Muscle transplantation between young and old rats: age of host determines recovery

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

Skeletal muscle satellite cells: Changes in proliferation potential as a function of age

Schultz, E., & Lipton, B. H. (1982) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(82)90105-1 · Cited by 335

Age‐related differences in absolute numbers of skeletal muscle satellite cells

Gibson, M. C., & Schultz, E. (1983) · Muscle & Nerve · doi:10.1002/mus.880060807 · Cited by 327

Myogenic cell formation in regenerating rat skeletal muscle injured by mincing II. An autoradiographic study

Snow, M. H. (1977) · The Anatomical Record · doi:10.1002/ar.1091880206 · Cited by 223

The effects of aging on satellite cells in skeletal muscles of mice and rats

Snow, M. H. (1977) · Cell and Tissue Research · doi:10.1007/bf00220299 · Cited by 201

Effects of age on contractile and enzyme‐histochemical properties of fast‐ and slow‐twitch single motor units in the rat.

Edström, L., & Larsson, L. (1987) · The Journal of Physiology · doi:10.1113/jphysiol.1987.sp016773 · Cited by 152

Reinnervation of long-term denervated rat muscle freely grafted into an innervated limb

Carlson, B. M., & Faulkner, J. A. (1988) · Experimental Neurology · doi:10.1016/0014-4886(88)90077-5 · Cited by 83

The Influence of Age on the Course of Reinnervation of Muscle

Drahota, Z., & GUTMANN, E. (2009) · Gerontologia · doi:10.1159/000211047 · Cited by 49

A rapid silver impregnation for central and peripheral nerve fibers in paraffin and frozen sections

Goshgarian, H. G. (1977) · Experimental Neurology · doi:10.1016/0014-4886(77)90065-6 · Cited by 46

The clustering of acetylcholine receptors and formation of neuromuscular junctions in regenerating mammalian muscle grafts

Womble, M. D., & Carlson, B. M. (1986) · American Journal of Anatomy · doi:10.1002/aja.1001760208 · Cited by 26

Sources for skeletal muscle repair: from satellite cells to reprogramming

Sirabella, D., Angelis, L. D., & Berghella, L. (2013) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1007/s13539-012-0098-y · Cited by 44

Transcriptional profiling of skeletal muscle reveals factors that are necessary to maintain satellite cell integrity during ageing

Scimè, A., Desrosiers, J., Trensz, F., Palidwor, G., Caron, A. Z., Andrade-Navarro, M. A., & Grenier, G. (2009) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2009.11.001 · Cited by 40

Regulation and Function of Skeletal Muscle Stem CellsPreprint

Cerletti, M., Shadrach, J. L., Jurga, S., Sherwood, R. I., & Wagers, A. J. (2008) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2008.73.054 · Cited by 40

Pro-Insulin-Like Growth Factor-II Ameliorates Age-Related Inefficient Regenerative Response by Orchestrating Self-Reinforcement Mechanism of Muscle Regeneration

Ikemoto‐Uezumi, M., Uezumi, A., Tsuchida, K., Fukada, S., Yamamoto, H., Yamamoto, N., Shiomi, K., & Hashimoto, N. (2015) · Stem Cells · doi:10.1002/stem.2045 · Cited by 39

Satellite cells are increasingly refractory to activation by nitric oxide and stretch in aged mouse-muscle cultures

Leiter, J., & Anderson, J. E. (2009) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2009.09.021 · Cited by 38

Age-related gene expression in luminal epithelial cells is driven by a microenvironment made from myoepithelial cells

Miyano, M., Sayaman, R. W., Stoiber, M. H., Lin, C., Stampfer, M. R., Brown, J., & LaBarge, M. A. (2017) · Aging · doi:10.18632/aging.101298 · Cited by 36

Delineating the relationship between immune system aging and myogenesis in muscle repair

Tobin, S. W., Alibhai, F. J., Wlodarek, L., Yeganeh, A., Millar, S., Wu, J., Li, S., Weisel, R. D., & Li, R. (2021) · Aging Cell · doi:10.1111/acel.13312 · Cited by 40

Intrinsic and Extrinsic Factors in Muscle Aging

Cannon, J. G. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb09893.x · Cited by 42

Satellite cell therapy – from mice to men

Bareja, A., & Billin, A. N. (2013) · Skeletal Muscle · doi:10.1186/2044-5040-3-2 · Cited by 35

Modulation of overload-induced inflammation by aging and anabolic steroid administration.

Thompson, R. W., McClung, J., Baltgalvis, K. A., Davis, J. M., & Carson, J. A. (2006) · Experimental Gerontology · doi:10.1016/j.exger.2006.08.013 · Cited by 41

Muscle precursor cells isolated from aged rats exhibit an increased tumor necrosis factor‐α response

Lees, S. J., Zwetsloot, K. A., & Booth, F. W. (2008) · Aging Cell · doi:10.1111/j.1474-9726.2008.00445.x · Cited by 36

Embryonic anti-aging niche.

Conboy, I. M., Yousef, H., & Conboy, M. J. (2011) · Aging · doi:10.18632/aging.100333 · Cited by 33

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 time course of myonuclear accretion during hypertrophy in young adult and older rat plantaris muscle

van der Meer, S. F. T., Jaspers, R. T., Jones, D. A., & Degens, H. (2010) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2010.08.004 · Cited by 35

Systemic milieu and age-related deterioration

Zhang, H., Cherian, R., & Jin, K. (2019) · GeroScience · doi:10.1007/s11357-019-00075-1 · Cited by 35

An altered response in macrophage phenotype following damage in aged human skeletal muscle: implications for skeletal muscle repair

Sorensen, J. R., Kaluhiokalani, J. P., Hafen, P. S., Deyhle, M. R., Parcell, A. C., & Hyldahl, R. D. (2019) · The FASEB Journal · doi:10.1096/fj.201900519r · Cited by 37

Mechanisms of skeletal muscle ageing; avenues for therapeutic intervention

Lightfoot, A. P., McCormick, R., Nye, G. A., & McArdle, A. (2014) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2014.05.005 · Cited by 34

Programmed ageing: decline of stem cell renewal, immunosenescence, and Alzheimer's disease

Lathe, R., & Clair, D. S. (2023) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12959 · Cited by 37

MEAT SCIENCE AND MUSCLE BIOLOGY SYMPOSIUM: Stem cell niche and postnatal muscle growth1,2

Bi, P., & Kuang, S. (2011) · Journal of Animal Science · doi:10.2527/jas.2011-4594 · Cited by 34

Muscle fiber branching — difference between grafts in old and young rats

Blaivas, M., & Carlson, B. M. (1991) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(91)90108-c · Cited by 34

Rejuvenating stem cells to restore muscle regeneration in aging

Bengal, E., Perdiguero, E., Serrano, A. L., & Muñoz‐Cánoves, P. (2017) · F1000Research · doi:10.12688/f1000research.9846.1 · Cited by 30

The systemic milieu as a mediator of dietary influence on stem cell function during ageing

Murphy, T., & Thuret, S. (2014) · Ageing Research Reviews · doi:10.1016/j.arr.2014.11.004 · Cited by 34

Determinants of Skeletal Muscle Hypertrophy and the Attenuated Hypertrophic Response at Old Age

Degens, H. (2012) · Journal of Sports Medicine & Doping Studies · doi:10.4172/2161-0673.s1-003 · Cited by 33

Evolutionary Explanations of the “Actuarial Senescence in the Wild” and of the “State of Senility”

Libertini, G. (2006) · The Scientific World JOURNAL · doi:10.1100/tsw.2006.209 · Cited by 31

Tissue aging: the integration of collective and variant responses of cells to entropic forces over time

Todhunter, M. E., Sayaman, R. W., Miyano, M., & LaBarge, M. A. (2018) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2018.05.016 · Cited by 32

Dose optimization of decellularized skeletal muscle extracellular matrix hydrogels for improving perfusion and subsequent validation in an aged hindlimb ischemia model

Hernandez, M. J., Zelus, E. I., Spang, M. T., Braden, R. L., & Christman, K. L. (2020) · Biomaterials Science · doi:10.1039/c9bm01963d · Cited by 32

Facial reanimation by transplantation of a microneurovascular muscle: long-term follow-up

Ylä-Kotola, T. M., Kauhanen, M. S. C., & Asko-Seljavaara, S. L. (2004) · Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery · doi:10.1080/02844310410029138 · Cited by 32

Concise Review: Translating Regenerative Biology into Clinically Relevant Therapies: Are We on the Right Path?

Simkin, J., & Seifert, A. W. (2017) · Stem Cells Translational Medicine · doi:10.1002/sctm.17-0213 · Cited by 29

Age‐Related Muscle Loss and Progressive Dysfunction in Mechanosensitive Growth Factor Signaling

Goldspink, G. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1297.050 · Cited by 31

Aging-associated oxidative stress modulates the acute inflammatory response in skeletal muscle after contusion injury

Ghaly, A., & Marsh, D. R. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.03.004 · Cited by 30

Aging and stem cell renewal

Conboy (2008) · StemBook · doi:10.3824/stembook.1.11.1 · Cited by 32

Skeletal muscle aging – Stem cells in the spotlight

Henze, H., Jung, M. J., Ahrens, H. E., Steiner, S., & von Maltzahn, J. (2020) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2020.111283 · Cited by 30

Stem cells and tissue niche: two faces of the same coin of muscle regeneration

Scicchitano, B. M., Sica, G., & Musarò, A. (2016) · European Journal of Translational Myology · doi:10.4081/ejtm.2016.6125 · Cited by 29

Mixing old and young: enhancing rejuvenation and accelerating aging

Lau, A., Kennedy, B. K., Kirkland, J. L., & Tullius, S. G. (2019) · Journal of Clinical Investigation · doi:10.1172/jci123946 · Cited by 29

Rejuvenating effect of pregnancy on the mother

Michaeli, T. F., Bergman, Y., & Gielchinsky, Y. (2015) · Fertility and Sterility · doi:10.1016/j.fertnstert.2015.02.034 · Cited by 28

Motor Unit Properties of Nerve-Intact Extensor Digitorum Longus Muscle Grafts In Young and Old Rats

Cederna, P. S., Asato, H., Gu, X., van der Meulen, J., Kuzon, W. M., Carlson, B. M., & Faulkner, J. A. (2001) · The Journals of Gerontology Series A · doi:10.1093/gerona/56.6.b254 · Cited by 28

Quantification of muscle loss in the doxorubicin-treated orbicularis oculi of the monkey. Effect of local injection of doxorubicin into the eyelid.

McLoon, L. K., Bauer, G., & Wirtschafter, J. D. (1991) · PubMed · Cited by 28

Satellite cell activation and retention of muscle regenerative potential after long-term denervation

Wong, A., Garcia, S. M., Tamaki, S. J., Striedinger, K., Barruet, E., Hansen, S. L., Young, D. M., & Pomerantz, J. H. (2020) · Stem Cells · doi:10.1002/stem.3316 · Cited by 27

Strategic outline of interventions targeting extracellular matrix for promoting healthy longevity

Park, J. Y. C., King, A., Björk, V., English, B. W., Fedintsev, A., & Ewald, C. Y. (2023) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00060.2023 · Cited by 32

Lactate dehydrogenase regulation in aged skeletal muscle: Regulation by anabolic steroids and functional overload

Washington, T. A., Healey, J. M., Thompson, R. W., Lowe, L. L., & Carson, J. A. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.05.003 · Cited by 28

Functional deficits and insulin-like growth factor-I gene expression following tourniquet-induced injury of skeletal muscle in young and old rats

Hammers, D. W., Merritt, E., Matheny, W., Adamo, M. L., Walters, J., Estep, J. S., & Farrar, R. P. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.90418.2008 · Cited by 27

Aging: A cell source limiting factor in tissue engineering

Khorraminejad‐Shirazi, M., Dorvash, M., Estedlal, A., Hoveidaei, A. H., Mazloomrezaei, M., & Mosaddeghi, P. (2019) · World Journal of Stem Cells · doi:10.4252/wjsc.v11.i10.787 · Cited by 28

MG53 Inhibits Necroptosis Through Ubiquitination-Dependent RIPK1 Degradation for Cardiac Protection Following Ischemia/Reperfusion Injury

Wang, Q., Park, K. H., Geng, B., Chen, P., Yang, C., Jiang, Q., Yi, F., Tan, T., Zhou, X., Bian, Z., et al. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.868632 · Cited by 26

CCAAT-Enhancer-Binding Protein-Beta (CEBPB) Expression In-Vivo is Associated with Muscle Strength

Harries, L. W., Pilling, L., Hernandez, L., Bradley-Smith, R. M., Henley, W., Singleton, A., Guralnik, J., Bandinelli, S., Ferrucci, L., & Melzer, D. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2011.00782.x · Cited by 31

Human muscle stem cells are refractory to aging

Novak, J. S., Mázala, D. A. G., Nearing, M., Hindupur, R., Uapinyoying, P., Habib, N. F., Dickson, T., Ioffe, O. B., Harris, B. T., Fidelia‐Lambert, M. N., et al. (2021) · Aging Cell · doi:10.1111/acel.13411 · Cited by 24

Decline of regenerative potential of old muscle stem cells: contribution to muscle aging

Sahinyan, K., Lazure, F., Blackburn, D. M., & Soleimani, V. D. (2022) · FEBS Journal · doi:10.1111/febs.16352 · Cited by 25

Hippo pathway effectors YAP and TAZ and their association with skeletal muscle ageing

Setiawan, I., Sanjaya, A., Lesmana, R., Yen, P. M., & Goenawan, H. (2021) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-021-00787-z · Cited by 25

Macrophage immunomodulation accelerates skeletal muscle functional recovery in aged mice following disuse atrophy

Ferrara, P. J., Yee, E. M., Petrocelli, J. J., Fix, D. K., Hauser, C. T., de Hart, N. M. M. P., Mahmassani, Z. S., Reidy, P. T., O’Connell, R. M., & Drummond, M. J. (2022) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00374.2022 · Cited by 23

Extrinsic Regulation of Satellite Cell Function and Muscle Regeneration Capacity during Aging

Chakkalakal, J. V. (2012) · Journal of Stem Cell Research & Therapy · doi:10.4172/2157-7633.s11-001 · Cited by 26

Mcad-mediated intercellular interactions activate satellite cell division

Martí, M., Montserrat, N., Pardo, C., Mulero, L., Miquel‐Serra, L., Rodrigues, A. M. C., Vaquero, J. A., Kuebler, B., Morera, C., Barrero, M. J., et al. (2013) · Journal of Cell Science · doi:10.1242/jcs.123562 · Cited by 23

Elderly mouse skeletal muscle fibres have a diminished capacity to upregulate NCAM production in response to denervation

Gillon, A., & Sheard, P. W. (2015) · Biogerontology · doi:10.1007/s10522-015-9608-6 · Cited by 21

Myeloid Cell Responses to Contraction-induced Injury Differ in Muscles of Young and Old Mice

Sloboda, D. D., Brown, L. A., & Brooks, S. V. (2018) · The Journals of Gerontology Series A · doi:10.1093/gerona/gly086 · Cited by 22

Physical Activity in the Elderly

Harridge, S. D. R., & Suominen, H. (2003) · doi:10.1002/9780470757277.ch16 · Cited by 22

Brain Aging and Regeneration after Injuries: an Organismal approach.

Buga, A.-M., Vintilescu, R., Pop, O. T., & Popa‐Wagner, A. (2011) · Europe PMC (PubMed Central) · Cited by 19

“Known Unknowns”: Current Questions in Muscle Satellite Cell Biology

Cornelison, D. (2017) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2017.08.006 · Cited by 20

Impairment of IGF-I expression and anabolic signaling following ischemia/reperfusion in skeletal muscle of old mice

Hammers, D. W., Matheny, R. W., Sell, C., Adamo, M. L., Walters, J., Estep, J. S., & Farrar, R. P. (2010) · Experimental Gerontology · doi:10.1016/j.exger.2010.11.002 · Cited by 21

Gene therapy for cardiac cachexia?

Rosenthal, N. A., & Musarò, A. (2002) · International Journal of Cardiology · doi:10.1016/s0167-5273(02)00253-x · Cited by 20

Pax7+ Satellite Cells in Human Skeletal Muscle After Exercise: A Systematic Review and Meta-analysis

Dewi, L., Lin, Y., Nicholls, A., Condello, G., Huang, C., & Kuo, C. (2022) · Sports Medicine · doi:10.1007/s40279-022-01767-z · Cited by 21

Skeletal Muscle Stem Cells in the Spotlight: The Satellite Cell

Yablonka‐Reuveni, Z., & Day, K. R. (2011) · Humana Press eBooks · doi:10.1007/978-1-61779-021-8_11 · Cited by 19

Skeletal Muscle Stem Cells

LaBarge, M. A., & Blau, H. M. (2004) · Elsevier eBooks · doi:10.1016/b978-012436643-5/50127-9 · Cited by 19

Regeneration and Repair

Friedman, R. S., & Krause, D. S. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04411.x · Cited by 18

Age-Dependent Changes Cooperatively Impact Skeletal Muscle Regeneration after Compartment Syndrome Injury

Zhou, Y., Lovell, D., Bethea, M. M., Wang, Z., Christ, G. J., Söker, S., & Criswell, T. L. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.03.018 · Cited by 18

Absence of CCR2 results in an inflammaging environment in young mice with age-independent impairments in muscle regeneration

Melton, D. W., Roberts, A. C., Wang, H., Sarwar, Z. U., Wetzel, M. D., Wells, J. T., Porter, L., Berton, M. T., McManus, L. M., & Shireman, P. K. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.3ma0316-104r · Cited by 19

Studies that shed new light on aging

Katcher, H. L. (2013) · Biochemistry (Moscow) · doi:10.1134/s0006297913090137 · Cited by 17

The lymphocyte secretome from young adults enhances skeletal muscle proliferation and migration, but effects are attenuated in the secretome of older adults

Al-Dabbagh, S., McPhee, J., Murgatroyd, C., Butler-Browne, G., Stewart, C., & Al-Shanti, N. (2015) · Physiological Reports · doi:10.14814/phy2.12518 · Cited by 15

Human primary skeletal muscle‐derived myoblasts and fibroblasts reveal different senescent phenotypes

Francis, T., Jaka, O., Ellison, G. M., Lazarus, N. R., & Harridge, S. D. R. (2022) · JCSM Rapid Communications · doi:10.1002/rco2.67 · Cited by 13

Preventing aging with stem cell rejuvenation: Feasible or infeasible?

Honoki, K. (2017) · World Journal of Stem Cells · doi:10.4252/wjsc.v9.i1.1 · Cited by 16

Insights into Skeletal Muscle Development and Applications in Regenerative Medicine

Tran, T., Andersen, R., Sherman, S. P., & Pyle, A. D. (2012) · International review of cytology · doi:10.1016/b978-0-12-405210-9.00002-3 · Cited by 18

Recovery of slow skeletal muscle after injury in the senescent rat

Vignaud, A. (2003) · Experimental Gerontology · doi:10.1016/s0531-5565(03)00007-x · Cited by 16

Gene transcripts associated with muscle strength: a CHARGE meta-analysis of 7,781 persons

Pilling, L. C., Joehanes, R., Kacprowski, T., Peters, M. J., Jansen, R., Karasik, D., Kiel, D. P., Harries, L. W., Teumer, A., Powell, J. E., et al. (2016) · Physiological Genomics · doi:10.1152/physiolgenomics.00054.2015 · Cited by 14

‘From Death, Lead Me to Immortality’ – Mantra of Ageing Skeletal Muscle

Saini, A. S., Mastana, S. S., Myers, F. A., & Lewis, M. P. (2013) · Current Genomics · doi:10.2174/1389202911314040004 · Cited by 14

Muscle satellite cells from GRMD dystrophic dogs are not phenotypically distinguishable from wild type satellite cells in ex vivo culture

Berg, Z., Beffa, L. R., Cook, D. P., & Cornelison, D. (2011) · Neuromuscular Disorders · doi:10.1016/j.nmd.2010.12.009 · Cited by 14

Increased Adipocyte Area in Injured Muscle With Aging and Impaired Remodeling in Female Mice

Fearing, C. M., Melton, D. W., Lei, X., Hancock, H. M., Wang, H., Sarwar, Z. U., Porter, L., McHale, M. J., McManus, L. M., & Shireman, P. K. (2015) · The Journals of Gerontology Series A · doi:10.1093/gerona/glv104 · Cited by 14

Muscle Regeneration in Animal Models

Carlson, B. M. (2008) · Springer eBooks · doi:10.1007/978-1-4020-6768-6_8 · Cited by 14

Capillary facilitation of skeletal muscle function in health and disease

Parise, G., Murrant, C. L., Cocks, M. S., Snijders, T., Baum, O., & Plyley, M. J. (2019) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2019-0416 · Cited by 14

The onset and duration of mobilization affect the regeneration in the rat muscle.

Faria, F. E. T., Ferrari, R., Distéfano, G., Ducatti, A. C., Soares, K. F. D. S., Montebelo, M. I. L., & Minamoto, V. B. (2008) · PubMed · doi:10.14670/hh-23.565 · Cited by 13

Can thrombin‐activated platelet releasate compensate the age‐induced decrease in cell proliferation of MSC?

Vogl, M., Fischer, J., Jäger, M., Zilkens, C., Krauspe, R., & Herten, M. (2013) · Journal of Orthopaedic Research® · doi:10.1002/jor.22433 · Cited by 13

Muscle Development and Regeneration in Normal and Pathological Conditions: Learning from Drosophila

Daczewska, M., Picchio, L., Jagla, T., Figeac, N., & Jagla, K. (2010) · Current Pharmaceutical Design · doi:10.2174/138161210790883462 · Cited by 12

Ovarian stem cells and aging

Hosni, W., & Baştu, E. (2011) · Climacteric · doi:10.3109/13697137.2011.636848 · Cited by 13

GDF11 and aging biology - controversies resolved and pending

Driss, L. B., Lian, J., Walker, R. G., Howard, J. A., Thompson, T. B., Rubin, L. L., Wagers, A. J., & Lee, R. T. (2023) · The Journal of Cardiovascular Aging · doi:10.20517/jca.2023.23 · Cited by 13

Effect of Age and Neurovascular Grafting on the Mechanical Function of Medial Gastrocnemius Muscles of Fischer 344 Rats

Larkin, L. M., Kuzon, W. M., Supiano, M. A., Galecki, A., & Halter, J. B. (1998) · The Journals of Gerontology Series A · doi:10.1093/gerona/53a.4.b252 · Cited by 12

Developmental Biology and Regenerative Medicine: Addressing the Vexing Problem of Persistent Muscle Atrophy in the Chronically Torn Human Rotator Cuff

Meyer, G. A., & Ward, S. R. (2016) · Physical Therapy · doi:10.2522/ptj.20150029 · Cited by 13

Phytoecdysteroids Accelerate Recovery of Skeletal Muscle Function Following in vivo Eccentric Contraction-Induced Injury in Adult and Old Mice

Zwetsloot, K. A., Shanely, R. A., Godwin, J. S., & Hodgman, C. F. (2021) · Frontiers in Rehabilitation Sciences · doi:10.3389/fresc.2021.757789 · Cited by 11

Embryonic stem cell microenvironment enhances proliferation of human retinal pigment epithelium cells by activating the PI3K signaling pathway

Liu, J., Yang, L., Wang, X., Wang, S., Huang, Z., Li, C., Liu, Y., Cheng, Y., Liu, C., & Wang, Z. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-01923-0 · Cited by 11

Host pre‐conditioning improves human adipose–derived stem cell transplantation in ageing rats after myocardial infarction: Role of NLRP3 inflammasome

Lee, T., Harn, H., Chiou, T., Chuang, M., Chen, C., Chuang, C., Lin, P., & Lin, S. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15403 · Cited by 11

The effects of age upon the expression of three miRNAs in muscle stem cells isolated from two different porcine skeletal muscles

Redshaw, Z., Sweetman, D., & Loughna, P. T. (2014) · Differentiation · doi:10.1016/j.diff.2014.12.001 · Cited by 10

Regenerative rehabilitation: a novel multidisciplinary field to maximize patient outcomes

Deng, C., Aldali, F., Luo, H., & Chen, H. (2024) · Medical Review · doi:10.1515/mr-2023-0060 · Cited by 11

Age-associated functional healing of musculoskeletal trauma through regenerative engineering and rehabilitation

Habing, K. M., Alcazar, C. A., Duke, V. R., Tan, Y. H., Willett, N. J., & Nakayama, K. H. (2024) · Biomaterials Science · doi:10.1039/d4bm00616j · Cited by 10

The Satellite Cell Niche in Skeletal Muscle

Brun, C. E., Chevalier, F. P., Dumont, N. A., & Rudnicki, M. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802734-9.00010-x · Cited by 11

Regenerative Medicine

Stocum, D. L. (2006) · Elsevier eBooks · doi:10.1016/b978-012369371-6/50030-7 · Cited by 10

Age‐related nitration/dysfunction of myogenic stem cell activator HGF

Elgaabari, A., Imatomi, N., Kido, H., Nakashima, T., Okuda, S., Manabe, Y., Sawano, S., Mizunoya, W., Kaneko, R., Tanaka, S., et al. (2023) · Aging Cell · doi:10.1111/acel.14041 · Cited by 10

Evaluation of skeletal muscle regeneration in experimental model after malnutrition.

Pertille, A., Moura, K., Matsumura, C. Y., Ferretti, R., Ramos, D. M., Petrini, A. C., Oliveira, P., & Silva, C. A. (2017) · Brazilian journal of biology = Revista brasleira de biologia · doi:10.1590/1519-6984.10415 · Cited by 6

The Critical Role of Insulin-Like Growth Factor-1 Isoforms in the Physiopathology of Skeletal Muscle

Musarò, A., & Rosenthal, N. A. (2006) · Current Genomics · doi:10.2174/138920206776389784 · Cited by 10

Skeletal muscle cell aging and stem cells

Rafi, S. T. M., Sambandam, Y., Sittadjody, S., Pathak, S., Ramachandran, I., & Kumaran, R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820071-1.00009-8 · Cited by 9

Short-term metformin ingestion by healthy older adults improves myoblast function

Mahmassani, Z. S., McKenzie, A. I., Petrocelli, J. J., de Hart, N. M. M. P., Reidy, P. T., Fix, D. K., Ferrara, P. J., Funai, K., & Drummond, M. J. (2021) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00469.2020 · Cited by 10

The Impact of Age on Skeletal Muscle Progenitor Cell Survival and Fate After Injury

Zhou, Y., Lovell, D., Bethea, M. M., Yoseph, B. P., Poteracki, J. M., Söker, S., & Criswell, T. L. (2017) · Tissue Engineering Part C Methods · doi:10.1089/ten.tec.2017.0216 · Cited by 9

Aging Effects in Skeletal Muscle Recovery After Reinnervation

Choi, S.-J., Harii, K., Asato, H., & Ueda, K. (1996) · Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery · doi:10.3109/02844319609056389 · Cited by 9

Reduced expression of calcitonin receptor is closely associated with age‐related loss of the muscle stem cell pool

Ikemoto‐Uezumi, M., Uezumi, A., Zhang, L., Zhou, H., Hashimoto, N., Okamura, K., Matsui, Y., Tsukazaki, K., Hosoyama, T., Nakatani, M., et al. (2019) · JCSM Rapid Communications · doi:10.1002/j.2617-1619.2019.tb00012.x · Cited by 8

Long-term adaptation of human microneurovascular muscle flaps to the paralyzed face: An immunohistochemical study

Kauhanen, S., Ylä-Kotola, T. M., Leivo, I. V. V., Tukiainen, E. J., & Asko-Seljavaara, S. L. (2006) · Microsurgery · doi:10.1002/micr.20288 · Cited by 8

Biological Basis of Exercise‐Based Treatments for Musculoskeletal Conditions

Ambrosio, F., Tarabishy, A., Kadi, F., Brown, E. H. P., & Sowa, G. (2011) · PM&R · doi:10.1016/j.pmrj.2011.05.001 · Cited by 8

Skeletal Muscle Regeneration in Very Old Rats

Carlson, B. M., Dedkov, E. I., Borisov, A. B., & Faulkner, J. A. (2001) · The Journals of Gerontology Series A · doi:10.1093/gerona/56.5.b224 · Cited by 119

Regeneration and transplantation of muscles in old rats and between young and old rats

Gutmann, E., & Carlson, B. M. (1976) · Life Sciences · doi:10.1016/0024-3205(76)90280-0 · Cited by 55

The Regeneration of Noninnervated Musele Grafts and Marcaine-Treated Muscles in Young and Old Rats

Carlson, B. M., & Faulkner, J. A. (1996) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/51a.1.b43 · Cited by 62

Aging and Regenerative Capacity of Skeletal Muscle in Rats

Kaasik, P., Aru, M., Alev, K., & Seene, T. (2012) · Current Aging Science · doi:10.2174/1874609811205020126 · Cited by 4

Effects of age on aneural regeneration of soleus muscle in rat.

Lewis, D. M., & Schmalbruch, H. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020982 · Cited by 8