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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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樓主: CHARY
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發(fā)表于 2025-3-25 07:15:33 | 只看該作者
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發(fā)表于 2025-3-25 11:08:36 | 只看該作者
Generation of T-Lineage Cells from iPS Cells and Its Application,on (DLI) therapy. DLI is an effective therapy for lymphoma or leukemia patient for the inhibition of relapses after bone marrow transplantation (BMT). However, DLI treatment depends on the availability of T lymphocytes isolated from a donor for the generation of lymphocytes. The application of cell
23#
發(fā)表于 2025-3-25 13:45:19 | 只看該作者
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 t
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發(fā)表于 2025-3-25 19:39:31 | 只看該作者
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發(fā)表于 2025-3-25 20:58:10 | 只看該作者
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發(fā)表于 2025-3-26 07:58:12 | 只看該作者
Generation of T-Lineage Cells from iPS Cells and Its Application,reprogramming technology facilitates the generation of lymphocytes without donor apheresis, offering a sustainable and repeatable DLI therapy. In this chapter, we show an instance of this new age immunotherapy that utilizes cell reprogramming technology.
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發(fā)表于 2025-3-26 10:16:58 | 只看該作者
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