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- W2945393772 abstract "In this issue of Blood , Xu et al describe a novel CRISPR/Cas approach for correcting β-thalassemias that result from aberrant donor or acceptor splice sites. 1 The authors designed guide RNA/Cas complexes that can be introduced efficiently into hematopoietic stem and progenitor cells (HSPCs) ex vivo without viral vectors and can create double-stranded DNA cuts at specific genomic sites. The cells rapidly repair these double-stranded breaks by nonhomologous end-joining, which typically results in small deletions around the cut site. If these deletions encompass the aberrant splice sites and avoid additional sequences necessary for efficient splicing (see figure), normal splicing can be restored." @default.
- W2945393772 created "2019-05-29" @default.
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- W2945393772 date "2019-05-23" @default.
- W2945393772 modified "2023-09-29" @default.
- W2945393772 title "A novel therapeutic strategy for β-thalassemia" @default.
- W2945393772 cites W2908873329 @default.
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- W2945393772 doi "https://doi.org/10.1182/blood-2019-02-900464" @default.
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