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Cited by 443

The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.

Cornerstones of CRISPR–Cas in drug discovery and therapy

Open access
Fellmann, Christof, Gowen, Benjamin G., Lin, Pei-Chun, Doudna, Jennifer A., Corn, Jacob E.·2017·Nature Reviews Drug Discovery

Abstract

The recent development of CRISPR–Cas systems as easily accessible and programmable tools for genome editing and regulation is spurring a revolution in biology. Paired with the rapid expansion of reference and personalized genomic sequence information, technologies based on CRISPR–Cas are enabling nearly unlimited genetic manipulation, even in previously difficult contexts, including human cells. Although much attention has focused on the potential of CRISPR–Cas to cure Mendelian diseases, the technology also holds promise to transform the development of therapies to treat complex heritable and somatic disorders. In this Review, we discuss how CRISPR–Cas can affect the next generation of drugs by accelerating the identification and validation of high-value targets, uncovering high-confidence biomarkers and developing differentiated breakthrough therapies. We focus on the promises, pitfalls and hurdles of this revolutionary gene-editing technology, discuss key aspects of different CRISPR–Cas screening platforms and offer our perspectives on the best practices in genome engineering.

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Crossref · 10.1038/nrd.2016.238

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Metadata

Authors
Fellmann, C., Gowen, B. G., Lin, P.-C., Doudna, J. A., & Corn, J. E.
Venue
Nature Reviews Drug Discovery
Published
2016-12-23
Volume
16
Issue
2
Pages
89-100
ISSN
  • 1474-1776 (ISSN-L)
  • 1474-1784
OpenAlex
W2565920990
Cited by
443
References
54
FWCI
3.70
Type
journal article
Language
en
Open access
green

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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.