A new study has developed a breakthrough biomedical tool that can deliver genetic material to edit faulty genes in fetal brain cells.

A new biomedical tool successfully delivers genetic material to edit faulty genes in developing fetal mouse brain cells. This might stop disease progression of genetic-based neurodevelopmental ...

A new study shows that a biomedical tool can successfully deliver genetic material to edit faulty genes in developing fetal ...

Researchers have developed a novel delivery system for sending CRISPR reagents to brain cells, where it performs its gene ...

A recent breakthrough in genetic research has introduced a tool capable of delivering genetic material to developing fetal ...

For the past decade, scientists have relied almost exclusively on CRISPR-Cas systems for genome editing. Now, a smaller but ...

People with myotonic dystrophy type 1 (DM1), the most common adult-onset form of muscular dystrophy, progressively lose ...

Prenatal gene therapy via mRNA LNPs fixes faulty genes in fetal brain cells in animal model of neurodevelopmental syndrome.