Mammals are vulnerable to a number of diseases that cause blindness through permanent retinal cell loss. Previous work has shown that expression of the proneural transcription factor Ascl1 in mouse […] Read More
As a Postdoctoral Fellow, McCloskey is part of a team developing gene therapeutics to treat Amyotrophic Lateral Sclerosis (ALS), a fatal neuromuscular disease. In order to combat challenges in drug […] Read More