Tushare Jinadasa

This paper develops a high-throughput platform to discover arginine-depleted cell-penetrating peptides for improved antisense delivery in Duchenne muscular dystrophy, showing reduced toxicity and enhanced efficacy.

The paper identifies distinct VIP interneuron subpopulations in the ACC that selectively encode anxiogenic, anxiolytic, social, or non-social stimuli in mice.

This study shows that increased C4 expression in mice causes prefrontal cortex hypoconnectivity and reduced social interaction, linking C4 to schizophrenia pathogenesis.