
Crispr genome editing in stem cells turns to gold
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Hematopoietic stem and progenitor cells have been engineered using gold nanoformulations conjugated with CRISPR capable of targeting two distinct genomic loci of therapeutic interest, with
potential engraftment in humanized mouse models. Access through your institution Buy or subscribe This is a preview of subscription content, access via your institution ACCESS OPTIONS Access
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INFORMATION AUTHORS AND AFFILIATIONS * Department of Surgery, Duke University, Durham, NC, USA Aravind Asokan * Department of Molecular Genetics and Microbiology, Duke University, Durham,
NC, USA Aravind Asokan * Department of Biomedical Engineering, Duke University, Durham, NC, USA Aravind Asokan Authors * Aravind Asokan View author publications You can also search for this
author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to Aravind Asokan. RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Asokan, A. CRISPR
genome editing in stem cells turns to gold. _Nat. Mater._ 18, 1038–1039 (2019). https://doi.org/10.1038/s41563-019-0491-4 Download citation * Published: 19 September 2019 * Issue Date:
October 2019 * DOI: https://doi.org/10.1038/s41563-019-0491-4 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a
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