RNA editing with CRISPR-Cas13
Precise transcriptome engineering
Abstract
Comprehensive characterization of Cas13 family members in mammalian cells
Specificity of Cas13 mammalian interference activity
Cas13-ADAR fusions enable targeted RNA editing
Defining the sequence parameters for RNA editing
Correction of disease-relevant human mutations using REPAIRv1
Transcriptome-wide specificity of REPAIRv1
Improving specificity of REPAIR through rational protein engineering
Discussion
Acknowledgments
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24 November 2017
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- David B. T. Cox et al.
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