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Duchenne muscular ... researchers in Germany have managed to use the CRISPR gene-editing tool to correct the condition in pigs, bringing the treatment ever closer to human trials.
Scientists have demonstrated a new gene therapy in mice that can treat muscular dystrophy, which could be ready for human use in two years Depositphotos View 1 Image ...
New muscular dystrophy treatment approach developed using human stem cells Date: May 4, 2012 Source: University of Minnesota Academic Health Center Summary: Researchers have effectively treated ...
Human protein improves muscle function of muscular dystrophy mice. ScienceDaily . Retrieved June 3, 2025 from www.sciencedaily.com / releases / 2010 / 12 / 101227203432.htm ...
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