base editing
| 3 min read
CRISPR-edited immune cells may help patients with T-cell leukemia, albeit with immunotherapy-related risks.
| 6 min read
Kan Cao studies the rare aging disorder progeria to find a cure, and she’s ready to solve the mysteries of healthy human aging along the way.
| 7 min read
Creative solutions may enable gene therapy for more common diseases.
| 6 min read
Recent advancements in mitochondrial genome editing technologies take scientists one step closer to developing viable treatments for mitochondrial diseases, which affect 1 in 4300 adults.
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