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Applied Category Filter (Click To Remove): Neuromuscular Disease


Induction of Dystrophin DelCH2 Isoform
TS-000308 — Absence of the dystrophin protein leads to the severe muscle disorder Duchenne Muscular Dystrophy (DMD). Nearly asymptomatic patients have been identified to produce a functional N-terminal truncated dystrophin protein. Gene therapy experts at Nationwide Children's Hospital are developing a U7-snRNA exon skipping strategy to facilitate expression of a truncated dystrophin protein for patients carrying mutations within exon 6 to 9 of the DMD gene, rendering their dystrophin nonfunctional. Our experts have effectively skipped exon 8 in patient-derived cell lines and in turn produced a functional truncated dystrophin protein product.
  • College:
  • Inventors: Wein, Nicolas; Flanigan, Kevin
  • Licensing Officer: Eidahl, Jocelyn

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