Discovery of a selective TC-PTP degrader for cancer immunotherapy
Discovery of a SHP2 degrader with in vivo anti-tumor activity
Small Molecule Degraders of Protein Tyrosine Phosphatase 1B and T-Cell Protein Tyrosine Phosphatase for Cancer Immunotherapy
PRL2 phosphatase enhances oncogenic FLT3 signaling via dephosphorylation of the E3 ubiquitinligase CBL at tyrosine371
Structure-Based Design of Active-Site-Directed, Highly Potent, Selective, and Orally Bioavailable Low-Molecular-Weight Protein Tyrosine Phosphatase Inhibitors
An Integrated Proteomic Strategy to Identify SHP2 Substrates
Cryo-electron microscopy structures of VCP/p97reveal a new mechanism of oligomerizationregulation
Functional interrogation and therapeutic targeting of protein tyrosine phosphatases
Systemic inhibition of PTPN22 augments anticancer immunity
SHP2 is a multifunctional therapeutic target in drug resistant metastatic breast cancer
Highly Potent and Selective N-Aryl Oxamic Acid-Based Inhibitors for Mycobacterium tuberculosis Protein Tyrosine Phosphatase B
Mechanism of PRL2 phosphatase-mediated PTEN degradation and tumorigenesis
Mechanistic insights explain the transforming potential of the T507K substitution in the protein-tyrosine phosphatase SHP2
Total Synthesis, Biological Evaluation, and Target Identification of Rare Abies Sesquiterpenoids
Regulatory Mechanisms and Novel Therapeutic Targeting Strategies for Protein Tyrosine Phosphatases