Accelerating development of genetic therapies for muscular dystrophies
The aim of MAGIC is to accelerate the development of gene therapies and genome editing strategies for muscular dystrophies by creating advanced humanized muscle models and innovative gene therapy approaches, ultimately improving the lives of individuals affected by these debilitating diseases.
Key Objectives
- Creating accurate humanized muscle models.
- Developing precise gene therapies and genome editing strategies.
- Engineering disease-specific muscle-on-chip devices.
- Assessing safety and efficacy of novel gene therapies.
- Exploring gene editing strategies for neuromuscular disorders.
- Facilitating translation and exploitation of project outputs.
- Ensuring patient perspectives remain central to the research.
See how MAGIC is working to reach these key objectives
Latest News
Meet Parent Project Italy: A Key Player in the MAGIC Project Consortium
We ask MAGIC partners why they are joining this project. This time, we are speaking with Ilaria Zito, molecular biologist and scientific coordinator of Parent Project aps Italy.
Join the MAGIC Team – recruitment opportunities
Join MAGIC vibrant team - Department of Biology, Maynooth University is recruiting for: Post-doctoral researcher- Immunology/Gene Therapy (24 month Temporary Contract). To know more about this...
Ilaria Zito Presents MAGIC at the 21st Interuniversity Institute of Myology Meeting
In September, Ilaria Zito from Parent Project Italy aps presented the MAGIC Project at the 21st Interuniversity Institute of Myology Meeting in Assisi, Italy.