Relevant bibliographies by topics / Stem cell

Academic literature on the topic 'Stem cell'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 July 2024

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Journal articles on the topic "Stem cell"

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Gupta, Dr Shalini, and Dr Shalini Gupta. "Dental Stem Cell: A Review." Indian Journal of Applied Research 3, no. 7 (October 1, 2011): 483–87. http://dx.doi.org/10.15373/2249555x/july2013/149.

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Kumar, Dr M. L. Harendra. "Stem Cell and Ethical Issues." JOURNAL OF CLINICAL AND BIOMEDICAL SCIENCES 04, no. 1 (March 15, 2014): 213–15. http://dx.doi.org/10.58739/jcbs/v04i1.13.

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Ahmed Elkammar, Hala. "Effect of human bone marrow derived mesenchymal stem cells on squamous cell carcinoma cell line." International Journal of Academic Research 6, no. 1 (January 30, 2014): 110–16. http://dx.doi.org/10.7813/2075-4124.2014/6-1/a.14.

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Holden, C. "STEM CELLS: Stem Cell Candidates Proliferate." Science 315, no. 5813 (February 9, 2007): 761. http://dx.doi.org/10.1126/science.315.5813.761.

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Mihaylova, Zornitsa. "Stem cells and mesenchymal stem cell markers." International Journal of Medical Science and Clinical invention 6, no. 08 (August 6, 2019): 4544–47. http://dx.doi.org/10.18535/ijmsci/v6i8.03.

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Stem cells are undifferentiated cell type characterized by colonogenic ability, self-renewal and multi-lineage differentiation. They are classified into the following categories: embryonic stem cells [ESC], somatic stem cells [or adult stem cells] and induced pluripotent stem cells [iPSC]. Stem cells represent area of interest for wide range of scientists, as they are promising tool for regenerative therapy. Their differentiation ability is significantly affected by various factors of the local environment. Additional research will provide more information about the optimal cell culture conditions when stem cells are cultivated for clinical purpose, to avoid side effects like uncontrolled cell proliferation and premature differentiation.
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Zerhouni, E. "EMBRYONIC STEM CELLS: Enhanced: Stem Cell Programs." Science 300, no. 5621 (May 9, 2003): 911–12. http://dx.doi.org/10.1126/science.1084819.

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Wang, Y., F. Yates, O. Naveiras, P. Ernst, and G. Q. Daley. "Embryonic stem cell-derived hematopoietic stem cells." Proceedings of the National Academy of Sciences 102, no. 52 (December 15, 2005): 19081–86. http://dx.doi.org/10.1073/pnas.0506127102.

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Adel, Ghadeer M., Ahmed A. Khalil, and Ahmed A. Moustafa. "Stem Cell with a Peri-implant Defects." NeuroQuantology 20, no. 4 (April 30, 2022): 466–68. http://dx.doi.org/10.14704/nq.2022.20.4.nq22288.

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Periodontal regeneration aims are restoring of the destructed bone, cementum and periodontal ligament. The new strategies of regeneration is very challenging, one of these strategies is tissue engineering, including stem cells and it's considered very promising solution. This paper aims to review the use of stem cells for the treatment of peri-implant defects. Nowadays, many types of mesenchymal stem cells (MSCs) have the ability of periodontal regeneration in animal studies. The bone marrow MSCs (BMMSCs), dental pulp stem cell (DPSC), periodontal ligament stem cells (PDLSCs), and gingival mesenchymal stem cells (GMSCs) are the most types that give very promising results in animal models.
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PANGESTY, Azizah intan, Takaaki ARAHIRA, and Mitsugu TODO. "1F42 Characterization of Osteochondral Cell Sheets of Human Mesenchymal Stem Cell." Proceedings of the Bioengineering Conference Annual Meeting of BED/JSME 2015.27 (2015): 253–54. http://dx.doi.org/10.1299/jsmebio.2015.27.253.

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Chukka, Kereena. "Current Status of Cancer Stem Cell Research." Journal of Embryology & Stem Cell Research 4, no. 1 (2020): 1–2. http://dx.doi.org/10.23880/jes-16000137.

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Dissertations / Theses on the topic "Stem cell"

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Falk, Anna. "Stem cells : proliferation, differentiation, migration /." Stockholm, 2005. http://diss.kib.ki.se/2006/91-7140-497-X/.

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Karnsund, Alice, and Elin Samuelsson. "Stem Cell Classification." Thesis, KTH, Skolan för teknikvetenskap (SCI), 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-214731.

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Machine learning and neural networks haverecently become hot topics in many research areas. They havealready proved to be useful in the fields of medicine andbiotechnology. In these areas, they can be used to facilitatecomplicated and time consuming analysis processes. Animportant application is image recognition of cells, tumours etc.,which also is the focus of this paper.Our project was to construct both Fully Connected NeuralNetworks and Convolutional Neural Networks with the ability torecognize pictures of muscular stem cells (MuSCs). We wanted toinvestigate if the intensity values in each pixel of the images weresufficient to use as indata for classification.By optimizing the structure of our networks, we obtained goodresults. Using only the pixel values as input, the pictures werecorrectly classified with up to 95.1% accuracy. If the image sizewas added to the indata, the accuracy was as best 97.9 %.The conclusion was that it is sensible and practical to use pixelintensity values as indata to classification programs. Importantrelationships exist and by adding some other easily accessiblecharacteristics, the success rate can be compared to a human’sability to classify these cells.
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Hunter, Susan MacLean. "Stem cell pluripotency." Thesis, Cardiff University, 2008. http://orca.cf.ac.uk/54712/.

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Embryonic stem cells (ES cells) are derived by explantation of the embryonic portion of the pre-implantation embryo into culture. These cells have unique properties which have made them invaluable in study of the function of genes in vivo and of cell differentiation in vitro. They can be grown in culture for extended periods of time in an undifferentiated state and induced to differentiate in vitro. While undifferentiated they can be genetically manipulated. Subsequent reintroduction of these cells into the blastocyst results in the cells being integrated and contributing to all the cells of the animal including the germ line thus leading to designed genetic change. The homology of these cells, however, to their tissue of origin is not unambiguous. The primary aim of this thesis was to apply global transcriptome analysis to investigate the homology of ES cells to the pluripotent compartment of the embryo. Although ES cells can be grown in bulk, the tissue of origin, the embryonic portion of the peri-implantation embryo are small and inaccessible. It was therefore necessary to develop methods which would allow the transcriptome to be amplified without distorting the transcript profile. A linear amplification method proved to give the best result. The best method for fluorescently labelling the cDNA was shown to be enzymatic incorporation of aminoallyl dUTP followed by coupling to monoreactive Cy dyes. With these tools it was then possible to amplify the transcriptome of both colonies of ES cells and the embryonic portion of various peri-implantation embryos and apply the labelled cDNA to microarray slides. Statistical analysis of the results proved that the transcriptome of ES cells most resembles that of the embryonic ectoderm on day 5.5 of development.
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Tsai, Filip, and Henrik Hellström. "Stem Cell Classification." Thesis, KTH, Skolan för elektro- och systemteknik (EES), 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-200606.

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Samuelsson, Elin, and Alice Karnsund. "Stem Cell Classification." Thesis, KTH, Skolan för teknikvetenskap (SCI), 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-210867.

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Machine learning and neural networks have recently become hot topics in many research areas. They have already proved to be useful in the fields of medicine and biotechnology. In these areas, they can be used to facilitate complicated and time consuming analysis processes. An important application is image recognition of cells, tumours etc., which also is the focus of this paper.Our project was to construct both Fully Connected Neural Networks and Convolutional Neural Networks with the ability to recognize pictures of muscular stem cells (MuSCs). We wanted to investigate if the intensity values in each pixel of the images were sufficient to use as indata for classification.By optimizing the structure of our networks, we obtained good results. Using only the pixel values as input, the pictures were correctly classified with up to 95.1% accuracy. If the image size was added to the indata, the accuracy was as best 97.9 %.The conclusion was that it is sensible and practical to use pixel intensity values as indata to classification programs. Important relationships exist and by adding some other easily accessible characteristics, the success rate can be compared to a human’s ability to classify these cells.
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Gilner, Jennifer Bushman Kirby Suzanne Lee. "Enrichment of therapeutic hematopoietic stem cell populations from embryonic stem cells." Chapel Hill, N.C. : University of North Carolina at Chapel Hill, 2007. http://dc.lib.unc.edu/u?/etd,1232.

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Thesis (Ph. D.)--University of North Carolina at Chapel Hill, 2007.
Title from electronic title page (viewed Mar. 26, 2008). "... in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Pathology and Laboratory Medicine." Discipline: Pathology and Laboratory Medicine; Department/School: Medicine.
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Sarvi, Sana. "Small cell lung cancer and cancer stem cell-like cells." Thesis, University of Edinburgh, 2014. http://hdl.handle.net/1842/9542.

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Small cell lung cancer (SCLC) is a highly aggressive malignancy with extreme mortality and morbidity. Although initially chemo- and radio-sensitive, almost inevitable recurrence and resistance occurs. SCLC patients often present with metastases, making surgery not feasible. Current therapies, rationally designed on underlying pathogenesis, produce in vitro results, however, these have failed to translate into satisfactory clinical outcomes. Recently, research into cancer stem cells (CSCs) has gained momentum and form an attractive target for novel therapies. Based on this concept, CSCs are the cause of neoplastic tissue development that are inherently resistant to chemotherapy, explaining why conventional therapies can shrink the tumour but are unable to eliminate the tumour completely, leading to eventual recurrence. Here I demonstrate that SCLC H345 and H69 cell lines contain a subset of cells expressing CD133, a known CSC marker. CD133+ SCLC sub-population maintained their stem cell-like phenotype over a prolonged period of culture, differentiated in appropriate conditions and expressed the embryonic stem cell marker Oct-4 indicating their stem-like phenotype. Additionally, these cells displayed augmented clonogenic efficacy, were chemoresistant and tumorigenic in vivo, distinct from the CD133- cells. Thus, the SCLC CD133 expressing cells fulfil most criteria of CSClike definition. The molecular mechanisms associated with CD133+ SCLC chemoresistance and growth is unknown. Up-regulated Akt activity, a known promoter of resistance with survival advantage, was observed in CD133+ SCLC cells. Likewise, these cells demonstrated elevated expression of Bcl-2, an anti-apoptotic protein compared to their negative counterpart explaining CD133+ cell chemoresistance phenotype. Additionally, CD133+ cells revealed greater expression of neuropeptide receptors, gastrin releasing peptide (GRP) and V1A receptors compared to the CD133- cells. Addition of exogenous GRP and arginine vasopressin (AVP) to CD133+ SCLC cells promoted their clonogenic growth in semi-solid medium, illustrating for the first time neuropeptide dependent growth of these cells. A novel peptide (peptide-1) was designed based on the known structure of the substance P analogues that have shown benefit in animal models and in early clinical trials. This compound inhibited the growth of SCLC cells in in vitro with improved potency and stability compared to previous analogues and reduced tumorigenicity in vivo. Interestingly, peptide-1 was more effective in CD133+ cells due to increased expression of neuropeptide receptors on these cells. In conclusion, my results show that SCLC cells retain a sub-population of cells that demonstrate CSC-like phenotype. Preferential activation of Akt and Bcl-2 survival pathways and enhanced expression of neuropeptide receptors contribute to CD133+ SCLC chemoresistance and growth. Therefore, it can be proposed that CD133+ cells are the possible cause of SCLC development, treatment resistance and disease recurrence. Despite being chemoresistant, CD133+ cells demonstrated sensitivity to peptide-1. The identification of such new analogue that demonstrates efficacy towards resistant CD133+ SCLC cells is a very exciting step forward in the identification of a potential new therapy for resistant disease.
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Eriksson, Malin. "Manipulating neural stem cells." Stockholm, 2010. http://diss.kib.ki.se/2010/978-91-7409-853-2/.

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Gupta, Gunjan. "Effect of chondrocyte-stem cell interactions on chondrogenesis of mesenchymal stem cells." Diss., [La Jolla] : University of California, San Diego, 2009. http://wwwlib.umi.com/cr/ucsd/fullcit?p1465607.

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Thesis (M.S.)--University of California, San Diego, 2009.
Title from first page of PDF file (viewed August 11, 2009). Available via ProQuest Digital Dissertations. Includes bibliographical references (p. 128-134).
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Zhang, Jiao, and 张姣. "Regulation of cell proliferation and modulation of differentiation in human induced pluripotent stem cell-derived mesenchumal stem cells." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B49617503.

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Functional mesenchymal stem cells (MSCs) derived from human induced pluripotent stem cells (iPSCs) may represent an unlimited cell source with superior therapeutic benefits for tissue regeneration to somatic tissue, such as bone marrow (BM)-derived MSC. In the first part of this project, I investigated whether the differential expression of ion channels in iPSC-MSCs was responsible for their higher proliferation capacity than that of BM-MSCs. The expression of ion channels for K+, Na+, Ca2+ and Cl- currents was assessed by reverse transcription-polymerase chain reaction (RT-PCR). The functional role of these ion channels were then verified by patch clamp experiments to compare the electrophysiological properties of iPSC-MSCs versus BM-MSCs. I detected significant mRNA expression of ion channel genes including KCa1.1, KCa3.1, KCNH1, Kir2.1, SCN9A, CACNA1C and Clcn3 in both human iPSC-MSCs and BM-MSCs; while Kir2.2 and Kir2.3 were only observed in human iPSC-MSCs. Furthermore, I identified five types of currents (BKCa, IKDR, IKir, IKCa and ICl) in iPSC-MSCs, while only four of them (BKCa, IKDR, IKir and IKCa) were observed in BM-MSCs. The rate of cell proliferation was 1.4 fold faster in iPSC-MSCs as compared to BM-MSCs. Interestingly, the proliferation rate of human iPSCMSCs was significantly reduced when inhibiting IKDR with shRNA and hEAG1 channel blockers, 4-AP and astemizole. Though to a lesser extent, the proliferation rate of human BM-MSCs also decreased by IKDR blockage. These results demonstrated that hEAG1 channel plays a crucial role in controlling the proliferation rate of human iPSC-MSCs but to a lesser extent in BM-MSCs. Next, I examined whether forced expression of a transcription factor- myocardin in iPSC-MSC using viral vectors (adenovirus or lentivirus) can further enhance their trans-differentiation to cardiomyocytes and improve their electrophysiological properties for cardiac regeneration. My results on RT-PCR and immunofluorescent staining revealed that myocardin induced the expression of several cardiac and smooth muscle cell markers, including α-MHC, cTnT, GATA4, α-actinin, and cardiac MHC, smooth muscle cell markers MYH11, calponin, and SM α-actin, but not the more mature cardiac markers such as β-MHC and MLC2v in iPSC-MSCs. These findings indicate that forced expression of myocardin in iPSC-MSC resulted in partial trans-differentiation into cardiomyocytes phenotype. Furthermore, I also discovered that myocardin altered the electrophysiological properties of iPSC-MSCs when examined by RT-PCR and patch clamp experiments. Forced expression of myocardin in iPSC-MSC enhanced the expression of Kv4.3, SCN9A and CACNA1C, but reduced that of KCa3.1 and Kir 2.2 in iPSC-MSCs. Moreover, BKCa, IKir, ICl, Ito and INa.TTX were detected in iPSC-MSC with ectopic expression of myocardin; while only BKCa, IKir, ICl, IKDR and IKCa were noted in iPSC-MSC transfected with green florescence protein. Furthermore, as measured by multi-electrode arrays recording plate, the conduction velocity of the neonatal rat ventricular cardiomyocytes cocultured iPSC-MSC monolayer was significantly increased after ectopic expression of myocardin. Taken together, I have demonstrated that hEAG1 channel is important in the regulation of iPSC-MSC proliferation and forced expression of myocardin in iPSC-MSC resulted in their partial transdifferentiation into cardiomyocytes phenotype and improved the electrical conduction during integration with mature cardiomyocytes.
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Medicine
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Books on the topic "Stem cell"

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Stem cell. [Milan, Italy]: Sperling & Kupfer, 2009.

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The cell biology of stem cells. New York: Springer Science+Business Media, 2010.

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Konopli︠a︡nnikov, A. G. Adult stem cell survival. Hauppauge, N.Y: Nova Science Publishers, 2009.

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Al-Rubeai, Mohamed, and Mariam Naciri, eds. Stem Cells and Cell Therapy. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-7196-3.

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V, Greer Erik, ed. Focus on stem cell research. Hauppauge, N.Y: Nova Biomedical Books, 2004.

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Koka, Prasad S. Stem cell research advancements. Hauppauge, N.Y: Nova Science Publishers, 2011.

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W, Masters J. R., Palsson Bernhard, and Thomson James A. Dr, eds. Embryonic stem cells. Dordrecht: Springer, 2007.

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Irina, Klimanskaya, and Lanza Robert, eds. Adult stem cells. Amsterdam: Elsevier Academic Press, 2006.

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V, Greer Erik, ed. Embryonic stem cell research. New York: Nova Science Publishers, 2006.

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S, Koka Prasad, ed. Developments in stem cell research. New York: Nova Science Publishers, 2008.

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Book chapters on the topic "Stem cell"

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Piscioneri, Antonella. "Stem Cell." In Encyclopedia of Membranes, 1822–26. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-44324-8_2144.

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Piscioneri, Antonella. "Stem Cell." In Encyclopedia of Membranes, 1–4. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-40872-4_2144-1.

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Silk, Alain, Anne E. Powell, Paige S. Davies, and Melissa H. Wong. "Cell Fusion and Stem Cells." In Cell Fusions, 277–314. Dordrecht: Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-90-481-9772-9_14.

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Cook, Matthew M. "Mesenchymal Stem Cells and Haematopoietic Stem Cell Culture." In Mesenchymal Stem Cell Therapy, 161–72. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-200-1_9.

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Horgan, Claire, and David Valcárcel. "Selection of Stem Cell Source." In The EBMT Handbook, 135–41. Cham: Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-44080-9_14.

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AbstractSelection of stem cell source is an important consideration for any physician planning an allogeneic haematopoietic cell transplant (HCT) and has evolved considerably since bone marrow (BM) was used as the stem cell source in the first successful allogeneic HCT in 1968 (Gatti et al. 1968). BM remained the only source of stem cells for the two decades that followed until experimental work demonstrating that peripheral blood (PB) stem cells can be enriched by pre-treatment with certain chemotherapy agents and haematopoietic growth factors (Richman et al. 1976; Socinski et al. 1988; Duhrsen et al. 1988) resulted in the first peripheral blood stem cell transplant in 1986 (Korbling and Freireich 2011). Alongside this, the recognition of cord blood (CB) as a rich source of stem cells (Prindull et al. 1978) led to the successful use of cord blood as a third stem cell source in allogeneic HCT in the late 80s (Gluckman et al. 1989).
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Chowdhury, Suchandra, and Shyamasree Ghosh. "Plant Stem Cell Biology." In Stem Cells, 253–66. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-1638-9_11.

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Mitra, Arindam. "Stem Cell Clinical Trials and Stem Cell Market." In Stem Cell Production, 257–72. Singapore: Springer Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-7589-8_11.

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Singh, Abhalaxmi, and Sanjeeb K. Sahoo. "Stem-Cell Nanoengineering." In Stem-Cell Nanoengineering, 87–95. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118540640.ch6.

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McNiece, Ian K., and Robert A. Briddell. "Stem Cell Factor." In Blood Cell Biochemistry, 363–79. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-0-585-31728-1_14.

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Spaggiari, Grazia Maria, and Lorenzo Moretta. "Mesenchymal Stem Cell-Natural Killer Cell Interactions." In Stem Cells and Cancer Stem Cells, Volume 4, 217–24. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-2828-8_19.

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Conference papers on the topic "Stem cell"

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Saito, Norihiko, Nozomi Hirai, Kazuya Aoki, Satoshi Fujita, Haruo Nakayama, Morito Hayashi, Takatoshi Sakurai, and Satoshi Iwabuchi. "Abstract 2621: OLIG2 regulates stem cell maintenance and cell cycle in glioma stem cells." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-2621.

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Saito, Norihiko, Nozomi Hirai, Kazuya Aoki, Satoshi Fujita, Haruo Nakayama, Morito Hayashi, Takatoshi Sakurai, and Satoshi Iwabuchi. "Abstract 2621: OLIG2 regulates stem cell maintenance and cell cycle in glioma stem cells." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-2621.

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Martin, Stephen. "Annual International Meeting on Stem Cell Research." In Annual International Meeting on Stem Cell Research. Global Science & Technology Forum (GSTF), 2011. http://dx.doi.org/10.5176/978-981-08-8227-3_scr2011.

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Thoson, J. "Embryonic stem cell research." In 2006 IEEE Aerospace Conference. IEEE, 2006. http://dx.doi.org/10.1109/aero.2006.1655714.

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ROEDER, INGO. "SYSTEMS STEM CELL BIOLOGY." In International Symposium on Mathematical and Computational Biology. WORLD SCIENTIFIC, 2007. http://dx.doi.org/10.1142/9789812708779_0001.

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Lobba, Aline RM, Maria Fernanda PAD Forni, Carolina Perozzi, Ana Claúdia O. Carreira, Leticia Labriola, and Mari Cleide Sogayar. "Abstract 3872: Differentially expressed stem cell markers in breast cancer stem cells." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-3872.

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Prudnikov, Igor, Anton Smirnov, and Volodymyr Tsyvkin. "Apoptosomes and proteasomes from exosomes generated by human hematopoietic stem cells." In Cell-to-Cell Metabolic Cross-Talk in Physiology and Pathology. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/cells2020-08924.

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Li, Lulu, Rene Schloss, Noshir Langrana, and Martin Yarmush. "Effects of Encapsulation Microenvironment on Embryonic Stem Cell Differentiation." In ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-192587.

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Pluripotent embryonic stem cells represent a promising renewable cell source to generate a variety of differentiated cell types. Although many investigators have described techniques to effectively differentiate stem cells into different mature cell lineages, their practicality is limited by the absence of large scale processing consideration and low yields of differentiated cells. Previously we have established a murine embryonic stem cell alginate-poly-l-lysine microencapsulation differentiation system. The three-dimensional alginate microenvironment maintains cell viability, is conducive to ES cell differentiation to hepatocyte lineage cells, and maintains differentiated cellular function. In the present work, we demonstrate that hepatocyte differentiation is mediated by cell-cell aggregation in the encapsulation microenvironment. Both cell aggregation and hepatocyte functions, such as urea and albumin secretion, as well as increased expression of cytokaratin 18 and cyp4507a, occur concomitantly with surface E-cadherin expression. Furthermore, by incorporating soluble inducers, such as retinoic acid, into the permeable microcapsule system, we demonstrate decreased cell aggregation and enhanced neuronal lineage differentiation with the expression of various neuronal specific markers, including neurofilament, A2B5, O1 and GFAP. Therefore, as a result of capsule parameter and microenvironment manipulation, we are capable of targeting cellular differentiation to both endodermal and ectodermal cell lineages.
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"11th International Meeting of the Portuguese Society for Stem Cells and Cell Therapies." In 11th International Meeting of the Portuguese Society for Stem Cells and Cell Therapies. Frontiers Media SA, 2019. http://dx.doi.org/10.3389/978-2-88945-675-8.

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Erlank, A. O., and C. P. Bridges. "The satellite stem cell architecture." In 2016 IEEE Symposium Series on Computational Intelligence (SSCI). IEEE, 2016. http://dx.doi.org/10.1109/ssci.2016.7850165.

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Reports on the topic "Stem cell"

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Sussman, Daniel J. Mammary Stem Cell Isolation. Fort Belvoir, VA: Defense Technical Information Center, August 2004. http://dx.doi.org/10.21236/ada429766.

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Cohen, Isaac. Megakaryocytopoiesis in Stem Cell Transplantation. Fort Belvoir, VA: Defense Technical Information Center, October 1997. http://dx.doi.org/10.21236/adb233503.

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Donohue, Henry J., Christopher Niyibizi, and Alayna Loiselle. Induced Pluripotent Stem Cell Derived Mesenchymal Stem Cells for Attenuating Age-Related Bone Loss. Fort Belvoir, VA: Defense Technical Information Center, September 2013. http://dx.doi.org/10.21236/ada606237.

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Donahue, Henry J. Induced Pluripotent Stem Cell Derived Mesenchymal Stem Cells for Attenuating Age-Related Bone Loss. Fort Belvoir, VA: Defense Technical Information Center, July 2012. http://dx.doi.org/10.21236/ada581680.

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Signoretti, Sabina. The Basal Cell Marker p63 and Prostate Stem Cells. Fort Belvoir, VA: Defense Technical Information Center, May 2002. http://dx.doi.org/10.21236/ada406963.

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Signoretti, Sabina. The Basal Cell Marker p63 and Prostate Stem Cells. Fort Belvoir, VA: Defense Technical Information Center, May 2004. http://dx.doi.org/10.21236/ada427706.

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Signoretti, Sabina. The Basal Cell Marker p63 and Prostate Stem Cells. Fort Belvoir, VA: Defense Technical Information Center, May 2003. http://dx.doi.org/10.21236/ada416722.

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8

Heffelfinger, Sue C. Mammary Stem Cell Susceptibility to Carcinogenesis. Fort Belvoir, VA: Defense Technical Information Center, July 2005. http://dx.doi.org/10.21236/ada443556.

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Watabe, Kounosuke. Identification of Metastatic Tumor Stem Cell. Fort Belvoir, VA: Defense Technical Information Center, September 2011. http://dx.doi.org/10.21236/ada554453.

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Watabe, Kounosuke. Identification of Metastatic Tumor Stem Cell. Fort Belvoir, VA: Defense Technical Information Center, September 2010. http://dx.doi.org/10.21236/ada554826.

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