ADAM17-deficient natural killer cells derived from induced pluripotent stem cells demonstrate increased cytotoxicity against tumor targets.
Converting non-hepatocytes to functional induced hepatocytes via transcription factor modulation overcomes primary cell scarcity for drug development.
Engineered pluripotent stem cells express tissue-specific cytotoxic genes to prevent unwanted differentiation into predetermined cell types.
A WAYNE293 cell line engineered for high-density suspension growth in serum-free media.
A co-culture lymphoid tissue equivalent combines T cells, B cells, and antigen-primed dendritic cells to model human immune responses in vitro.
A non-static bioreactor enables scalable T cell expansion using varying rocking rates.
ETV2 transcription factor reprograms endothelial cells to self-assemble into stable vessels, eliminating scaffold complexity and perfusion requirements.
Adding specific inhibitors to the medium prevents differentiation pathways, enabling stable self-renewal of rat embryonic stem cells.