Regulation of Myogenesis and Skeletal Muscle Regeneration: Effects of Oxygen Levels on Satellite Cell Activity

Cellular and Molecular Regulation of Muscle Regeneration

CHARGÉ, S. B. P., & Rudnicki, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00019.2003 · Cited by 2,691 · see citing works

Satellite Cells and the Muscle Stem Cell Niche

Yin, H., Price, F., & Rudnicki, M. A. (2013) · Physiological Reviews · doi:10.1152/physrev.00043.2011 · Cited by 2,166 · see citing works

Oxygen Sensing, Hypoxia-Inducible Factors, and Disease Pathophysiology

Semenza, G. L. (2013) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-012513-104720 · Cited by 1,159 · see citing works

Hypoxia requires Notch signaling to maintain the undifferentiated cell state

Gustafsson, M. V., Zheng, X., Pereira, T., Gradin, K., Jin, S., Lundkvist, J., Ruas, J. L., Poellinger, L., Lendahl, U., & Bondesson, M. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.09.010 · Cited by 1,109 · see citing works

The role of oxygen availability in embryonic development and stem cell function

Simon, M. C., & Keith, B. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2354 · Cited by 966 · see citing works

Distribution of hematopoietic stem cells in the bone marrow according to regional hypoxia

Parmar, K., Mauch, P., Vergilio, J.-A., Sackstein, R., & Down, J. D. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701152104 · Cited by 867 · see citing works

HIF‐1 is expressed in normoxic tissue and displays an organ‐specific regulation under systemic hypoxia

Stroka, D., Burkhardt, T., Desbaillets, I., Wenger, R. H., Neil, D., Bauer, C., GASSMANN, M., & Candinas, D. (2001) · The FASEB Journal · doi:10.1096/fj.01-0125com · Cited by 716 · see citing works

The Role of Hypoxia in Development of the Mammalian Embryo

Dunwoodie, S. L. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.11.008 · Cited by 651 · see citing works

Myoglobin O2 desaturation during exercise. Evidence of limited O2 transport.

Richardson, R. S., Noyszewski, E. A., Kendrick, K. F., Leigh, J. S., & Wagner, P. D. (1995) · Journal of Clinical Investigation · doi:10.1172/jci118237 · Cited by 647 · see citing works

Functional muscle regeneration with combined delivery of angiogenesis and myogenesis factors

Borselli, C., Storrie, H., Benesch, F., Shvartsman, D. E., Cezar, C. A., Lichtman, J. W., Vandenburgh, H. H., & Mooney, D. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903875106 · Cited by 448 · see citing works

Cellular and molecular mechanisms underlying age-related skeletal muscle wasting and weakness

Ryall, J. G., Schertzer, J. D., & Lynch, G. S. (2008) · Biogerontology · doi:10.1007/s10522-008-9131-0 · Cited by 423 · see citing works

Wnt signaling in myogenesis

von Maltzahn, J., Chang, N. C., Bentzinger, C. F., & Rudnicki, M. A. (2012) · Trends in Cell Biology · doi:10.1016/j.tcb.2012.07.008 · Cited by 393 · see citing works

The p38 MAPK signaling pathway: A major regulator of skeletal muscle development

Keren, A., Tamir, Y., & Bengal, E. (2006) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2006.03.017 · Cited by 372 · see citing works

Cardiovascular disease in obstructive sleep apnoea syndrome: the role of intermittent hypoxia and inflammation

Garvey, J., Taylor, C. T., & McNicholas, W. T. (2009) · European Respiratory Journal · doi:10.1183/09031936.00111208 · Cited by 356 · see citing works

Oxygen homeostasis

Semenza, G. L. (2009) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.69 · Cited by 311 · see citing works

Complications and side effects of hyperbaric oxygen therapy.

Plafki, C., Peters, P., Almeling, M., Welslau, W., & Busch, R. (2000) · PubMed · Cited by 280 · see citing works

Common micro‐RNA signature in skeletal muscle damage and regeneration induced by Duchenne muscular dystrophy and acute ischemia

Greco, S., Simone, M. C. D., Colussi, C., Zaccagnini, G., Fasanaro, P., Pescatori, M., Cardani, R., Perbellini, R., Isaia, E., Sale, P., et al. (2009) · The FASEB Journal · doi:10.1096/fj.08-128579 · Cited by 253 · see citing works

Catabolic/Anabolic Balance and Muscle Wasting in Patients With COPD

Debigaré, R., Marquis, K., Côt́e, C. H., Tremblay, R. R., Michaud, A., Leblanc, P., & Maltais, F. (2003) · CHEST Journal · doi:10.1378/chest.124.1.83 · Cited by 240 · see citing works

Oxygen‐mediated regulation of skeletal muscle satellite cell proliferation and adipogenesis in culture

CSETE, M. E., Walikonis, J., Slawny, N. A., Wei, Y., Korsnes, S. J., Doyle, J. C., & Wold, B. J. (2001) · Journal of Cellular Physiology · doi:10.1002/jcp.10016 · Cited by 228 · see citing works

Operation Everest. II: Nutrition and body composition

Rose, M. S., Houston, C. S., Fulco, C. S., Coates, G., Sutton, J. R., & Cymerman, A. (1988) · Journal of Applied Physiology · doi:10.1152/jappl.1988.65.6.2545 · Cited by 220 · see citing works

Human skeletal muscle intracellular oxygenation: the impact of ambient oxygen availability

Richardson, R. S., Duteil, S., Wary, C., Wray, D. W., Hoff, J., & Carlier, P. G. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2005.102327 · Cited by 217 · see citing works

Hif-1α regulates differentiation of limb bud mesenchyme and joint development

Provot, S., Zinyk, D. L., Güneş, Y., Kathri, R., Le, Q., Kronenberg, H. M., Johnson, R. S., Longaker, M. T., Giaccia, A. J., & Schipani, E. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200612023 · Cited by 199 · see citing works

Hypoxia promotes satellite cell self-renewal and enhances the efficiency of myoblast transplantation

Liu, W., Wen, Y., Bi, P., Lai, X., Liu, X., Liu, X., & Kuang, S. (2012) · Development · doi:10.1242/dev.079665 · Cited by 198 · see citing works

A systematic review of the literature reporting the application of hyperbaric oxygen prevention and treatment of delayed radiation injuries: an evidence based approach.

Feldmeier, J. J., & Hampson, N. B. (2002) · PubMed · Cited by 193 · see citing works

Satellite Cells

Chang, N. C., & Rudnicki, M. A. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-416022-4.00006-8 · Cited by 180 · see citing works

Effect of pulmonary rehabilitation on muscle remodelling in cachectic patients with COPD

Vogiatzis, I., Simoes, D. C. M., Stratakos, G. K., Kourepini, E., Terzis, G. D., Manta, P., Athanasopoulos, D., Roussos, C., Wagner, P. D., & Zakynthinos, S. G. (2010) · European Respiratory Journal · doi:10.1183/09031936.00112909 · Cited by 173 · see citing works

Effects of different acute hypoxic regimens on tissue oxygen profiles and metabolic outcomes

Reinke, C., Bevans‐Fonti, S., Drager, L. F., Shin, M., & Polotsky, V. Y. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00492.2011 · Cited by 170 · see citing works

Hyperbaric oxygen therapy for chronic wounds

Kranke, P., Bennett, M. H., Debus, S. E., Roeckl-Wiedmann, I., & Schnabel, A. (2004) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd004123.pub2 · Cited by 167 · see citing works

Triggers and mechanisms of skeletal muscle wasting in chronic obstructive pulmonary disease

LANGEN, R. C. J., Gosker, H. R., Remels, A. H. V., & Schols, A. M. W. J. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.06.015 · Cited by 159 · see citing works

Control of the hypoxic response through regulation of mRNA translation

Wouters, B. G., van den Beucken, T., Magagnin, M. G., Koritzinsky, M., Fels, D. R., & Koumenis, C. (2005) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2005.03.009 · Cited by 154 · see citing works

mTOR regulates skeletal muscle regeneration in vivo through kinase-dependent and kinase-independent mechanisms

Ge, Y., Wu, A.-L., Warnes, C., Liu, J., Zhang, C., Kawasome, H., Terada, N., Boppart, M. D., Schoenherr, C. J., & Chen, J. (2009) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00248.2009 · Cited by 152 · see citing works

Myotoxic phospholipases A2 and the regeneration of skeletal muscles

Harris, J. B. (2003) · Toxicon · doi:10.1016/j.toxicon.2003.11.011 · Cited by 150 · see citing works

Does Oxidative Stress Modulate Limb Muscle Atrophy in Severe COPD Patients?

Fermoselle, C., Rabinovich, R., Ausín, P., Puig-Vilanova, E., Coronell, C., Sanchez, F., Roca, J., Gea, J., & Barreiro, E. (2012) · European Respiratory Journal · doi:10.1183/09031936.00137211 · Cited by 148 · see citing works

Adaptive Myogenesis under Hypoxia

Yun, Z., Lin, Q., & Giaccia, A. J. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.8.3040-3055.2005 · Cited by 145 · see citing works

Hypoxia Inhibits Myogenic Differentiation through Accelerated MyoD Degradation

Carlo, A. D., Mori, R. D., Martelli, F., Pompilio, G., Capogrossi, M. C., & Germani, A. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313931200 · Cited by 142 · see citing works

Sarcopenia is a prognostic factor for overall survival in patients with critical limb ischemia.

Matsubara, Y., Matsumoto, T., Aoyagi, Y., Tanaka, S., Okadome, J., Morisaki, K., Shirabe, K., & Maehara, Y. (2015) · Journal of Vascular Surgery · doi:10.1016/j.jvs.2014.10.094 · Cited by 137 · see citing works

HIF-1-driven skeletal muscle adaptations to chronic hypoxia: molecular insights into muscle physiology

Favier, F. B., Britto, F. A., Freyssenet, D. G., Bigard, X. A., & Benoit, H. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2025-9 · Cited by 129 · see citing works

Downregulation of Akt/Mammalian Target of Rapamycin Pathway in Skeletal Muscle Is Associated with Increased REDD1 Expression in Response to Chronic Hypoxia

Favier, F. B., Costes, F., Defour, A., Bonnefoy, R., Lefai, E., Baugé, S., Peinnequin, A., Benoit, H., & Freyssenet, D. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00550.2009 · Cited by 127 · see citing works

Hyperbaric oxygen therapy for acute ischaemic stroke

Bennett, M. H., Weibel, S., Wasiak, J., Schnabel, A., French, C. R., & Kranke, P. (2014) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd004954.pub3 · Cited by 124 · see citing works

Selective control of skeletal muscle differentiation by Akt1

Wilson, E. M., & Rotwein, P. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.c600315200 · Cited by 118 · see citing works

Time course of skeletal muscle repair and gene expression following acute hind limb ischemia in mice

Paoni, N. F., Peale, F. V., Jr., Wang, F., Errett-Baroncini, C., Steinmetz, H., Toy, K. J., Bai, W., Williams, P. M., Bunting, S., Gerritsen, M. E., et al. (2002) · Physiological Genomics · doi:10.1152/physiolgenomics.00110.2002 · Cited by 113 · see citing works

Hypoxia converts the myogenic action of insulin-like growth factors into mitogenic action by differentially regulating multiple signaling pathways

Ren, H., Accili, D., & Duan, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909570107 · Cited by 100 · see citing works

Culture in low levels of oxygen enhances in vitro proliferation potential of satellite cells from old skeletal muscles

Chakravarthy, M. V., Spangenburg, E. E., & Booth, F. W. (2001) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000929 · Cited by 98 · see citing works

O 2 Regulates Skeletal Muscle Progenitor Differentiation through Phosphatidylinositol 3-Kinase/AKT Signaling

Majmundar, A. J., Skuli, N., Mesquita, R. C., Kim, M. N., Yodh, A. G., Nguyen-McCarty, M., & Simon, M. C. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.05857-11 · Cited by 75 · see citing works

Myogenesis and muscle regeneration

Yusuf, F., & Brand‐Saberi, B. (2012) · Histochemistry and Cell Biology · doi:10.1007/s00418-012-0972-x · Cited by 74 · see citing works

Satellite Cells Senescence in Limb Muscle of Severe Patients with COPD

Thériault, M., Paré, M., Maltais, F., & Debigaré, R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0039124 · Cited by 71 · see citing works

Hyperbaric Oxygen Induces Basic Fibroblast Growth Factor and Hepatocyte Growth Factor Expression, and Enhances Blood Perfusion and Muscle Regeneration in Mouse Ischemic Hind Limbs

Asano, T., Kaneko, E., Shinozaki, S., Imai, Y., Shibayama, M., Chiba, T., Ai, M., Kawakami, A., Asaoka, H., Nakayama, T., et al. (2007) · Circulation Journal · doi:10.1253/circj.71.405 · Cited by 69 · see citing works

HIF modulation of Wnt signaling regulates skeletal myogenesis <i>in vivo</i>

Majmundar, A. J., Lee, D. S. M., Skuli, N., Mesquita, R. C., Kim, M. N., Yodh, A. G., Nguyen-McCarty, M., Li, B., & Simon, M. C. (2015) · Development · doi:10.1242/dev.123026 · Cited by 67 · see citing works

Myosin heavy chain composition of skeletal muscles in young rats growing under hypobaric hypoxia conditions

Bigard, A. X., Sanchez, H., Birot, O., & Serrurier, B. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.88.2.479 · Cited by 67 · see citing works

Hypoxia Promotes Proliferation of Human Myogenic Satellite Cells: A Potential Benefactor in Tissue Engineering of Skeletal Muscle

Koning, M., Werker, P. M. N., van Luyn, M. J. A., & Harmsen, M. C. (2011) · Tissue Engineering Part A · doi:10.1089/ten.tea.2010.0624 · Cited by 65 · see citing works

Hyperbaric oxygen therapy does not affect recovery from delayed onset muscle soreness

Mekjavić, I. B., EXNER, J. A., Tesch, P. A., & Eiken, O. (2000) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-200003000-00002 · Cited by 65 · see citing works

Treatment of exercise-induced muscle injury via hyperbaric oxygen therapy

Harrison, B. C., ROBINSON, D., DAVISON, B. J., FOLEY, B., SEDA, E., & Byrnes, W. C. (2001) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-200101000-00007 · Cited by 65 · see citing works

Skeletal muscle atrophy: disease-induced mechanisms may mask disuse atrophy

Malavaki, C. J., Sakkas, G. K., Mitrou, G. I., Kalyva, A., Stefanidis, I., Myburgh, K. H., & Karatzaferi, C. (2015) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-015-9439-8 · Cited by 61 · see citing works

Reduced myotube diameter, atrophic signalling and elevated oxidative stress in cultured satellite cells from <scp>COPD</scp> patients

Pomiès, P., Rodriguez, J., Blaquière, M., Sedraoui, S., Gouzi, F., Carnac, G., Laoudj‐Chenivesse, D., Mercier, J., Préfaut, C., & Hayot, M. (2015) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12390 · Cited by 61 · see citing works

Hypoxia Inhibits Myogenic Differentiation through p53 Protein-dependent Induction of Bhlhe40 Protein

Wang, C., Liu, W., Liu, Z., Chen, L., Liu, X., & Kuang, S. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.688671 · Cited by 59 · see citing works

Hyperbaric Oxygen in the Treatment of Acute Muscle Stretch Injuries

Best, T. M., Loitz-Ramage, B., Corr, D. T., & Vanderby, R. (1998) · The American Journal of Sports Medicine · doi:10.1177/03635465980260030401 · Cited by 57 · see citing works

Hypoxia affects positively the proliferation of bovine satellite cells and their myogenic differentiation through up‐regulation of MyoD

Kook, S., Son, Y., Lee, K., Lee, H., Chung, W., Choi, K., & Lee, J. (2008) · Cell Biology International · doi:10.1016/j.cellbi.2008.03.017 · Cited by 57 · see citing works

Exposure to hypobaric hypoxia results in higher oxidative stress compared to normobaric hypoxia

Ribon‐Demars, A., Pialoux, V., SAUGY, J. J., Rupp, T., Faiss, R., Debevec, T., & Millet, G. P. (2015) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2015.12.008 · Cited by 56 · see citing works

Effects of Hyperbaric Oxygen on a Human Model of Injury

Staples, J. R., Clement, D. B., Taunton, J. E., & McKenzie, D. C. (1999) · The American Journal of Sports Medicine · doi:10.1177/03635465990270050901 · Cited by 55 · see citing works

Enhancement of satellite cell differentiation and functional recovery in injured skeletal muscle by hyperbaric oxygen treatment

Horie, M., Enomoto, M., Shimoda, M., Okawa, A., Miyakawa, S., & Yagishita, K. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00235.2013 · Cited by 53 · see citing works

Regenerative defect in vastus lateralis muscle of patients with chronic obstructive pulmonary disease

Thériault, M., Paré, M., Lemire, B. B., Maltais, F., & Debigaré, R. (2014) · Respiratory Research · doi:10.1186/1465-9921-15-35 · Cited by 51 · see citing works

Knockdown of hypoxia‐inducible factor‐1α by siRNA inhibits C2C12 myoblast differentiation

Ono, Y., Sensui, H., Sakamoto, Y., & Nagatomi, R. (2006) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20804 · Cited by 50 · see citing works

Hypoxia Increases Mouse Satellite Cell Clone Proliferation Maintaining both In Vitro and In Vivo Heterogeneity and Myogenic Potential

Urbani, L., Piccoli, M., Franzin, C., Pozzobon, M., & Coppi, P. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049860 · Cited by 50 · see citing works

Ambient hypoxia enhances the loss of muscle mass after extensive injury

Chaillou, T., Koulmann, N., Meunier, A., Pugnière, P., McCarthy, J. J., Beaudry, M., & Bigard, X. A. (2013) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-013-1336-7 · Cited by 48 · see citing works

Accumulation and nuclear import of HIF1 alpha during high and low oxygen concentration in skeletal muscle cells in primary culture

Kubis, H., Hanke, N., Scheibe, R. J., & Gros, G. (2005) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2005.05.007 · Cited by 47 · see citing works

Hypoxia transiently affects skeletal muscle hypertrophy in a functional overload model

Chaillou, T., Koulmann, N., Simler, N., Meunier, A., Serrurier, B., Chapot, R., Peinnequin, A., Beaudry, M., & Bigard, X. A. (2011) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00262.2011 · Cited by 43 · see citing works

Blunting effect of hypoxia on the proliferation and differentiation of human primary and rat L6 myoblasts is not counteracted by Epo

Launay, T., Hagström, L., Lottin, S., Marchant, D., Quidu, P., Favret, F., Duvallet, A. L., Darribère, T., Richalet, J., & Beaudry, M. (2009) · Cell Proliferation · doi:10.1111/j.1365-2184.2009.00648.x · Cited by 42 · see citing works

Hypoxia alters contractile protein homeostasis in L6 myotubes

Caron, M., Thériault, M., Paré, M., Maltais, F., & Debigaré, R. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.04.006 · Cited by 40 · see citing works

Hypoxia and muscle maintenance regulation

de Theije, C. C., Costes, F., LANGEN, R. C. J., Pison, C. M., & Gosker, H. R. (2011) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e32834b6e79 · Cited by 39 · see citing works

Hyperbaric Oxygen Therapy in Sports Injuries

James, P., Scott, B., & Allen, M. W. (1993) · Physiotherapy · doi:10.1016/s0031-9406(10)60302-1 · Cited by 38 · see citing works

p21Cip1 expression is increased in ambient oxygen, compared to estimated physiological (5%) levels in rat muscle precursor cell culture

Lees, S. J., Childs, T. E., & Booth, F. W. (2008) · Cell Proliferation · doi:10.1111/j.1365-2184.2008.00512.x · Cited by 32 · see citing works

Hyperbaric oxygen improves contractile function of regenerating rat skeletal muscle after myotoxic injury

Gregorevic, P., Lynch, G. S., & Williams, D. A. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.89.4.1477 · Cited by 29 · see citing works

Effects of Transient Hypoxia versus Prolonged Hypoxia on Satellite Cell Proliferation and Differentiation In Vivo

Jash, S., & Adhya, S. (2015) · Stem Cells International · doi:10.1155/2015/961307 · Cited by 26 · see citing works

Oxygen Modulates the Glutathione Peroxidase Activity during the L6 Myoblast Early Differentiation Process

Hidalgo, M., Marchant, D., Quidu, P., Youcef-Ali, K., Richalet, J., Beaudry, M., BESSE, S., & Launay, T. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000356650 · Cited by 26 · see citing works

Hyperbaric oxygen increases the contractile function of regenerating rat slow muscles

Gregorevic, P., WILLIAMS, D. A., & Lynch, G. S. (2002) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-200204000-00011 · Cited by 24 · see citing works

Cellular and molecular responses of human skeletal muscle exposed to hypoxic environment.

Mancinelli, R., Pietrangelo, T., Rovere, R. L., Toniolo, L., Fanò, G., Reggiani, C., & Fulle, S. (2011) · PubMed · Cited by 24 · see citing works

Effects of Hyperbaric Oxygen at 1.25 Atmospheres Absolute with Normal Air on Macrophage Number and Infiltration during Rat Skeletal Muscle Regeneration

Fujita, N., Ono, M., Tomioka, T., & Deie, M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0115685 · Cited by 23 · see citing works

Effect of hypoxia exposure on the recovery of skeletal muscle phenotype during regeneration

Chaillou, T., Koulmann, N., Meunier, A., Chapot, R., Serrurier, B., Beaudry, M., & Bigard, X. A. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-013-1952-8 · Cited by 22 · see citing works

Atmospheric Oxygen Tension Slows Myoblast Proliferation via Mitochondrial Activation

Duguez, S., Duddy, W. J., Gnocchi, V. F., Bowe, J., Dadgar, S., & Partridge, T. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043853 · Cited by 20 · see citing works

The Effect of Hyperbaric Oxygen Treatment on the Healing of Burn Wounds in Nicotinized and Nonnicotinized Rats

Selçuk, C. T., Özalp, B., Durğun, M., Tekin, A., Akkoç, M. F., Alabalık, U., & İlgezdi, S. (2012) · Journal of Burn Care & Research · doi:10.1097/bcr.0b013e318270092e · Cited by 19 · see citing works

The translational repressor 4E-BP mediates the hypoxia-induced defects in myotome cells

Hidalgo, M., Bouffant, R. L., Bello, V., Buisson, N., Cormier, P., Beaudry, M., & Darribère, T. (2012) · Journal of Cell Science · doi:10.1242/jcs.097998 · Cited by 17 · see citing works

Effect of hypoxia exposure on the phenotypic adaptation in remodelling skeletal muscle submitted to functional overload

Chaillou, T., Koulmann, N., Meunier, A., Malgoyre, A., Serrurier, B., Beaudry, M., & Bigard, X. A. (2013) · Acta Physiologica · doi:10.1111/apha.12110 · Cited by 17 · see citing works

Therapeutic use of hyperbaric oxygen therapy for children with autism spectrum disorder.

Halepoto, D. M., AL-Ayadhi, L. Y., & Salam, A. A. A. (2014) · PubMed · Cited by 11 · see citing works

Effects of hyperbaric oxygen therapy on rabbit skeletal muscle during extremity lengthening

Atesalp, A. S., Yurttaş, Y., Köse, Ö., Demiralp, B., Yıldız, C., Kürklü, M., Kurt, B., Karaçalioğlu, Ö., Özgürtaş, T., Öztaş, E., et al. (2007) · Archives of Orthopaedic and Trauma Surgery · doi:10.1007/s00402-007-0525-2 · Cited by 9 · see citing works

Neurological decompression illness (DCI) responds favorably to hyperbaric oxygen treatment (HBOT) even when treatment is substantially delayed.

Kizer, K. W. (2008) · PubMed · Cited by 1 · see citing works

To the editor UHM

Kizer, K. W. (2008) · Undersea and Hyperbaric Medicine · Cited by 1 · see citing works

The Hyperoxic-Hypoxic Paradox

Hadanny, A., & Efrati, S. (2020) · Biomolecules · doi:10.3390/biom10060958 · Cited by 216 · see citing works

Maintaining bovine satellite cells stemness through p38 pathway

Ding, S., Swennen, G., Meßmer, T., Gagliardi, M., Molin, D. G. M., Li, C., Zhou, G., & Post, M. J. (2018) · Scientific Reports · doi:10.1038/s41598-018-28746-7 · Cited by 176 · see citing works

Hypoxia-Induced ROS Contribute to Myoblast Pyroptosis during Obstructive Sleep Apnea via the NF-κB/HIF-1α Signaling Pathway

Yu, L., Zhang, W., Han, X., Li, Y., Lu, Y., Pan, J., Mao, J.-Q., Zhu, L., Deng, J., Huang, W., et al. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/4596368 · Cited by 100 · see citing works

Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting

Henrot, P., Dupin, I., Schilfarth, P., Esteves, P., Blervaque, L., Zysman, M., Gouzi, F., Hayot, M., Pomiès, P., & Berger, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076454 · Cited by 85 · see citing works

Transient HIF2A inhibition promotes satellite cell proliferation and muscle regeneration

Xie, L., Yin, A., Nichenko, A. S., Beedle, A. M., Call, J. A., & Yin, H. (2018) · Journal of Clinical Investigation · doi:10.1172/jci96208 · Cited by 81 · see citing works

Skeletal Muscle Fiber Type in Hypoxia: Adaptation to High-Altitude Exposure and Under Conditions of Pathological Hypoxia

Chaillou, T. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01450 · Cited by 80 · see citing works

Hypoxia preconditioned bone marrow-derived mesenchymal stromal/stem cells enhance myoblast fusion and skeletal muscle regeneration

Archacka, K., Grabowska, I., Mierzejewski, B., Graffstein, J., Górzyńska, A., Krawczyk, M., Różycka, A. M., Kalaszczyńska, I., Muras, G., Stremińska, W., et al. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02530-3 · Cited by 66 · see citing works

Oxygen therapy attenuates neuroinflammation after spinal cord injury

Sunshine, M. D., Bindi, V. E., Nguyen, B. L., Doerr, V., Boeno, F. P., Chandran, V., Smuder, A. J., & Fuller, D. D. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-023-02985-6 · Cited by 55 · see citing works

Bovine Satellite Cells Isolated after 2 and 5 Days of Tissue Storage Maintain the Proliferative and Myogenic Capacity Needed for Cultured Meat Production

Skrivergaard, S., Rasmussen, M. K., Therkildsen, M., & Young, J. F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22168376 · Cited by 46 · see citing works

Hyperbaric Oxygen Therapy in Sports Musculoskeletal Injuries

Moghadam, N., Hieda, M., Ramey, L. N., Levine, B. D., & Guilliod, R. (2019) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000002257 · Cited by 46 · see citing works

Hypoxia and Hypoxia-Inducible Factor Signaling in Muscular Dystrophies: Cause and Consequences

Nguyen, T.-H., Conotte, S., Belayew, A., Declèves, A., Legrand, A., & Tassin, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137220 · Cited by 45 · see citing works

Critical Limb Ischemia Induces Remodeling of Skeletal Muscle Motor Unit, Myonuclear-, and Mitochondrial-Domains

Mohiuddin, M., Lee, N. H., Moon, J. Y., Han, W. M., Anderson, S. E., Choi, J. J., Shin, E.-J., Nakhai, S. A., Trần, T. H., Aliya, B., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-45923-4 · Cited by 36 · see citing works

PDH‐mediated metabolic flow is critical for skeletal muscle stem cell differentiation and myotube formation during regeneration in mice

Hori, S., Hiramuki, Y., Nishimura, D., Sato, F., & Sehara‐Fujisawa, A. (2019) · The FASEB Journal · doi:10.1096/fj.201802479r · Cited by 36 · see citing works

Hyperbaric Oxygen Prevents Cognitive Impairments in Mice Induced by d-Galactose by Improving Cholinergic and Anti-apoptotic Functions

Chen, C., Huang, L., Nong, Z., Li, Y., Chen, W., Huang, J., Pan, X., Wu, G., & Lin, Y. (2017) · Neurochemical Research · doi:10.1007/s11064-016-2166-8 · Cited by 35 · see citing works

Vertebrate cell culture as an experimental approach – limitations and solutions

Abbas, M., Moradi, F., Hu, W., Regudo, K. L., Osborne, M., Pettipas, J., Atallah, D. S., Hachem, R., Ott-Peron, N., & Stuart, J. A. (2021) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2021.110570 · Cited by 32 · see citing works

Acute environmental hypoxia potentiates satellite cell‐dependent myogenesis in response to resistance exercise through the inflammation pathway in human

Britto, F. A., Gnimassou, O., Groote, E. D., Balan, E., Warnier, G., Everard, A., Cani, P. D., & Deldicque, L. (2019) · The FASEB Journal · doi:10.1096/fj.201902244r · Cited by 30 · see citing works

Environmental hypoxia favors myoblast differentiation and fast phenotype but blunts activation of protein synthesis after resistance exercise in human skeletal muscle

Gnimassou, O., Fernández‐Verdejo, R., Brook, M. S., Naslain, D., Balan, E., Sayda, M. H., Cegielski, J., Nielens, H., Decottignies, A., Demoulin, J., et al. (2018) · The FASEB Journal · doi:10.1096/fj.201800049rr · Cited by 28 · see citing works

Deaccelerated Myogenesis and Autophagy in Genetically Induced Pulmonary Emphysema

Balnis, J., Drake, L. A., Singer, D. V., Vincent, C. E., Korponay, T. C., D’Armiento, J., Lee, C. G., Elias, J. A., Singer, H. A., & Jaitovich, A. (2022) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2021-0351oc · Cited by 27 · see citing works

Graphene Oxide Scaffold Stimulates Differentiation and Proangiogenic Activities of Myogenic Progenitor Cells

Wierzbicki, M., Hotowy, A., Kutwin, M., Jaworski, S., Bałaban, J., Sosnowska, M., Wójcik, B., Wędzińska, A., Chwalibóg, A., & Sawosz, E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21114173 · Cited by 25 · see citing works

Photosynthetic biomaterials: applications of photosynthesis in algae as oxygenerator in biomedical therapies

Wang, Y., Xue, Y., Zhang, T., Fang, Q., Jin, M.-Y., Wang, X., Wang, Z., Hu, Y., Zhao, W., Lou, D., et al. (2021) · Bio-Design and Manufacturing · doi:10.1007/s42242-021-00129-4 · Cited by 25 · see citing works

Mitochondrial NDUFA4L2 is a novel regulator of skeletal muscle mass and force

Liu, Z., Chaillou, T., Alves, E. S., Mader, T., Jude, B., Ferreira, D. M. S., Hynynen, H., Cheng, A. J., Jonsson, W. O., Pironti, G., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202100066r · Cited by 22 · see citing works

Titanium decorated iron oxide (Ti@Fe2O3) regulates the proliferation of bovine muscle satellite cells through oxidative stress

Ramalingam, V., Mohan, H., & Hwang, I. (2020) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2020.104459 · Cited by 21 · see citing works

Critical role of the mTOR pathway in poultry skeletal muscle physiology and meat quality: an opinion paper

Xu, J., & Velleman, S. G. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1228318 · Cited by 21 · see citing works

Chronic hypoxia impairs skeletal muscle repair via HIF‐2α stabilization

Yin, A., Fu, W., Elengickal, A. J., Kim, J., Liu, Y., Bigot, A., Mamchaoui, K., Call, J. A., & Yin, H. (2024) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.13436 · Cited by 21 · see citing works

Cobalt chloride, a chemical hypoxia-mimicking agent, suppresses myoblast differentiation by downregulating myogenin expression

Wagatsuma, A., Arakawa, M., Matsumoto, H., Matsuda, R., Hoshino, T., & Mabuchi, K. (2020) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-020-03762-2 · Cited by 20 · see citing works

Downregulated miR‐204 Promotes Skeletal Muscle Regeneration

Tan, Y., Shen, L., Gan, M., Fan, Y., Xiao, C., Zheng, T., Niu, L., Chen, L., Jiang, D., Li, X., et al. (2020) · BioMed Research International · doi:10.1155/2020/3183296 · Cited by 20 · see citing works

Primary bovine skeletal muscle cells enters apoptosis rapidly via the intrinsic pathway when available oxygen is removed

Rønning, S. B., Andersen, P. V., Pedersen, M. E., & Hollung, K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182928 · Cited by 19 · see citing works

Bioengineering strategies for the treatment of peripheral arterial disease

Li, C., Kitzerow, O., Nie, F., Dai, J., Liu, X., Carlson, M. A., Casale, G. P., Pipinos, I. I., & Li, X. (2020) · Bioactive Materials · doi:10.1016/j.bioactmat.2020.09.007 · Cited by 19 · see citing works

Nuclear Factor Erythroid 2-Related Factor 2 and Its Targets in Skeletal Muscle Repair and Regeneration

Łoboda, A., & Dulak, J. (2023) · Antioxidants and Redox Signaling · doi:10.1089/ars.2022.0208 · Cited by 18 · see citing works

NRF2 Regulates Viability, Proliferation, Resistance to Oxidative Stress, and Differentiation of Murine Myoblasts and Muscle Satellite Cells

Bronisz-Budzyńska, I., Kozakowska, M., Pietraszek‐Gremplewicz, K., Madej, M., Józkowicz, A., Łoboda, A., & Dulak, J. (2022) · Cells · doi:10.3390/cells11203321 · Cited by 18 · see citing works

Pattern of myogenesis and vascular repair in early and advanced lesions of juvenile dermatomyositis.

Baumann, M., Gumpold, C., Mueller-Felber, W., Schoser, B., Haberler, C., Loescher, W., Rostásy, K., Fischer, M., & Wanschitz, J. (2018) · Neuromuscular Disorders · doi:10.1016/j.nmd.2018.09.002 · Cited by 18 · see citing works

Gintonin-enriched fraction protects against sarcopenic obesity by promoting energy expenditure and attenuating skeletal muscle atrophy in high-fat diet-fed mice

Jin, H., Oh, H., Nah, S.-Y., & Lee, B.-Y. (2021) · Journal of Ginseng Research · doi:10.1016/j.jgr.2021.10.003 · Cited by 17 · see citing works

Hyperbaric oxygen therapy as an adjunt treatment for glioma and brain metastasis: a literature review

Cai, T. (2025) · Medical Gas Research · doi:10.4103/mgr.medgasres-d-24-00096 · Cited by 16 · see citing works

Impact of Different Methods of Induction of Cellular Hypoxia: Focus on Protein Homeostasis Signaling Pathways and Morphology of C2C12 Skeletal Muscle Cells Differentiated into Myotubes

Bensaid, S., Fabre, C., Fourneau, J., & Cieniewski-Bernard, C. (2019) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-019-00687-3 · Cited by 16 · see citing works

Hypoxia mediates Hif-1α to affect myofiber development and Vc regulates the influence by activating Shh-Gli pathway in channel catfish (Ictalurus punctatus)

Xiao, K., Wang, X., Dai, Y., Huang, Y., Wang, M.-M., Guo, H., Liu, W., Li, X., Abasubong, K. P., & Jiang, G. (2022) · Aquaculture · doi:10.1016/j.aquaculture.2022.738849 · Cited by 15 · see citing works

Effects of Ecklonia stolonifera extract on the obesity and skeletal muscle regeneration in high-fat diet-fed mice

Jin, H., Oh, H., Kim, J., Lee, K., Han, X., Lee, O., & Lee, B.-Y. (2021) · Journal of Functional Foods · doi:10.1016/j.jff.2021.104511 · Cited by 15 · see citing works

Impaired regenerative capacity contributes to skeletal muscle dysfunction in chronic obstructive pulmonary disease

Jaitovich, A. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00292.2022 · Cited by 14 · see citing works

Linoleic acid-induced ANGPTL4 inhibits C2C12 skeletal muscle differentiation by suppressing Wnt/β-catenin

Son, Y., Lorenz, W. W., & Paton, C. M. (2023) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2023.109324 · Cited by 13 · see citing works

Hypoxia promotes proliferation and inhibits myogenesis in broiler satellite cells

Jung, U., Kim, M., Dowker-Key, P., Noë, S., Bettaieb, A., Shepherd, E., & Voy, B. (2024) · Poultry Science · doi:10.1016/j.psj.2023.103203 · Cited by 13 · see citing works

Electrical Stimulation of Cultured Myotubes in vitro as a Model of Skeletal Muscle Activity: Current State and Future Prospects

Vepkhvadze, T. F., Vorotnikov, A. V., & Викторович, П. Д. (2021) · Biochemistry (Moscow) · doi:10.1134/s0006297921050084 · Cited by 12 · see citing works

Loss of miR-451a enhances SPARC production during myogenesis

Munk, R. B., Martindale, J. L., Yang, X., Yang, J., Grammatikakis, I., Germanio, C. D., Mitchell, S. J., de Cabo, R., Lehrmann, E., Zhang, Y., et al. (2019) · PLoS ONE · doi:10.1371/journal.pone.0214301 · Cited by 12 · see citing works

Higher strength gain after hypoxic vs normoxic resistance training despite no changes in muscle thickness and fractional protein synthetic rate

de ten Ryen, S. V. D., Warnier, G., Gnimassou, O., Belhaj, M. R., Benoit, N., Naslain, D., Brook, M. S., Smith, K., Wilkinson, D. J., Nielens, H., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202100654rr · Cited by 12 · see citing works

High‐fat diet pre‐conditioning improves microvascular remodelling during regeneration of ischaemic mouse skeletal muscle

Nwadozi, E., Rudnicki, M., Ciantis, M. D., Milkovich, S., Pulbere, A., Roudier, E. A., Birot, O., Gustafsson, T. P., Ellis, C. G., & Haas, T. L. (2020) · Acta Physiologica · doi:10.1111/apha.13449 · Cited by 11 · see citing works

Anemic hypoxemia reduces myoblast proliferation and muscle growth in late-gestation fetal sheep

Rozance, P. J., Wesolowski, S. R., Jonker, S. S., & Brown, L. D. (2021) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00342.2020 · Cited by 11 · see citing works

Oxygen in Metabolic Dysfunction and Its Therapeutic Relevance

López-Pascual, A., Trayhurn, P., Martínez, J. A., & González‐Muniesa, P. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2019.7901 · Cited by 13 · see citing works

Effects of hyperoxia and hypoxia on the proliferation of C2C12 myoblasts

Horiike, M., Ogawa, Y., & Kawada, S. (2021) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00269.2020 · Cited by 9 · see citing works

DOCK3 regulates normal skeletal muscle regeneration and glucose metabolism

Samani, A., Karuppasamy, M., English, K. G., Siler, C. A., Wang, Y., Widrick, J. J., & Alexander, M. S. (2023) · The FASEB Journal · doi:10.1096/fj.202300386rr · Cited by 9 · see citing works

Coordinated expression of Jumonji and AHCY under OCT transcription factor control to regulate gene methylation in wood frogs during anoxia

Gupta, A., & Storey, K. B. (2021) · Gene · doi:10.1016/j.gene.2021.145671 · Cited by 9 · see citing works

Simvastatin Enhances Muscle Regeneration Through Autophagic Defect-Mediated Inflammation and mTOR Activation in G93ASOD1 Mice

Wang, Y., Bai, L., Li, S., Wen, Y., Liu, Q., Li, R., & Liu, Y. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-02216-6 · Cited by 7 · see citing works

Regulation of satellite cells by exercise in hypoxic conditions: a narrative review

de ten Ryen, S. V. D., Francaux, M., & Deldicque, L. (2021) · European Journal of Applied Physiology · doi:10.1007/s00421-021-04641-4 · Cited by 8 · see citing works

Exercise improves hypobaric hypoxia-induced skeletal muscle dysfunction via Sirt1-Mediated myotube and mitochondrial remodeling

Wang, C., Chen, W., Chen, H., Zhao, J., He, J., Hu, Y., He, M., Zhang, Y., Lin, C.-S., Chang, J., et al. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.08.022 · Cited by 9 · see citing works

Utility of hypoxic modalities for musculoskeletal injury rehabilitation in athletes: A narrative review of mechanisms and contemporary perspectives

Narang, B. J., Drole, K., Barber, J. F. P., Goods, P. S. R., & Debevec, T. (2024) · Journal of Sports Sciences · doi:10.1080/02640414.2024.2416779 · Cited by 7 · see citing works

Skeletal muscle-specific Bambi deletion induces hypertrophy and oxidative switching coupling with adipocyte thermogenesis against metabolic disorders

Yao, X., Mai, X., Tian, Y., Liu, Y., Jin, G., Li, Z., Chen, S., Dai, X., Huang, L., Fan, Z., et al. (2025) · Science China Life Sciences · doi:10.1007/s11427-023-2586-x · Cited by 7 · see citing works

Donepezil, an anti-Alzheimer's disease drug, promotes differentiation and regeneration in injured skeletal muscle through the elevation of the expression of myogenic regulatory factors

Todaka, H., Arikawa, M., Noguchi, T., Ichikawa, A., & Sato, T. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174528 · Cited by 7 · see citing works

Cholesterol and Sphingomyelin Polarize at the Leading Edge of Migrating Myoblasts and Involve Their Clustering in Submicrometric Domains

Vanderroost, J., Avalosse, N., Mohammed, D., Hoffmann, D., Henriet, P., Pierreux, C. E., Alsteens, D., & Tyteca, D. (2023) · Biomolecules · doi:10.3390/biom13020319 · Cited by 7 · see citing works

Acute hypoxia attenuates resistance exercise-induced ribosome signaling but does not impact satellite cell pool expansion in human skeletal muscle

Horwath, O., Nordström, F., von Walden, F., Apró, W., & Moberg, M. (2023) · The FASEB Journal · doi:10.1096/fj.202202065rr · Cited by 6 · see citing works

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 · see citing works

Intermittent Hypoxic Exposure with High Dose of Arginine Impact on Circulating Mediators of Tissue Regeneration

Zembroń-Łacny, A., Gramacki, A., Wawrzyniak-Gramacka, E., Tylutka, A., Hertmanowska, N., Kasperska, A., & Czuba, M. (2020) · Nutrients · doi:10.3390/nu12071933 · Cited by 6 · see citing works

Activation of the Hippo Pathway in Rana sylvatica: Yapping Stops in Response to Anoxia

Gupta, A., & Storey, K. B. (2021) · Life · doi:10.3390/life11121422 · Cited by 5 · see citing works

Echinacoside stimulates myogenesis and ATP-dependent thermogenesis in the skeletal muscle via the activation of D1-like dopaminergic receptors

Haddish, K., & Yun, J. W. (2024) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2024.109886 · Cited by 4 · see citing works

Modulation of the Cellular Microenvironment by Mechanical Fluid Shear Stress and Hypoxia Alters the Differentiation Capacity of Skeletal Muscle-Derived Stem Cells

Hawlitschek, P., Klymiuk, M. C., Eldaey, A., Wenisch, S., Arnhold, S., & Elashry, M. I. (2024) · Applied Sciences · doi:10.3390/app14073047 · Cited by 4 · see citing works

Rosa canina Extract Attenuates Muscle Atrophy in L6 Myotubes and Immobilized Mice

Lee, H., Kim, M., Kang, J.-K., Hwang, J., & Kim, B. (2025) · Nutrients · doi:10.3390/nu17213462 · Cited by 3 · see citing works

Iron Deficiency Impairs Muscle Stem Cell Proliferation and Skeletal Muscle Regeneration via HIF‐2α Stabilization

Fu, W., Liu, Y., Yin, A., Xie, L., & Yin, H. (2025) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.70124 · Cited by 3 · see citing works

Hyperbaric oxygen therapy enhances restoration of physical functional in patients with recurrent glioma: A case report

Cai, T., Jin, T., Guan, Y., Zou, W., Wang, X., & Zhu, Y. (2024) · Oncology Letters · doi:10.3892/ol.2024.14716 · Cited by 3 · see citing works

Investigation on the Effect of Cyclic Stretch and Hypoxia on Recovery of Damaged Skeletal Muscle Cells Using Microfluidic System

Kim, J., Kim, W., Ahn, J., Jang, Y. J., Park, H., & Jeon, J. S. (2021) · Advanced Materials Technologies · doi:10.1002/admt.202100465 · Cited by 3 · see citing works

Mapping the global research landscape and hotspot of exercise therapy and chronic obstructive pulmonary disease: A bibliometric study based on the web of science database from 2011 to 2020

Zhou, Y., Liu, X., & Wu, W. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.947637 · Cited by 3 · see citing works

RNA Sequencing Reveals the Inhibitory Effect of High Levels of Arachidonic Acid and Linoleic Acid on C2C12 Differentiation and Myogenic Biomarkers

Wang, W., Abdelrahman, M., Yang, Y., Lv, H., & Yang, L. (2024) · Nutrients · doi:10.3390/nu16050706 · Cited by 3 · see citing works

Muscle oxygenation induced by cycling exercise does not accelerate recovery kinetics following exercise-induced muscle damage in humans: A randomized cross-over study

Abaïdia, A., Cosyns, S., & Dupont, G. (2019) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2019.05.005 · Cited by 3 · see citing works

Hyperbaric Oxygen Therapy

Moghadam, N., Amiri, A. A., & Amiri, A. A. (2025) · Springer eBooks · doi:10.1007/978-3-031-44270-4_30 · Cited by 2 · see citing works

Hypoxia-driven Dental Pulp Stem Cells as a Promising Strategy for Tissue Regeneration

Liao, C., Chen, L., Xiang, M., Long, S., Xiang, M., Xiao, L., Long, Q., Liu, J., & Guan, X. (2024) · Current Stem Cell Research & Therapy · doi:10.2174/011574888x312892240625091241 · Cited by 1 · see citing works

Transient hypoxia followed by progressive reoxygenation is required for muscle repair

Quétin, M., Der Vartanian, A., Dubois, C., Berthier, J., Ledoux, M., Michineau, S., Drayton-Libotte, B., Prola, A., Sotiropoulos, A., Relaix, F., et al. (2026) · EMBO Reports · doi:10.1038/s44319-025-00679-z · Cited by 1 · see citing works

PINK1/Parkin-Mediated Mitophagy Participates in High-Altitude Hypoxia Adaptation in Yaks via Energy Metabolism Remodeling

Li, Z.-B., Li, T.-S., Li, M. Y., Li, Z.-D., Wang, J.-L., Li, G.-X., Lv, J.-S., Li, L.-X., Ye, X.-D., & Ling, X.-D. (2026) · Animals · doi:10.3390/ani16142121 · Cited by 1 · see citing works

Maintaining the stemness of satellite cells during long-term culture

Ding (2019) · doi:10.26481/dis.20190327sd · Cited by 1 · see citing works

Электростимуляция миотуб как модель сократительной активности мышц in vitro: текущее состояние и перспективы развития

Vepkhvadze, T. F., Vorotnikov, A. V., & Викторович, П. Д. (2021) · Biochemistry (Moscow) · doi:10.31857/s0320972521050080

Dysregulated myogenesis and autophagy in genetically induced pulmonary emphysemaPreprint

Balnis, J., Drake, L. A., Singer, D. V., Vincent, C. E., Korponay, T. C., D'Armiento, J. M., Lee, C. G., Elias, J. A., Singer, H. A., & Jaitovich, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.08.450201

Complex Yet Coordinated: Regulation of Transcriptional Factors and Cell Signaling Pathways to Endure Anoxia in Rana sylvatica

Gupta, A. (2022) · doi:10.22215/etd/2022-15335

A muscle hypertrophy-derived myokine reprograms the stromal vascular fractions differentiation towards thermogenic adipocytes in subcutaneous adipose tissuePreprint

Yao, X., Mai, X., Tian, Y., Liu, Y., Jin, G., Li, Z., Chen, S., Dai, X., Jin, X., Huang, L., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.20.558627

Transient hypoxia followed by progressive reoxygenation is required for efficient skeletal muscle repair through Rev-ERBα modulationPreprint

Quétin, M., Vartanian, A. D., Dubois, C., Berthier, J., Ledoux, M., Michineau, S., Drayton‐Libotte, B., Sotiropoulos, A., Relaix, F., & Gervais, M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.02.592180

Additional file 1 of Hypoxia preconditioned bone marrow-derived mesenchymal stromal/stem cells enhance myoblast fusion and skeletal muscle regeneration

Archacka, K., Grabowska, I., Mierzejewski, B., Graffstein, J., Górzyńska, A., Krawczyk, M., Różycka, A. M., Kalaszczyńska, I., Muras, G., Stremińska, W., et al. (2021) · Figshare · doi:10.6084/m9.figshare.15139553

Additional file 1 of Oxygen therapy attenuates neuroinflammation after spinal cord injury

Sunshine, M. D., Bindi, V. E., Nguyen, B. L., Doerr, V., Boeno, F. P., Chandran, V., Smuder, A. J., & Fuller, D. D. (2023) · Figshare · doi:10.6084/m9.figshare.24864181

Establishing Molecular Mechanism of Carnosine Against Hypobaric Hypoxia Induced Muscle Protein Loss via In‐Silico and In‐Vivo Approach

Kumar, A., Suryakumar, G., & Rathor, R. (2026) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.70690

Influence of hypoxia and reoxygenation on muscle stem cell fate and myogenesis during skeletal muscle repair

Quétin, M. (2019) · doi:10.70675/b9963449z4ba2z4f62z9991z66974e549c9c

Distribution and regenerative potential of muscle stem cells in patients with chronic limb- threatening ischemia

Touma, J. (2020) · doi:10.70675/49923de1z1bc9z4535zbd1azb3d9cce68e6d

Regulation of Satellite Cells and Myogenesis in Response to Eccentric Resistance Exercise in Hypoxic Conditions in Healthy Young Men

de ten Ryen, S. V. D., Warnier, G., Antoine, N., Boyer, E., Kienlen‐Campard, P., Copine, S., Francaux, M., & Deldicque, L. (2026) · The FASEB Journal · doi:10.1096/fj.202600405rr

Hypoxic Signaling in Skeletal Muscle Maintenance and Regeneration: A Systematic Review

Pircher, T., Wackerhage, H., Aszódi, A., Kammerlander, C., Böcker, W., & Saller, M. M. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.684899 · Cited by 54 · see citing works

Effects of hypoxia on proliferation and differentiation of myoblasts

Li, X., Zhu, L., Chen, X., & Fan, M. (2007) · Medical Hypotheses · doi:10.1016/j.mehy.2006.12.050 · Cited by 32 · see citing works

The hypoxia-inducible factors HIF1α and HIF2α are dispensable for embryonic muscle development but essential for postnatal muscle regeneration

Yang, X., Yang, S., Wang, C., & Kuang, S. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.756312 · Cited by 85 · see citing works

Hypoxia promotes satellite cell self-renewal and enhances the efficiency of myoblast transplantation

Liu, W., Wen, Y., Bi, P., Lai, X., Liu, X., Liu, X., & Kuang, S. (2012) · Development · doi:10.1242/dev.079665 · Cited by 198 · see citing works

The Role of Hypoxia and Hypoxia Signaling in Skeletal Muscle Physiology

Endo, Y., Zhu, C., Giunta, E., Guo, C. R., Koh, D. J., & Sinha, I. (2023) · Advanced Biology · doi:10.1002/adbi.202200300 · Cited by 10 · see citing works