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Establishing iPSCs as a method to model neurodevelopment in Down’s syndromeBartish, Margarita January 2012 (has links)
The derivation of pluripotent stem cells (now termed induced pluripotent stem cells, iPSC) from mature somatic cells was a finding of seminal importance to fundamental cell biology. Thus established iPSC technology has been predicted to advance fields that previously relied on the ethically disputed use of embryonic stem cells. Being pluripotent (able to differentiate into every cell type present in the human body) and sharing most other characteristics with embryonic stem cells, but being much readier obtainable and their derivation free from ethical restraints, human induced pluripotent stem cells (hiPSC) provide access to cell types and insights into cell processes previously unattainable to researches. For this thesis, a hiPSC line was established from a skin biopsy donated by a Down’s syndrome patient. Most of what is known today about the molecular neurobiology behind this disease has been gathered from mice models or human post mortem studies, but this has a limited extrapolation potential to early human brain development in DS patients, as Down’s syndrome is an inherently human disease whose defining phenotype is established early during embryonic development. Having access to human pluripotent cells able to recapitulate the events of early neurogenesis is thus invaluable to the understanding of the mechanisms of this disorder. In parallel, work has been performed on optimizing iPSC reprogramming protocol. By exchanging one of the transcription factors used for reprogramming with a reporter gene, genomic integration of reprogramming factors has become possible to be traced visually, enabling more efficient selection of reprogrammed iPSC colonies.
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ESTABLISHMENT AND OPTIMAL CULTURE CONDITIONS OF MICRORNA-INDUCED PLURIPOTENT STEM CELLS GENERATED FROM HEK293 CELLS VIA TRANSFECTION OF MICRORNA-302S EXPRESSION VECTORTAKEI, YOSHIFUMI, KADOMATSU, KENJI, YASUDA, KAORI, KOIDE, NAOSHI 02 1900 (has links)
No description available.
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Nuclear organization of mouse Hox cluster paralogs during mouse embryonic stem cell differentiation to neural stem cellPanicker, Priya, January 2009 (has links)
Thesis (M.S.)--Rutgers University, 2009. / "Graduate Program in Biomedical Engineering." Includes bibliographical references (p. 53-55).
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The development of surrogate marker-tagged ES cell technology to study haematopoietic commitmentCheng, Yi-Han January 2013 (has links)
No description available.
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Human mesenchymal stem cell engraftment in the chimeric sheep modelColletti, Evan. January 2006 (has links)
Thesis (Ph. D.)--University of Nevada, Reno, 2006. / "May, 2006." Includes bibliographical references. Online version available on the World Wide Web.
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Studies on adult stem cells /Meletis, Konstantinos, January 2006 (has links)
Diss. (sammanfattning) Stockholm : Karolinska institutet, 2006. / Härtill 6 uppsatser.
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The influence of osteoblasts and growth factors on the proliferation and differentiation of OMA-AML-1 cells a report submitted in partial fulfillment ... for the degree of Master of Science (School of Dentistry) ... /Korsnes, Maria Isabel. January 1998 (has links)
Thesis (M.S.)--University of Michigan, 1998. / Includes bibliographical references.
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Stem cells, TGF-[beta], and the adenoviral mediated overexpression of fibromodulin to promote incisional wound healingMoore, Steven T. January 2006 (has links) (PDF)
Thesis (M.S.)--University of Alabama at Birmingham, 2006. / Description based on contents viewed Jan. 29, 2007; title from title screen. Includes bibliographical references (p. 51-54).
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Effects of intrinsic & extrinsic factors on the growth and differentiation of human mesenchymal stem cells /Li, Jing, January 2006 (has links)
Thesis (Ph. D.)--University of Hong Kong, 2006. / Also available online.
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Transcriptional regulation of Runx1 in the developing haematopoietic systemNottingham, Wade January 2007 (has links)
No description available.
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