By Ellen Capon (Drug Target Review)2024-06-18T10:00:30
As the industry looks beyond CRISPR to safely introduce therapeutic genomic changes anywhere in the body, in vivo gene editing holds immense potential to address diseases with a genetic basis. Boston-based biotech Tessera Therapeutics is pioneering the next generation of genetic medicines with its Gene Writing™ platform. At this year’s ...
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Sponsored by Sartorius
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Sponsored by Revvity
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Sponsored by Cellistic
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Sponsored by Bio-Techne
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Sponsored by Bio-Techne
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