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Titlebook: Stem Cell Therapy for Diabetes; Shimon Efrat Book 2010 Humana Press 2010 Diabetes.Immunity.Pancreas.Regulation.Tissue Engineering.cell bio

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發(fā)表于 2025-3-21 18:38:06 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Stem Cell Therapy for Diabetes
編輯Shimon Efrat
視頻videohttp://file.papertrans.cn/878/877219/877219.mp4
概述Leading experts in the field.Thorough description and analysis of research.Includes supplementary material:
叢書名稱Stem Cell Biology and Regenerative Medicine
圖書封面Titlebook: Stem Cell Therapy for Diabetes;  Shimon Efrat Book 2010 Humana Press 2010 Diabetes.Immunity.Pancreas.Regulation.Tissue Engineering.cell bio
描述.Stem Cell Therapy for Diabetes, one of the latest installments of the Stem Cell Biology and Regenerative Medicine series, reviews the three main approaches for generation of sufficient numbers of insulin-producing cells for restoration of an adequate beta-cell mass: beta-cell expansion, stem-cell differentiation, and nuclear reprogramming. Adeptly collecting the research of the leading scientists in the field, Stem Cell Therapy for Diabetes compares the merits of employing autologous versus banked allogeneic cell sources for generation of surrogate beta cells, and addresses tissue engineering and ways for cell protection from recurring autoimmunity and graft rejection. Stem Cell Therapy for Diabetes provides essential reading for those especially interested in tracking the progress in applying of one of the most exciting new developments in bio-medicine towards a cure for diabetes..
出版日期Book 2010
關(guān)鍵詞Diabetes; Immunity; Pancreas; Regulation; Tissue Engineering; cell biology; insulin
版次1
doihttps://doi.org/10.1007/978-1-60761-366-4
isbn_softcover978-1-61779-669-2
isbn_ebook978-1-60761-366-4Series ISSN 2196-8985 Series E-ISSN 2196-8993
issn_series 2196-8985
copyrightHumana Press 2010
The information of publication is updating

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Adult Cell Reprogramming: Using Nonpancreatic Cell Sources to Generate Surrogate Beta Cells for Trea adult tissue, specifically liver and bone marrow, to provide a source of tissue for generating functional insulin-producing cells. This approach might generate custom-made autologous surrogate β cells for treatment of diabetes and possibly circumvent both the shortage of cadaveric human donor tissu
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Xiaobo Xu,Joke D’Hoker,Nico De Leu,Xiangwei Xiao,Yves Heremans,Mark Van De Casteele,Harry Heimberg
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