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

Function of Membrane-Associated Proteoglycans in the Regulation of Satellite Cell Growth

Song, Y. Y. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-27511-6_4 · Cited by 7

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

Systemic low-grade inflammation does not decrease skeletal muscle mass and protein synthesis in old rats.

Mayot, G., Breuillé, D., Jarret, A. R., Obled, C., & Papet, I. (2008) · PubMed · Cited by 8

Thyroid disease and vertical rectus muscle overaction after retrobulbar anesthesia

Han, S. K., & Hwang, J. (2003) · Journal of Cataract & Refractive Surgery · doi:10.1016/s0886-3350(02)01437-2 · Cited by 7

Oxidative stress and the pathogenesis of sarcopenia

Lopez, M. E., Zainal, T. A., Chung, S. S., Aiken, J. M., & Weindruch, R. H. (2000) · Elsevier eBooks · doi:10.1016/b978-044482650-3/50029-8 · Cited by 7

Age-Dependent Changes in Skeletal MuscleRegeneration

Brack, A. S., & Rando, T. A. (2008) · Springer eBooks · doi:10.1007/978-1-4020-6768-6_16 · Cited by 7

Replacement as an aging intervention

Lore, S., Poganik, J. R., Atala, A., Church, G. M., Gladyshev, V. N., Scheibye‐Knudsen, M., & Verdin, E. M. (2025) · Nature Aging · doi:10.1038/s43587-025-00858-6 · Cited by 6

Sex-specific preservation of neuromuscular function and metabolism following systemic transplantation of multipotent adult stem cells in a murine model of progeria

Thompson, S. D., Barrett, K. L., Rugel, C. L., Redmond, R. S., Rudofski, A., Kurian, J., Curtin, J. L., Dayanidhi, S., & Lavasani, M. (2023) · GeroScience · doi:10.1007/s11357-023-00892-5 · Cited by 6

Aging of Stem Cells

Liu, L. A., & Rando, T. A. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-378638-8.00006-3 · Cited by 7

Depletion of NIMA-related kinase Nek2 induces aberrant self-renewal and apoptosis in stem/progenitor cells of aged muscular tissues

Mori, T., Onodera, Y., Itokazu, M., Takehara, T., Shigi, K., Iwawaki, N., Akagi, M., & Teramura, T. (2022) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2022.111619 · Cited by 6

An organismal view of cellular aging

Carnes, B. A., Staats, D. O., Vaughan, M. B., & Witten, T. M. (2010) · Médecine & longévité · doi:10.1016/j.mlong.2010.06.002 · Cited by 6

Muscle Stem Cells: A Model System for Adult Stem Cell Biology

Cornelison, D., & Perdiguero, E. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6771-1_1 · Cited by 6

Ex-vivo Expansion of Muscle-Regenerative Cells for the Treatment of Muscle Disorders

Schaaf, G. (2012) · Journal of Stem Cell Research & Therapy · doi:10.4172/2157-7633.s11-003 · Cited by 5

Skeletal Muscle Stem Cells

Blau, H. M., Sacco, A., & Gilbert, P. M. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374729-7.00030-5 · Cited by 5

Skeletal Muscle Aging

Broome, C. S., Vasilaki, A., & McArdle, A. (2003) · Springer eBooks · doi:10.1007/978-94-017-0673-5_3 · Cited by 5

Recovery of muscle transfers replacing the total plantar flexor muscle group in rats

Miller, S. W., Hassett, C. A., & Faulkner, J. A. (1998) · Journal of Applied Physiology · doi:10.1152/jappl.1998.84.6.1865 · Cited by 5

Systemic Rejuvenating Interventions: Perspectives on Neuroinflammation and Blood–Brain Barrier Integrity

de Rezende, V. L., da Costa, M. D. A., Martins, C. D., Mathias, K., Gonçalves, C. L., Barichello, T., & Petronilho, F. C. (2025) · Neurochemical Research · doi:10.1007/s11064-025-04361-7 · Cited by 5

Altered senescence and mitochondrial transcriptome defines age-related changes in satellite cells

Rahman, F. A., & Quadrilatero, J. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1699206 · Cited by 5

Semaphorins: Missing Signals in Age-dependent Alteration of Neuromuscular Junctions and Skeletal Muscle Regeneration

Fard, D., Barbiera, A., Dobrowolny, G., Tamagnone, L., & Scicchitano, B. M. (2023) · Aging and Disease · doi:10.14336/ad.2023.0801 · Cited by 4

Stem Cell Aging and Rejuvenation in the Skeletal Muscle System

Libergoli, M., & Almada, A. E. (2025) · Rejuvenation Research · doi:10.1089/rej.2025.0028 · Cited by 4

Cellular Senescence and Stem Cell Niche

Krause, A., Conboy, M. J., & Conboy, I. M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802734-9.00012-3 · Cited by 4

Observation of Age‐Related Decline in the Performance of the Transverse Abdominis Muscle

Davies, P. A., Grace, F., Lewis, M. P., & Sculthorpe, N. F. (2015) · PM&R · doi:10.1016/j.pmrj.2015.05.023 · Cited by 4

Myogenic precursor cells

Grounds, M. D., & Relaix, F. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511674747.006 · Cited by 4

Enhanced Satellite Cell Activity in Aging Skeletal Muscle after Manual Acupuncture-Induced Injury

Sobrian, S. K., & Walters, E. (2014) · Chinese Medicine · doi:10.4236/cm.2014.51004 · Cited by 4

Norepinephrine-induced atriopeptin release in conscious dogs is mediated by alterations in atrial pressure

Zhu, J. L., Leadley, R. J., Geer, P. G., Wang, B. C., & Goetz, K. L. (1990) · Life Sciences · doi:10.1016/0024-3205(90)90046-t · Cited by 4

Decoding the forces that shape muscle stem cell function

Nguyen, J., & Gilbert, P. M. (2024) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2024.02.009 · Cited by 3

Aging and Gait

Singhal, K., & Casebolt, J. B. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-805376-8.00008-3 · Cited by 3

Atrial natriuretic peptide serum concentration decreases in donors undergoing discontinuous plasmapheresis involving a large extracorporeal blood volume

Karger, R., Halbe, M., Giffhorn‐Katz, S., Katz, N. R., & Kretschmer, V. (2007) · Transfusion · doi:10.1111/j.1537-2995.2007.01347.x · Cited by 3

Factors Influencing Satellite Cell Activity during Skeletal Muscle Development in Avian and Mammalian Species

Nierobisz, L. S., & Mozdziak, P. E. (2008) · Asian-Australasian Journal of Animal Sciences · doi:10.5713/ajas.2008.r.02 · Cited by 3

Biomaterial Applications in the Adult Skeletal Muscle Satellite Cell Niche: Deliberate Control of Muscle Stem Cells and Muscle Regeneration in the Aged Niche

Jabart, E., & Conboy, I. M. (2010) · Studies in mechanobiology, tissue engineering and biomaterials · doi:10.1007/8415_2010_12 · Cited by 3

Developmental Mechanisms of Regeneration

Stocum, D. L. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-385942-6.00015-9 · Cited by 3

Une vue organismique du vieillissement cellulaire

Carnes, B. A., Staats, D. O., Vaughan, M. B., & Witten, T. M. (2010) · Médecine & longévité · Cited by 3

Strategies of Regenerative Medicine

Stocum, D. L. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-384860-4.00009-5 · Cited by 3

Developmental Mechanisms of Regeneration

Stocum, D. L. (2008) · Elsevier eBooks · doi:10.1016/b978-012369410-2.50008-5 · Cited by 3

Skeletal muscle transplantation

Carlson, B. M. (1996) · Springer eBooks · doi:10.1007/978-94-009-0165-0_7 · Cited by 3

Metabolic slowdown as the proximal cause of ageing and deathPreprint

Wordsworth, J., Yde, P., Fielder, E., Chandrasegaran, S., & Shanley, D. P. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.01.551537 · Cited by 6

Muscle Repair after Injury and Disease

Ambrosio, F., Li, Y., Ūsas, A., Boninger, M. L., & Huard, J. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-239-7_22 · Cited by 3

Aging and Skeletal Muscle

Lynch, G. S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.11434-5 · Cited by 2

Effect of Porphyromonas gingivalis Infection on Healing of Skeletal Muscle Injury: An In Vivo Study

Shimizu, S., Hayashi, K., Takeuchi, Y., Tanabe, G., Churei, H., Kobayashi, H., Ueno, T., & Fueki, K. (2024) · Dentistry Journal · doi:10.3390/dj12110346 · Cited by 2

The biological time calendar

Duc, H. T. (2014) · Biomedicine & Aging Pathology · doi:10.1016/j.biomag.2014.03.006 · Cited by 2

Impairment of Host Liver Repopulation by Transplanted Hepatocytes in Aged Rats and the Release by Short-Term Growth Hormone Treatment

Stock, P., Bielohuby, M., Staege, M. S., Hsu, M., Bidlingmaier, M., & Christ, B. (2017) · American Journal Of Pathology · doi:10.1016/j.ajpath.2016.11.016 · Cited by 2

Innovations in Human Stem Cell Research: A Holy Grail for Regenerative Medicine

Liao, Y., Zhu, H., Ivanova, L. B., & Cairo, M. S. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.88790 · Cited by 2

Skeletal Muscle Stem Cells

LaBarge, M. A., & Blau, H. M. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-385942-6.00055-x · Cited by 2

Description of muscle disease – specific diseases

Karpati, G. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511674747.014 · Cited by 2

Skeletal muscle aging

Close, G. L., Haggan, P., & McArdle, A. (2007) · Reviews in Clinical Gerontology · doi:10.1017/s0959259808002360 · Cited by 2

Biological Pathways Impacting Cancer Survival: Exercise as a Countermeasure for the Development and Progression of Cachexia

Carson, J. A., & Puppa, M. (2012) · Springer eBooks · doi:10.1007/978-1-4614-4493-0_5 · Cited by 2

Cellular regulators of myoblast migration and myogenesis

Dimchev, G. A. (2026) · e-space (Manchester Metropolitan University) · doi:10.83056/mmu.32434632 · Cited by 2

Biomedical Research in Aging

González-Meljem, J. M., Haston, S., Gallage, S., & Innes, A. J. (2018) · Springer eBooks · doi:10.1007/978-3-319-95387-8_3 · Cited by 1

Secretome Profiling of Young Multipotent Stem Cells Reveals Angiogenic and Immunomodulatory Mechanisms Supporting Aged Neuromuscular Health

Thompson, S. D., Rugel, C. L., Haller, M. R., Curtin, J. L., Dayanidhi, S., & Lavasani, M. (2026) · Aging Cell · doi:10.1111/acel.70408 · Cited by 1

Blood to Blood: A New Therapeutic Opportunity for Age-Related Diseases

Totey, S. M. (2017) · Springer eBooks · doi:10.1007/978-981-10-3701-6_26 · Cited by 1

Soluble factors released from activated T-lymphocytes regulate C2C12 myoblast proliferation and cellular signalling, but effects are blunted in the elderly.

Al-Dabbagh, S., McPhee, J., Piasecki, M., Stewart, C., & Al-Shanti, N. (2018) · The journals of gerontology. Series A, Biological sciences and medical sciences · doi:10.1093/gerona/gly238 · Cited by 2

The scientific basis of muscle disease

Karpati, G. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511674747.005 · Cited by 2

Heterotopic bone formation derived from multipotent stromal cells is not inhibited in aged mice

Carbonneau, C. L., Despars, G., Moquin‐Beaudry, G., Benabdallah, B., Bouhanik, S., Dépôt, J., Moreau, A., & Beausejour, C. M. (2014) · Cytotherapy · doi:10.1016/j.jcyt.2014.03.004 · Cited by 1

Rejuvenation on the Road to Pluripotency

Sarkar, T. J., & Sebastiano, V. (2016) · InTech eBooks · doi:10.5772/63219 · Cited by 1

Aging of Epidermal Stem Cells

Charruyer, A., & Ghadially, R. (2016) · Springer eBooks · doi:10.1007/978-3-662-47398-6_19 · Cited by 1

Rejuvenating Stem Cells to Restore Muscle Regeneration in Aging

Bengal, E., & Odeh, M. (2019) · Springer eBooks · doi:10.1007/978-3-030-19962-3_22 · Cited by 1

Excitability and Contractility of Skeletal Muscle: Measurements and Interpretations

Faulkner, J. A., & Dennis, R. G. (2003) · Springer eBooks · doi:10.1007/0-387-21547-6_5 · Cited by 1

Myosin light chain 1 isoform expression remains constant during ageing in Wistar F455 rats

Dunathan, A. L., Lomax, M. I., & Barald, K. F. (1991) · Mechanisms of Ageing and Development · doi:10.1016/0047-6374(91)90014-q · Cited by 1

The role of myostatin during postnatal myogenesis and sarcopenia

Siriett, V. (2007) · Research Commons (University of Waikato) · Cited by 1

Modelling the mesenchymal stem cell niche in vitro using magnetic nanoparticles

Lewis, E. E. (2016) · Enlighten: Theses (The University of Glasgow) · Cited by 1

Derivation and Characterization of Pax7 Positive Skeletal Muscle Precursor Cells from Control and HGPS-derived induced Pluripotent Stem Cells

Kocharyan, A. (2018) · uO Research (University of Ottawa) · doi:10.20381/ruor-21786 · Cited by 1

Degradation of ribosome and chaperone proteins is attenuated during the Differentiation of Replicatively Aged C2C12 MyoblastsPreprint

Brown, A. D., Stewart, C. E., & Burniston, J. G. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.18.464830 · Cited by 1

Stem Cells and Aging

Perdiguero, E., García‐Prat, L., Sousa‐Victor, P., & Muñoz‐Cánoves, P. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00138-3 · Cited by 1

Editorial: Immunosenescence in organ transplantation

Iske, J., & Zhou, H. (2024) · Frontiers in Transplantation · doi:10.3389/frtra.2024.1422358 · Cited by 1

Stem Cells and Aging

Perdiguero, E., García‐Prat, L., Sousa‐Victor, P., & Muñoz‐Cánoves, P. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.30115-8 · Cited by 1

THE ROLE OF STEM CELL ANTIGEN-1(Sca-1) IN MUSCLE AGING

Richards-Malcolm, S. A. (2008) · UKnowledge (University of Kentucky)

Old-age muscle atrophy : Cellular mechanisms and behavioral consequenses

Altun, M. (2007) · Figshare

Muscle Stem Cells: Their Discovery, Properties, andIn-VitroManipulation

McFarland, S., Pagani, I., & Conboy, I. M. (2013) · Encyclopedia of Molecular Cell Biology and Molecular Medicine · doi:10.1002/3527600906.mcb.201200001

Expression profile of Wnt isoforms during differentiation of aging C2C12 myoblast cells.

Lin, C. (2010) · ResearchSpace (University of KwaZulu-Natal)

Effects of age and Pax6 deficiency on mouse limbal stem cell function

Douvaras, P. (2010) · ERA

Satellite cells and skeletal muscle characteristics in sarcopenia

Verdijk, L. B. (2009) · doi:10.26481/dis.20091016lv

Aging of Epidermal Stem Cells

Charruyer, A., & Ghadially, R. (2009) · Springer eBooks · doi:10.1007/978-3-540-89656-2_19

Response to stimulation-evoked eccentric muscle contractions in hypertensive rats

Willett, J. A., Gray, S. D., & Carlsen, R. C. (2000) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-200008000-00006

The Universal Stem Cell Source: Does It Exist?

Gallego, G. A., Grande, E., & Aparicio, L. A. (2014) · Springer eBooks · doi:10.1007/978-94-017-8754-3_1

CELLULAR CARDIOMYOPLASTY BASED ON MUSCLE STEM CELLS: IMPLICATIONS FOR THERAPY

Drowley, L. (2009) · D-Scholarship@Pitt (University of Pittsburgh)

Treinamento de força e morbidades geriátricas: uma revisão

Antonini, T. C., Fiamoncini, R. L., & da Cruz, I. B. M. (2010) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)

EFFECTS OF CONJUGATED LINOLEIC ACID ON BODY COMPOSITION PARAMETERS IN AGED AND CACHECTIC MICE

Carroll, S. H. (2007) · UA Campus Repository (The University of Arizona)

Microneurovascular free muscle transfer with cross-over nerve grafts in facial reanimation

Ylä-Kotola, T. M. (2008) · Työväentutkimus Vuosikirja

Calibrating Notch/TGF-β Signaling for Youthful, Healthy Tissue Maintenance and Repair

Carlson, M. E., & Conboy, I. M. (2010) · Springer eBooks · doi:10.1007/978-90-481-3999-6_13

young and older humans from the contractile properties of skeletal muscle fibers Effects of high- and low-velocity resistance training on

Carlson, M. E., Faulkner, J. A., Ashton‐Miller, J. A., Cole, N. M., Gałecki, A., Shu, C., NYQUIST, L. V., Claflin, R., Larkin, L. M., Cederna, P. S., et al. (2015)

Molecular Mechanisms of Muscle Stem Cell Aging

Baig, A. H., & Tümpel, S. (2012) · Else Kröner-Fresenius Symposia · doi:10.1159/000338030

Human population studies of transcriptome-wide expression in age-related traits

Pilling, L. C. (2015) · Open Research Exeter (University of Exeter)

Role of Myostatin in oxidative stress in skeletal muscle

Sandhya, S. (2013) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/53725

Regulation of postnatal skeletal muscle growth and metabolism by peroxisome proliferator-activated receptor??/??

Chandrashekar, P. (2016) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/67320

senescenceincreases CCN1 expression leading to muscle

Du, J., Klein, J. D., Hassounah, F., Zhang, J., Zhang, C., & Wang, X. H. (2016)

Exercise-Induced Fatigue and Recovery in the Ageing Athlete

Fell, J. W. (2006) · Griffith Research Online · doi:10.25904/1912/1059

Using Antibodies to Characterize Healthy, Disease, and Age States

Whittemore, K. (2014)

Neuromuscular Tissue Engineering

Avin, K. G., Badylak, S. F., & Ambrosio, F. (2014) · Orthopaedic Section, APTA, Inc. eBooks · doi:10.17832/isc.2014.23.2.2

Embryonic and Adult Stem Cells Explored through Microfluidics and Biological Manipulation

Jabart, E. (2013) · eScholarship (California Digital Library)

Unique localization patterns for E2F5 and LEK1 in skeletal muscle

Ouellette, S. E. (2007)

A Multi-angled Approach to Discover and Improve Skeletal Muscle Stem Cell Therapies

Davoudi, S. (2019) · TSpace (University of Toronto)

The α7β1 integrin accelerates exercise-induced myogenesis

Lueders, T. N. (2010) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign)

Control of muscle fibre size: a crucial factor in ageing: Muscle fibre size control

Hughes, S. M., & Schiaffino (1999) · Acta Physiologica Scandinavica

Therapeutic approaches for the treatment of aging-induced stem cell dysfunction

Bizzaro, D., Russo, F. P., & Burra, P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-820071-1.00018-9

Mechanisms of adipose-derived stem cell aging and the impact on therapeutic potential

Shan, X., & Percec, I. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819376-1.00017-2

Serum Hs-CRP in elderly women affects the proliferative capacity of human myoblast

Ewen, J. (2012) · KTH Publication Database DiVA (KTH Royal Institute of Technology)

Aging of Epidermal Stem Cells

Charruyer, A., & Ghadially, R. (2015) · Springer eBooks · doi:10.1007/978-3-642-27814-3_19-2

References

(2007) · Elsevier eBooks · doi:10.1016/b978-012369439-3/50018-0

Contractility and myosin heavy chain content of skeletal muscle engineered from adult and aged rats

Dennis, R. G., & Kosnik, P. E. (2021) · The Journal of Science and Medicine · doi:10.37714/josam.v3i2.88

Sarcopenia

Lynch, G. S. (2012) · Springer eBooks · doi:10.1007/978-3-540-29807-6_143

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