A team of researchers at Columbia, Harvard and University of Minnesota has developed a gene editing technique they say could ...

The personalized CRISPR treatment could be the future of gene therapy, but hurdles remain before everyone has access.

Genetic defects are exceedingly common, which is not surprising considering just how many cells make up our bodies, including our reproductive cells. While most of these defects have no or only ...

Cytosine base editors use an uracil-containing intermediate to introduce C•G to T•A and C•G to G•C point mutations ... which uses CRISPR/Cas9 to target and remove certain ubiquitous ...