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New paper published in 'Cells' (17/08/2026)

In this study, we have identified a previously uncharacterised regulatory element within the LMTK3 C-terminus that can modulate its kinase domain interactions and LMTK3-driven oncogenic functions. Ultimately, by understanding and potentially blocking this switch, the study opens up a new avenue for developing therapies that could stop breast cancer from progressing.



 
 
 

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