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- W3204120268 endingPage "181" @default.
- W3204120268 startingPage "171" @default.
- W3204120268 abstract "CRISPR-dependent genome editing enables the study of genes and mutations on a large scale. Here we review CRISPR-based functional genomics technologies that generate gene knockouts and single nucleotide variants (SNVs) and discuss how their use has provided new important insights into the function of homologous recombination (HR) genes. In particular, we highlight discoveries from CRISPR screens that have contributed to define the response to PARP inhibition in cells deficient for the HR genes BRCA1 and BRCA2, uncover genes whose loss causes synthetic lethality in combination with BRCA1/2 deficiency, and characterize the function of BRCA1/2 SNVs of uncertain clinical significance. Further use of these approaches, combined with next-generation CRISPR-based technologies, will aid to dissect the genetic network of the HR pathway, define the impact of HR mutations on cancer etiology and treatment, and develop novel targeted therapies for HR-deficient tumors." @default.
- W3204120268 created "2021-10-11" @default.
- W3204120268 creator A5024098581 @default.
- W3204120268 creator A5029782413 @default.
- W3204120268 date "2021-12-01" @default.
- W3204120268 modified "2023-10-01" @default.
- W3204120268 title "Towards a CRISPeR understanding of homologous recombination with high-throughput functional genomics" @default.
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