CRISPR-Cas9 has revolutionized gene editing due to its precision, efficiency, and versatility. It has been used in a wide range of applications, from basic research to potential clinical therapies.
‘Cutting edge’ is, for once, a truly apt description when it comes to gene editing – both because the field is pushing medicine into areas we might never have dreamed possible, and because ...
Researchers have developed a gene-editing treatment for prion disease that extends lifespan by about 50 percent in a mouse model of the fatal neurodegenerative condition. The treatment ...
Researchers have developed a highly efficient gene editing therapy that could potentially treat Stargardt disease, the most common form of inherited macular degeneration. This groundbreaking study ...
Researchers at the Broad Institute of MIT and Harvard have developed a gene-editing treatment for prion disease that extends lifespan by about 50 percent in a mouse model of the fatal ...
Gene editing using base editing has been shown to extend the lifespan of mice with prion disease by approximately 50%. This approach involves a single-letter DNA change that reduces prion protein ...