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In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration

In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5331785

In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

A method for CRISPR-based genome editing that harnesses cellular non-homologous end joining activity to achieve targeted DNA knock-in in non-dividing tissues.
A novel method for knock-in gene integration
A current challenge in genome editing is achieving efficient targeted integration of transgenes in post-mitotic cells. These authors develop...

Alternative Titles

Full title

In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5331785

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5331785

Other Identifiers

ISSN

0028-0836

E-ISSN

1476-4687

DOI

10.1038/nature20565

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