Academic literature on the topic 'Muscle stem cell'

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Journal articles on the topic "Muscle stem cell"

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Liu, Qi, Su Pan, Shijie Liu, Sui Zhang, James T. Willerson, James F. Martin, and Richard A. F. Dixon. "Suppressing Hippo signaling in the stem cell niche promotes skeletal muscle regeneration." Stem Cells 39, no. 6 (February 18, 2021): 737–49. http://dx.doi.org/10.1002/stem.3343.

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Abstract Lack of blood flow to the lower extremities in peripheral arterial disease causes oxygen and nutrient deprivation in ischemic skeletal muscles, leading to functional impairment. Treatment options for muscle regeneration in this scenario are lacking. Here, we selectively targeted the Hippo pathway in myofibers, which provide architectural support for muscle stem cell niches, to facilitate functional muscle recovery in ischemic extremities by promoting angiogenesis, neovascularization, and myogenesis. We knocked down the core Hippo pathway component, Salvador (SAV1), by using an adeno-a
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Wang, Shuaiyu, Bao Zhang, Gregory C. Addicks, Hui Zhang, Keir J. Menzies, and Hongbo Zhang. "Muscle Stem Cell Immunostaining." Current Protocols in Mouse Biology 8, no. 3 (August 14, 2018): e47. http://dx.doi.org/10.1002/cpmo.47.

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Yin, Hang, Feodor Price, and Michael A. Rudnicki. "Satellite Cells and the Muscle Stem Cell Niche." Physiological Reviews 93, no. 1 (January 2013): 23–67. http://dx.doi.org/10.1152/physrev.00043.2011.

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Adult skeletal muscle in mammals is a stable tissue under normal circumstances but has remarkable ability to repair after injury. Skeletal muscle regeneration is a highly orchestrated process involving the activation of various cellular and molecular responses. As skeletal muscle stem cells, satellite cells play an indispensible role in this process. The self-renewing proliferation of satellite cells not only maintains the stem cell population but also provides numerous myogenic cells, which proliferate, differentiate, fuse, and lead to new myofiber formation and reconstitution of a functional
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Kodaka, Yusaku, Gemachu Rabu, and Atsushi Asakura. "Skeletal Muscle Cell Induction from Pluripotent Stem Cells." Stem Cells International 2017 (2017): 1–16. http://dx.doi.org/10.1155/2017/1376151.

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Embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) have the potential to differentiate into various types of cells including skeletal muscle cells. The approach of converting ESCs/iPSCs into skeletal muscle cells offers hope for patients afflicted with the skeletal muscle diseases such as the Duchenne muscular dystrophy (DMD). Patient-derived iPSCs are an especially ideal cell source to obtain an unlimited number of myogenic cells that escape immune rejection after engraftment. Currently, there are several approaches to induce differentiation of ESCs and iPSCs to skeletal m
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Memczak, Sebastian, and Juan CI Belmonte. "Overcoming muscle stem cell aging." Current Opinion in Genetics & Development 83 (December 2023): 102127. http://dx.doi.org/10.1016/j.gde.2023.102127.

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Ishii, Kana, Nobuharu Suzuki, Yo Mabuchi, Naoki Ito, Naomi Kikura, So-ichiro Fukada, Hideyuki Okano, Shin'ichi Takeda, and Chihiro Akazawa. "Muscle Satellite Cell Protein Teneurin-4 Regulates Differentiation During Muscle Regeneration." STEM CELLS 33, no. 10 (June 28, 2015): 3017–27. http://dx.doi.org/10.1002/stem.2058.

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Torrente, Yuan, Jacques-P. Tremblay, Federica Pisati, Marzia Belicchi, Barbara Rossi, Manuela Sironi, Franco Fortunato, et al. "Intraarterial Injection of Muscle-Derived Cd34+Sca-1+ Stem Cells Restores Dystrophin in mdx Mice." Journal of Cell Biology 152, no. 2 (January 22, 2001): 335–48. http://dx.doi.org/10.1083/jcb.152.2.335.

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Duchenne muscular dystrophy is a lethal recessive disease characterized by widespread muscle damage throughout the body. This increases the difficulty of cell or gene therapy based on direct injections into muscles. One way to circumvent this obstacle would be to use circulating cells capable of homing to the sites of lesions. Here, we showed that stem cell antigen 1 (Sca-1), CD34 double-positive cells purified from the muscle tissues of newborn mice are multipotent in vitro and can undergo both myogenic and multimyeloid differentiation. These muscle-derived stem cells were isolated from newbo
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Borok, Matthew, Nathalie Didier, Francesca Gattazzo, Teoman Ozturk, Aurelien Corneau, Helene Rouard, and Frederic Relaix. "Progressive and Coordinated Mobilization of the Skeletal Muscle Niche throughout Tissue Repair Revealed by Single-Cell Proteomic Analysis." Cells 10, no. 4 (March 28, 2021): 744. http://dx.doi.org/10.3390/cells10040744.

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Background: Skeletal muscle is one of the only mammalian tissues capable of rapid and efficient regeneration after trauma or in pathological conditions. Skeletal muscle regeneration is driven by the muscle satellite cells, the stem cell population in interaction with their niche. Upon injury, muscle fibers undergo necrosis and muscle stem cells activate, proliferate and fuse to form new myofibers. In addition to myogenic cell populations, interaction with other cell types such as inflammatory cells, mesenchymal (fibroadipogenic progenitors—FAPs, pericytes) and vascular (endothelial) lineages a
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Wagers, Amy J. "Stem Cell Rejuvenation." Blood 124, no. 21 (December 6, 2014): SCI—42—SCI—42. http://dx.doi.org/10.1182/blood.v124.21.sci-42.sci-42.

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Effective functioning of the body’s tissues and organs depends upon innate regenerative processes that maintain proper cell numbers during homeostasis and replace damaged cells after injury. In many tissues, regenerative potential is determined by the presence and functionality of dedicated populations of stem and progenitor cells, which respond to exogenous cues to produce replacement cells when needed. Understanding how these unspecialized precursors are maintained and regulated is essential for understanding the fundamental biology of tissues. In addition, this knowledge has practical impli
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Heslop, L., J. E. Morgan, and T. A. Partridge. "Evidence for a myogenic stem cell that is exhausted in dystrophic muscle." Journal of Cell Science 113, no. 12 (June 15, 2000): 2299–308. http://dx.doi.org/10.1242/jcs.113.12.2299.

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Injection of the myotoxin notexin, was found to induce regeneration in muscles that had been subjected to 18 Gy of radiation. This finding was unexpected as irradiation doses of this magnitude are known to block regeneration in dystrophic (mdx) mouse muscle. To investigate this phenomenon further we subjected mdx and normal (C57Bl/10) muscle to irradiation and notexin treatment and analysed them in two ways. First by counting the number of newly regenerated myofibres expressing developmental myosin in cryosections of damaged muscles. Second, by isolating single myofibres from treated muscles a
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Dissertations / Theses on the topic "Muscle stem cell"

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Woodhouse, Samuel. "The role of Ezh2 in adult muscle stem cell fate." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610201.

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Theret, Marine. "Cell and non-cell autonomous regulations of metabolism on muscle stem cell fate and skeletal muscle homeostasis." Thesis, Sorbonne Paris Cité, 2015. http://www.theses.fr/2015USPCB120/document.

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A l’état basal, les cellules souches musculaires sont quiescentes. Après blessure, ces cellules s’activent, s’amplifient et se différencient afin de réparer les myofibres lésées. Cependant, une petite population de ces cellules myogéniques activées ne va pas entrer dans la voie de la myogenèse, mais va retourner en quiescence par un phénomène appelé auto-renouvellement. Cette étape est cruciale afin de maintenir une réserve de cellules souches musculaires tout au long de la vie. Mais, les mécanismes cellulaires et moléculaires régulant ce phénomène sont peu décrits dans la littérature. La régé
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Wang, Yu Xin. "Molecular Regulation of Muscle Stem Cell Self-Renewal." Thesis, Université d'Ottawa / University of Ottawa, 2016. http://hdl.handle.net/10393/35207.

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Muscle stem cells self-renew to maintain the long-term capacity for skeletal muscles to regenerate. However, the homeostatic regulation of muscle stem cell self-renewal is poorly understood. By utilizing high-throughput screening and transcriptomic approaches, we identify the critical function of dystrophin, the epidermal growth factor receptor (EGFR), and fibronectin in the establishment of cell polarity and in determining symmetric and asymmetric modes of muscle stem cell self-renewal. These findings reveal an orchestrated network of paracrine signaling that regulate muscle stem cell homeost
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Victor, Pedro Sousa. "Skeletal muscle aging: stem cell function and tissue homeostasis." Doctoral thesis, Universitat Pompeu Fabra, 2012. http://hdl.handle.net/10803/81933.

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Muscle aging, in particular, is characterized by the reduction of tissue mass and function, which are particularly prominent in geriatric individuals undergoing sarcopenia. The age-associated muscle wasting is also associated with a decline in regenerative ability and a reduction in resident muscle stem cell (satellite cell) number and function. Although sarcopenia is one of the major contributors to the general loss of physiological function, the mechanisms involved in age-related loss of muscle homeostasis and satellite cell activity are yet poorly understood. Using a microarray-based tran
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Richards-Malcolm, Sonia Angela. "THE ROLE OF STEM CELL ANTIGEN-1(Sca-1) IN MUSCLE AGING." UKnowledge, 2008. http://uknowledge.uky.edu/gradschool_theses/519.

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Muscle aging is associated with a decrease in the number of satellite cells and their progeny, muscle progenitor cells (MPCs) that are available for muscle repair and regeneration. However, there is an increase in non-immuno-hematopoietic cells (CD45 negative) in regenerating muscle from aged mice characterized by high stem cell antigen -1(Sca-1) expression. In aged regenerating muscle, 14.2% of cells are CD45neg Sca-1pos while 7.2% of cells are CD45neg Sca-1pos in young adult muscle. In vitro, CD45neg Sca-1pos cells over express genes associated with fibrosis, potentially controlled by Wnt2.
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Feige, Peter. "Molecular Regulation of Satellite Cell Fate." Thesis, Université d'Ottawa / University of Ottawa, 2020. http://hdl.handle.net/10393/40804.

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Muscle homeostasis and regeneration are complex cellular processes orchestrated by muscle stem cells and their interaction with their stem cell microenvironment. The fate of a muscle stem cell is influenced by different conditions such as muscle injury, cold stress, or disease. During extensive muscle repair and in the context of muscular dystrophy, we identified the critical function of the Epidermal Growth Factor Receptor (EGFR) in establishing cell polarity and in turn the efficient formation of myogenic progeny able to repair muscle. Using a novel drug screen, we identified the p53 protein
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Pannerec, Alice. "The skeletal muscle stem cell niche : defining hierarchies based upon the stem cell marker PW1 to identify therapeutic target cells." Paris 6, 2012. http://www.theses.fr/2012PA066440.

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Les cellules satellites permettent la réparation des muscles squelettiques, mais chez les patients atteints de myopathies ces cellules ne fonctionnent pas correctement ce qui conduit à l’atrophie musculaire. Nos travaux ont montré qu’une nouvelle population de cellules souches musculaires, les PICs, favorisent la prolifération des cellules satellites par l’intermédiaire de la follistatine qui contrebalance l’effet négatif de la myostatine. Lorsque la myostatine est inactivée chez des souris par injection d’inhibiteur, le nombre de PICs augmente considérablement et les animaux présentent des mu
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Pannérec, Alice. "The skeletal muscle stem cell niche : defining hierarchies based upon the stem cell marker PW1 to identify therapeutic target cells." Phd thesis, Université Pierre et Marie Curie - Paris VI, 2012. http://tel.archives-ouvertes.fr/tel-00833422.

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Les cellules satellites permettent la réparation des muscles squelettiques, mais chez les patients atteints de myopathies ces cellules ne fonctionnent pas correctement ce qui conduit à l'atrophie musculaire. Nos travaux ont montré qu'une nouvelle population de cellules souches musculaires, les PICs, favorisent la prolifération des cellules satellites par l'intermédiaire de la follistatine qui contrebalance l'effet négatif de la myostatine. Lorsque la myostatine est inactivée chez des souris par injection d'inhibiteur, le nombre de PICs augmente considérablement et les animaux présentent des mu
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Cahill, Kevin Scott. "Enhancement of stem-cell transplantation strategies for muscle regeneration." [Gainesville, Fla.] : University of Florida, 2003. http://purl.fcla.edu/fcla/etd/UFE0002319.

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Zhang, Ting [Verfasser]. "Epigenetic regulation of muscle stem cell expansion / Ting Zhang." Gießen : Universitätsbibliothek, 2015. http://d-nb.info/1076980325/34.

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Books on the topic "Muscle stem cell"

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A, Sassoon D., ed. Stem cells and cell signalling in skeletel myogenesis. Amsterdam: Elsevier, 2002.

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Perdiguero, Eusebio, and DDW Cornelison, eds. Muscle Stem Cells. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6771-1.

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Asakura, Atsushi, ed. Skeletal Muscle Stem Cells. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3036-5.

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Sassoon, D. A. Stem Cells and Cell Signalling in Skeletal Myogenesis (Advances in Developmental Biology and Biochemistry, V. 11). Elsevier Science, 2002.

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Bonnie Fagan, Melinda. Individuality, Organisms, and Cell Differentiation. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780190636814.003.0006.

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This chapter builds on earlier arguments concerning the individuality of stem cells. The author has argued in previous work that stem cells are not biological individuals in the same way as specialized cells of multicellular organisms (e.g., neurons, red blood cells, muscle cells) but that some stem cells (cultured pluripotent stem cells) can be considered biological individuals by analogy with multicellular organisms. More precisely, the author claims that cultured pluripotent stem cells can be considered model organisms for studying early mammalian development. An important objection to this
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Rudnicki, Michael, and Jeffrey Dilworth. Muscle Stem Cells. Elsevier Science & Technology Books, 2024.

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Perdiguero, Eusebio, and Dawn Cornelison. Muscle Stem Cells: Methods and Protocols. Springer New York, 2017.

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Perdiguero, Eusebio, and D. D. W. Cornelison. Muscle Stem Cells: Methods and Protocols. Springer New York, 2018.

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Douglas, Kenneth. Bioprinting. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780190943547.001.0001.

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Abstract: This book describes how bioprinting emerged from 3D printing and details the accomplishments and challenges in bioprinting tissues of cartilage, skin, bone, muscle, neuromuscular junctions, liver, heart, lung, and kidney. It explains how scientists are attempting to provide these bioprinted tissues with a blood supply and the ability to carry nerve signals so that the tissues might be used for transplantation into persons with diseased or damaged organs. The book presents all the common terms in the bioprinting field and clarifies their meaning using plain language. Readers will lear
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Asakura, Atsushi. Skeletal Muscle Stem Cells: Methods and Protocols. Springer, 2023.

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Book chapters on the topic "Muscle stem cell"

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Kuang, Shihuan, and Michael A. Rudnicki. "Muscle Stem Cells." In Cell Cycle Regulation and Differentiation in Cardiovascular and Neural Systems, 105–20. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-60327-153-0_6.

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Abou-Khalil, Rana, Fabien Le Grand, and Bénédicte Chazaud. "Human and Murine Skeletal Muscle Reserve Cells." In Stem Cell Niche, 165–77. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-508-8_14.

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Negroni, Elisa, Maximilien Bencze, Stéphanie Duguez, Gillian Butler-Browne, and Vincent Mouly. "Skeletal Muscle Stem Cells." In Stem Cell Biology and Regenerative Medicine, 415–28. New York: River Publishers, 2022. http://dx.doi.org/10.1201/9781003339601-19.

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Brand-Saberi, Beate, and Eric Bekoe Offei. "Skeletal Muscle Stem Cells." In Essential Current Concepts in Stem Cell Biology, 77–97. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-33923-4_5.

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Marra, Kacey G., Candace A. Brayfield, and J. Peter Rubin. "Adipose Stem Cell Differentiation into Smooth Muscle Cells." In Adipose-Derived Stem Cells, 261–68. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-61737-960-4_19.

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Goel, Aviva J., and Robert S. Krauss. "Ex Vivo Visualization and Analysis of the Muscle Stem Cell Niche." In Stem Cell Niche, 39–50. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/7651_2018_177.

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Boldrin, Luisa, and Jennifer E. Morgan. "Modulation of the Host Skeletal Muscle Niche for Donor Satellite Cell Grafting." In Stem Cell Niche, 179–90. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-508-8_15.

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McKay, Bryon R., and Gianni Parise. "Aging of Muscle Stem Cells." In Stem Cell Aging: Mechanisms, Consequences, Rejuvenation, 195–226. Vienna: Springer Vienna, 2015. http://dx.doi.org/10.1007/978-3-7091-1232-8_10.

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Sambasivan, Ramkumar, and Shahragim Tajbakhsh. "Adult Skeletal Muscle Stem Cells." In Results and Problems in Cell Differentiation, 191–213. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-44608-9_9.

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Duelen, Robin, Domiziana Costamagna, and Maurilio Sampaolesi. "Stem Cell Therapy in Muscle Degeneration." In The Plasticity of Skeletal Muscle, 55–91. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-3292-9_3.

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Conference papers on the topic "Muscle stem cell"

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Cassino, Theresa R., Masaho Okada, Lauren Drowley, Johnny Huard, and Philip R. LeDuc. "Mechanical Stimulation Improves Muscle-Derived Stem Cell Transplantation for Cardiac Repair." In ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-192941.

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Muscle-derived stem cells (MDSCs) have been successfully transplanted into both skeletal (1) and cardiac muscle (2) of dystrophin-deficient (mdx) mice, and show potential for improving cardiac and skeletal dysfunction in diseases like Duchenne muscular dystrophy (DMD). Our previous study explored the regeneration of dystrophin-expressing myocytes following MDSC transplantation into environments with distinct blood flow and chemical/mechanical stimulation attributes. After MDSC transplantation within left ventricular myocardium and gastrocnemius (GN) muscles of the same mdx mice, significantly
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Ahsan, Taby, Adele M. Doyle, Garry P. Duffy, Frank Barry, and Robert M. Nerem. "Stem Cells and Vascular Regenerative Medicine." In ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-193591.

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Vascular applications in regenerative medicine include blood vessel substitutes and vasculogenesis in ischemic or engineered tissues. For these repair processes to be successful, there is a need for a stable supply of endothelial and smooth muscle cells. For blood vessel substitutes, the immediate goal is to enable blood flow, but vasoactivity is necessary for long term success. In engineered vessels, it is thought that endothelial cells will serve as an anti-thrombogenic lumenal layer, while smooth muscle cells contribute to vessel contractility. In other clinical applications, what is needed
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Yuste, Yaiza, Juan A. Serrano, Alberto Olmo, Andres Maldonado-Jacobi, Pablo Pérez, Gloria Huertas, Sheila Pereira, Fernando de la Portilla, and Alberto Yúfera. "Monitoring Muscle Stem Cell Cultures with Impedance Spectroscopy." In 11th International Conference on Biomedical Electronics and Devices. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0006712300960099.

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Soker, Shay, Dawn Delo, Samira Neshat, and Anthony Atala. "Amniotic Fluid Derived Stem Cells for Cardiac Muscle Therapies." In ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-192492.

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Many forms of pediatric and adult heart disease are accompanied by high morbidity and mortality, as the heart muscle has limited regenerative potential. Cell therapy has been proposed as a means to promote the regeneration of injured heart muscle. We have established lines of broad spectrum multipotent stem cells derived from primitive fetal cells present in human amniotic fluid (hAFS) cells (1). AFS cells offer several advantages: They are easy to isolate and grow (no feeder layers needed), are highly expansive including clonal growth and they can differentiate into all germ layers. In the cu
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Tsvankin, Vadim, Dmitry Belchenko, Devon Scott, and Wei Tan. "Anisotropic Strain Effects on Vascular Smooth Muscle Cell Physiology." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-176284.

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Biological development is a complex and highly-regulated process, a significant part of which is controlled by mechanostimulus, or the strain imparted on a cell by its environment. Mechanostimulus is important for stem cell differentiation, from cytoskeletal assembly to cell-cell and cell-matrix adhesion [1]. The mechanics of cells and tissues play a critical role in organisms, under both physiological and pathological conditions; abnormal mechanotransduction — the mechanism by which cells sense and respond to strain — has been implicated in a wide range of clinical pathologies [2,3].
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Cassino, Theresa R., Masaho Okada, Lauren M. Drowley, Joseph Feduska, Johnny Huard, and Philip R. LeDuc. "Using Mechanical Environment to Enhance Stem Cell Transplantation in Muscle Regeneration." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-176545.

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Muscle-derived stem cell (MDSC) transplantation has shown potential as a therapy for cardiac and skeletal muscle dysfunction in diseases such as Duchenne muscular dystrophy (DMD). In this study we explore mechanical environment and its effects on MDSCs engraftment into cardiac and skeletal muscle in mdx mice and neoangiogenesis within the engraftment area. We first looked at transplantation of the same number of MDSCs into the heart and gastrocnemius (GN) muscle of dystrophic mice and the resulting dystrophin expression. We then explored neoangiogenesis within the engraftments through quantifi
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Li, Zhizhong. "Abstract A58: HMGA2 controls muscle stem cell activation and rhabdomyosarcoma progression." In Abstracts: AACR Special Conference: Pediatric Cancer at the Crossroads: Translating Discovery into Improved Outcomes; November 3-6, 2013; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.pedcan-a58.

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Monteiro, Gary A., and David I. Shreiber. "Guiding Stem Cell Differentiation Into Neural Lineages With Tunable Collagen Biomaterials." In ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-206752.

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The long-term objective of this research is to develop tunable collagen-based biomaterial scaffolds for directed stem cell differentiation into neural lineages to aid in CNS diseases and trauma. Type I collagen is a ubiquitous protein that provides mechanostructural and ligand-induced biochemical cues to cells that attach to the protein via integrin receptors. Previous studies have demonstrated that the mechanical properties of a substrate or tissue can be an important regulator of stem cell differentiation. For example, the mechanical properties polyacrylamide gels can be tuned to induce neur
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Barğı, Gülşah, Meral Boşnak Güçlü, and Gülsan Türköz Sucak. "Stem cell recipients versus healthy subjects regarding exercise tolerance and muscle strength." In ERS International Congress 2018 abstracts. European Respiratory Society, 2018. http://dx.doi.org/10.1183/13993003.congress-2018.pa1485.

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Kallifatidis, Georgios, Diandra K. Smith, Jie Gao, Richard Pearce, Jiemin Li, Vinata Lokeshwar, and Balakrishna L. Lokeshwar. "Abstract 86: Beta-arrestins regulate basal cell and cancer stem cell phenotype in muscle-invasive bladder cancer." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-86.

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Reports on the topic "Muscle stem cell"

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Huard, Johnny, Ira Fox, and David Perlmutter. Muscle Stem Cell Therapy for the Treatment of DMD Associated Cardiomyopathy. Fort Belvoir, VA: Defense Technical Information Center, October 2012. http://dx.doi.org/10.21236/ada576384.

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Gonzalez-Cadavid, Nestor F. Modulation of Stem Cell Differentiation and Myostatin as an Approach to Counteract Fibrosis in Muscle Dystrophy and Regeneration After Injury. Addendum. Fort Belvoir, VA: Defense Technical Information Center, March 2012. http://dx.doi.org/10.21236/ada586854.

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Halevy, Orna, Sandra Velleman, and Shlomo Yahav. Early post-hatch thermal stress effects on broiler muscle development and performance. United States Department of Agriculture, January 2013. http://dx.doi.org/10.32747/2013.7597933.bard.

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In broilers, the immediate post-hatch handling period exposes chicks to cold or hot thermal stress, with potentially harmful consequences to product quantity and quality that could threaten poultry meat marketability as a healthy, low-fat food. This lower performance includes adverse effects on muscle growth and damage to muscle structure (e.g., less protein and more fat deposition). A leading candidate for mediating the effects of thermal stress on muscle growth and development is a unique group of skeletal muscle cells known as adult myoblasts (satellite cells). Satellite cells are multipote
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Yahav, Shlomo, John McMurtry, and Isaac Plavnik. Thermotolerance Acquisition in Broiler Chickens by Temperature Conditioning Early in Life. United States Department of Agriculture, 1998. http://dx.doi.org/10.32747/1998.7580676.bard.

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Abstract:
The research on thermotolerance acquisition in broiler chickens by temperature conditioning early in life was focused on the following objectives: a. To determine the optimal timing and temperature for inducing the thermotolerance, conditioning processes and to define its duration during the first week of life in the broiler chick. b. To investigate the response of skeletal muscle tissue and the gastrointestinal tract to thermal conditioning. This objective was added during the research, to understand the mechanisms related to compensatory growth. c. To evaluate the effect of early thermo cond
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Funkenstein, Bruria, and Cunming Duan. GH-IGF Axis in Sparus aurata: Possible Applications to Genetic Selection. United States Department of Agriculture, November 2000. http://dx.doi.org/10.32747/2000.7580665.bard.

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Abstract:
Many factors affect growth rate in fish: environmental, nutritional, genetics and endogenous (physiological) factors. Endogenous control of growth is very complex and many hormone systems are involved. Nevertheless, it is well accepted that growth hormone (GH) plays a major role in stimulating somatic growth. Although it is now clear that most, if not all, components of the GH-IGF axis exist in fish, we are still far from understanding how fish grow. In our project we used as the experimental system a marine fish, the gilthead sea bream (Sparus aurata), which inhabits lagoons along the Mediter
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