Björn von Eyß

This study shows that transient YAP/TAZ inhibition can suppress tumor growth in advanced cancers and enhances immunotherapy when combined with immune checkpoint blockade.

This study shows Hippo-YAP1/TAZ-TEAD signaling coordinates myoblast fusion and sarcomere assembly in skeletal muscle development through transcriptional regulation.

This study shows TRPS1 maintains luminal progenitors in the mammary gland by repressing SRF/MRTF activity, linking it to mechanotransduction and breast cancer initiation.

The paper identifies YIPF5 and GOT1A/B as components of ER export and shows ATF6 has a transcription-independent role in ER export inhibition by FLI-06.

This study identifies c-JUN as a noncanonical repressor of YAP/TAZ that suppresses their oncogenic activity in liver cancer.