The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
Reprogramming Cellular Identity for Regenerative Medicine
Open accessAbstract
The choreographed development of over 200 distinct differentiated cell types from a single zygote is a complex and poorly understood process. Whereas development leads unidirectionally towards more restricted cell fates, recent work in cellular reprogramming has proven that striking conversions of one cellular identity into another can be engineered, promising countless applications in biomedical research and paving the way for modeling disease with patient-derived stem cells. To date, there has been little discussion of which disease models are likely to be most informative. We here review evidence demonstrating that because environmental influences and epigenetic signatures are largely erased during reprogramming, patient-specific models of diseases with strong genetic bases and high penetrance are likely to prove most informative in the near term. However, manipulating in vitro culture conditions may ultimately enable cell-based models to recapitulate gene-environment interactions. Here, we discuss the implications of the new reprogramming paradigm in biomedicine and outline how reprogramming of cell identities is enhancing our understanding of cell differentiation and prospects for cellular therapies and in vivo regeneration.
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Self-citationIn vivo reprogramming of adult pancreatic exocrine cells to β-cells
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Cited by
Super-enhancers in the control of cell identity and disease
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Emerging trends and new developments in regenerative medicine: a scientometric update (2000 – 2014)
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Direct Reprogramming of Human Fibroblasts to Functional and Expandable Hepatocytes
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Chemical reprogramming of human somatic cells to pluripotent stem cells.
Guan, J., Wang, G., Wang, J., Zhang, Z., Fu, Y., Cheng, L., Meng, G., Lyu, Y., Zhu, J., Li, Y., et al. (2022) · Nature · doi:10.1038/s41586-022-04593-5 · Cited by 388
Metadata
- Authors
- Cherry, A. B. C., & Daley, G. Q.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2012-03
- Volume
- 148
- Issue
- 6
- Pages
- 1110-1122
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2081143491
- Cited by
- 191
- References
- 22
- FWCI
- 10.80
- Type
- journal article
- Language
- en
- Open access
- bronze
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