tang, Y., Li, J., Gao, C., Xu, Y., Li, Y., Xiao, Y., Wang, J., Liu, L., & Yao, P. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/8696587 · Cited by 45 · see citing works

Impact of exercise on pain perception in women with endometriosis: A systematic review

Hansen, S., Sverrisdóttir, U. Á., & Rudnicki, M. (2021) · Acta Obstetricia Et Gynecologica Scandinavica · doi:10.1111/aogs.14169 · Cited by 44 · see citing works

Factors associated with increased irisin levels in the type 1 diabetes mellitus

Ateş, İ., Arikan, M. F., Erdogan, K., Kaplan, M., Yuksel, M., Topçuoğlu, C., Yilmaz, N., & Guler, S. (2017) · Endocrine Regulations · doi:10.1515/enr-2017-0001 · Cited by 38 · see citing works

Peroxisome proliferator‐activated receptor‐γ coactivator‐1α in muscle links metabolism to inflammation

Handschin, C. (2009) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2009.05275.x · Cited by 38 · see citing works

Role of Metabolic Stress and Exercise in Regulating Fibro/Adipogenic Progenitors

Collao, N., Farup, J., & Lisio, M. D. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00009 · Cited by 37 · see citing works

Impact of Physical Activity on Pain Perception in an Animal Model of Endometriosis

Hernández, S., Cruz, M. L., Torres-Reverón, A., & Appleyard, C. B. (2015) · Journal of Endometriosis and Pelvic Pain Disorders · doi:10.5301/je.5000231 · Cited by 33 · see citing works

Changes in circulating cytokines and markers of muscle damage in elite cyclists during a multi‐stage competition

Córdova, A., Martorell, M., Sureda, A., Marí, J. A. T., & Pons, A. (2014) · Clinical Physiology and Functional Imaging · doi:10.1111/cpf.12170 · Cited by 30 · see citing works

Comparisons of the Prevalence, Severity, and Risk Factors of Dysmenorrhea between Japanese Female Athletes and Non-Athletes in Universities

Momma, R., Nakata, Y., Sawai, A., Takeda, M., Natsui, H., Mukai, N., & Watanabe, K. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph19010052 · Cited by 29 · see citing works

Docosahexanoic acid diet supplementation attenuates the peripheral mononuclear cell inflammatory response to exercise following LPS activation

Capó, X., Martorell, M., Llompart, I., Sureda, A., Tur, J. A., & Pons, A. (2014) · Cytokine · doi:10.1016/j.cyto.2014.05.026 · Cited by 26 · see citing works

Effect of a 12-week walking exercise program on body composition and immune cell count in patients with breast cancer who are undergoing chemotherapy

Kim, J. J., Shin, Y. A., & Suk, M. H. (2015) · Physical Activity and Nutrition · doi:10.5717/jenb.2015.15092812 · Cited by 23 · see citing works

Toll-Like Receptors: Are They Taking a Toll on the Heart in Viral Myocarditis?

Favere, K., Bosman, M., Klingel, K., Heymans, S. R. B., Linthout, S. V., Delputte, P., SUTTER, J. D., Heidbüchel, H., & Guns, P. (2021) · Viruses · doi:10.3390/v13061003 · Cited by 21 · see citing works

Cardiometabolic Risk Factors in Children

McMurray, R. G., & Ondrak, K. S. (2013) · American Journal of Lifestyle Medicine · doi:10.1177/1559827613481429 · Cited by 19 · see citing works

A defect in the activities of Δ6 and Δ5 desaturases and pro-resolution bioactive lipids in the pathobiology of non-alcoholic fatty liver disease

Das, U. N. (2011) · World Journal of Diabetes · doi:10.4239/wjd.v2.i11.176 · Cited by 18 · see citing works

Dietary supplementation of aSaccharomyces cerevisiaefermentation product attenuates exercise-induced stress markers in young horses

Valigura, H. C., Leatherwood, J. L., Martinez, R. E., Norton, S. A., & White-Springer, S. H. (2021) · Journal of Animal Science · doi:10.1093/jas/skab199 · Cited by 19 · see citing works

White matter pathways as both a target and mediator of health behaviors

Porter, A., Leckie, R. L., & Verstynen, T. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13708 · Cited by 8 · see citing works

Physiotherapy for endometriosis-associated pelvic pain: a systematic review and meta-analysis

Can, G., das Virgens, I. P. A., Fehér, B., Orbán, E. P., Fehérvári, P., Bánhidy, F. G., Hegyi, P. J., Mayer, Á. A., & Ács, N. (2025) · Pain Medicine · doi:10.1093/pm/pnaf083 · Cited by 7 · see citing works

Körperliche Aktivität zur Primärprävention des Prostatakarzinoms

Heitkamp, H., & Jelas, I. (2012) · Der Urologe · doi:10.1007/s00120-011-2799-9 · Cited by 6 · see citing works

The effects of exercise on macrophage function

Kizaki, T., Sato, S., Sakurai, T., Ogasawara, J., Imaizumi, K., Izawa, T., Nagasawa, J., Saitoh, D., Haga, S., & Ohno, H. (2012) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.1.113 · Cited by 6 · see citing works

HMB Supplementation and Resistance Training: Current Overview on Inflammation, Oxidative Stress and Cardiovascular Risk Factors

Arazi, H., Taati, B., & Suzuki, K. (2021) · Recent Research Advances in Biology Vol. 5 · doi:10.9734/bpi/rrab/v5/7486d · Cited by 6 · see citing works

Physical Activity and Menstrual Health Symptoms and Characteristics: A Systematic Review and Meta-Analysis of Observational Studies

Buchanan-Smith, L. I. M., Pang, A. H., Yeshitila, N., Parsons, E. N., & Blodgett, J. M. (2025) · Journal of Women s Health · doi:10.1177/15409996251365804 · Cited by 5 · see citing works

Ex vivo LPS-stimulated cytokine production is associated with hydration status in community-dwelling middle-to-older-aged adults

Davis, K. M., Rosinger, A. Y., & Murdock, K. W. (2023) · European Journal of Nutrition · doi:10.1007/s00394-023-03105-z · Cited by 5 · see citing works

How Inflamed Is the Horse in Training? Insights into Exercise-Induced Acute Phase Response in Endurance Horses

Rakowska, A., Biazik, A. K., Sobuś, M., & Cywińska, A. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27052328 · Cited by 4 · see citing works

Effect of high-intensity exercise on endoplasmic reticulum stress and proinflammatory cytokine levels

Korkmaz, K., Düzova, H., Taşlıdere, A. Ç., Koç, A., Karaca, Z. M., & Durmuş, K. (2023) · Science & Sports · doi:10.1016/j.scispo.2022.04.009 · Cited by 4 · see citing works

Whole blood stimulation provides preliminary evidence of altered immune function following SRC

Battista, A. P. D., Rhind, S. G., Shiu, M. Y., & Hutchison, M. G. (2024) · BMC Immunology · doi:10.1186/s12865-023-00595-8 · Cited by 4 · see citing works

Spezielle Trainingstherapie zur Reduktion der Inflammation bei Anti-Jo-1-Syndrom

Greulich, T., Müller, S., Fechtel, J., Nell, C., Holland, A., Bach, J., Tackenberg, B., Schubert, H., Kenn, K., Vogelmeier, C. F., et al. (2011) · Pneumologie · doi:10.1055/s-0030-1256669 · Cited by 3 · see citing works

Holistic approach to care for patients with endometriosis

Molina, A., Carter, A. S., Alexander, L. M., Davé, A., & Riley, K. A. (2024) · Current Opinion in Obstetrics & Gynecology · doi:10.1097/gco.0000000000000970 · Cited by 3 · see citing works

The Effects of Diet, Exercise, and Sleep on Brain Metabolism and Function

Farooqui, A. A. (2014) · Springer eBooks · doi:10.1007/978-3-319-04111-7_1 · Cited by 3 · see citing works

New trends in food science: the use of nutraceuticals as an antiinflammatory therapeutic tool in exercise

Teixeira‐Lemos, E., de Oliveira, J. B. F., Teixeira-Lemos, L. P., Lima, M. J., & Pinheiro, J. P. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804305-9.00017-8 · Cited by 3 · see citing works

The association of activity patterns on female reproductive diseases: a prospective cohort study of UK biobank

Guo, H., Sun, Y., Gao, W., Liu, Y., Han, T., & Zhang, D. (2025) · BMC Public Health · doi:10.1186/s12889-025-21576-z · Cited by 2 · see citing works

Exercise-evoked immunometabolic niches coordinate context-dependent muscle metabolism

Kanzaki, M. (2026) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2026.06.008 · Cited by 1 · see citing works

Association of irisin hormone with some physiological and inflammatory parameters of type 1 diabetic mellitus (TIDM) patiens in Thi-Qar province, Iraq

Al-Badry, S. H., & Al-Fartosi, K. G. (2019) · Journal of Physics Conference Series · doi:10.1088/1742-6596/1279/1/012011 · Cited by 1 · see citing works

Inflammatory cytokine expression in the quadriceps of rats with posttraumatic knee stiffness: A preliminary study

Liu, K., Wang, F., Cui, Z., Liu, S., & Han, X. (2015) · Cytokine · doi:10.1016/j.cyto.2014.12.018 · Cited by 1 · see citing works

PGC-1a in muscle links metabolism to inflammation

Handschin, C. (2009) · edoc (University of Basel) · doi:10.5451/unibas-ep33741 · Cited by 1 · see citing works

Influência do exercício sobre a resposta imunológica de ratos desnutridos.

Cunha, W. D. D. S. (2009) · doi:10.11606/t.42.2009.tde-18112009-115338

Exercise-induced alterations in melanocortin receptor expression and inflammation

Henagan, T. (2010) · doi:10.31390/gradschool_dissertations.1018

Modulation of Hallmarks of Brain Aging by Environmental Enrichment

Bartolotti, N., & Lazarov, O. (2016) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-3-319-33486-8_16

Effect of 7 Days Aerobic Exercise on Insulin Sensitivity, Oxidative Stress, TLR2/TLR4 Cell Surface Expression and Cytokine Secretion in Sedentary Obese Adults

Patrick-Melin, A. J. (2011) · OhioLink ETD Center (Ohio Library and Information Network)

Physical Inactivity is not the Same as Sedentarism: The Harm of Prolonged Sitting to Human Health

Nouailhetas, V. L. (2017) · MOJ Anatomy & Physiology · doi:10.15406/mojap.2017.03.00110

The frequent exacerbator phenotype of Chronic Obstructive Pulmonary Disease in pulmonary rehabilitation – assessment of clinical outcomes and inflammation

Jenkins, A. R. (2019) · Lincoln Repository (University of Lincoln) · doi:10.24385/lincoln.24326113

The Tasks for Diagnosis and Treatment of Chronic Pain

Konno, S. (2021) · リハビリテーション医学 : 日本リハビリテーション医学会誌 · doi:10.2490/jjrmc.58.661

Defining the impact of clinically modeled hindlimb stretching, exercise, and inactivity on functional recovery after spinal cord injury.

Cesarz, G. M. (2022) · doi:10.18297/etd/4018

Endothelial Function

Katsagoni, C. N., Kokkinos, P. F., & Sidossis, L. S. (2023) · Wiley eBooks · doi:10.1002/9781119833475.ch14

On the use of Raman Blood Spectroscopy and Prediction Machines for Enhanced Care of Endometriosis Patients

Nsugbe, E. (2023) · Digital Technologies Research and Applications · doi:10.54963/dtra.v2i1.94

Review on Diagnosis, Treatment and Medication for Dysmenorrhea for Young to Old Age Women

Sothu, K., Kori, A., & Patil, S. (2025) · Journal for Research in Applied Sciences and Biotechnology · doi:10.55544/jrasb.4.1.5

Menstrual Symptom Differences Between Adolescent Volleyball Athletes and Nonathletes

Uluşahin, S. B., Ozkutlu, O., & Kafa, N. (2025) · Pediatric Exercise Science · doi:10.1123/pes.2025-0025

Additional file 2 of Whole blood stimulation provides preliminary evidence of altered immune function following SRC

Battista, A. P. D., Rhind, S. G., Shiu, M. Y., & Hutchison, M. G. (2024) · Figshare · doi:10.6084/m9.figshare.24995612

Additional file 1 of Whole blood stimulation provides preliminary evidence of altered immune function following SRC

Battista, A. P. D., Rhind, S. G., Shiu, M. Y., & Hutchison, M. G. (2024) · Figshare · doi:10.6084/m9.figshare.24995519

Additional file 3 of Whole blood stimulation provides preliminary evidence of altered immune function following SRC

Battista, A. P. D., Rhind, S. G., Shiu, M. Y., & Hutchison, M. G. (2024) · Figshare · doi:10.6084/m9.figshare.26667574

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