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Cited by 397

The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.

Sox2, a key factor in the regulation of pluripotency and neural differentiation

Open access
Zhang, Shuchen·2014·World Journal of Stem Cells

Abstract

Sex determining region Y-box 2 (Sox2), a member of the SoxB1 transcription factor family, is an important transcriptional regulator in pluripotent stem cells (PSCs). Together with octamer-binding transcription factor 4 and Nanog, they co-operatively control gene expression in PSCs and maintain their pluripotency. Furthermore, Sox2 plays an essential role in somatic cell reprogramming, reversing the epigenetic configuration of differentiated cells back to a pluripotent embryonic state. In addition to its role in regulation of pluripotency, Sox2 is also a critical factor for directing the differentiation of PSCs to neural progenitors and for maintaining the properties of neural progenitor stem cells. Here, we review recent findings concerning the involvement of Sox2 in pluripotency, somatic cell reprogramming and neural differentiation as well as the molecular mechanisms underlying these roles.

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Metadata

Authors
Zhang, S.
Venue
World Journal of Stem Cells
Published
2014
Volume
6
Issue
3
Pages
305
ISSN
1948-0210 (ISSN-L)
OpenAlex
W2010573097
Cited by
397
References
50
FWCI
7.54
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Sox2, a key factor in the regulation of pluripotency and neural differentiation. https://app.cochat.ai/papers/10.4252/wjsc.v6.i3.305
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Zhang, S. (2014). Sox2, a key factor in the regulation of pluripotency and neural differentiation. World Journal of Stem Cells. https://doi.org/10.4252/wjsc.v6.i3.305

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.