Markers of Human Skeletal Muscle Mitochondrial Biogenesis and Quality Control: Effects of Age and Aerobic Exercise Training

Exercise capacity and mortality among men referred for exercise testing

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Adaptations of skeletal muscle to endurance exercise and their metabolic consequences

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Decline in skeletal muscle mitochondrial function with aging in humans

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Mitochondria and the Autophagy–Inflammation–Cell Death Axis in Organismal Aging

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Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations

Chen, H., Vermulst, M., Wang, Y. E., Chomyn, A., Prolla, T. A., McCaffery, J. M., & Chan, D. C. (2010) · Cell · doi:10.1016/j.cell.2010.02.026 · Cited by 1,211

Mitofusin-2 Determines Mitochondrial Network Architecture and Mitochondrial Metabolism

Bach, D., Pich, S., Soriano, F. X., Vega, N., Baumgartner, B., Oriola, J., Daugaard, J. R., Lloberas, J., Camps, M., Zierath, J. R., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m212754200 · Cited by 832

Effects of treadmill exercise on the regulatory mechanisms of mitochondrial dynamics and oxidative stress in the brains of high-fat diet fed rats

Koo, J., & Kang, E. (2019) · Physical Activity and Nutrition · doi:10.20463/jenb.2019.0005 · Cited by 26

Mild aerobic training with blood flow restriction increases the hypertrophy index and MuSK in both slow and fast muscles of old rats: Role of PGC-1α

Bahreinipour, M.-A., Joukar, S., Hovanloo, F., Najafipour, H., Naderi-Boldaji, V., Raji-Amirhasani, A., & Esmaeili‐Mahani, S. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.03.051 · Cited by 25

Nutri-stress, mitochondrial dysfunction, and insulin resistance—role of heat shock proteins

Jayashree, K., & Senthilkumar, G. P. (2022) · Cell Stress and Chaperones · doi:10.1007/s12192-022-01314-9 · Cited by 29

Caffeoylquinic Acid-Rich Extract ofAster glehniF. Schmidt Ameliorates Nonalcoholic Fatty Liver through the Regulation of PPARδand Adiponectin in ApoE KO Mice

Lee, Y.-J., Jang, Y. N., Han, Y.-M., Kim, H. M., Jeong, J.-M., Son, M. J., Jin, C., Kim, H. J., & Seo, H. S. (2017) · PPAR Research · doi:10.1155/2017/3912567 · Cited by 24

Energy transfer between the mitochondrial network and lipid droplets in insulin resistant skeletal muscle

Parry, H. A., & Glancy, B. C. (2021) · Current Opinion in Physiology · doi:10.1016/j.cophys.2022.100487 · Cited by 22

The role of exercise in Parkinson’s Disease

Almikhlafi, M. A. (2023) · Neurosciences · doi:10.17712/nsj.2023.1.20220105 · Cited by 22

The physiological impact of high‐intensity interval training in octogenarians with comorbidities

Blackwell, J., Gharahdaghi, N., Brook, M. S., Watanabe, S., Boereboom, C., Doleman, B., Lund, J. N., Wilkinson, D. J., Smith, K., Atherton, P. J., et al. (2021) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12724 · Cited by 24

Effect of age on in vivo oxidative capacity in two locomotory muscles of the leg

Tevald, M. A., Foulis, S. A., & Kent, J. A. (2014) · AGE · doi:10.1007/s11357-014-9713-5 · Cited by 22

Effect of aquatic exercise on mental health, functional autonomy, and oxidative dysfunction in hypertensive adults

Silva, L. A. D., Menguer, L., Motta, J. V. D. S., Dieke, B., Mariano, S., Tasca, G. M., Zaccaron, R. P., Silveira, P. C. L., & Pinho, R. A. (2017) · Clinical and Experimental Hypertension · doi:10.1080/10641963.2017.1407331 · Cited by 22

Effects of Treadmill Exercise on the Expression Level of BAX, BAD, BCL-2, BCL-XL, TFAM, and PGC-1α in the Hippocampus of Thimerosal-Treated Rats

Navazani, P., Vaseghi, S., Hashemi, M., Shafaati, M., & Nasehi, M. (2021) · Neurotoxicity Research · doi:10.1007/s12640-021-00370-w · Cited by 20

CYB5R3 overexpression preserves skeletal muscle mitochondria and autophagic signaling in aged transgenic mice

Lopez-Bellón, S., Rodríguez-López, S., González-Reyes, J. A., Burón, M. I., de Cabo, R., & Villalba, J. M. (2022) · GeroScience · doi:10.1007/s11357-022-00574-8 · Cited by 19

Age-dependent impact of two exercise training regimens on genomic and metabolic remodeling in skeletal muscle and liver of male mice

Bernier, M., Navas‐Enamorado, I., Gómez‐Cabrera, M. C., Calvo‐Rubio, M., González-Reyes, J. A., Price, N. L., Cortés-Rodríguez, A. B., Rodríguez‐Aguilera, J. C., Rodríguez-López, S., Mitchell, S. J., et al. (2022) · npj Aging · doi:10.1038/s41514-022-00089-8 · Cited by 20

Aerobic exercise attenuates neurodegeneration and promotes functional recovery – Why it matters for neurorehabilitation & neural repair

Zhang, D., Lu, Y., Zhao, X., Zhang, Q., & Li, L. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104862 · Cited by 21

Ameliorating Effects of Lifelong Physical Activity on Healthy Aging and Mitochondrial Function in Human White Adipose Tissue

Gudiksen, A., Qoqaj, A., Ringholm, S., Wojtaszewski, J. F. P., Plomgaard, P., & Pilegaard, H. (2021) · The Journals of Gerontology Series A · doi:10.1093/gerona/glab356 · Cited by 21

The mediating role of inflammaging between mitochondrial dysfunction and sarcopenia in aging: a review.

Xu, X., & Wen, Z. (2023) · PubMed Central · Cited by 21

Influence of Amino Acids and Exercise on Muscle Protein Turnover, Particularly in Cancer Cachexia

Pradhan, R., Dieterich, W., Natarajan, A., Schwappacher, R., Reljic, D., Herrmann, H. J., Neurath, M. F., & Zopf, Y. (2024) · Cancers · doi:10.3390/cancers16101921 · Cited by 18

Higher Daily Physical Activities Continue to Preserve Muscle Strength After Mid-Life, But Not Muscle Mass After Age of 75

Hwang, A., Zhan, Y.-R., Lee, W., Peng, L., Chen, L.-Y., Lin, M., Liu, L.-K., & Chen, L. (2016) · Medicine · doi:10.1097/md.0000000000003809 · Cited by 20

Autophagy gene expression in skeletal muscle of older individuals is associated with physical performance, muscle volume and mitochondrial function in the study of muscle, mobility and aging ( SOMMA )

Coen, P. M., Huo, Z., Tranah, G. J., Barnes, H. N., Zhang, X., Wolff, C. A., Wu, K., Cawthon, P. M., Hepple, R. T., Toledo, F. G. S., et al. (2024) · Aging Cell · doi:10.1111/acel.14118 · Cited by 17

Mitochondrial Adaptations in Aged Skeletal Muscle: Effect of Exercise Training

Ziaaldini, M. M., Hosseini, S. R. A., & Fathi, M. (2017) · Physiological Research · doi:10.33549/physiolres.933329 · Cited by 18

Effects of a single bout of exercise on mitochondria-mediated apoptotic signaling in rat cardiac and skeletal muscles

Yoo, S.-Z., No, M., Heo, J., Chang, E., Park, D., Kang, J., Seo, D. Y., Han, J., Jung, S., Hwang-Bo, K., et al. (2019) · Journal of Exercise Rehabilitation · doi:10.12965/jer.1938380.190 · Cited by 16

Exercise reduces the protein abundance of TXNIP and its interacting partner REDD1 in skeletal muscle: potential role for a PKA-mediated mechanism

Chaves, A., Miranda, E. R., Mey, J. T., Blackburn, B. K., Fuller, K. N. Z., Stearns, B., Ludlow, A., Williamson, D. L., Houmard, J. A., & Haus, J. M. (2021) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00229.2021 · Cited by 15

Small-Scale Randomized Controlled Trial to Explore the Impact of β-Hydroxy-β-Methylbutyrate Plus Vitamin D3 on Skeletal Muscle Health in Middle Aged Women

Fairfield, W. D., Minton, D. M., Elliehausen, C. J., Nichol, A. D., Cook, T. L., Rathmacher, J. A., Pitchford, L. M., Paluska, S. A., Kuchnia, A. J., Allen, J. M., et al. (2022) · Nutrients · doi:10.3390/nu14214674 · Cited by 13

Skeletal muscle adaptations to high‐intensity, low‐volume concurrent resistance and interval training in recreationally active men and women

Sterczala, A. J., Rodriguez‐Ortiz, N., Feigel, E. D., Krajewski, K. T., Martin, B. J., Sekel, N. M., Lovalekar, M. T., Kargl, C. K., Koltun, K. J., van Eck, C. F., et al. (2024) · Physiological Reports · doi:10.14814/phy2.15953 · Cited by 13

Age and sex-specific changes in mitochondrial quality control in skeletal and cardiac muscle

Springer, C. B., Ogbara, O., Silva, M. C. D., Henderson, A., Liu, Y., Prior, S. J., & Kuzmiak‐Glancy, S. (2025) · Frontiers in Aging · doi:10.3389/fragi.2025.1606110 · Cited by 13

Effects of Interval Exercise Training on Serum Biochemistry and Bone Mineral Density in Dogs

Lee, H. S., Kim, J. H., Oh, H. J., & Kim, J. H. (2021) · Animals · doi:10.3390/ani11092528 · Cited by 13

Multifidus Muscles Lipid Content Is Associated with Intervertebral Disc Degeneration: A Quantitative Magnetic Resonance Imaging Study

Ogon, I., Takebayashi, T., Takashima, H., Morita, T., Oshigiri, T., Terashima, Y., Yoshimoto, M., & Yamashita, T. (2019) · Asian Spine Journal · doi:10.31616/asj.2018.0258 · Cited by 13

Mitochondria‐associated membranes contribution to exercise‐mediated alleviation of hepatic insulin resistance: Contrasting high‐intensity interval training with moderate‐intensity continuous training in a high‐fat diet mouse model

Li, X., Yang, J., Hu, W., Ruan, Y., Chen, H. Y., Zhang, Q., Zhang, Z., & Ding, Z. S. (2024) · Journal of Diabetes · doi:10.1111/1753-0407.13540 · Cited by 12

Mitochondrial dynamics: roles in exercise physiology and muscle mass regulation

Djalalvandi, A., & Scorrano, L. (2022) · Current Opinion in Physiology · doi:10.1016/j.cophys.2022.100550 · Cited by 14

Trade-Offs Between Anti-Aging Dietary Supplementation and Exercise

Mendelsohn, A. R., & Larrick, J. W. (2013) · Rejuvenation Research · doi:10.1089/rej.2013.1484 · Cited by 11

Prospective Intervention Strategies Between Skeletal Muscle Health and Mitochondrial Changes During Aging

Zhang, X., Liao, S., Huang, L., & Wang, J. (2024) · Advanced Biology · doi:10.1002/adbi.202400235 · Cited by 11

Late life maintenance and enhancement of functional exercise capacity in low and high responding rats after low intensity treadmill training

Brown, L. A., Macpherson, P. C. D., Koch, L. G., Qi, N., Britton, S. L., & Brooks, S. V. (2019) · Experimental Gerontology · doi:10.1016/j.exger.2019.110657 · Cited by 9

Exercise-Induced Circulating microRNAs: Potential Key Factors in the Control of Breast Cancer

Telles, G. D., Conceição, M. S., VECHIN, F. C., Libardi, C. A., Mori, M. A., Derchain, S., & Ugrinowitsch, C. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.800094 · Cited by 8

Mechanisms of Exercise in Improving Sarcopenia

Su, M., Shao, Y., Fang, Q., Li, Y., Qiu, F., Che, T., & Zhang, S. (2025) · Comprehensive physiology · doi:10.1002/cph4.70030 · Cited by 9

Sarcopenia: an Aging Perspective and Management Options

Teixeira, A. M., Nosrani, S. E., Parvani, M., Viola, J., & Mohammadi, S. (2025) · International Journal of Sports Medicine · doi:10.1055/a-2577-2577 · Cited by 10

Effects of Intermittent Fasting and Calorie Restriction on Exercise Performance: A Systematic Review and Meta-Analysis

Kazeminasab, F., Sharafifard, F., Kerchi, A. B., Bagheri, R., Carteri, R. B., Kirwan, R., Santos, H. O., & Dutheil, F. (2025) · Nutrients · doi:10.3390/nu17121992 · Cited by 13

Mitochondrial quality control in human ageing and longevity

Picca, A., & Ferrucci, L. (2026) · Nature Metabolism · doi:10.1038/s42255-026-01563-3 · Cited by 10

Cycle exercise training and muscle mass: A preliminary investigation of 17 lower limb muscles in older men

Naruse, M., Vincenty, C. S., Konopka, A. R., Trappe, S. W., Harber, M. P., & Trappe, T. A. (2023) · Physiological Reports · doi:10.14814/phy2.15781 · Cited by 7

Effect of Short-Term Endurance Exercise on COX IV and PGC-1a mRNA Expression Levels in Rat Skeletal Muscle

Sylviana, N., Christina, N., Goenawan, H., Pratiwi, Y. S., Setiawan, I. B., Tarawan, V. M., Nurhayati, T., Rezano, A., Juliati, J., Purba, A., et al. (2019) · Biomedical & Pharmacology Journal · doi:10.13005/bpj/1759 · Cited by 8

Effects of chronic alcohol intoxication on aerobic exercise-induced adaptations in female mice

Tice, A. L., Gordon, B. S., Fletcher, E., McNeill, A., Laskin, G. R., Laudato, J. A., Rossetti, M. L., Koutakis, P., & Steiner, J. L. (2024) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00599.2023 · Cited by 6

Targeting Mitochondria with Sweat: Improving Mitochondrial Function with Physical Activity

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Markers of clinical and mitochondrial adaptation in response to moderate intensity continuous training: A systematic review and meta-analysis

Vabishchevich, V., Smith, R. T., & Bittel, A. J. (2026) · PLoS ONE · doi:10.1371/journal.pone.0339902 · Cited by 5

NOR ‐1 Overexpression Elevates Myoglobin Expression via PERM1 and Enhances Mitochondrial Function and Endurance in Skeletal Muscles of Aged Mice

Paez, H. G., Pitzer, C. R., Ferrandi, P. J., Mohamed, J. S., & Alway, S. E. (2025) · The FASEB Journal · doi:10.1096/fj.202500375r · Cited by 5

46th Walter J. Zeiter Lecture, Exercise Is Rehabilitation Medicine: Our History and Future

Becker, B. E. (2015) · PM&R · doi:10.1016/j.pmrj.2015.02.013 · Cited by 6

Protective Effect of Aerobic Training along with Resveratrol on Mitochondrial Dynamics of Cardiac Myocytes in Animal Model of Non-alcoholic Fatty Liver Disease

delroz, H., Abdi, A., Barari, A., & Farzanegi, P. (2019) · مجله دانشگاه علوم پزشکی اردبیل · doi:10.29252/jarums.19.3.272 · Cited by 6

Mitochondrial remodelling supports migration in white-crowned sparrows ( Zonotrichia leucophrys )

Mesquita, P. H. C., Rhodes, E. A., Yap, K. N., Mueller, B. J., Hill, G. E., Hood, W. R., & Kavazis, A. N. (2024) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2024.2409 · Cited by 7

Increased cardiorespiratory fitness and skeletal muscle size following single-leg knee extension exercise training

Wolff, C. A., Konopka, A. R., Suer, M. K., Trappe, T. A., Kaminsky, L. A., & Harber, M. P. (2019) · The Journal of Sports Medicine and Physical Fitness · doi:10.23736/s0022-4707.18.08590-0 · Cited by 5

Three-week sprint interval training (SIT) reduces cell-free DNA and low-frequency fatigue but does not induce VO2max improvement in older men

Juškevičiūtė, E., Neuberger, E. W. I., Eimantas, N., Venckūnas, T., Kamandulis, S., Simon, P. D., & Brazaitis, M. (2023) · European Journal of Applied Physiology · doi:10.1007/s00421-023-05366-2 · Cited by 5

Antioxidants and Polyphenols Mediate Mitochondrial Mediated Muscle Death Signaling in Sarcopenia

Alway, S. E. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-810422-4.00026-9 · Cited by 6

Exercising heart failure patients: cardiac protection through preservation of mitochondrial function and substrate utilization?

Nijholt, K. T., Voorrips, S. N., Sánchez-Aguilera, P., & Westenbrink, B. D. (2023) · Current Opinion in Physiology · doi:10.1016/j.cophys.2023.100656 · Cited by 4

Voluntary wheel running activates Akt/AMPK/eNOS signaling cascades without improving profound endothelial dysfunction in mice deficient in α-galactosidase A

Kang, J. J., Treadwell, T., Bodary, P. F., & Shayman, J. A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0217214 · Cited by 4

Regenerative Rehabilitation in Sarcopenia, Dynapenia, and Frailty

Baumann, C. W., Clark, B. C., Phillips, B. E., Szewczyk, N. J., & Consitt, L. A. (2022) · Physiology in health and disease · doi:10.1007/978-3-030-95884-8_5 · Cited by 4

Exercise training and changes in skeletal muscle mitochondrial proteins: from blots to “omics”

Reisman, E. G., Caruana, N. J., & Bishop, D. J. (2024) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2024.2383408 · Cited by 3

Aqueous extract of Atractylodes macrocephala Koidz. improves dexamethasone-induced skeletal muscle atrophy in mice by enhancing mitochondrial biological function

Ye, M., Lai, P., Fang, Y., Li, Y., Wang, F., Yu, J., Zhang, Y., Yang, Q., Zhu, J., Xie, X., et al. (2025) · Experimental Gerontology · doi:10.1016/j.exger.2025.112693 · Cited by 3

Role Of Exercise Intensity in Skeletal Muscle Hypertrophy

Irawati, N. A. V., Sylviana, N., & Lubis, L. (2024) · Jurnal Biomedika dan Kesehatan · doi:10.18051/jbiomedkes.2024.v7.124-132 · Cited by 3

Muscle oxidative capacity but not specific force is greater in aerobic versus resistance trained young adults

Perlet, M. R., Batman, G. B., Ransom, K. V., Bailey, M. D., & Keller, J. L. (2025) · European Journal of Applied Physiology · doi:10.1007/s00421-025-05771-9 · Cited by 3

Molecular Mechanisms and Nutritional Modulation in Sarcopenia: A Narrative Review

Chin, H. S., Liu, L., Liao, P.-J., Wee, A. L. R. M., Kwek, X.-Y., Teh, B. T., & Koh, F. H.-X. (2026) · Nutrients · doi:10.3390/nu18071161 · Cited by 3

Comparison of the Effects of Endurance Training on Alternate Days and on Consecutive 4 Days Each Week for 8 Weeks on the Abundance of PGC-1α, CaMKII, NRF-1, mtTFA, and COXIV Proteins in Rat Skeletal Muscle

Qiu, J., Huang, L., Davie, A. J., & Zhou, S. (2017) · The Journal of Strength and Conditioning Research · doi:10.1519/jsc.0000000000002407 · Cited by 2

Treadmill training impacts the skeletal muscle molecular clock after ischemia stroke in rats

Mai, L., Yin, Y., & Qin, D. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e27430 · Cited by 2

Mitochondrial quality control in exercise-mitigated muscular atrophy

Fan, J., Wen, X., Duan, X., Zhu, X., Bai, J., & Zhang, T. (2025) · Mitochondrion · doi:10.1016/j.mito.2025.102074 · Cited by 2

THE ROLE OF MACROPHAGES IN EXERCISE AND INSULIN RESISTANCE IN HUMAN SKELETAL MUSCLE

Groshong, J. S. (2013) · UKnowledge (University of Kentucky) · Cited by 2

Molecular mechanisms of adaptive and therapeutic effects of physical activity in patients with cardiovascular diseases

Vladimirsky, V. E., Vladimirsky, E. V., Lunina, A. N., Fesyun, A. D., Rachin, A. P., Lebedeva, O. D., Yakovlev, M. Y., & Tubekova, M. (2022) · Problems of Balneology Physiotherapy and Exercise Therapy · doi:10.17116/kurort20229902169 · Cited by 2

Cardiomyocyte mitochondrial dynamics in health and disease and the role of exercise training: A brief review

Naderi, N., Ebadi, B., Damirchi, A., Alamdari, K. A., & Darbandi-Azar, A. (2018) · Research in Cardiovascular Medicine · doi:10.4103/rcm.rcm_11_18 · Cited by 2

The effectiveness of physical activity in cardiorehabilitation

Yakovlev, M. Y., Lebedeva, O. D., Vladimirsky, V. E., Vladimirsky, E. V., & Lunina, A. N. (2022) · Sports medicine research and practice · doi:10.47529/2223-2524.2022.1.1 · Cited by 1

Impact of two-month sodium citrate supplementation along with moderate-intensity continuous training on PGC-1α and Nrf2 expression in diabetic rats

Nabilpour, M., Seifi-Skishahr, F., Ghouroghchi, A. P., & Nobarı, H. (2024) · Physiology and Pharmacology · doi:10.61186/phypha.28.2.157 · Cited by 1

The effect of sarcopenia on postoperative adverse events after endoscopic submucosal dissection for early gastrointestinal cancer

Sun, Y., Zhang, Y., Tian, B., Liu, T., Wang, N., Han, S., Xuan, M., Zhang, R., Liu, K., Liu, S., et al. (2025) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365521.2025.2594784 · Cited by 1

Effect of Polyphenol-Rich Diet Combined with Leucine, Vitamin D3, and Magnesium Supplementation on Self-Reported Mobility and Health Perception in Adults at Risk of Sarcopenia: A 3-Months Quasi-Experimental Study

Tache-Codreanu, D.-L., Tache-Codreanu, A.-M., Ștefan, G., Trăistaru, M. R., Rusu, E., Tache-Codreanu, A., & Sporea, C. (2026) · Life · doi:10.3390/life16040554 · Cited by 1

ITCH ‐Mediated Ubiquitination and Degradation of THBS1 : A Key Mechanism for Enhancing Mitochondrial Biogenesis and Alleviating Mouse Skeletal Muscle Atrophy

Yu, W., Wang, Y., Li, N., & Wang, D. (2026) · Acta Physiologica · doi:10.1111/apha.70299 · Cited by 1

Linking mitochondrial dysfunction to sarcopenia

Alway, S. E. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822146-4.00004-1 · Cited by 1

The Effect of Eight Weeks of Aerobic Training Combined With Resveratrol on MFn1 and MFn2 Expression in Cardiac Myocytes in a Non-alcoholic Fatty Liver Animal Model

delroz, H., Abdi, A., Barari, A., & Farzanegi, P. (2020) · Complementary Medicine Journal · doi:10.32598/cmja.9.3.627.3 · Cited by 1

Rehabilitation of Patients with Severe Disability after coVID-19 in Rehabilitation Department. Multiple Case Study

Vladimirsky, V. E., Vladimirsky, E. V., Lunina, A. N., Fesyun, A. D., Rachin, A. P., Lebedeva, O. D., & Yakovlev, M. Y. (2021) · Bulletin of Rehabilitation Medicine · doi:10.38025/2078-1962-2021-20-3-16-25 · Cited by 1

Combining in vivo 2-photon imaging with photoactivatable fluorescent labeling reveals strikingly low rates of mitochondrial dynamics in skeletal musclePreprint

O’Reilly, C. L., Davidyan, A., Cizio, K., Doidge, S. M., Bubak, M. P., Borowik, A., Lewis, T. L., & Miller, B. F. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.10.627796 · Cited by 1

Estudio de la mitofagia en respuesta a un programa de entrenamiento de fuerza en personas mayores = Study of mitophagy in response to a strength training program for older people

Moreira, O. C. (2018) · Buleria (Universidad de León) · doi:10.18002/10612/8008

The Effects of Acute Aerobic and Resistance Exercise on mTOR Signaling and Autophagy in Human Skeletal Muscle

Mazo, C. E. (2019) · Arizona State University Library Digital Repository (Arizona State University)

Feeding recombinant Royalactin: Measures of improved lifespan and mitochondrial function in Caenorhabditis elegansPreprint

Li, X., Ingram, T. L., Wang, Y., Derecka, K., Courtier, N., Piana, M., Hardy, I. C. W., Chakrabarti, L., & Stöger, R. J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.14.296053

Control of Mitochondrial Homeostasis In Disused and Aging Skeletal Muscle: Role of Pgc-1Alpha and Sirtuins

Yeo, D. (2020) · University of Minnesota Digital Conservancy (University of Minnesota)

Efeitos de uma sessão de treinamento concorrente nos níveis de metilação e expressão de genes fatores regulatórios miogênicos

Telles, G. D. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.39.2019.tde-22102021-122843

Skeletal muscle health in aging

Grevendonk, L. (2021) · Research Publications (Maastricht University) · doi:10.26481/dis.20211006lg

Hybrid HIIT/isometrics strength training programs: a paradigm shift for physical exercise

Wyche, L., Rojo-Gil, G., Marín-Peiró, M., Perez-Turpin, J. A., Gómez-Paternina, J. E., Elvira, C., & Ayers, D. (2022) · Scientific Journal of Sport and Performance · doi:10.55860/dfxo4471

Exercise: Thermodynamic and Bioenergetic Principles

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