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Titlebook: Hematopoietic Differentiation of Human Pluripotent Stem Cells; Tao Cheng Book 2015 The Author(s) 2015 Crispr/Cas9-Mediated Genome Editing.

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發(fā)表于 2025-3-21 16:52:08 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Hematopoietic Differentiation of Human Pluripotent Stem Cells
編輯Tao Cheng
視頻videohttp://file.papertrans.cn/426/425561/425561.mp4
概述Includes cutting-edge methods and protocols in blood cell differentiation.Provides step-by-step detail essential for reproducible results.Written by experts in hematology.Includes supplementary materi
叢書名稱SpringerBriefs in Stem Cells
圖書封面Titlebook: Hematopoietic Differentiation of Human Pluripotent Stem Cells;  Tao Cheng Book 2015 The Author(s) 2015 Crispr/Cas9-Mediated Genome Editing.
描述This book features the most cutting-edge work from the world’s leading laboratories in this field and provides practical methods for differentiating pluripotent stem cells into hematopoietic lineages in the blood system. Pluripotent stem cells have attracted major interest from a fast-growing and multidisciplinary community of researchers who are developing new techniques for the derivation and differentiation of these cells into specific cell lineages. These direct differentiation methods hold great promise for the translational applications of these cells. This book is an essential reference work for researchers at all levels in the fields of hematology and stem cell biology, as well as clinical practitioners in regenerative medicine.
出版日期Book 2015
關(guān)鍵詞Crispr/Cas9-Mediated Genome Editing; Pluripotent stem cells; T cells; hematopoietic differentiation; pro
版次1
doihttps://doi.org/10.1007/978-94-017-7312-6
isbn_softcover978-94-017-7311-9
isbn_ebook978-94-017-7312-6Series ISSN 2192-8118 Series E-ISSN 2192-8126
issn_series 2192-8118
copyrightThe Author(s) 2015
The information of publication is updating

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Jian-Ping Zhang,Amanda Neises,Tao Cheng,Xiao-Bing Zhangbout intention-to-treat analysis, per protocol analysis, and as treated analysis. Furthermore, this chapter informs the readers about the simplicity of the equations used and how to obtain the datasets used in the examples.
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Reprogramming of Human Cord Blood CD34+ Cells into Induced MSCs,orted that induced MSCs (iMSCs) can be efficiently generated with OCT4 under defined conditions and iMSCs can be immortalized by overexpression of OCT4. Here, we detail the protocol for generating integration-free iMSCs from cord blood CD34. cells using an episomal vector and describe the approach to immortalizing iMSCs.
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Hematopoietic Differentiation of Human Pluripotent Stem Cells978-94-017-7312-6Series ISSN 2192-8118 Series E-ISSN 2192-8126
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SpringerBriefs in Stem Cellshttp://image.papertrans.cn/h/image/425561.jpg
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