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Delta-like ligand 3 (DLL3) is a transmembrane protein and a member of the Notch ligand family. Unlike other Notch ligands, DLL3 primarily acts as an inhibitor of Notch signaling within the same cell. It is highly expressed during fetal development and is often overexpressed in high-grade neuroendocrine tumors, making it a therapeutic target. Loss-of-function mutations cause spondylocostal dysostosis.
Antibody-drug conjugate targeting DLL3, Bispecific T-cell engager targeting DLL3
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