Carlo Corona

This study combines APOE4 and TREM2R47H in female tauopathy mice to identify pathways activated by AD risk factors, finding cGAS-STING signaling and microglial senescence as potential drivers.

This study investigates RS1 deficiency in mice, identifying aberrant neuro-glial activity and signaling disruptions that may inform therapeutic strategies for XLRS.

The paper uses AAV-BR1 to target endothelial cells in the mouse retina, identify their morphology, and deliver Cx43 for studying microvascular function.

The paper uses mouse retinal models to characterize pericyte diversity and demonstrate targeted control of capillary blood flow through optogenetic manipulation.