Physical Exercise: A Novel Tool to Protect Mitochondrial Health

Repertoires of Autophagy in the Pathogenesis of Ocular Diseases

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The Hallmarks of Aging

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Quantity and Quality of Exercise for Developing and Maintaining Cardiorespiratory, Musculoskeletal, and Neuromotor Fitness in Apparently Healthy Adults

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AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1

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Progression Models in Resistance Training for Healthy Adults

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Guidelines for the use and interpretation of assays for monitoring autophagy

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Mitochondrial Fission, Fusion, and Stress

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Progression Models in Resistance Training for Healthy Adults

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PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1

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Mitochondria: It is all about energy

Casanova, A., Wevers, A., Ledesma, S. N., & Pruimboom, L. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1114231 · Cited by 350

Signatures of Mitochondrial Dysfunction and Impaired Fatty Acid Metabolism in Plasma of Patients with Post-Acute Sequelae of COVID-19 (PASC)

Guntur, V. P., Nemkov, T. G., de Boer, E., Mohning, M. P., Baraghoshi, D., Cendali, F. I., San-Millán, I., Petrache, I., & D’Alessandro, A. (2022) · Metabolites · doi:10.3390/metabo12111026 · Cited by 159

Role of Impaired Mitochondrial Dynamics Processes in the Pathogenesis of Alzheimer’s Disease

Blagov, A. V., Grechko, A. V., Nikiforov, N. G., Borisov, E. E., Sadykhov, N. K., & Orekhov, A. N. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23136954 · Cited by 70

Positive Aspects of Oxidative Stress at Different Levels of the Human Body: A Review

Jîtcă, G., Ősz, B. E., Tero-Vescan, A., Miklos, A., Rusz, C.-M., Bătrînu, M.-G., & Vari, C.-E. (2022) · Antioxidants · doi:10.3390/antiox11030572 · Cited by 67

Age-associated inflammation and implications for skeletal muscle responses to exercise

Kunz, H. E., & Lanza, I. R. (2023) · Experimental Gerontology · doi:10.1016/j.exger.2023.112177 · Cited by 56

Mechanisms, Mediators, and Moderators of the Effects of Exercise on Chemotherapy-Induced Peripheral Neuropathy

Chung, K., Park, S. B., Streckmann, F., Wiskemann, J., Mohile, N. A., Kleckner, A. S., Colloca, L., Dorsey, S. G., & Kleckner, I. R. (2022) · Cancers · doi:10.3390/cancers14051224 · Cited by 95

A cross-talk between sestrins, chronic inflammation and cellular senescence governs the development of age-associated sarcopenia and obesity

Livshits, G., & Kalinkovich, A. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101852 · Cited by 56

Exercise improves vascular health: Role of mitochondria

Zhang, X., & Gao, F. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.11.002 · Cited by 52

Impact of Exercise and Aging on Mitochondrial Homeostasis in Skeletal Muscle: Roles of ROS and Epigenetics

Li, J., Wang, Z., Li, C., Song, Y., Wang, Y., Hai, B., & Zhang, Y. (2022) · Cells · doi:10.3390/cells11132086 · Cited by 56

An Overview of Physical Exercise and Antioxidant Supplementation Influences on Skeletal Muscle Oxidative Stress

Taherkhani, S., Valaei, K., Arazi, H., & Suzuki, K. (2021) · Antioxidants · doi:10.3390/antiox10101528 · Cited by 54

Exercise mitigates age-related metabolic diseases by improving mitochondrial dysfunction

Jia, D., Tian, Z., & Wang, R. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102087 · Cited by 50

From mitochondrial dysfunction to neuroinflammation in Parkinson’s disease: Pathogenesis and mitochondrial therapeutic approaches

Ebadpour, N., Mahmoudi, M., Kheder, R. K., Abavisani, M., Baridjavadi, Z., Abdollahi, N., & Esmaeili, S. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113015 · Cited by 48

Mitochondrial-derived peptides in cardiovascular disease: Novel insights and therapeutic opportunities

Li, Y., Li, Z., Ren, Y., Lei, Y., Yang, S., Shi, Y., Peng, H., Yang, W., Guo, T., Yu, Y., et al. (2023) · Journal of Advanced Research · doi:10.1016/j.jare.2023.11.018 · Cited by 43

Association of Accelerometer-Measured Physical Activity Level With Risks of Hospitalization for 25 Common Health Conditions in UK Adults

Watts, E. L., Saint‐Maurice, P. F., Doherty, A., Fensom, G. K., Freeman, J. R., Gorzelitz, J., Jin, D., McClain, K. M., Papier, K., Patel, S., et al. (2023) · JAMA Network Open · doi:10.1001/jamanetworkopen.2022.56186 · Cited by 42

The Effects of Exercise Training on Mitochondrial Function in Cardiovascular Diseases: A Systematic Review and Meta-Analysis

Lim, A. Y., Chen, Y.-C., Hsu, C., Fu, T., & Wang, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012559 · Cited by 38

Brown adipose tissue and aging: A potential role for exercise

Nirengi, S., & Stanford, K. I. (2023) · Experimental Gerontology · doi:10.1016/j.exger.2023.112218 · Cited by 38

Blood-based mitochondrial respiratory chain function in major depression

Fernström, J., Mellon, S. H., McGill, M. A., Picard, M. A., Reus, V. I., Hough, C. M., Lin, J., Epel, E. S., Wolkowitz, O. M., & Lindqvist, D. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01723-x · Cited by 39

Exercise-Induced Neuroplasticity: Adaptive Mechanisms and Preventive Potential in Neurodegenerative Disorders

Mansoor, M. A., Ibrahim, A., Hamide, A., Tran, T., Candreva, E., & Baltaji, J. (2025) · Physiologia · doi:10.3390/physiologia5020013 · Cited by 38

Association between regular physical activity and the protective effect of vaccination against SARS-CoV-2 in a South African case–control study

Collie, S., Saggers, R. T., Bandini, R. M., Steenkamp, L., Champion, J., Gray, G., Bekker, L., Goga, A. E., Garrett, N., & Patricios, J. (2022) · British Journal of Sports Medicine · doi:10.1136/bjsports-2022-105734 · Cited by 29

Exercise intolerance associated with impaired oxygen extraction in patients with long COVID

Norweg, A. M., Yao, L., Barbuto, S., Nordvig, A. S., Tarpey, T., Collins, E. G., Whiteson, J. H., Sweeney, G., Haas, F., & Leddy, J. J. (2023) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2023.104062 · Cited by 27

Perspectives on mitochondrial dysfunction in the regeneration of aging skeletal muscle

Wang, K., Gan, M., Lei, Y., Liao, T., Li, J., Niu, L., Zhao, Y., Chen, L., Wang, Y., Zhu, L., et al. (2025) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-025-00771-1 · Cited by 34

The Therapeutic Role of Exercise and Probiotics in Stressful Brain Conditions

Martínez‐Guardado, I., Arboleya, S., Pérez, F. J. G., Kaliszewska, A., Gueimonde, M., & Arias, N. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073610 · Cited by 27

Mitochondrial Aging and Senolytic Natural Products with Protective Potential

Deledda, A., Giordano, E., Velluzzi, F., Flore, G., Franceschelli, S., Speranza, L., & Ripari, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232416219 · Cited by 27

Exerkines and Sarcopenia: Unveiling the Mechanism Behind Exercise-Induced Mitochondrial Homeostasis

Wang, J., Jia, D., Zhang, Z., & Wang, D. (2025) · Metabolites · doi:10.3390/metabo15010059 · Cited by 23

COVID-19 induced liver injury from a new perspective: Mitochondria

Akbari, H., & Taghizadeh‐Hesary, F. (2023) · Mitochondrion · doi:10.1016/j.mito.2023.04.001 · Cited by 24

Physiological Approaches Targeting Cellular and Mitochondrial Pathways Underlying Adipose Organ Senescence

de Lange, P., Lombardi, A., Silvestri, E., Cioffi, F., Giacco, A., Iervolino, S., Petito, G., Senese, R., Lanni, A., & Moreno, M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241411676 · Cited by 26

Mitochondrial Dysfunction in Cardiac Disease: The Fort Fell

PARASKEVAIDIS, I. A., Kourek, C., Farmakis, D. T., & Tsougos, E. (2024) · Biomolecules · doi:10.3390/biom14121534 · Cited by 22

Forced treadmill running modifies gut microbiota with alleviations of cognitive impairment and Alzheimer's disease pathology in 3xTg-AD mice

Jin, Y., Kim, T., & Kang, H. (2023) · Physiology & Behavior · doi:10.1016/j.physbeh.2023.114145 · Cited by 18

Moderate-Intensity Exercise Enhances Mitochondrial Biogenesis Markers in the Skeletal Muscle of a Mouse Model Affected by Diet-Induced Obesity

Jun, L., Knight, E., Broderick, T. L., Al‐Nakkash, L., Tobin, B. L., Geetha, T., & Babu, J. R. (2024) · Nutrients · doi:10.3390/nu16121836 · Cited by 17

Converging protective pathways: Exploring the linkage between physical exercise, extracellular vesicles and oxidative stress

Lisi, V., Senesi, G., & Balbi, C. (2023) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2023.09.021 · Cited by 18

Aerobic Capacity Beyond Cardiorespiratory Fitness Linking Mitochondrial Function, Disease Resilience and Healthy Aging

Gao, T., Hu, Y., Zhang, H., Shi, R., Song, Y., Ding, M., & Gao, F. (2025) · The FASEB Journal · doi:10.1096/fj.202500554r · Cited by 16

Validation of Amazon Halo Movement: a smartphone camera-based assessment of movement health

Fanton, M., Harari, Y., Giffhorn, M., Lynott, A., Alshan, E., Mendley, J., Czerwiec, M., Macaluso, R., Ideses, I., Oks, E., et al. (2022) · npj Digital Medicine · doi:10.1038/s41746-022-00684-9 · Cited by 15

Hypothesis: Enhanced glucose availability and insulin resistance enhances an activated immune system and accounts for the obesity paradox

Bradley, P. J. (2022) · Clinical Obesity · doi:10.1111/cob.12521 · Cited by 13

The Molecular Mechanisms of Fuel Utilization during Exercise

Pi, A., Villivalam, S. D., & Kang, S. (2023) · Biology · doi:10.3390/biology12111450 · Cited by 15

Exercise-Boosted Mitochondrial Remodeling in Parkinson’s Disease

Magaña, J. C., Deus, C. M., Giné‐Garriga, M., Montané, J., & Pereira, S. P. (2022) · Biomedicines · doi:10.3390/biomedicines10123228 · Cited by 15

Effects of intermittent hypoxia and whole-body vibration training on health-related outcomes in older adults

Timón, R., González-Custodio, A., Gusi, N., & Olcina, G. J. (2024) · Aging Clinical and Experimental Research · doi:10.1007/s40520-023-02655-w · Cited by 12

Physical Activity and Cancer Incidence and Mortality: Current Evidence and Biological Mechanisms

Kruk, J., Aboul-Enein, B. H., Gołębiewska, M. E., Duchnik, E., Czerniak, U., & Marchlewicz, M. (2025) · Cancers · doi:10.3390/cancers17091410 · Cited by 13

Changing ROS, NAD and AMP: A path to longevity via mitochondrial therapeutics

Lushchak, O. V., Gospodaryov, D. V., Strilbytska, O. M., & Bayliak, M. M. (2023) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2023.03.005 · Cited by 11

Exercise-modulated IL-6 in cancer cachexia: molecular mechanisms and therapeutic potential

Wei, S., Lv, X., Xu, Y., & Ding, S. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-026-07690-5 · Cited by 12

The Role of Skeletal Muscle Mitochondria in Colorectal Cancer Related Cachexia: Friends or Foes?

van de Haterd, B., Verboven, K., Vandenabeele, F., & Agten, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232314833 · Cited by 10

Skeletal Muscle mRNA Splicing Variants Association With Four Different Fitness and Energetic Measures in the GESTALT Study

Donegà, S., Banskota, N., Gupta, E., González‐Freire, M., Moore, A. Z., Ubaida‐Mohien, C., Munk, R. B., Zukley, L. M., Piao, Y., Bergeron, C., et al. (2024) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13603 · Cited by 10

Mitochondrial Dysfunction in Cardiac Diseases: Insights into Pathophysiology and Clinical Outcomes

Ahmad, S. S., Ansari, J. A., Ansari, T. M., & Zaidi, S. M. H. (2025) · Current Cardiology Reviews · doi:10.2174/011573403x379197250417061904 · Cited by 9

Moderate-intensity exercise training uniquely modulates circulating lipid species beyond classical lipid levels in humans

Zhang, Y., Zhang, Z., Martínez‐Téllez, B., Di, X., Kindt, A. S. D., Köhler, I., Osuna‐Prieto, F. J., Clark, C., Drouin, N., Harms, A. C., et al. (2025) · EBioMedicine · doi:10.1016/j.ebiom.2025.105849 · Cited by 10

Exercise-mediated regulation of mitochondrial dynamics in aging muscle: implications for mitochondrial diseases

Zhang, C., Zheng, X., Xiang, L., & Su, Z. (2025) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05441-6 · Cited by 10

Induction of Cardiac Pathology: Endogenous versus Exogenous Nrf2 Upregulation

Mathis, B. J., Kato, H., & Hiramatsu, Y. (2022) · Cells · doi:10.3390/cells11233855 · Cited by 9

Sepsis-like Energy Deficit Is Not Sufficient to Induce Early Muscle Fiber Atrophy and Mitochondrial Dysfunction in a Murine Sepsis Model

Pierre, A., Bourel, C., Favory, R., Brassart, B., Wallet, F., Daussin, F., Normandin, S., Howsam, M., Romien, R., Lemaire, J., et al. (2023) · Biology · doi:10.3390/biology12040529 · Cited by 9

Effects of exercise on cardiorespiratory fitness in children and adolescents with overweight and obesity: a systematic review and meta-analysis of 72 randomized controlled trials

Men, J., Yu, Z., An, W., Wang, P., Hou, X., Zhang, Y., Wu, S., Zhu, G., Wang, P., Cui, C., et al. (2025) · BMC Public Health · doi:10.1186/s12889-025-25254-y · Cited by 9

Oxidative Stress in Military Missions—Impact and Management Strategies: A Narrative Analysis

Rădulescu, D., Mihai, F.-D., Trasca, M. E.-T., Căluianu, E. I., Calafeteanu, C. D. M., Radulescu, P.-M., Mercuţ, R., Ciupeanu-Călugăru, E. D., Marinescu, G.-A., Siloşi, C. A., et al. (2024) · Life · doi:10.3390/life14050567 · Cited by 7

Replacing sedentary time with sleep and physical activity: associations with physical function and wellbeing in Type 2 diabetes

Covenant, A., Yates, T. E., Rowlands, A. V., Dempsey, P. C., Edwardson, C. L., Hall, A. P., Davies, M. J., & Henson, J. J. (2024) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2024.111886 · Cited by 8

Piperine Enhances Mitochondrial Biogenesis to Mitigate Stress in SH ‐ SY5Y Neuroblastoma Cells

Saikachain, N., Charoensawat, P., Tuntoolavest, O., Vejsureeyakul, N., Kunpittaya, T., Poolsri, W., Sungkaworn, T., Saeeng, R., Muanprasat, C., & Asavapanumas, N. (2025) · Food Science & Nutrition · doi:10.1002/fsn3.70637 · Cited by 6

Salutogenic Effects of Greenspace Exposure: An Integrated Biopsychological Perspective on Stress Regulation, Mental and Physical Health in the Urban Population

Varadarajan, S., Herchet, M., Mack, M., Hofmann, M., Bisle, E., Sayer, E. J., & Kolassa, I. (2025) · Open Psychology · doi:10.1515/psych-2024-0003 · Cited by 6

Identification of novel genes associated with exercise and calorie restriction effects in skeletal muscle

Kang, J. S., Kim, M. J., Kwon, E., Lee, K., Kim, C., Kwon, K., & Yang, Y. R. (2023) · Aging · doi:10.18632/aging.204793 · Cited by 5

SomaModules: A Pathway Enrichment Approach Tailored to SomaScan Data

Candia, J., Fantoni, G., Delgado‐Peraza, F., Shehadeh, N., Tanaka, T., Moaddel, R., Walker, K. A., & Ferrucci, L. (2025) · Journal of Proteome Research · doi:10.1021/acs.jproteome.4c01114 · Cited by 4

Role of L-carnitine in exercise training: Anti-inflammatory, antioxidant, and metabolic interactions

Aminizadeh, S., Zarezadehmehrizi, A., Deh-Ahmadi, M. A., & Shahouzehi, B. (2025) · Advances in Redox Research · doi:10.1016/j.arres.2025.100149 · Cited by 4

Mitochondrial Health, Physical Functioning, and Daily Affect: Bioenergetic Mechanisms of Dementia Caregiver Well-Being

Wu‐Chung, E. L., Medina, L. D., Paoletti, J., Lai, V., Stinson, J. M., Mahant, I., Schulz, P. E., Heijnen, C. J., & Fagundes, C. P. (2024) · Psychosomatic Medicine · doi:10.1097/psy.0000000000001312 · Cited by 6

Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application

Sun, X., Bulekova, K., Yang, J., Lai, M. M., Pitsillides, A., Liu, X., Zhang, Y., Guo, X., Yong, Q., Raffield, L. M., et al. (2024) · Mitochondrion · doi:10.1016/j.mito.2024.101954 · Cited by 4

Dementia and Cognitive Decline: A HEALM Approach

Jaqua, E. E., Tran, M.-L. N., Alvarez, P., Gupta, M., & Yoong, J. (2024) · American Journal of Lifestyle Medicine · doi:10.1177/15598276241291508 · Cited by 4

Brown adipose tissue: a potential target for aging interventions and healthy longevity

Li, H., Li, J., Song, C., Yang, H., Luo, Q., & Chen, M. (2024) · Biogerontology · doi:10.1007/s10522-024-10137-3 · Cited by 6

Mitotherapy in Alzheimer’s and Parkinson’s diseases: A systematic review of preclinical studies

Modiri, A., Hosseini, L., Abolhasanpour, N., Azizi, H., & Sadeh, R. N. (2025) · BMC Neurology · doi:10.1186/s12883-025-04241-1 · Cited by 4

Analyzing Superoxide Dismutase as A Molecular Signal Transducer that is Beneficial for Health during Physical Exercise: A Systematic Review

Ayubi, N., Wibawa, J. C., Aljunaid, M., Dafun, P. B., & Ming, J. (2024) · AL-Kindy College Medical Journal · doi:10.47723/rxr2gb93 · Cited by 3

Training-Induced Metabolic Adaptations in Skeletal Muscle

García-Domínguez, E., Gómez‐Cabrera, M. C., & González, G. O. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-88361-3_21 · Cited by 3

Effectiveness of Otago Exercise Program on Successful Aging within Older Women with Migrant Children Referring to Public Health Centers in Shiraz City, Iran

Ghaedi, M., Kashfi, S. M., Ghahremani, L., & Asadollahi, A. (2023) · Gerontology and Geriatric Medicine · doi:10.1177/23337214231172640 · Cited by 3

Physical exercise induces increased translocation of type 4 glucose transporters (GLUT4): a systematic review

Ayubi, N., Wibawa, J. C., Lesmana, H. S., Callixte, C., & Dafun, P. B. (2024) · Retos · doi:10.47197/retos.v59.104078 · Cited by 3

Near Infrared‐Mediated Intracellular NADH Delivery Strengthens Mitochondrial Function and Stability in Muscle Dysfunction Model

Cho, H. B., Kim, H., Lee, S., Cho, C. W., Park, J., Youn, S., So, G., Kang, S., Kim, H. J., & Park, K. (2025) · Advanced Science · doi:10.1002/advs.202415303 · Cited by 3

The vital role of exercise and nutrition in COVID-19 rehabilitation: synergizing strength

Peterson, B. M., Unger, I., Sun, S., Park, J.-Y., Kim, J., Gunasekera, R. S., Wilson, J., & Galbadage, T. (2023) · Frontiers in Sports and Active Living · doi:10.3389/fspor.2023.1305175 · Cited by 3

A mito-centric view on muscle aging and function

Burtscher, J., Strasser, B., & Burtscher, M. (2024) · Frontiers in Public Health · doi:10.3389/fpubh.2023.1330131 · Cited by 3

Exercise-induced cardiac mitochondrial reorganization and enhancement in spontaneously hypertensive rats

Coto, J. G., Pereyra, E., Cavalli, F. A., Valverde, C. A., Caldiz, C. I., Maté, S. M., Yeves, A. M., & Ennis, I. L. (2024) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-024-02956-7 · Cited by 3

Assessing the joint effects of mitochondrial genes and physical activity on the psychiatric phenotype of subjective well-being based on the UK Biobank data

Shi, P., Wang, B., Shi, S., Chu, X., Liu, C., Kang, M., Hui, J., Gou, Y., Zhou, R., Liu, Y., et al. (2024) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-024-01822-y · Cited by 3

Early Mobilization in the Intensive Care Unit: To Rest or to Test?

Wang, D. S., Moitra, V. K., & Flynn, B. C. (2023) · Journal of Cardiothoracic and Vascular Anesthesia · doi:10.1053/j.jvca.2023.02.004 · Cited by 3

Caring While Moving: Case Studies on Physical Activity and Dementia Caregiver Well-Being

Boon, J. T., Maxwell, C. A., & Layne, D. M. (2025) · Healthcare · doi:10.3390/healthcare13172205 · Cited by 2

Cardiorespiratory fitness responses to a Daily Mile program in overweight youth from a low-income Colombian school

la Rosa, A. D., Ojeda-Aravena, A., Cruz, G. I. N., Díaz-Marín, I. J., Quintero, A. M., Ramírez, P. C., & Villa, M. A. C. (2026) · Scientific Reports · doi:10.1038/s41598-026-38361-6 · Cited by 2

Physical activity and risk of thyroid cancer: a systematic review and meta-analysis of prospective cohort studies

Cho, H., Park, Y., & Myung, S. (2025) · International Journal of Clinical Oncology · doi:10.1007/s10147-025-02907-x · Cited by 2

ATPase Inhibitory Factor 1—A Novel Marker of Cellular Fitness and Exercise Capacity?

Domin, R., Pytka, M., Niziński, J., Żołyński, M., Zybek‐Kocik, A., Wrotkowska, E., Zieliński, J., Guzik, P., & Ruchała, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315303 · Cited by 2

Long COVID: current management and future prospects

Liew, F., & Openshaw, P. (2024) · European Respiratory Society eBooks · doi:10.1183/2312508x.10021523 · Cited by 2

Manifold epigenetics: A conceptual model that guides engineering strategies to improve whole-body regenerative health

Ung, C. Y., Correia, C., Billadeau, D. D., Zhu, S., & Li, H. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1122422 · Cited by 4

The integrative role of physical exercise and muscle satellite cells in remodeling muscle structure and function

Lu, Y., Xu, K., Kong, J., & Liu, C. (2025) · Molecular & cellular biomechanics · doi:10.62617/mcb1298 · Cited by 1

Impacts of aging on brain metabolism

Rodrigues, B. A., Santiago, T. C., & Silva, J. D. N. (2025) · Progress in brain research · doi:10.1016/bs.pbr.2025.05.009 · Cited by 2

Purinergic signaling by ATP induces exercise‐like effects and ameliorates insulin resistance in HT22 mouse hippocampal cells

Reddy, I., & Dey, C. S. (2025) · FEBS Letters · doi:10.1002/1873-3468.70158 · Cited by 1

Environmental Influences on Genetic Aging Processes: Experimental Evidence from Model Systems

Molla, A. (2025) · European Journal of Clinical and Biomedical Sciences · doi:10.11648/j.ejcbs.20251104.12 · Cited by 1

Impact of exercise-induced DNA damage repair on age-related muscle weakness and sarcopenia

朱, 玲., Su, Y., & Su, Z. (2026) · Frontiers in Genetics · doi:10.3389/fgene.2025.1639224 · Cited by 2

Physical Therapist Management of Cardiovascular Diseases

Ahmed, A. S., Balogun, J. A., & Balogun, O. I. (2026) · Springer eBooks · doi:10.1007/978-3-031-86558-9_21 · Cited by 1

Strategic targeting of mitochondria in ischemic heart disease: mechanisms and emerging therapies

Kurian, G. A., & Gino, E. R. (2026) · Expert Review of Cardiovascular Therapy · doi:10.1080/14779072.2026.2637751 · Cited by 1

Exerkines in diabetic retinopathy: from mechanisms to therapeutic prospects

Zhu, J. (2026) · Frontiers in Endocrinology · doi:10.3389/fendo.2026.1762255 · Cited by 1

Is the muscle post-ACL injury ready to rebuild or is it limited by mitochondrial dysfunction?

Stoneback, L., Buchanan, B., Weishuhn, B. D., Macpherson, P. C. D., & Lepley, L. K. (2026) · Journal of science and medicine in sport · doi:10.1016/j.jsams.2026.03.017 · Cited by 1

Exercise prevents fatal stress-induced myocardial injury in obese mice

Dun, Y., Hu, Z., You, B., Du, Y., Zeng, L., Zhao, Y., Liu, Y., Wu, S., Cui, N., Yang, F., et al. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1223423 · Cited by 1

The Future of Chemotherapy: The Mechanisms and Benefits of Exercise in Taxane-Induced Peripheral Neuropathy

Shastry, S., Mizrahi, D., & Kanzawa-Lee, G. A. (2023) · Physiologia · doi:10.3390/physiologia3040042 · Cited by 1

Salivary proteomic profile of response to different resistance training protocols: A case report

Santos, K. O., Filho, D. M. P., Ventura, T. M. O., Grizzo, L. T., Macedo, A. G., Buzalaf, M. A. R., Braga, A. S., Faria, M. H., & Magalhães, A. C. (2024) · Cell Biochemistry and Function · doi:10.1002/cbf.3936 · Cited by 1

Moderate-intensity training can ameliorate the process of cardiac apoptosis induced by lithium drug consumption in male Wistar rats

Roholamini, Z., Abbaspoor, M., Aminizadeh, S., & Saberi, S. (2024) · Toxicology Reports · doi:10.1016/j.toxrep.2024.101802 · Cited by 1

Efficacy and Safety of Photobiomodulation in MELAS: Protocol for a Series of N-of-1 Trials

Laakso, E., Ewais, T., McMahon, K. L., Forbes, J. M., & Phillips, L. K. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14062047 · Cited by 1

Exercise training improves sarcopenic muscle function via restoration of mitochondrial quality controlPreprint

Alldritt, I., Sligar, J., Campelj, D. G., Padilha, C. S., Ritenis, E. J., Mantamadiotis, T., Widodo, S. S., Dinevska, M., Nielsen, J., Philp, A. M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.03.686168 · Cited by 1

The effect of eight weeks of high-intensity interval training with caloric restriction and spirulina supplementation on inflammatory factors in heart tissue of rats under high-fat diet

khirabadi, J., Etemad, Z., Azizbeigi, K., & Salamat, K. M. (2023) · Journal of Sport and Exercise Physiology · doi:10.52547/joeppa.16.1.67

The Acute Effects of Exercise on Saliva-Derived Regional Mitochondrial DNA from Trained Runners

McGlynn, M. L., Rosales, A. M., Collins, C. W., & Slivka, D. R. (2023) · Exercise Sport and Movement · doi:10.1249/esm.0000000000000009

Evaluating the molecular drivers of physical inactivity and muscle atrophy as initiating factors in cognitive impairment

Kerr, N. R. (2023) · MOspace Institutional Repository (University of Missouri) · doi:10.32469/10355/97056

The role of mitochondria in the pathogenesis of sarcopenia: a concise review

Greggi, C., & Tarantino, U. (2023) · International Journal of Bone Fragility · doi:10.57582/ijbf.230302.050

Parkinson's and physical activity: the what, why and how

Peel, C. (2024) · British Journal of Neuroscience Nursing · doi:10.12968/bjnn.2024.20.2.54

Aging: Generation of oxidative stress

Rehman, R., Zulkipli, I. N., & Khan, H. N. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-18807-7.00007-7

Mitochondrial defects in sporadic inclusion body myositis—causes and consequences

Iu, E. C. Y., So, H., & Chan, C. B. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1403463

Integrating Cluster Analysis and Predictive Modeling for COVID-19 Treatment Outcomes: A Machine Learning Framework

Feretzakis, G., Sakagianni, A., Paxinou, E., & Verykios, V. S. (2024) · International Conference on Information, Intelligence, Systems & Applications (IISA) · doi:10.1109/iisa62523.2024.10786641

Ionic and Molecular Regulation of Mitochondrial Bioenergetics

Stowe, D. F. (2025) · Springer eBooks · doi:10.1007/978-3-031-76668-8_7

Exercise and the Mitochondria

Gidlund, E. (2019) · Springer eBooks · doi:10.1007/978-3-030-04816-7_3 · Cited by 4

Mitochondrial dysfunction in cardiovascular disease: Towards exercise regulation of mitochondrial function

Li, K., Wan, B., Li, S., Chen, Z., Jia, H., Song, Y., Zhang, J., Ju, W., Ma, H., & Wang, Y. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1063556 · Cited by 21

Mitochondria as a Target for Exercise-Induced Cardioprotection

Ascensão, A. A. M. R., Lumini‐Oliveira, J., Oliveira, P. J., & Magalhães, J. (2011) · Current Drug Targets · doi:10.2174/138945011795529001 · Cited by 36

Exercise-Induced Mitochondrial Adaptations in Addressing Heart Failure

Marquez, J. C., & Han, J. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-981-10-4304-8_17 · Cited by 3

Mitochondrial quality control as a therapeutic target in cardiovascular disease: Mechanistic insights and future directions

Zhang, M., Zhang, T., Zou, R., He, K., Huang, R., Feng, J., Hu, J., Ge, T., Fan, X., Zhou, H., et al. (2025) · Journal of Translational Internal Medicine · doi:10.1515/jtim-2025-0030 · Cited by 26