No doubt 2025 will usher in many more advances in CRISPR therapies, thanks to the FDA’s new Platform Technology Designation ...
Potent in vivo gene editing in skeletal muscle of non-human primates by a novel, ultracompact CRISPR system delivered via a single AAV vector.
Gene therapies to treat rheumatoid arthritis have evolved slowly, but one is ready to move into human trials and an ...
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AZoLifeSciences on MSNCRISPR-Cas9 Off-Target Effects: Challenges and SolutionsThe CRISPR-Cas9 system offers groundbreaking genome editing capabilities, yet off-target cleavage raises concerns about ...
Akribion Therapeutics emerges from stealth with €8 million in seed funding to develop a novel cancer RNA-guided approach ...
CRISPR is an example of gene editing ... virus kills a cancer cell by replicating inside cancer cells and breaking them open. The cancer-related antigens are then exposed to the body’s immune ...
Padilla et al, Branched endosomal disruptor (BEND) lipids mediate delivery of mRNA and CRISPR-Cas9 ribonucleoprotein complex for hepatic gene editing and T cell engineering, Nature Communications ...
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