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本文引用的文献

1
Oxidative stress tolerance of early stage diabetic endothelial progenitor cell.早期糖尿病内皮祖细胞的氧化应激耐受性
Regen Ther. 2015 Feb 23;1:38-44. doi: 10.1016/j.reth.2014.11.001. eCollection 2015 Jun.
2
Xenogeneic-free defined conditions for derivation and expansion of human embryonic stem cells with mesenchymal stem cells.用于人胚胎干细胞与间充质干细胞的衍生和扩增的无异种动物成分的限定条件。
Regen Ther. 2015 Feb 19;1:18-29. doi: 10.1016/j.reth.2014.12.004. eCollection 2015 Jun.
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Flow-dependent regulation of genome-wide mRNA and microRNA expression in endothelial cells in vivo.血流依赖性调节内皮细胞中全基因组 mRNA 和 microRNA 的表达。
Sci Data. 2014 Oct 28;1:140039. doi: 10.1038/sdata.2014.39. eCollection 2014.
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Regulators of pluripotency and their implications in regenerative medicine.多能性调控因子及其在再生医学中的意义。
Stem Cells Cloning. 2015 Apr 21;8:67-80. doi: 10.2147/SCCAA.S80157. eCollection 2015.
5
An alternative pluripotent state confers interspecies chimaeric competency.一种替代性多能状态赋予种间嵌合能力。
Nature. 2015 May 21;521(7552):316-21. doi: 10.1038/nature14413. Epub 2015 May 6.
6
Origin of cells and network information.细胞起源与网络信息。
World J Stem Cells. 2015 Apr 26;7(3):535-40. doi: 10.4252/wjsc.v7.i3.535.
7
Elimination of tumorigenic human pluripotent stem cells by a recombinant lectin-toxin fusion protein.重组凝集素-毒素融合蛋白消除致瘤性人多能干细胞。
Stem Cell Reports. 2015 May 12;4(5):811-20. doi: 10.1016/j.stemcr.2015.02.016. Epub 2015 Apr 9.
8
Structure-based discovery of NANOG variant with enhanced properties to promote self-renewal and reprogramming of pluripotent stem cells.基于结构的具有增强特性的NANOG变体发现,以促进多能干细胞的自我更新和重编程。
Proc Natl Acad Sci U S A. 2015 Apr 14;112(15):4666-71. doi: 10.1073/pnas.1502855112. Epub 2015 Mar 30.
9
Using induced pluripotent stem cells as a tool for modelling carcinogenesis.利用诱导多能干细胞作为致癌建模的工具。
World J Stem Cells. 2015 Mar 26;7(2):461-9. doi: 10.4252/wjsc.v7.i2.461.
10
A continuous molecular roadmap to iPSC reprogramming through progression analysis of single-cell mass cytometry.通过单细胞质谱流式细胞术的进程分析获得诱导多能干细胞重编程的连续分子路线图。
Cell Stem Cell. 2015 Mar 5;16(3):323-37. doi: 10.1016/j.stem.2015.01.015.

干细胞重编程和分化过程中涉及的信号传导。

Signaling involved in stem cell reprogramming and differentiation.

作者信息

Tanabe Shihori

机构信息

Shihori Tanabe, National Institute of Health Sciences, Tokyo 158-8501, Japan.

出版信息

World J Stem Cells. 2015 Aug 26;7(7):992-8. doi: 10.4252/wjsc.v7.i7.992.

DOI:10.4252/wjsc.v7.i7.992
PMID:26328015
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4550631/
Abstract

Stem cell differentiation is regulated by multiple signaling events. Recent technical advances have revealed that differentiated cells can be reprogrammed into stem cells. The signals involved in stem cell programming are of major interest in stem cell research. The signaling mechanisms involved in regulating stem cell reprogramming and differentiation are the subject of intense study in the field of life sciences. In this review, the molecular interactions and signaling pathways related to stem cell differentiation are discussed.

摘要

干细胞分化受多种信号事件调控。最近的技术进展表明,分化细胞可被重编程为干细胞。参与干细胞编程的信号是干细胞研究的主要关注点。调控干细胞重编程和分化的信号机制是生命科学领域深入研究的课题。在本综述中,将讨论与干细胞分化相关的分子相互作用和信号通路。