Targeting genome-editing tools to the right part of the body could become much easier thanks to delivery vehicles made from a viral protein shell 1. Gene-editing methods such as CRISPR and ...
Northwestern scientists have developed a new nanostructure that supercharges CRISPR’s ability to safely and efficiently enter cells, potentially unlocking its full power to treat genetic diseases. By ...
CRISPR has the power to correct genetic mutations, but current delivery methods are either unsafe or inefficient, keeping the technology from reaching its full medical potential. With the power to ...
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