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Characterization and differentiation of peripheral blood derived multipotent adult progenitor cellsAddagarla, Hari Satya Shankar. January 1900 (has links)
Thesis (degree.)--Marshall University, 2009. / Title from document title page. Includes abstract. Document formatted into pages: contains 57 p. Includes bibliographical references p. 51-57.
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Stem cell research embryonic and adult stem cells : the ethical pursuit of dignity for human life /Hannasch, Matthew R. January 1900 (has links)
Thesis (M.A.)--Catholic Theological Union at Chicago, 2007. / Vita. Includes bibliographical references (leaves 42-47).
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Stem cell research embryonic and adult stem cells : the ethical pursuit of dignity for human life /Hannasch, Matthew R. January 1900 (has links)
Thesis (M.A.)--Catholic Theological Union at Chicago, 2007. / Vita. Includes bibliographical references (leaves 42-47).
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Model of Joint Immunoregulation via Stem Cell Educated MacrophagesJanuary 2019 (has links)
archives@tulane.edu / I would like to thank the Tulane Department of Biomedical Engineering and the Tulane Center for Stem Cell Research and Regenerative Medicine for the support and means to conduct such meaningful research. I am also thankful for the continued support and encouragement from Dr. Bruce Bunnell, whose enthusiasm and inexhaustible drive is a source of inspiration. To my fellow lab members, and particularly Ben O’Donnell, I attribute the technical skills I have learned and the joy of coming to work every day in such a welcoming environment. I am grateful for the additional help from our cohort of research assistants, including Tia Monjure, Brooke Santagato, Michael L’Ecuyer, and Mitchell Couldwell. Additionally, much of my work is in part attributed to the team of specialized core personnel, Alan Tucker in flow cytometry and Dina Gaupp in histology. I am grateful for the American Association of University Women which provided funding for my master’s coursework. In affiliation with the University and Pittsburgh and Stanford University, this project is the collaborative effort of many great minds. It was financially supported by the National Institute of Health under the project number 1UG3TR002136-01. / 1 / Clara Ives
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Stem Cells Derived from Umbilical Cord Blood (UCB)—A Promise for the FutureAndreasen, Debra S. January 2011 (has links) (PDF)
No description available.
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A study of primary neural stem cell differentiation in vitro, focusing on the Three Amino acid Loop Extension (TALE) homeobox transcription factorsBarber, Benjamin A. 26 March 2012 (has links)
Neural stem cells are capable of self-renewal and multilineage differentiation into the main cell types of the central nervous system, which are the neurons, astrocytes, and oligodendrocytes. These properties make neural stem cells an attractive cell source for potential cell-based therapies; however, thoroughly describing their gene expression programs is required to predict their safety and efficacy. In this study, we reveal that mouse embryonic day (E14) forebrain-derived primary neural stem cells have an astrocytic gene expression profile. We show that the NOTCH and BMP signalling pathways exhibit transcription profiles that are specific to the proliferation and differentiation of this neural stem cell source. Finally, we report the expression patterns of the Hox and TALE family homeobox genes in the E14 forebrain, E14 forebrain-derived primary neural stem cells, and their differentiating progeny. Protein expression analysis suggests that PREP2 is involved in neural stem cell proliferation and neuronogenesis, and that MEIS1 is involved in astrocyte differentiation. This is the first report on the expression patterns of TALE genes in forebrain-derived NSC differentiated in vitro, which provides a starting point to investigate the role of TALE genes in forebrain neurogenesis.
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Epigenetic reprogramming of epiblast stem cells to a naïve pluripotent stateGillich, Astrid January 2012 (has links)
No description available.
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A study of primary neural stem cell differentiation in vitro, focusing on the Three Amino acid Loop Extension (TALE) homeobox transcription factorsBarber, Benjamin A. 26 March 2012 (has links)
Neural stem cells are capable of self-renewal and multilineage differentiation into the main cell types of the central nervous system, which are the neurons, astrocytes, and oligodendrocytes. These properties make neural stem cells an attractive cell source for potential cell-based therapies; however, thoroughly describing their gene expression programs is required to predict their safety and efficacy. In this study, we reveal that mouse embryonic day (E14) forebrain-derived primary neural stem cells have an astrocytic gene expression profile. We show that the NOTCH and BMP signalling pathways exhibit transcription profiles that are specific to the proliferation and differentiation of this neural stem cell source. Finally, we report the expression patterns of the Hox and TALE family homeobox genes in the E14 forebrain, E14 forebrain-derived primary neural stem cells, and their differentiating progeny. Protein expression analysis suggests that PREP2 is involved in neural stem cell proliferation and neuronogenesis, and that MEIS1 is involved in astrocyte differentiation. This is the first report on the expression patterns of TALE genes in forebrain-derived NSC differentiated in vitro, which provides a starting point to investigate the role of TALE genes in forebrain neurogenesis.
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A comparative study of how high school students understand stem cells /Moyer, Jonathan Christian Rabe, January 2007 (has links) (PDF)
Thesis (M.S.) in Teaching--University of Maine, 2007. / Includes vita. Includes bibliographical references (leaves 63-64).
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Natural and modified variations in human induced pluripotent stem cellsRouhani, Foad Jafari January 2015 (has links)
No description available.
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