Research teams have created a versatile set of gene delivery systems that can reach different neural cell types in the human brain and spinal cord with exceptional accuracy. These delivery systems are ...

The development of efficient delivery technologies has lagged behind significant advancements in nucleic acid therapeutics, such as antisense oligonucleotids (ASOs), short interfering RNA (siRNA), ...

CRISPR has the power to correct genetic mutations, but current delivery methods are either unsafe or inefficient, keeping the technology from reaching its full medical potential. With the power to ...