In the Press
Media Appearances
- UCLA Duchenne muscular dystrophy research receives grant from California’s stem cell agency
- Duchenne MD Gene Therapy Project Awarded More Than $2M from Stem Cell Agency
- With a deft snip, potential treatment emerges for deadly childhood Duchenne Muscular Dystrophy
- Stem cell gene therapy could be key to treating Duchenne muscular dystrophy
- Duchenne MD Therapy by Gene Editing of Stem Cells May Be Possible in Next Decade
- Family ties help drive UCLA’s search for a stem cell treatment for Duchenne muscular dystrophy
- CRISPR Getting Closer to Correcting Gene Defect in Duchenne Muscular Dystrophy
- Scientists reveal how osteopontin ablation ameliorates muscular dystrophy
- Removing immunomodulatory protein improves symptoms of muscular dystrophy in mice
- Two Scientists Vow to Find a Cure for Their Son's Rare and Fatal Disease: 'I'm Proud of the Work My Parents Are Doing,' Says Teen
- Neurologist receives $2.8 million grant to develop gene therapy for muscular dystrophy
- New Gene Therapy Project for Adolescent-Onset Muscular Dystrophy
- C3 Awards Research Grant to Drs. Melissa Spencer and Jeffrey Chamberlain to Develop Gene Therapy Vectors for LGMD2A/R1
