Genetics

'CRISPR-Gold' fixes Duchenne muscular dystrophy mutation in mice

Scientists at the University of California, Berkeley, have engineered a new way to deliver CRISPR-Cas9 gene-editing technology inside cells and have demonstrated in mice that the technology can repair the mutation that causes ...

Medical research

Researchers replicate FSH muscular dystrophy in mice

A new study published in the journal Nature Communications describes a breakthrough in research related to facioscapulohumeral muscular dystrophy (FSHD). The debilitating genetic disease - which has no approved treatment ...

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