SPLICER Gene Editing Tool Holds A Lot of Potential to Treat Duchenne Muscular Dystrophy
A new gene editing tool that helps cellular machinery skip parts of genes responsible for diseases has been applied to reduce the formation of...
Researchers Discover 18-Digit Code (Wnt7a) that Allows Proteins to Hitch a Ride Around the Body
Researchers from the University of Ottawa and The Ottawa Hospital have found an 18-digit code (Wnt7a) that proteins can use to bind to exosomes,...
Capricor Therapeutics Submits Application for Treatment of DMD Cardiomyopathy
Capricor Therapeutics, a biotechnology company developing transformative cell and exosome-based therapeutics for the treatment of rare diseases, announced today that it has initiated its...
Satellos Produced Near-Normal Levels of Dystrophin in Experiment with Dogs with DMD with SAT-3247
According to the announcement made by Satellos Bioscience Inc., in an experiment conducted on dogs with DMD, it was seen that dystrophin was produced...
CRISPR-Cas13 Could Accelerate Studies on RNA-Targeted Therapies
In recent years, the scientific community has made significant strides in the field of gene editing, particularly through the development of the CRISPR (Clustered...