CRISPR-Cas9 technology precisely targets miR-21a, significantly extending the survival time of glioma mice
It reveals the function of SVTg as a new brainstem reward center, which processes emotional value by integrating inputs from cortical and subcortical regions.
In the long exploration of epilepsy treatment, adeno-associated virus (AAV) vectors have served as a precise “genetic scalpel,” offering new hope to countless patients.
CRISPR-Cas9 has been widely applied in gene editing, facilitating gene knockouts, knock-ins, and transcriptional activation.