Satellite cell content is specifically reduced in type II skeletal muscle fibers in the elderly

Homeostasis model assessment: insulin resistance and ?-cell function from fasting plasma glucose and insulin concentrations in man

Matthews, D. R., Hosker, J. P., Rudenski, A. S., Naylor, B. A., Treacher, D. F., & Turner, R. C. (1985) · Diabetologia · doi:10.1007/bf00280883 · Cited by 31,502

SATELLITE CELL OF SKELETAL MUSCLE FIBERS

Mauro, A. (1961) · The Journal of Cell Biology · doi:10.1083/jcb.9.2.493 · Cited by 3,683

Pax7 Is Required for the Specification of Myogenic Satellite Cells

Seale, P., Sabourin, L. A., Girgis-Gabardo, A., Mansouri, A., Gruß, P., & Rudnicki, M. A. (2000) · Cell · doi:10.1016/s0092-8674(00)00066-0 · Cited by 2,345

Rejuvenation of aged progenitor cells by exposure to a young systemic environment

Conboy, I. M., Conboy, M. J., Wagers, A. J., Girma, E. R., Weissman, I. L., & Rando, T. A. (2005) · Nature · doi:10.1038/nature03260 · Cited by 2,287

Muscle Fiber Types: How Many and What Kind?

Brooke, M. H., & Kaiser, K. K. (1970) · Archives of Neurology · doi:10.1001/archneur.1970.00480280083010 · Cited by 2,179

What is the cause of the ageing atrophy?

Lexell, J. E., Taylor, C. C., & Sjöstróm, M. (1988) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(88)90132-3 · Cited by 2,080

Myogenic satellite cells: physiology to molecular biology

Hawke, T. J., & Garry, D. J. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.2.534 · Cited by 1,646

High-Intensity Strength Training in Nonagenarians: Effects on Skeletal Muscle

Fiatarone, M. A. (1990) · JAMA · doi:10.1001/jama.1990.03440220053029 · Cited by 1,593

Human aging, muscle mass, and fiber type composition.

Evans, W. J., & Lexell, J. (1995) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/50a.special_issue.11 · Cited by 1,308

Percutaneous Needle Biopsy of Skeletal Muscle in Physiological and Clinical Research

Bergström, J. P. (1975) · Scandinavian Journal of Clinical and Laboratory Investigation · doi:10.3109/00365517509095787 · Cited by 1,173

Proliferation of Human Primary Myoblasts Is Associated with Altered Energy Metabolism in Dependence on Ageing In Vivo and In Vitro

Pääsuke, R., Eimre, M., Piirsoo, A., Peet, N., Liidia, L., Kadaja, L., Roosimaa, M., Pääsuke, M., Märtson, A., Seppet, E. K., et al. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/8296150 · Cited by 42

Preserved stem cell content and innervation profile of elderly human skeletal muscle with lifelong recreational exercise

Soendenbroe, C., Dahl, C. L., Meulengracht, C., Tamáš, M., Svensson, R. B., Schjerling, P., Kjaer, M., Andersen, J. L., & Mackey, A. L. (2022) · The Journal of Physiology · doi:10.1113/jp282677 · Cited by 36

Effect of Different Frequencies of Creatine Supplementation on Muscle Size and Strength in Young Adults

Candow, D. G., Chilibeck, P. D., Burke, D. G., Mueller, K. D., & Lewis, J. D. (2011) · The Journal of Strength and Conditioning Research · doi:10.1519/jsc.0b013e3181e7419a · Cited by 36

Effect of age on the processing and import of matrix-destined mitochondrial proteins in skeletal muscle

Huang, J. H., Joseph, A.-M., Ljubicic, V., Iqbal, S., & Hood, D. A. (2010) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glp201 · Cited by 35

Sera from young and older humans equally sustain proliferation and differentiation of human myoblasts

George, T., Velloso, C. P., Alsharidah, M. S., Lazarus, N. R., & Harridge, S. D. R. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.07.006 · Cited by 35

The role of DNA ‐ PK in aging and energy metabolism

Chung, J. H. (2018) · FEBS Journal · doi:10.1111/febs.14410 · Cited by 34

Impaired Function and Altered Morphology in the Skeletal Muscles of Adult Men and Women With Type 1 Diabetes

Dial, A. G., Monaco, C. M. F., Grafham, G. K., Patel, T. P., Tarnopolsky, M. A., & Hawke, T. J. (2021) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgab261 · Cited by 37

Protein Availability and Satellite Cell Dynamics in Skeletal Muscle

Shamim, B., Hawley, J. A., & CAMERA, D. M. (2018) · Sports Medicine · doi:10.1007/s40279-018-0883-7 · Cited by 42

Cellular and Physiological Effects of Dietary Supplementation with β-Hydroxy-β-Methylbutyrate (HMB) and β-Alanine in Late Middle-Aged Mice

Vallejo, J. A., Spence, M., Cheng, A., Brotto, L. S., Edens, N. K., Garvey, S. M., & Brotto, M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0150066 · Cited by 34

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 34

Acute extracellular matrix, inflammatory and MAPK response to lengthening contractions in elderly human skeletal muscle

Sorensen, J. R., Skousen, C., Holland, A., Williams, K., & Hyldahl, R. D. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.02.013 · Cited by 34

Age‐related changes to the satellite cell niche are associated with reduced activation following exercise

Nederveen, J. P., Joanisse, S., Thomas, A. C. Q., Snijders, T., Manta, K., Bell, K. E., Phillips, S. M., Kumbhare, D. A., & Parise, G. (2020) · The FASEB Journal · doi:10.1096/fj.201900787r · Cited by 35

Premature senescence in primary muscle cultures of myotonic dystrophy type 2 is not associated with p16 induction

Renna, L. V., Cardani, R., Botta, A., Rossi, G., Fossati, B., Costa, E., & Meola, G. (2014) · European Journal of Histochemistry · doi:10.4081/ejh.2014.2444 · Cited by 34

Micro(RNA)-managing muscle wasting

Sannicandro, A. J., Soriano‐Arroquia, A., & Goljanek‐Whysall, K. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00961.2018 · Cited by 32

Sod2 overexpression preserves myoblast mitochondrial mass and function, but not muscle mass with aging

Lee, S., Remmen, H. V., & CSETE, M. E. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00477.x · Cited by 33

Fibre type‐specific satellite cell content in two models of muscle disease

Bankolé, L.-C., Féasson, L., Ponsot, E., & Kadi, F. (2013) · Histopathology · doi:10.1111/his.12231 · Cited by 33

The Function of Metformin in Aging-Related Musculoskeletal Disorders

Song, Y., Wu, Z., & Zhao, P. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.865524 · Cited by 32

Sarcopenia and piscines: the case for indeterminate-growing fish as unique genetic model organisms in aging and longevity research

Froehlich, J. M., Fowler, Z. G., Galt, N. J., Smith, D. L., & Biga, P. R. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00159 · Cited by 33

Absence of an aging‐related increase in fiber type grouping in athletes and non‐athletes

Messa, G. A. M., Piasecki, M., Rittweger, J., McPhee, J. S., Koltai, E., Radak, Z. O., Šimunič, B., Heinonen, A. O., Suominen, H., Korhonen, M. T., et al. (2020) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/sms.13778 · Cited by 32

Rotator Cuff Health, Pathology, and Repair in the Perspective of Hyperlipidemia

Yazdani, A. N., Rai, V., & Agrawal, D. K. (2022) · Journal of Orthopaedics and Sports Medicine · doi:10.26502/josm.511500063 · Cited by 31

Chapter 2 Calcineurin Signaling and the Slow Oxidative Skeletal Muscle Fiber Type

Mallinson, J. E., Meissner, J., & Chang, K. (2009) · International review of cytology · doi:10.1016/s1937-6448(09)77002-9 · Cited by 32

Cultured myoblasts from patients affected by myotonic dystrophy type 2 exhibit senescence-related features: ultrastructural evidence

Malatesta, M., Giagnacovo, M., Renna, L. V., Cardani, R., Meola, G., & Pellicciari, C. (2011) · European Journal of Histochemistry · doi:10.4081/ejh.2011.e26 · Cited by 31

Hallmarks of frailty and osteosarcopenia in prematurely aged PolgA (D257A/D257A) mice

Scheuren, A. C., D’Hulst, G., Kuhn, G. A., Masschelein, E., Wehrle, E., Bock, K. D., & Müller, R. (2020) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12588 · Cited by 28

Matters of fiber size and myonuclear domain: Does size matter more than age?

Karlsen, A., Couppé, C., Andersen, J. L., Mikkelsen, U. R., Nielsen, R. H., Magnusson, S. P., Kjær, M., & Mackey, A. L. (2015) · Muscle & Nerve · doi:10.1002/mus.24669 · Cited by 30

β-Hydroxy-β-Methylbutyrate Did Not Enhance High Intensity Resistance Training-Induced Improvements in Myofiber Dimensions and Myogenic Capacity in Aged Female Rats

Kim, J., Park, Y., Lee, S.-R., Masad, I. S., Khamoui, A. V., Jo, E., Park, B., Arjmandi, B. H., Panton, L. B., Lee, W. J., et al. (2012) · Molecules and Cells · doi:10.1007/s10059-012-0196-x · Cited by 30

Emerging role of MyomiRs as biomarkers and therapeutic targets in skeletal muscle diseases

Srivastava, S., Rathor, R., Singh, S. N., & Suryakumar, G. (2021) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00057.2021 · Cited by 31

[Benefits of strength training for the prevention and treatment of sarcopenia].

Colón, C. J. P., Collado, P. S., & Cuevas, M. J. (2014) · PubMed · doi:10.3305/nh.2014.29.5.7313 · Cited by 46

Nuclei of aged myofibres undergo structural and functional changes suggesting impairment in RNA processing

Malatesta, M., Perdoni, F., Muller, S., Zancanaro, C., & Pellicciari, C. (2009) · European Journal of Histochemistry · doi:10.4081/ejh.2009.106 · Cited by 28

The satellite cell in skeletal muscle: A story of heterogeneity

Guilhot, C., Catenacci, M., Lofaro, S., & Rudnicki, M. A. (2024) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2024.01.018 · Cited by 27

Hypovitaminosis D and frailty: Epiphenomenon or causal?

Wong, Y. Y., & Flicker, L. A. (2015) · Maturitas · doi:10.1016/j.maturitas.2015.07.027 · Cited by 27

Impacto del ejercicio físico en variables relacionadas con el bienestar emocional y funcional en adultos mayores

Darraz, S. B., González‐Roldán, A. M., Arrebola, J. D. M., & Montoro, C. I. (2021) · Revista Española de Geriatría y Gerontología · doi:10.1016/j.regg.2021.01.006 · Cited by 43

The Aging Athlete: Paradigm of Healthy Aging

Gries, K. J., & Trappe, S. W. (2022) · International Journal of Sports Medicine · doi:10.1055/a-1761-8481 · Cited by 33

Plantaris muscle weakness in old mice: relative contributions of changes in specific force, muscle mass, myofiber cross-sectional area, and number

Ballak, S. B., Degens, H., Busé-Pot, T., HAAN, A. D., & Jaspers, R. T. (2014) · AGE · doi:10.1007/s11357-014-9726-0 · Cited by 27

Pre-mRNA Processing Is Partially Impaired in Satellite Cell Nuclei from Aged Muscles

Malatesta, M., Perdoni, F., Muller, S., Pellicciari, C., & Zancanaro, C. (2010) · BioMed Research International · doi:10.1155/2010/410405 · Cited by 27

The Combination of Physical Exercise with Muscle‐Directed Antioxidants to Counteract Sarcopenia: A Biomedical Rationale for Pleiotropic Treatment with Creatine and Coenzyme Q10

Guescini, M., Tiano, L., Genova, M. L., Polidori, E., Silvestri, S., Orlando, P., Fimognari, C., Calcabrini, C., Stocchi, V., & Sestili, P. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/7083049 · Cited by 32

From molecular to physical function: The aging trajectory

Janssen, T., Lowisz, C. V., & Phillips, S. M. (2024) · Current Research in Physiology · doi:10.1016/j.crphys.2024.100138 · Cited by 31

MuRF-1 and Atrogin-1 Protein Expression and Quadriceps Fiber Size and Muscle Mass in Stable Patients with COPD

Natanek, S. A., Riddoch-Contreras, J., Marsh, G. S., Hopkinson, N. S., Moxham, J., Man, W. D.-C., Kemp, P. R., & Polkey, M. I. (2013) · COPD: Journal of Chronic Obstructive Pulmonary Disease · doi:10.3109/15412555.2013.781577 · Cited by 32

Increased CaVβ1a expression with aging contributes to skeletal muscle weakness

Taylor, J. R., Zheng, Z., Wang, Z., Payne, A. M., Messi, M. L., & Delbono, O. (2009) · Aging Cell · doi:10.1111/j.1474-9726.2009.00507.x · Cited by 25

Current Status of Sarcopenia in Korea: A Focus on Korean Geripausal Women

Park, H. M. (2018) · Annals of Geriatric Medicine and Research · doi:10.4235/agmr.2018.22.2.52 · Cited by 25

Low‐Grade Systemic Inflammation Interferes with Anabolic and Catabolic Characteristics of the Aged Human Skeletal Muscle

Draganidis, D., Jamurtas, A. Z., Chondrogianni, N., Mastorakos, G. P., Jung, T., Grune, T., Papadopoulos, C., Παπανικολάου, Κ., Papassotiriou, I., Papaevgeniou, N., et al. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/8376915 · Cited by 30

Does an NSAID a day keep satellite cells at bay?

Mackey, A. L. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00044.2013 · Cited by 25

Developmental specificity in skeletal muscle of late-term avian embryos and its potential manipulation

Chen, W., Lv, Y. T., Zhang, H. X., Ruan, D., Wang, S., & Lin, Y. C. (2013) · Poultry Science · doi:10.3382/ps.2013-03099 · Cited by 27

Steep Increase in Myonuclear Domain Size During Infancy

Delhaas, T., van der Meer, S. F. T., Schaart, G., Degens, H., & Drost, M. R. (2012) · The Anatomical Record · doi:10.1002/ar.22631 · Cited by 25

Preparation and Culture of Myogenic Precursor Cells/Primary Myoblasts from Skeletal Muscle of Adult and Aged Humans

Soriano‐Arroquia, A., Clegg, P., Molloy, A., & Goljanek‐Whysall, K. (2017) · Journal of Visualized Experiments · doi:10.3791/55047 · Cited by 26

Muscle mass, muscle morphology and bone health among community-dwelling older men: Findings from the Hertfordshire Sarcopenia Study (HSS)

Patel, H. P., Dawson, A., Westbury, L. D., Hasnaoui, G., Syddall, H. E., Shaw, S., Sayer, A. A., Cooper, C., & Dennison, E. M. (2018) · Calcified Tissue International · doi:10.1007/s00223-018-0388-2 · Cited by 24

Hypoxic preconditioning-engineered bone marrow mesenchymal stem cell-derived exosomes promote muscle satellite cell activation and skeletal muscle regeneration via the miR-210-3p/KLF7 mechanism

Guo, R., Wu, Z., Liu, A., Li, Q., Han, T., & Shen, C. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113143 · Cited by 24

Aging in Rats Differentially Affects Markers of Transcriptional and Translational Capacity in Soleus and Plantaris Muscle

Mobley, C. B., Mumford, P. W., Kephart, W. C., Haun, C. T., Holland, A. M., Beck, D. T., Martin, J. S., Young, K. C., Anderson, R. G., Patel, R. K., et al. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00518 · Cited by 24

Isokinetic Dynamometry in Healthy Versus Sarcopenic and Malnourished Elderly: Beyond Simple Measurements of Muscle Strength

Cramer, J. T., Jenkins, N. D. M., Mustad, V. A., & Weir, J. P. (2015) · Journal of Applied Gerontology · doi:10.1177/0733464815584669 · Cited by 24

Biomarkers of sarcopenia: an unmet need

Sebaie, M. A. E., & Elwakil, W. (2023) · Egyptian Rheumatology and Rehabilitation · doi:10.1186/s43166-023-00213-w · Cited by 25

Estradiol deficiency reduces the satellite cell pool by impairing cell cycle progression

Larson, A. A., Shams, A. S., McMillin, S. L., Sullivan, B. P., Vue, C., Roloff, Z. A., Batchelor, E., Kyba, M., & Lowe, D. A. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00429.2021 · Cited by 23

Use of alfacalcidol in osteoporotic patients with low muscle mass might increase muscle mass: An investigation using a patient database

Ito, S., Harada, A., Kasai, T., Sakai, Y., Takemura, M., Matsui, Y., Hida, T., & Ishiguro, N. (2014) · Geriatrics and gerontology international/Geriatrics & gerontology international · doi:10.1111/ggi.12222 · Cited by 23

Histochemical and ultrastructural changes of sternomastoid muscle in aged wistar rats

Ciena, A. P., de Almeida, S. R. Y., Alves, P. H. D. M., Matos, R. D. S. B., Días, F. J., Issa, J. P. M., Iyomasa, M. M., & Watanabe, I. (2011) · Micron · doi:10.1016/j.micron.2011.06.003 · Cited by 23

Alterations in Skeletal Muscle Oxidative Phenotype in Mice Exposed to 3 Weeks of Normobaric Hypoxia

Slot, I. G. M., Schols, A. M. W. J., de Theije, C. C., Snepvangers, F. J. M., & Gosker, H. R. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25083 · Cited by 23

Yin Yang 1 Expression and Localisation in Quadriceps Muscle in COPD

Natanek, S. A., Riddoch‐Contreras, J., Marsh, G. S., Hopkinson, N. S., Man, W. D., Moxham, J., Polkey, M. I., & Kemp, P. R. (2011) · Archivos de Bronconeumología · doi:10.1016/j.arbr.2011.02.004 · Cited by 22

Muscle Stem Cell and Physical Activity: What Point is the Debate at?

Ceccarelli, G., Benedetti, L., Arcari, M., Carubbi, C., & Galli, D. (2017) · Open Medicine · doi:10.1515/med-2017-0022 · Cited by 12

Differing Effects of Younger and Older Human Plasma on C2C12 Myocytes in Vitro

Kalampouka, I., van Bekhoven, A., & Elliott, B. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00152 · Cited by 22

Isolation and characterization of muscle stem cells, fibro-adipogenic progenitors, and macrophages from human skeletal muscle biopsies

Jensen, J., Møller, A. B., Just, J., Mose, M., de Paoli, F. V., Billeskov, T. B., Fred, R. G., Pers, T. H., Pedersen, S. B., Petersen, K. K., et al. (2021) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00127.2021 · Cited by 21

Musclin Is Related to Insulin Resistance and Body Composition, but Not to Body Mass Index or Cardiorespiratory Capacity in Adults

Sánchez, Y. L., Yepes-Calderón, M., Valbuena, L. H., Milán, A. F., Almanza, M. C. T., Granados, S., Peña, M., Estrada-Castrillón, M., Aristizábal, J. C., Narvez-Sanchez, R., et al. (2021) · Endocrinology and Metabolism · doi:10.3803/enm.2021.1104 · Cited by 21

The non-modifiable factors age, gender, and genetics influence resistance exercise

Viecelli, C., & Ewald, C. Y. (2022) · Frontiers in Aging · doi:10.3389/fragi.2022.1005848 · Cited by 26

The importance of serial sarcomere addition for muscle function and the impact of aging

Hinks, A., Hawke, T. J., Franchi, M. V., & Power, G. A. (2023) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00205.2023 · Cited by 21

Satellite cell count, VO 2max, and p 38 MAPK in inactive to moderately active young men

Macaluso, F., Brooks, N. E., van de Vyver, M., van Tubbergh, K., Niesler, C. U., & Myburgh, K. H. (2011) · Scandinavian Journal of Medicine and Science in Sports · doi:10.1111/j.1600-0838.2011.01389.x · Cited by 21

Satellite cell function, intramuscular inflammation and exercise in chronic kidney disease

O’Sullivan, T. F., Smith, A. C., & Watson, E. L. (2018) · Clinical Kidney Journal · doi:10.1093/ckj/sfy052 · Cited by 22

Resistance exercise: a mighty tool that adapts, destroys, rebuilds and modulates the molecular and structural environment of skeletal muscle

Bersiner, K., Park, S., Schaaf, K., Yang, W., Theis, C., Jacko, D., & Gehlert, S. (2023) · Physical Activity and Nutrition · doi:10.20463/pan.2023.0021 · Cited by 20

Resistance Training as Treatment for Sarcopenia: Examining Sex-Related Differences in Physiology and Response

Cheng, R., Maloney, A., Moran, J. T., Newman, T. H., & Gardner, E. C. (2021) · Clinical Therapeutics · doi:10.1016/j.clinthera.2021.11.012 · Cited by 23

Molecular and Structural Alterations of Skeletal Muscle Tissue Nuclei during Aging

Cisterna, B., & Malatesta, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031833 · Cited by 27

Moving human muscle physiology research forward: an evaluation of fiber type-specific protein research methodologies

Tobias, I. S., & Galpin, A. J. (2020) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00107.2020 · Cited by 21

Prioritizing movement to address the frailty phenotype in heart failure

Laddu, D., Ozemek, C., Sabbahi, A., Severin, R. S., Phillips, S. A., & Arena, R. A. (2021) · Progress in Cardiovascular Diseases · doi:10.1016/j.pcad.2021.01.005 · Cited by 20

Microbiopsy Sampling for Examining Age-Related Differences in Skeletal Muscle Fiber Morphology and Composition

Hester, G. M., VanDusseldorp, T. A., Ha, P. L., Kiani, K., Olmos, A. A., Jabbari, M., Kalladanthyil, S., An, S., Bailly, A. R., Dalton, B. E., et al. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2021.756626 · Cited by 19

Shared and Divergent Epigenetic Mechanisms in Cachexia and Sarcopenia

Yedigaryan, L., Gatti, M., Marini, V., Maraldi, T., & Sampaolesi, M. (2022) · Cells · doi:10.3390/cells11152293 · Cited by 19

Cucurbitacin IIb attenuates cancer cachexia induced skeletal muscle atrophy by regulating the IL ‐6/ STAT3 / FoxO signaling pathway

Wang, Y., Sun, X., Yang, Q., & Guo, C. (2023) · Phytotherapy Research · doi:10.1002/ptr.7811 · Cited by 19

Expresión y localización del factor de transcripción Yin Yang 1 en el músculo cuádriceps en la enfermedad pulmonar obstructiva crónica

Natanek, S. A., Riddoch‐Contreras, J., Marsh, G. S., Hopkinson, N. S., Man, W. D., Moxham, J., Polkey, M. I., & Kemp, P. R. (2011) · Archivos de Bronconeumología · doi:10.1016/j.arbres.2011.02.015 · Cited by 19

Structural and functional alterations of the cell nucleus in skeletal muscle wasting: the evidence in situ

Malatesta, M., & Meola, G. (2010) · European Journal of Histochemistry · doi:10.4081/ejh.2010.e44 · Cited by 19

Comparison of the influence of age on cycling efficiency and the energy cost of running in well-trained triathletes

Peiffer, J. J., Abbiss, C. R., Sultana, F., Bernard, T., & Brisswalter, J. (2015) · European Journal of Applied Physiology · doi:10.1007/s00421-015-3264-z · Cited by 20

Myotendinous junction plasticity in aged ovariectomized rats submitted to aquatic training

Sierra, L. R., Fávaro, G., Cerri, B. R., Rocha, L. C., de Almeida, S. R. Y., Watanabe, I., & Ciena, A. P. (2018) · Microscopy Research and Technique · doi:10.1002/jemt.23040 · Cited by 19

The Crossroads of Aging: An Intersection of Malnutrition, Frailty, and Sarcopenia

Severin, R., Berner, P. M., Miller, K. L., & Mey, J. (2019) · Topics in Geriatric Rehabilitation · doi:10.1097/tgr.0000000000000218 · Cited by 19

Consistent expression pattern of myogenic regulatory factors in whole muscle and isolated human muscle satellite cells after eccentric contractions in humans

Nederveen, J. P., Fortino, S. A., Baker, J. M., Snijders, T., Joanisse, S., McGlory, C., McKay, B. R., Kumbhare, D. A., & Parise, G. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01123.2018 · Cited by 21

Satellite cell activation and number following acute and chronic exercise: A mini review

Martin, N. R., & Lewis, M. P. (2012) · Cellular and Molecular Exercise Physiology · doi:10.7457/cmep.v1i1.e3 · Cited by 20

Quantifying the Effects of Aging on Morphological and Cellular Properties of Human Female Pelvic Floor Muscles

Rieger, M. M., Duran, P., Cook, M. S., Schenk, S., Shah, M. M., Jacobs, M. B., Christman, K. L., Kado, D. M., & Alperin, M. (2021) · Annals of Biomedical Engineering · doi:10.1007/s10439-021-02748-5 · Cited by 18

Muscle characteristics in patients with chronic systemic inflammation

Beenakker, K. G. M., Duijnisveld, B. J., van der Linden, H. M. J., Visser, C. P. J., Westendorp, R. G. J., Butler-Browne, G. S., Nelissen, R. G. H. H., & Maier, A. B. (2012) · Muscle & Nerve · doi:10.1002/mus.23291 · Cited by 18

Unlocking diagnosis of sarcopenia: The role of circulating biomarkers – A clinical systematic review

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