Highly effective treatments for HIV keep people healthy, but we do not yet have a safe and scalable way to completely rid the ...
StitchR makes it possible to deliver larger payloads with current vectors, expanding the list of diseases targetable by gene therapies.
StitchR, a new gene therapy technique, delivers large genes in two parts to treat muscular dystrophies by restoring critical proteins in animal models.
Gene therapy can effectively treat various diseases, but for some debilitating conditions like muscular dystrophies there is a big problem: size.
CRISPR-Cas9 is a powerful gene-editing tool that allows scientists to modify DNA in living organisms precisely. It works like ...
Gene therapy can effectively treat various diseases, but for some debilitating conditions like muscular dystrophies there is a big problem: size. The ...
Scientists at Vilnius University have developed a novel gene silencing method using a type IV-A CRISPR system that silences ...
Life Sciences Center (LSC) have discovered a unique way for cells to silence specific genes without cutting DNA. This ...
A research team led by Professor Lee Sang-hwa of the Synthetic Biology Project Group of the Catholic Central Medical Center's ...