Recognized in the Biotechnology category of the 2025 Top Innovations contest, small Cas12l nucleases are versatile, ...
The goal of gene therapy is to permanently cure hereditary diseases. One of the most promising technologies for this is the ...
urning genes on and off is like flipping a light switch, controlling whether genes in a cell are active. When a gene is turned on, the production of proteins or other substances is promoted; when it's ...
In a first for adults in Singapore, scientists are conducting gene editing trials on heart patients to correct defects at ...
In previous studies, researchers have investigated the use of CRISPR-Cas9 gene editing technology to create gene drives in mosquitos. Gene drives are genetic elements introduced into the genome that ...
A new study has revealed that the gene HMGN1 is a key driver of congenital heart defects (CHDs) in Down syndrome. Using ...
Pairwise has licensed its Fulcrum® gene editing platform to the International Rice Research Institute (IRRI), a non-profit agricultural research organization. The agreement will enable IRRI to apply ...
An infant with a rare metabolic disease became the world’s first patient to be treated with a personalized CRISPR gene-editing treatment in a landmark study between Penn Medicine and the Children’s ...
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