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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