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CRISPR–Cas9 genome editing in human cells occurs via the Fanconi anemia pathway

CRISPR–Cas9 genome editing in human cells occurs via the Fanconi anemia pathway

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2078579437

CRISPR–Cas9 genome editing in human cells occurs via the Fanconi anemia pathway

About this item

Full title

CRISPR–Cas9 genome editing in human cells occurs via the Fanconi anemia pathway

Publisher

New York: Nature Publishing Group US

Journal title

Nature genetics, 2018-08, Vol.50 (8), p.1132-1139

Language

English

Formats

Publication information

Publisher

New York: Nature Publishing Group US

More information

Scope and Contents

Contents

CRISPR–Cas genome editing creates targeted DNA double-strand breaks (DSBs) that are processed by cellular repair pathways, including the incorporation of exogenous DNA via single-strand template repair (SSTR). To determine the genetic basis of SSTR in human cells, we developed a coupled inhibition-cutting system capable of interrogating multiple ed...

Alternative Titles

Full title

CRISPR–Cas9 genome editing in human cells occurs via the Fanconi anemia pathway

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2078579437

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2078579437

Other Identifiers

ISSN

1061-4036

E-ISSN

1546-1718

DOI

10.1038/s41588-018-0174-0

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