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CRISPR/Cas9-mediated genome editing induces exon skipping by alternative splicing or exon deletion
CRISPR is widely used to disrupt gene function by inducing small insertions and deletions. Here, we show that some single-guide RNAs (sgRNAs) can induce exon skipping or large genomic deletions that delete exons. For example, CRISPR-mediated editing of β-catenin exon 3, which encodes an autoinhibito...
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| Publicat a: | Genome Biol |
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| Autors principals: | , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5470253/ https://ncbi.nlm.nih.gov/pubmed/28615073 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13059-017-1237-8 |
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