Search alternatives:
degrader therapeutics » derived therapeutics (Expand Search), dental therapeutics (Expand Search)
decrease therapeutic » increased therapeutic (Expand Search), great therapeutic (Expand Search), directed therapeutic (Expand Search)
host resistance » plant resistance (Expand Search)
decrease host » decreases short (Expand Search)
degrader therapeutics » derived therapeutics (Expand Search), dental therapeutics (Expand Search)
decrease therapeutic » increased therapeutic (Expand Search), great therapeutic (Expand Search), directed therapeutic (Expand Search)
host resistance » plant resistance (Expand Search)
decrease host » decreases short (Expand Search)
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Discovery of Oral Degraders of the ROS1 Fusion Protein with Potent Activity against Secondary Resistance Mutations
Published 2024“…More importantly, the degradation-based therapeutic modality can overcome on-target mutation resistance to tyrosine kinase inhibitors by efficient degradation of the mutated kinase to achieve greater potency than inhibition.…”
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Expression of hCAP-18/LL-37 mRNA in 1α,25(OH)<sub>2</sub>D<sub>3</sub>-pretreated A549 cells.
Published 2023Subjects: -
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Development of Oral, Potent, and Selective CK1α Degraders for AML Therapy
Published 2024“…These findings indicate that phenotypic drug discovery campaigns, in combination with chemically distinct CRBN ligand libraries, can accelerate the development of therapeutically relevant MGDs. Furthermore, the development of dCK1α-1 and dCK1α-2 provides new therapeutic options for cancers with functional p53 signaling and offers valuable chemical tools for future investigations into the role of CK1α.…”
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Development of Oral, Potent, and Selective CK1α Degraders for AML Therapy
Published 2024“…These findings indicate that phenotypic drug discovery campaigns, in combination with chemically distinct CRBN ligand libraries, can accelerate the development of therapeutically relevant MGDs. Furthermore, the development of dCK1α-1 and dCK1α-2 provides new therapeutic options for cancers with functional p53 signaling and offers valuable chemical tools for future investigations into the role of CK1α.…”
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Development of Oral, Potent, and Selective CK1α Degraders for AML Therapy
Published 2024“…These findings indicate that phenotypic drug discovery campaigns, in combination with chemically distinct CRBN ligand libraries, can accelerate the development of therapeutically relevant MGDs. Furthermore, the development of dCK1α-1 and dCK1α-2 provides new therapeutic options for cancers with functional p53 signaling and offers valuable chemical tools for future investigations into the role of CK1α.…”
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DataSheet_1_NtrBC Selectively Regulates Host-Pathogen Interactions, Virulence, and Ciprofloxacin Susceptibility of Pseudomonas aeruginosa.docx
Published 2021“…Here, we demonstrated that NtrBC, the master of nitrogen control, had a selective role in host colonization and a substantial role in determining intrinsic resistance to ciprofloxacin. …”