UT Southwestern scientists successfully employed a new type of gene therapy to treat mice with Duchenne muscular dystrophy (DMD), uniquely
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UI team is developing new delivery tools for gene editing
News of advances in gene-editing technology raises the prospect of actually using this approach to treat disease in patients. But
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Are humans immune to the CRISPR-Cas9 gene editing scissors?
The CRISPR-Cas9 gene editing system has been generating excitement within the field of gene therapy, inspiring hopes of molecular tools
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Gene ‘Editing’ in Dog Study Shows Promise for Kids With Muscular Dystrophy
THURSDAY, Aug. 30, 2018 — For the first time, scientists report using gene-editing technology to halt the progression of muscular
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Gene editing shown to lower cholesterol in monkeys
Hypercholesterolemia, which is a cardiovascular condition, puts people at an extremely high risk of coronary artery disease due to the
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