• Mashup Score: 6

    Kita et al. utilize the dual CRISPR-Cas3 system to induce a large deletion (∼340 kb) at the dystrophin exon 45–55 region for multi-exon skipping (MES) in various Duchenne muscular dystrophy (DMD) mutation patterns. Dual-Cas3-based MES restored dystrophin protein in DMD-iPSCs without significant off-target deletion. Dual CRISPR-Cas3 is a promising tool for MES induction to restore dystrophin protein in DMD.

    Tweet Tweets with this article
    • Dual #CRISPR-Cas3 restores dystrophin function in #stemcells derived from patients with Duchenne muscular dystrophy. Read more in @stemcellreports https://t.co/NkL5DsSduL @CiRA_KU_J Akitsu Hotta https://t.co/IKPi0S3KrF

  • Mashup Score: 8

    Kita et al. utilize the dual CRISPR-Cas3 system to induce a large deletion (∼340 kb) at the dystrophin exon 45–55 region for multi-exon skipping (MES) in various Duchenne muscular dystrophy (DMD) mutation patterns. Dual-Cas3-based MES restored dystrophin protein in DMD-iPSCs without significant off-target deletion. Dual CRISPR-Cas3 is a promising tool for MES induction to restore dystrophin protein in DMD.

    Tweet Tweets with this article
    • Dual #CRISPR-Cas3 restores dystrophin function in #stemcells derived from patients with Duchenne muscular dystrophy. Read more in @stemcellreports https://t.co/NkL5DsSduL @CiRA_KU_J Akitsu Hotta https://t.co/fmQeCP7jiZ