References
- Agapitou V., Tzanis G., Dimopoulos S., Karatzanos E., Karga H., Nanas S.: Effect of combined endurance and resistance training on exercise capacity and serum anabolic steroid concentration in patients with chronic heart failure. Hellenic. J. Cardiol., 2018; 59: 179–181
- Allen D.L., Teitelbaum D.H., Kurachi K.: Growth factor stimulation of matrix metalloproteinase expression and myoblast migration and invasion in vitro. Am. J. Physiol. Cell. Physiol., 2003; 284: C805–C815
- Amir R., Ben-Sira D., Sagiv M.: IGF-I and FGF-2 responses to Win-gate anaerobic test in older men. J. Sports. Sci. Med., 2007; 6: 227–232
- Annibalini G., Lucertini F., Agostini D., Vallorani L., Gioacchini A., Barbieri E., Guescini M., Casadei L., Passalia A., Del Sal M., Piccoli G., Andreani M., Federici A., Stocchi V.: Concurrent aerobic and resistance training has anti-inflammatory effects and increases both plasma and leukocyte levels of IGF-1 in late middle-aged type 2 diabetic patients. Oxid. Med. Cell. Longev, 2017; 2017: 3937842
- Archacka K., Kowalski K.K., Brzóska-Wójtowicz E.: Czy komórki satelitowe są macierzyste? Post. Bioch., 2013; 59: 205–218
- Archacka K., Moraczewski J., Grabowska I.: Udział niemięśniowych komórek macierzystych w regeneracji mięśni szkieletowych. Post. Biol. Komórki, 2010; 37: 187–207
- Basualto-Alarcón C., Varela D., Duran J., Maass R., Estrada M.: Sarcopenia and androgens: A link between pathology and treatment. Front. Endocrinol., 2014; 5: 217
- Beauchamp J.R., Morgan J.E., Pagel C.N., Partridge T.A.: Dynamics of myoblast transplantation reveal a discrete minority of precursors with stem cell-like properties as the myogenic source. J. Cell. Biol., 1999; 144: 1113–1122
- Bhasin S., Storer T., Berman N., Callegari C., Clevenger B., Phillips J., Bunnell T.J., Tricker R., Shirazi A., Casaburi R.: The effects of supraphysiologic doses of testosterone on muscle size and strength in normal men. N. Engl. J. Med., 1996; 335: 1–7
- Bosiacki M., Lubkowska A.: Starzenie się a ekspresja metaloproteinaz macierzy zewnątrzkomórkowej w mięśniach. Pomeranian J. Life. Sci., 2019; 65: 105–112
- Burdzińska A., Berwid S., Orzechowski A.: Transplantacje komórek mięśniowych – oczekiwania, możliwości i ograniczenia. Postępy Hig. Med. Dośw., 2005; 59: 299–308
- Carmeli E., Moas M., Lennon S., Powers S.K.: High intensity exercise increases expression of matrix metalloproteinases in fast skeletal muscle fibres. Exp. Physiol., 2005; 90: 613–619
- Charifi N., Kadi F., Féasson L., Denis C.: Effects of endurance traning on satellite cell frequency in skeletal muscle of old men. Muscle Nerve, 2003; 28: 87–92
- Chaudhary S., Shenoy S.: Analysis of hormonal responses to aerobic and anaerobic zone training. J. M. S. C. R., 2015; 3: 4677–4683
- Chen H.T., Chung Y.C., Chen Y.J., Ho S.Y., Wu H.J.: Effects of different types of exercise on body composition, muscle strength, and IGF-1 in the elderly with sarcopenic obesity. J. Am. Geriatr. Soc., 2017; 65: 827–832
- Chen X., Li Y.: Role of matrix metalloproteinases in skeletal muscle: Migration, differentiation, regeneration and fibrosis. Cell. Adh. Migr., 2009; 3: 337–341
- Chernausek S.D., Backeljauw P.F., Frane J., Kuntze J., Underwood L.E., GH Insensitivity Syndrome Collaborative Group: Long-term treatment with recombinant insulin-like growth factor (IGF)-I in children with severe IGF-I deficiency due to growth hormone insensitivity. J. Clin. Endocrinol. Metab., 2007; 92: 902–910
- Cho S.Y., Roh H.T.: Taekwondo enhances cognitive function as a result of increased neurotrophic growth factors in elderly women. Int. J. Environ. Res. Public Health, 2019; 16: 962
- Chyu M.C., Zhang Y., Brismée J.M., Dagda R.Y., Chaung E., Von Bergen V., Doctolero S., Shen C.L.: Effects of martial arts exercise on body composition, serum biomarkers and quality of life in overweight/obese premenopausal women: A pilot study. Clin. Med. Insights Womens Health, 2013; 6: 55–65
- Clemmons D.R.: Role of IGF-binding proteins in regulating IGF responses to changes in metabolism. J. Mol. Endocrinol., 2018; 61: T139–T169
- Collins C.A., Olsen I., Zammit P.S., Heslop L., Petrie A., Partridge T.A., Morgan J.E.: Stem cell function, self-renewal, and behavioral heterogeneity of cells from the adult muscle satellite cell niche. Cell, 2005; 122: 289–301
- Corotchi M.C., Popa M.A., Simionescu M.: Testosterone stimulates proliferation and preserves stemness of human adult mesenchymal stem cells and endothelial progenitor cells. Rom. J. Morphol. Embryol., 2016; 57: 75–80
- Cottle B.J., Lewis F.C., Shone V., Ellison-Hughes G.M.: Skeletal muscle-derived interstitial progenitor cells (PICs) display stem cell properties, being clonogenic, self-renewing, and multi-potent in vitro and in vivo. Stem Cell. Res. Ther., 2017; 8: 158
- Cui S.F., Li W., Niu J., Zhang C.Y., Chen X., Ma J.Z.: Acute responses of circulating microRNAs to low-volume sprint interval cycling. Front Physiol., 2015; 6: 311
- Cunha P.M., Nunes J.P., Tomeleri C.M., Nascimento M.A., Schoenfeld B.J., Antunes M., Gobbo L.A., Teixeira D., Cyrino E.S.: Resistance training performed with single and multiple sets induces similar improvements in muscular strength, muscle mass, muscle quality, and IGF-1 in older women: A randomized controlled trial. J. Strength Cond. Res., 2020; 34: 1008–1016
- Deane C.S., Hughes D.C., Sculthorpe N., Lewis M.P., Stewart C.E., Sharples A.P.: Impaired hypertrophy in myoblasts is improved with testosterone administration. J. Steroid. Biochem. Mol. Biol., 2013; 138: 152–161
- Dreyer H.C., Blanco C.E., Sattler F.R., Schroeder E.T., Wiswell R.A.: Satellite cell numbers in young and older men 24 hours after eccentric exercise. Muscle Nerve, 2006; 33: 242–253
- Englund D.A., Peck B.D., Murach K.A., Neal A.C., Caldwell H.A., McCarthy J.J., Peterson C.A., Dupont-Verteegden E.E.: Resident muscle stem cells are not required for testosterone-induced skeletal muscle hypertrophy. Am. J. Physiol. Cell Physiol., 2019; 317: C719–C724
- Forcales S.V.: Potential of adipose-derived stem cells in muscular regenerative therapies. Front. Aging Neurosci., 2015; 7: 123
- Fukada S.I.: The roles of muscle stem cells in muscle injury, atrophy and hypertrophy. J. Biochem., 2018; 163: 353–358
- Gomes R.V., Moreira A., Lodo L., Nosaka K., Coutts A.J., Aoki M.S.: Monitoring training loads, stress, immune-endocrine responses and performance in tennis players. Biol. Sport, 2013; 30: 173–180
- Grabowska I., Zimowska M., Maciejewska K., Jablonska Z., Bazga A., Ozieblo M., Streminska W., Bem J., Brzoska E., Ciemerych M.A.: Adi-pose tissue-derived stromal cells in matrigel impacts the regeneration of severely damaged skeletal muscles. Int. J. Mol. Sci., 2019; 20: 3313
- Harridge S.D.: Plasticity of human skeletal muscle: Gene expression to in vivo function. Exp. Physiol., 2007; 92: 783–797
- Hashimoto H., Rebagliati M., Ahmad N., Muraoka O., Kurokawa T., Hibi M., Suzuki T.: The Cerberus/Dan-family protein Charon is a negative regulator of Nodal signaling during left-right patterning in zebrafish. Development, 2004; 131: 1741–1753
- Hayes L.D., Grace F.M., Sculthorpe N., Herbert P., Ratcliffe J.W., Kilduff L.P., Baker J.S.: The effects of a formal exercise training programme on salivary hormone concentrations and body composition in previously sedentary aging men. Springerplus, 2013; 2: 18
- Heatwole C.R., Eichinger K.J., Friedman D.I., Hilbert J.E., Jackson C.E., Logigian E.L., Martens W.B., McDermott M.P., Pandya S.K., Quinn C., Smirnow A.M., Thornton C.A., Moxley R.T.3rd: Open-label trial of recombinant human insulin-like growth factor-1/recombinant human insulin-like growth factor binding protein-3 (rhIGF-1/rhIGFBP-3) in myotonic dystrophy type 1. Arch. Neurol., 2011; 68: 37–44
- Hejazi K., Hosseini S.R.: Influence of selected exercise on serum immunoglobulin, testosterone and cortisol in semi-endurance elite runners. Asian J. Sports Med., 2012; 3: 185–192
- Higashi Y., Gautam S., Delafontaine P., Sukhanov S.: IGF-1 and cardiovascular disease. Growth. Horm. IGF Res., 2019; 45: 6–16
- Huard J., Gharaibeh B., Usas A.: Regenerative medicine based on muscle-derived stem cells. Oper. Tech. Orthop., 2010; 20: 119–126
- Itariu B.K., Zeyda M., Prager G., Stulnig T.M.: Insulin-like growth factor 1 predicts post-load hypoglycemia following bariatric surgery: A prospective cohort study. PLoS One, 2014; 9: e94613
- Jung P., Zimowska M.: Metaloproteinazy macierzy zewnątrzkomórkowej w rozwoju, fizjologii i procesach degeneracyjnych mięśni szkieletowych. Post. Bioch., 2016; 62: 25–35
- Junnila R.K., List E.O., Berryman D.E., Murrey J.W., Kopchick J.J.: The GH/IGF-1 axis in ageing and longevity. Nat. Rev. Endocrinol., 2013; 9: 366–376
- Jȕrimäe J., Jȕrimäe T.: Leptin responses to short term exercise in college level male rowers. Br. J. Sports Med., 2005; 39: 6–9
- Kadi F., Schjerling P., Andersen L.L., Charifi N., Madsen J.L., Christensen L.R., Andersen J.L.: The effects of heavy resistance training and detraining on satellite cells in human skeletal muscles. J. Physiol., 2004; 558: 1005–1012
- Kilian Y., Engel F., Wahl P., Achtzehn S., Sperlich B., Mester J.: Markers of biological stress in response to a single session of high-intensity interval training and high-volume training in young athletes. Eur. J. Appl. Physiol., 2016; 116: 2177–2186
- Kim T., Chang J.S., Kim H., Lee K.H., Kong I.D.: Intense walking exercise affects serum IGF-1 and IGFBP3. J. Lifestyle Med., 2015; 5: 21–25
- Kraemer W.J., Ratamess N.A., Hymer W.C., Nindl B.C., Fragala M.S.: Growth hormone(s), testosterone, insulin-like growth factors, and cortisol: Roles and integration for cellular development and growth with exercise. Front. Endocrinol., 2020; 11: 33
- Kvorning T., Andersen M., Brixen K., Schjerling P., Suetta C., Madsen K.: Suppression of testosterone does not blunt mRNA expression of myoD, myogenin, IGF, myostatin or androgen receptor post strength training in humans. J. Physiol., 2007; 578: 579–593
- Liu W., Wen Y., Bi P., Lai X., Liu X.S., Liu X., Kuang S.: Hypoxia promotes satellite cell self-renewal and enhances the efficiency of myo-blast transplantation. Development, 2012; 139: 2857–2865
- Maass A., Düzel S., Brigadski T., Goerke M., Becke A., Sobieray U., Neumann K., Lövdén M., Lindenberger U., Bäckman L., Braun-Dullaeus R., Ahrens D., Heinze H.J., Müller N.G., Lessmann V., Sendtner M., Düzel E.: Relationships of peripheral IGF-1, VEGF and BDNF levels to exercise-related changes in memory, hippocampal perfusion and volumes in older adults. Neuroimage, 2016; 131: 142–154
- Mackey A., Kjaer M., Dandanell S., Mikkelsen K.H., Holm L., Døssing S., Kadi F., Koskinen S.O., Jensen C.H., Schrøder H.D., Langberg H.: The influence of anti-inflammatory medication on exercise-induced myogenic precursor cell response in humans. J. Appl. Physiol., 2007; 103: 425–431
- Mañes S., Mira E., Barbacid M.M., Ciprés A., Fernández-Resa P., Buesa J.M., Mérida I., Aracil M., Márquez G., Martìnez-A C.: Identification of insulin-like growth factor-binding protein-1 as a potential physiological substrate for human stromelysin-3. J. Biol. Chem., 1997; 272: 25706–25712
- Marcell T.J., Harman S.M., Urban R.J., Metz D.D., Rodgers B.D., Blackman M.R.: Comparison of GH, IGF-I, and testosterone with mRNA of receptors and myostatin in skeletal muscle in older men. Am. J. Physiol. Endocrinol. Metab., 2001; 281: E1159–E1164
- Mendell J.R., Kissel J.T., Amato A.A., King W., Signore L., Prior T.W., Sahenk Z., Benson S., McAndrew P.E., Rice R., Nagaraja H., Stephens R., Lantry L., Morris G.E., Burghes A.H.: Myoblast transfer in the treatment of Duchenne’s muscular dystrophy. N. Engl. J. Med., 1995; 333: 832–838
- Meng J., Muntoni F., Morgan J.: CD133+ cells derived from skeletal muscles of Duchenne muscular dystrophy patients have a compromised myogenic and muscle regenerative capability. Stem. Cell Res., 2018; 30: 43–52
- Mierzejewski B., Archacka K., Grabowska I., Florkowska A., Ciemerych M.A., Brzoska E.: Human and mouse skeletal muscle stem and progenitor cells in health and disease. Semin. Cell. Dev. Biol., 2020; 104: 93–104
- Milewska M., Grabiec K., Grzelkowska-Kowalczyk K.: Interakcje szlaków sygnałowych proliferacji i różnicowania w biogenezie. Postępy Hig. Med. Dośw., 2014; 68: 516–526
- Miller R.G., Sharma K.R., Pavlath G.K, Gussoni E., Mynhier M., Lanctot A.M., Greco C.M., Steinman L., Blau H.M.: Myoblast implantation in Duchenne muscular dystrophy: The San Francisco study. Muscle Nerve, 1997; 20: 469–478
- Mitchell K.J., Pannérec A., Cadot B., Parlakian A., Besson V., Gomes E.R., Marazzi G., Sassoon D.A.: Identification and characterization of a non-satellite cell muscle resident progenitor during postnatal development. Nat. Cell Biol., 2010; 12: 257–266
- Molsted S., Andersen J.L., Eidemak I., Harrison A.P., Jørgensen N.: Resistance training and testosterone levels in male patients with chronic kidney disease undergoing dialysis. Biomed. Res. Int., 2014; 2014: 121273
- Molsted S., Andersen J.L., Harrison A.P., Eidemak I., Mackey A.L.: Fiber type-specific response of skeletal muscle satellite cells to high-intensity resistance training in dialysis patients. Muscle Nerve, 2015; 52: 736–745
- Montarras D., Morgan J., Collins C., Relaix F., Zaffran S., Cumano A., Partridge T., Buckingham M.: Direct isolation of satellite cells for skeletal muscle regeneration. Science, 2005; 309: 2064–2067
- Morawin B.: Rola testosteronu w regeneracji mięśni szkieletowych po wysiłku fizycznym. Rocznik Lubuski, 2014; 40: 95–105
- Møller A.B., Lønbro S., Farup J., Voss T.S., Rittig N., Wang J., Højris I., Mikkelsen U.R., Jessen N.: Molecular and cellular adaptations to exercise training in skeletal muscle from cancer patients treated with chemotherapy. J. Cancer Res. Clin. Oncol., 2019; 145: 1449–1460
- Mueller S.M., Mihaylova V., Frese S., Petersen J.A., Ligon-Auer M., Aguayo D., Flück M., Jung H.H., Toigo M.: Satellite cell content in Huntington’s disease patients in response to endurance training. Orphanet J. Rare Dis., 2019; 14: 135
- Mukund K., Subramaniam S.: Skeletal muscle: A review of molecular structure and function, in health and disease. Wiley Interdiscip. Rev. Syst. Biol. Med., 2020; 12: e1462
- Negaresh R., Ranjbar R., Baker J.S., Habibi A., Mokhtarzade M., Gharibvand M.M., Fokin A.: Skeletal muscle hypertrophy, insulin-like growth factor 1, myostatin and follistatin in healthy and sarcopenic ederly men: The effect of whole-body resistance training. Int. J. Prev. Med., 2019; 10: 29
- Nemet D., Portal S., Zadik Z., Pilz-Burstein R., Adler-Portal D., Meckel Y., Eliakim A.: Training increases anabolic response and reduces inflammatory response to a single practice in elite male adolescent volleyball players. J. Pediatr. Endocrinol. Metab., 2012; 25: 875–880
- Nindl B.C., Alemany J.A., Tuckow A.P., Rarick K.R., Staab J.S., Kraemer W.J., Maresh C.M., Spiering B.A., Hatfield D.L., Flyvbjerg A., Frystyk J.: Circulating bioactive and immunoreactive IGF-I remain stable in women, despite physical fitness improvements after 8 weeks of resistance, aerobic, and combined exercise training. J. Appl. Physiol., 2010; 109: 112–120
- Onambele-Pearson G.L., Pearson S.J.: The magnitude and character of resistance-training-induced increase in tendon stiffness at old age is gender specific. Age, 2012; 34: 427–438
- Partridge T.: Myoblast transplantation. Neuromuscul. Disord., 2002; 12: S3–S6
- Peng H., Huard J.: Muscle-derived stem cells for musculoskeletal tissue regeneration and repair. Transpl. Immunol., 2004; 12: 311–319
- Petriz B.A., Gomes C.P., Almeida J.A., De Oliveria G.P.Jr., Ribeiro F.M., Pereira R.W., Franco O.L.: The effects of acute and chronic exercise on skeletal muscle proteome. J. Cell Physiol., 2017; 232: 257–269
- Pronsato L., Milanesi L., Vasconsuelo A., La Colla A.: Testosterone modulates FoxO3a and p53-related genes to protect C2C12 skeletal muscle cells against apoptosis. Steroids, 2017; 124: 35–45
- Qu Z., Balkir L., van Deutekom J.C., Robbins P.D., Pruchnic R., Huard J.: Development of approaches to improve cell survival in myoblast transfer therapy. J. Cell Biol., 1998; 142: 1257–1267
- Rando T.A, Blau H.M.: Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy. J. Cell Biol., 1994; 125: 1275–1287
- Renault V., Thornell L.E., Eriksson P.O., Butler-Browne G., Mouly W.: Regenerative potential of human skeletal muscle during aging. Aging Cell, 2002; 1: 132–139
- Riederer I., Negroni E., Bencze M., Wolff A., Aamiri A., Di Santo J.P., Silva-Barbosa S.D., Butler-Browne G., Savino W., Mouly V.: Slowing down differentiation of engrafted human myoblasts into immunodeficient mice correlates with increased proliferation and migration. Mol. Ther., 2012; 20: 146–154
- Rodriguez A.M., Pisani D., Dechesne C.A., Turc-Carel C., Kurzenne J.Y., Wdziekonski B., Villageois A., Bagnis C., Breittmayer J.P., Groux H., Ailhaud G., Dani C.: Transplantation of a multipotent cell population from human adipose tissue induces dystrophin expression in the immunocompetent mdx mouse. J. Exp. Med., 2005; 201: 1397–1405
- Sacco A., Doyonnas R., Kraft P., Vitorovic S., Blau H.M.: Self-renewal and expansion of single transplanted muscle stem cells. Nature, 2008; 456: 502–506
- Saini A., Mastana S., Myers F., Lewis M.P.: ‘From death, lead me to immortality’ - mantra of ageing skeletal muscle. Curr. Genomics, 2013; 14: 256–267
- Sato K., Iemitsu M., Katayama K., Ishida K., Kanao Y., Saito M.: Responses of sex steroid hormones to different intensities of exercise in endurance athletes. Exp. Physiol., 2016; 101: 168–175
- Schmidt M., Schüler S.C., Hüttner S.S., von Eyss B., von Maltzahn J.: Adult stem cells at work: Regenerating skeletal muscle. Cell. Mol. Life Sci., 2019; 76: 2559–2570
- Schoenfeld B.J.: The mechanisms of muscle hypertrophy and their application to resistance training. J. Strength Cond. Res., 2010; 24: 2857–2872
- Schulze M., Belema-Bedada F., Technau A., Braun T.: Mesenchymal stem cells are recruited to striated muscle by NFAT/IL-4-mediated cell fusion. Genes. Dev., 2005; 19: 1787–1798
- Snijders T., Nederveen J.P., Bell K.E., Lau S.W., Mazara N., Kumbhare D.A., Phillips S.M., Parise G.: Prolonged exercise training improves the acute type II muscle fibre satellite cell response in healthy older men. J. Physiol., 2019; 597: 105–119
- Song T., Sadayappan S.: Featured characteristics and pivotal roles of satellite cells in skeletal muscle regeneration. J. Muscle. Res. Cell. Motil., 2020; 41: 341–353
- Streuli C.: Extracellular matrix remodelling and cellular differentiation. Curr. Opin. Cell Biol., 1999; 11: 634–640
- Sutkowy P.B., Augustyńska B., Woźniak A., Rakowski A.: Physical exercise combined with whole-body cryotherapy in evaluating the level of lipid peroxidation products and other oxidant stress indicators in kayakers. Oxid. Med. Cell. Longev., 2014; 2014: 402631
- Thompson J.L., Butterfield G.E., Marcus R., Hintz R.L., Van Loan M., Ghiron L., Hoffman A.R.: The effects of recombinant human insulin-like growth factor-I and growth hormone on body composition in elderly women. J. Clin. Endocrinol. Metab., 1995; 80: 1845–1852
- Torrente Y., Belicchi M., Sampaolesi M., Pisati F., Meregalli M., D’Antona G., Tonlorenzi R., Porretti L., Gavina M., Mamchaoui K., Pellegrino M.A., Furling D., Mouly V., Butler-Browne G.S., Bottinelli R. i wsp.: Human circulating AC133+ stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle. J. Clin. Invest., 2004; 114: 182–195
- Tota Ł., Piotrowska A., Pałka T., Morawska M., Mikuľáková W., Mucha D., Żmuda-Pałka M., Pilch W.: Muscle and intestinal damage in triathletes. PLoS One, 2019; 14: e0210651
- Tsuchiya Y., Sakuraba K., Ochi E.: High force eccentric exercise enhances serum tartrate-resistant acid phosphatase-5b and osteocalcin. J. Musculoskelet. Neuronal. Interact., 2014; 14: 50–57
- Vassilakos G., Barton E.R.: Insulin-like growth factor I regulation and its actions in skeletal muscle. Compr. Physiol., 2018; 9: 413–438
- Velloso C.P.: Regulation of muscle mass by growth hormone and IGF-I. Br. J. Pharmacol. 2008; 154: 557–568
- Vlachopapadopoulou E., Zachwieja J.J., Gertner J.M., Manzione D., Bier D.M., Matthews D.E., Slonim A.E.: Metabolic and clinical response to recombinant human insulin-like growth factor I in myotonic dystrophy - a clinical research center study. J. Clin. Endocrinol. Metab., 1995; 80: 3715–3723
- Wegner M., Koedijker J.M., Budde H.: The effect of acute exercise and psychosocial stress on fine motor skills and testosterone concentration in the saliva of high school students. PLoS One, 2014; 9: e92953
- Wennberg A.M., Hagen C.E., Machulda M.M., Hollman J.H., Roberts R.O., Knopman D.S., Petersen R.C., Mielke M.M.: The association between peripheral total IGF-1, IGFBP-3, and IGF-1/IGFBP-3 and functional and cognitive outcomes in the Mayo Clinic Study of Aging. Neurobiol. Aging, 2018; 66: 68–74
- Wennberg A.M., Hagen C.E., Petersen R.C., Mielke M.M.: Trajectories of plasma IGF-1, IGFBP-3, and their ratio in the Mayo Clinic Study of Aging. Exp. Gerontol., 2018; 106: 67–73
- Wędrychowicz A., Dziatkowiak H., Sztefko K., Nazim J.: Zachowanie się IGF-I i jego białek wiążących IGFBP-1 i IGFBP-3 u dzieci i młodzieży chorych na cukrzycę typu 1 oraz ich zależność od kontroli metabolicznej cukrzycy. Diabetol. Dośw. Klin. 2003; 3: 489–499
- Wiewelhove T., Schneider C., Döweling A., Hanakam F., Rasche C., Meyer T., Kellmann M., Pfeiffer M., Ferrauti A.: Effects of different recovery strategies following a half-marathon on fatigue markers in recreational runners. PLoS One, 2018; 13: e0207313
- Yamakawa H., Kusumoto D., Hashimoto H., Yuasa S.: Stem cell aging in skeletal muscle regeneration and disease. Int. J. Mol. Sci., 2020; 21: 1830
- Zammit P.S., Relaix F., Nagata Y., Ruiz A.P., Collins C.A., Partridge T.A., Beauchamp J.R.: Pax7 and myogenic progression in skeletal muscle satellite cells. J. Cell Sci., 2006; 119: 1824–1832
- Zembroń-Łacny A., Krzywański J., Ostapiuk-Karolczuk J., Kasperska A.: Cell and molecular mechanisms of regeneration and reorganization of skeletal muscles. Ortop. Traumatol. Rehabil., 2012; 14: 1–11
- Zhang Y., Zhu Y., Li Y., Cao J., Zhang H., Chen M., Wang L., Zhang C.: Long-term engraftment of myogenic progenitors from adipose-derived stem cells and muscle regeneration in dystrophic mice. Hum. Mol. Genet., 2015; 24: 6029–6040
- Żebrowska A., Gąsior Z., Langfort J.: Serum IGF-I and hormonal responses to incremental exercise in athletes with and without left ventricular hypertrophy. J. Sports. Sci. Med., 2009; 8: 67–76