Randall J. Armstrong

This study investigates how lipid tail length in peptide amphiphile nanostructures affects their interactions with biological systems, showing that molecular design can control biointeractions and tumor accumulation.

This study functionally characterizes mutant ASXL1 in human hematopoietic stem cells, showing it drives transcriptional activation and repression through interactions with BRD4 and MECOM, with implications for therapy.

This study isolates extracellular vesicles from human milk and neonatal digestive fluid and shows they are taken up by intestinal epithelial cells.