The DOI matches its Crossref record; 126 of the 126 references it cites were found in a registry or an index.
Progress in understanding reprogramming to the induced pluripotent state
Open accessAbstract
Induction of pluripotency by transcription factors has become a commonplace method to produce pluripotent stem cells. Great strides have been made in our understanding of the mechanism by which this occurs — particularly in terms of transcriptional and chromatin-based events — yet only a small part of the complete picture has been revealed. Understanding the mechanism of reprogramming to pluripotency will have important implications for improving the efficiency and quality of reprogramming and advancing therapeutic application of induced pluripotent stem cells. It will also help to reveal the machinery that stabilizes cell identity and to instruct the design of directed differentiation or lineage switching strategies. To inform the next phase in understanding reprogramming, we review the latest findings, highlight ongoing debates and outline future challenges.
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Cites
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Cited by
m6A RNA methylation promotes XIST-mediated transcriptional repression
Patil, D. P., Chen, C.-K., Pickering, B. F., Chow, A., Jackson, C., Guttman, M., & Jaffrey, S. R. (2016) · Nature · doi:10.1038/nature19342 · Cited by 1,747
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Robust cellular reprogramming occurs spontaneously during liver regeneration
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H3K9 methylation is a barrier during somatic cell reprogramming into iPSCs
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Wang, T., Chen, K., Zeng, X., Yang, J., Wu, Y., Shi, X., Qin, B., Zeng, L., Esteban, M. A., Pan, G., et al. (2011) · Cell Stem Cell · doi:10.1016/j.stem.2011.10.005 · Cited by 458
Metadata
- Authors
- Plath, K., & Lowry, W. E.
- Venue
- Nature Reviews Genetics
- Published
- 2011-03-18
- Volume
- 12
- Issue
- 4
- Pages
- 253-265
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W1964224339
- Cited by
- 289
- References
- 126
- FWCI
- 2.96
- Type
- journal article
- Language
- en
- Open access
- green
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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).
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