Back to search

Article

Genome-wide and high-density CRISPR-Cas9 screens identify point mutations in <i>PARP1</i> causing PARP inhibitor resistance

2017-10-14

Abstract excerpt

PARP inhibitors (PARPi) target homologous recombination defective tumour cells via synthetic lethality. Genome-wide and high-density CRISPR-Cas9 “tag, mutate and enrich” mutagenesis screens identified single amino acid mutations in PARP1 that cause profound PARPi-resistance. These included PARP1 mutations outside of the DNA interacting regions of the protein, such as mutations in solvent exposed regions of the cat...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
7669a21c-7af7-5997-ad2d-1c1aff0d1244
DOI
10.1101/203224
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Genome-wide and high-density CRISPR-Cas9 screens identify point mutations in <i>PARP1</i> causing PARP inhibitor resistanceDOI 10.1101/203224
Select a neighboring publication to make it the new centre.