Relevant bibliographies by topics / Mesenchym

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Mesenchym'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Mesenchym"

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MASCHKILLEISSON, L. N., and L. A. ABRAMOWITSCH. "Die Wirkung der antisyphilitisclien Mittel auf das aktive Mesenchym." Acta Medica Scandinavica 93, no. 3 (2009): 248–52. http://dx.doi.org/10.1111/j.0954-6820.1937.tb17609.x.

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Nogawa, H., and Y. Nakanishi. "Mechanical aspects of the mesenchymal influence on epithelial branching morphogenesis of mouse salivary gland." Development 101, no. 3 (1987): 491–500. http://dx.doi.org/10.1242/dev.101.3.491.

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Three activities of mesenchymes from mouse embryonic submandibular gland, lung, stomach, mandible and skin were comparatively studied. The first ability was the induction of branching of submandibular epithelial lobes. Epithelial lobes branched well in recombination with submandibular or lung mesenchyme, less well with stomach mesenchyme, but never with mandibular or dermal mesenchyme. The second behavioural aspect studied was the contraction of collagen gels. When respective mesenchymal cells were dispersed at 2á0×105cellsml-1 in collagen gels (1á5mgml-1) and incubated, dermal mesenchymal cel
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Barasch, J., L. Pressler, J. Connor, and A. Malik. "A ureteric bud cell line induces nephrogenesis in two steps by two distinct signals." American Journal of Physiology-Renal Physiology 271, no. 1 (1996): F50—F61. http://dx.doi.org/10.1152/ajprenal.1996.271.1.f50.

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Nephrons develop from mesenchymal cells that have contacted the ureteric bud (UB). To determine whether cell associated or secreted ureteric molecules induce the mesenchyme, we have isolated UB cell lines from mice transgenic for T antigen. These cells express epithelial and ureteric (Dolichos lectin staining, c-ret, c-met without hepatocyte growth factor) specific markers, which identifies them as authentic UB cells. Medium conditioned by our cells rescues mesenchyme from apoptosis without inducing the appearance of epithelial aggregates. The same was found by culturing mesenchymes upon the a
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Fukuda, K., Y. Ishii, H. Saiga, K. Shiokawa, and S. Yasugi. "Mesenchymal regulation of epithelial gene expression in developing avian stomach: 5′-flanking region of pepsinogen gene can mediate mesenchymal influence on its expression." Development 120, no. 12 (1994): 3487–95. http://dx.doi.org/10.1242/dev.120.12.3487.

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The expression of a gene encoding an embryonic chick pepsinogen was investigated in developing avian gut. Expression is restricted to the epithelial layer of the embryonic proventriculus (glandular stomach). We can therefore regard this gene as a marker gene for proventricular epithelial differentiation. There is some considerable evidence in favour of epithelial-mesenchymal interactions being important during the development of the gastrointestinal system; for example, pepsinogen expression is induced in proventricular and gizzard (muscular stomach) epithelial by the proventricular mesenchyme
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Colvin, Jennifer S., Andrew C. White, Stephen J. Pratt, and David M. Ornitz. "Lung hypoplasia and neonatal death inFgf9-null mice identify this gene as an essential regulator of lung mesenchyme." Development 128, no. 11 (2001): 2095–106. http://dx.doi.org/10.1242/dev.128.11.2095.

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Mammalian lung develops as an evagination of ventral gut endoderm into the underlying mesenchyme. Iterative epithelial branching, regulated by the surrounding mesenchyme, generates an elaborate network of airways from the initial lung bud. Fibroblast growth factors (FGFs) often mediate epithelial-mesenchymal interactions and mesenchymal Fgf10 is essential for epithelial branching in the developing lung. However, no FGF has been shown to regulate lung mesenchyme. In embryonic lung, Fgf9 is detected in airway epithelium and visceral pleura at E10.5, but is restricted to the pleura by E12.5. We r
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Provot, Sylvain, Dawn Zinyk, Yasemin Gunes та ін. "Hif-1α regulates differentiation of limb bud mesenchyme and joint development". Journal of Cell Biology 177, № 3 (2007): 451–64. http://dx.doi.org/10.1083/jcb.200612023.

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Recent evidence suggests that low oxygen tension (hypoxia) may control fetal development and differentiation. A crucial mediator of the adaptive response of cells to hypoxia is the transcription factor Hif-1α. In this study, we provide evidence that mesenchymal condensations that give origin to endochondral bones are hypoxic during fetal development, and we demonstrate that Hif-1α is expressed and transcriptionally active in limb bud mesenchyme and in mesenchymal condensations. To investigate the role of Hif-1α in mesenchymal condensations and in early chondrogenesis, we conditionally inactiva
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Kramer, P. R., S. Nares, S. F. Kramer, D. Grogan, and M. Kaiser. "Mesenchymal Stem Cells Acquire Characteristics of Cells in the Periodontal Ligament in vitro." Journal of Dental Research 83, no. 1 (2004): 27–34. http://dx.doi.org/10.1177/154405910408300106.

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Mesenchymal stem cells differentiate into multiple types of cells derived from mesenchyme. Periodontal ligament cells are primarily derived from mesenchyme; thus, we expected mesenchymal stem cells to differentiate into periodontal ligament. Using a combination of immunohistochemistry and in situ hybridization on co-cultures of mesenchymal stem cells and periodontal ligament, we observed a significant increase in mesenchymal stem cells’ expression of osteocalcin and osteopontin and a significant decrease in expression of bone sialoprotein, characteristics of periodontal ligament in vivo. Incre
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Barasch, Jonathan, Jizeng Qiao, Glenn McWilliams, De Chen, Juan A. Oliver, and Doris Herzlinger. "Ureteric bud cells secrete multiple factors, including bFGF, which rescue renal progenitors from apoptosis." American Journal of Physiology-Renal Physiology 273, no. 5 (1997): F757—F767. http://dx.doi.org/10.1152/ajprenal.1997.273.5.f757.

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Kidney development requires reciprocal interactions between the ureteric bud and the metanephrogenic mesenchyme. Whereas survival of mesenchyme and development of nephrons from mesenchymal cells depends on signals from the invading ureteric bud, growth of the ureteric bud depends on signals from the mesenchyme. This codependency makes it difficult to identify molecules expressed by the ureteric bud that regulate mesenchymal growth. To determine how the ureteric bud signals the mesenchyme, we previously isolated ureteric bud cell lines (UB cells). These cells secrete soluble factors which rescu
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Vainio, S., M. Jalkanen, and I. Thesleff. "Syndecan and tenascin expression is induced by epithelial-mesenchymal interactions in embryonic tooth mesenchyme." Journal of Cell Biology 108, no. 5 (1989): 1945–53. http://dx.doi.org/10.1083/jcb.108.5.1945.

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Morphogenesis of embryonic organs is regulated by epithelial-mesenchymal interactions associating with changes in the extracellular matrix (ECM). The response of the cells to the changes in the ECM must involve integral cell surface molecules that recognize their matrix ligand and initiate transmission of signal intracellularly. We have studied the expression of the cell surface proteoglycan, syndecan, which is a matrix receptor for epithelial cells (Saunders, S., M. Jalkanen, S. O'Farrell, and M. Bernfield. J. Cell Biol. In press.), and the matrix glycoprotein, tenascin, which has been propos
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Li, J., J. Xu, Y. Cui, et al. "Mesenchymal Sufu Regulates Development of Mandibular Molars via Shh Signaling." Journal of Dental Research 98, no. 12 (2019): 1348–56. http://dx.doi.org/10.1177/0022034519872679.

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Sonic hedgehog ( Shh) in dental epithelium regulates tooth morphogenesis by epithelial-mesenchymal signaling transduction. However, the action of Shh signaling regulation in this process is not well understood. Here we find that mesenchymal Suppressor of Fused ( Sufu), a major negative regulator of Shh signaling, plays an important role in modulating the tooth germ morphogenesis during the bud-to-cap stage transition. Deletion of Sufu in dental mesenchyme by Dermo1-Cre mice leads to delayed development of mandibular molar into cap stage with defect of primary enamel knot (EK) formation. We sho
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Dissertations / Theses on the topic "Mesenchym"

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Meadows, Kafi, Seema Iyer, Mark Stevens, et al. "Akt promotes Endocardial-Mesenchyme Transition." BioMed Central, 2009. http://hdl.handle.net/10150/610167.

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Endothelial to mesenchyme transition (EndMT) can be observed during the formation of endocardial cushions from the endocardium, the endothelial lining of the atrioventricular canal (AVC), of the developing heart at embryonic day 9.5 (E9.5). Many regulators of the process have been identified<br>however, the mechanisms driving the initial commitment decision of endothelial cells to EndMT have been difficult to separate from processes required for mesenchymal proliferation and migration. We have several lines of evidence that suggest a central role for Akt signaling in committing endothelial cel
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Vujovic, Sonja. "Transcriptional profiling of mesenchymal stem cells, undergoing chondrogenesis, and mesenchymal tumours." Thesis, University College London (University of London), 2006. http://discovery.ucl.ac.uk/1445141/.

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Mesenchymal stem cells (MSC) represent an adult stem cell population isolated from the bone marrow with the ability to differentiate down various mesenchymal lineages including cartilage. The development of cartilage is a complex multiphase process regulated by the interplay of factors such as cell density and oxygen availability as well as many signalling pathways including TGFp, MAPK, FGF and Wnt. Using microarrays, the temporal transcriptional changes occurring in the in vitro MSC chondrogenesis model were analysed. The results obtained support the validity of the MSC model system for the s
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Teague, Warwick J. "Mesenchyme-to-epithelial transition in pancreatic organogenesis." Thesis, University of Oxford, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.670115.

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Suniara, Ravinder K. "The role of mesenchyme in early thymic development." Thesis, University of Birmingham, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.270080.

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Jayanthi, Naga Venkatesh Gupta. "The role of pancreatic mesenchyme in islet development." Thesis, University of Newcastle upon Tyne, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.437249.

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Wong, Yin-kwai, and 王現葵. "Characterization of hMSCs transmigrated through collagen barrier." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B47869720.

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Stem cell therapy is a promising approach for tissue regeneration but there exists a problem of low engraftment rate to the injury site. Our laboratory has shown that hMSCs that were capable to penetrate through collagen barrier have higher migration capacity and engraftment efficiency than those remained inside the collagen matrix and those in traditional 2D culture. These cells capable of penetrating through collagen barrier might be hopeful candidate for improving engraftment efficacy. Major processes of engraftment, such as transmigration through basement membrane and invasion to t
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Karystinou, Alexandra. "YAP in mesenchymal stem cells." Thesis, University of Aberdeen, 2012. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=192255.

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MSCs are the most studied subtype of adult stem cells and have been derived from most postnatal organs and tissues. MSCs are defined as having the capacity to self-renew and to differentiate into both mesodermal and non-mesodermal lineages, and are immunosuppressive. For these properties, MSCs have been considered ideal candidates for regenerative medicine and have been used in several clinical trials. The difficulty, however, to preserve the potency of the cells during culture expansion and to monitor differentiation are obstacles in their use in the clinic and have emphasized the need to inv
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Hahnel, Mark. "Trafficking of mesenchymal stem cells." Thesis, Imperial College London, 2012. http://hdl.handle.net/10044/1/14559.

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In adult life mesenchymal stem cells (MSCs) reside primarily in the bone marrow and are defined according to their ability to self-renew and differentiate into tissues of mesodermal origin. Due to their immuno-modulatory properties and ability to form cartilage and bone, MSCs have clinical potential, for the treatment of autoimmune diseases and tissue repair. This project determines the chemokine receptor profile on murine bone marrow MSCs at early and late passage and on human MSCs derived from a range of fetal tissues including fetal blood, bone marrow, amniotic fluid and placenta. The overw
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De, Arpan. "Circadian clock regulation of epithelial-mesenchymal and mesenchymal-epithelial transitions in glioma and breast cancer cells." Bowling Green State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1566494866910786.

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陳德華 and Tak-wah Chan. "Epithelial-mesenchymal interactions in development and cytodifferentiation of seminal vesicle." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1994. http://hub.hku.hk/bib/B31211239.

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Books on the topic "Mesenchym"

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Thompson, Erik W. Epithelial-mesenchymal transitions: new advances in development, fibrosis and cancer: 9 tables. Karger, 2011.

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Gnecchi, Massimiliano, ed. Mesenchymal Stem Cells. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3584-0.

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Prockop, Darwin J., Bruce A. Bunnell, and Donald G. Phinney, eds. Mesenchymal Stem Cells. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1.

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Hematti, Peiman, and Armand Keating, eds. Mesenchymal Stromal Cells. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-5711-4.

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Xiao, Yin. Mesenchymal stem cells. Nova Science Publishers, 2011.

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Chase, Lucas G., and Mohan C. Vemuri, eds. Mesenchymal Stem Cell Therapy. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-200-1.

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Mesenchymal stem cell assays and applications. Humana Press/Springer, 2011.

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Sŏnggyun'gwan Taehakkyo (Seoul, Korea). Sanhak Hyŏmnyŏktan. TGF-beta e ŭihan oncogenic Epithelial-Mesenchymal Transition (EMT) yubal inja rosŏ hangsanhwa tanbaekchildŭl ŭi yŏkhal kyumyŏng kwa kijŏn yŏn'gu =: Molecular characterization of distinct roles of anti-oxidative proteins and their signaling mechanism in the oncogenic epithelial-mesenchymal transition by TGF-beta. Pogŏn Pokchi Kajokpu, 2009.

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Campbell, Kyra, and Eric Theveneau, eds. The Epithelial-to Mesenchymal Transition. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-0779-4.

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Goldberg, I. D., and E. M. Rosen, eds. Epithelial-Mesenchymal Interactions in Cancer. Birkhäuser Basel, 1995. http://dx.doi.org/10.1007/978-3-0348-9070-0.

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Book chapters on the topic "Mesenchym"

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Krstić, R. V. "Mesenchym (embryonales Bindegewebe). Beispiel: Dorsales Mesogastrium eines 14 Tage alten Mäusefetus." In Die Gewebe des Menschen und der Säugetiere. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-61380-7_50.

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Wolfe, Margaret, Radhika Pochampally, William Swaney, and Roxanne L. Reger. "Isolation and Culture of Bone Marrow-Derived Human Multipotent Stromal Cells (hMSCs)." In Mesenchymal Stem Cells. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_1.

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Ylőstalo, Joni, Radhika Pochampally, and Darwin J. Prockop. "Assays of MSCs with Microarrays." In Mesenchymal Stem Cells. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_10.

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Izadpanah, Reza, and Bruce A. Bunnell. "Gene Delivery to Mesenchymal Stem Cells." In Mesenchymal Stem Cells. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_11.

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Phinney, Donald G. "Isolation of Mesenchymal Stem Cells from Murine Bone Marrow by Immunodepletion." In Mesenchymal Stem Cells. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_12.

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Pittenger, Mark F. "Mesenchymal Stem Cells from Adult Bone Marrow." In Mesenchymal Stem Cells. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_2.

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Gronthos, Stan, and Andrew C. W. Zannettino. "A Method to Isolate and Purify Human Bone Marrow Stromal Stem Cells." In Mesenchymal Stem Cells. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_3.

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Fraser, John K., Min Zhu, Isabella Wulur, and Zeni Alfonso. "Adipose-Derived Stem Cells." In Mesenchymal Stem Cells. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_4.

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Dubois, Severine G., Elizabeth Z. Floyd, Sanjin Zvonic, et al. "Isolation of Human Adipose-derived Stem Cells from Biopsies and Liposuction Specimens." In Mesenchymal Stem Cells. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_5.

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Pochampally, Radhika. "Colony Forming Unit Assays for MSCs." In Mesenchymal Stem Cells. Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-169-1_6.

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Conference papers on the topic "Mesenchym"

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Sudama, Hiroki, Atsushi Ogawa, Kei Saito, Wataru Ando, Norimasa Nakamura, and Hiromichi Fujie. "Effect of Shear Stress on Extracellular Matrix Production of Synovium-Derived Cells." In ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-206331.

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It is well known that various fibrous tissue such as tendons and ligaments functionally adapt to dynamic and static loads. Although a variety of biomechanical studies have been done to deterimine the mechanism of remodeling in fibrous tissues, it was difficult to obtain detailed information because of complicated condstitution of the tissues. We have developed a stem cell-based self-assembled tissue (scSAT) [1] for tissue engineering. Since the scSAT is consisted of synovium-derived mesenchyaml stem cells and their native extracellular matrix, it is a good experimental model to determine the p
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Zielinski, Rachel, Cosmin Mihai, and Samir Ghadiali. "Multi-Scale Modeling of Cancer Cell Migration and Adhesion During Epithelial-to-Mesenchymal Transition." In ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-53511.

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Cancer is a leading cause of death in the US, and tumor cell metastasis and secondary tumor formation are key factors in the malignancy and prognosis of the disease. The regulation of cell motility plays an important role in the migration and invasion of cancer cells into surrounding tissues. The primary modes of increased motility in cancerous tissues may include collective migration of a group of epithelial cells during tumor growth and single cell migration of mesenchymal cells after detachment from the primary tumor site [1]. In epithelial cancers, metastasizing cells lose their cell-cell
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Van Dyke, William S., Ozan Akkus, and Eric Nauman. "Murine Osteochondral Stem Cells Express Collagen Type I More Strongly on PDMS Substrates Than on Tissue Culture Plastic." In ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14272.

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The discovery of the multipotent lineage of mesenchymal stem cells has dawned a new age in tissue engineering, where an autologous cell-seeded scaffold can be implanted into different therapeutic sites. Mesenchymal stem cells have been reported to differentiate into numerous anchorage-dependent cell phenotypes, including neurons, adipocytes, myoblasts, chondrocytes, tenocytes, and osteoblasts. A seminal work detailing that mesenchymal stem cells can be directed towards differentiation of different cell types by substrate stiffness alone [1] has led to numerous studies attempting to understand
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Chen, Jing, and Sihong Wang. "Thermal Effects on Osteogenesis of Human Mesenchymal Stem Cells." In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80885.

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Intensive studies were reported on the osteogenesis of mesenchymal stem cells (MSC) using chemicals and mechanical loading. However, the maturity of differentiated osteoblasts is not same as that of isolated adult osteoblasts. Thermal treatment could be a missing factor in stem cell differentiation. It was reported that mild heat stimulated bone growth in animal experiments [1–2]. Thermal treatment is also used as a therapy to promote bone repair after injury [3]. In addition, hot shower daily is recommended to osteoarthritis patients. However, the mechanisms for the heat-induced osteogenesis
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Kozaki, Ken-ichi, Yasuhiro Kurasawa, Tomoki Muramatsu, et al. "Abstract 2415: Phenotypic stabilization of mesenchymal-like cancer cells through mesenchymal-specific DNA hypermethylation." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-2415.

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Satelli, Arun, Abhisek Mitra, Jeffery J. Cutrera, et al. "Abstract 1469: Specific detection tool for mesenchymal and epithelial-mesenchymal transformed circulating tumor cells." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-1469.

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Soucy, A., J. D. Campbell, T. Hu, I. M. C. Martin, and J. P. Mizgerd. "Lung Mesenchymal Cell Responses to Pneumonia." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a7723.

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Bonfield, Tracey L., Mary Kolze, Donald Lennon, and Arnold Caplan. "Mesenchymal Stem Cells Attenuate Asthma Inflammation." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a5585.

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"A glance to Mesenchymal stem cells, and Mesenchymal stem cells, which can derive from adipose tissue." In International Conference on Medicine, Public Health and Biological Sciences. CASRP Publishing Company, Ltd. Uk, 2016. http://dx.doi.org/10.18869/mphbs.2016.119.

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Juncosa-Melvin, Natalia, Karl S. Matlin, Robert W. Holdcraft, Victor S. Nirmalanandhan, and David L. Butler. "Mechanical Stimulation Increases Collagen Type I and Collagen Type III Gene Expression of Stem Cell: Collagen Sponge Constructs for Patellar Tendon Repair." In ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-175807.

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Tendons (rotator cuff, Achilles and patellar tendons) are among the most commonly injured soft tissues [1]. Many repairs/reconstructions have been attempted using sutures, resorbable biomaterials, autografts, and allografts, but with varying success. A tissue engineered repair using mesenchymal stem cells (MSCs) is attractive [2–4] but often lacks initial stiffness and strength [5].
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Reports on the topic "Mesenchym"

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Song, Yao-Hua. Role of Mesenchymal Stem Cells In Tumorigenesis. Defense Technical Information Center, 2009. http://dx.doi.org/10.21236/ada541309.

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Krause, Silva. Promotion of Epithelial to Mesenchymal Transformation by Hyaluronan. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada485556.

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Karp, Jeffrey, and John Isaacs. Mesenchymal Stem Cell-Based Therapy for Prostate Cancer. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada612823.

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Krause, Silva, and Alexandra Zoltan-Jones. Promotion of Epithelial to Mesenchymal Transformation by Hyaluronan. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada429933.

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Krause, Silva. Promotion of Epithelial to Mesenchymal Transition by Hyaluronan. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada462484.

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Krause, Silva. Promotion of Epithelial to Mesenchymal Transition by Hyaluronan. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada463843.

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Kah, Kong J. Signature and Mechanism of the Epithelial-to-Mesenchymal Transition. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada541945.

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Thompson, Erik W. Functional Genomics for Epithelial-Mesenchymal Transition in Breast Cancer. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada542255.

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Kah, Kong J. Signature and Mechanism of the Epithelial-to-Mesenchymal Transition. Defense Technical Information Center, 2009. http://dx.doi.org/10.21236/ada504655.

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Tyner, Angela L. Regulation of the Epithelial-Mesenchymal Transition in Prostate Cancer. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada594294.

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