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- W3134747076 endingPage "106" @default.
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- W3134747076 abstract "CRISPR/Cas technology has been successfully designed for genome edition in numerous biological systems. Additionally, the re-engineering of Cas nucleases for purposes other than genome editing has resulted in the generation of, for example, catalytically inactive dead Cas9 or dCas12 nucleases, no longer able to cut any DNA strand, but with the ability to strongly bind the target sequence. Consequently, the different modifications to Cas9 and Cas12 nucleases offer a valuable platform to generate plant disease resistance against pathogens. In this chapter, we highlight some of the different modifications used to re-engineer Cas nucleases for targeted genome and epigenome editing, and their importance to modulate chromatin activity and gene expression." @default.
- W3134747076 created "2021-03-15" @default.
- W3134747076 creator A5003298091 @default.
- W3134747076 creator A5030073581 @default.
- W3134747076 creator A5072068183 @default.
- W3134747076 date "2021-01-01" @default.
- W3134747076 modified "2023-09-27" @default.
- W3134747076 title "CRISPR-Cas epigenome editing: improving crop resistance to pathogens" @default.
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