Showing 141 - 160 results of 2,307 for search '(( decrease host resistance ) OR ( ((decrease therapeutic) OR (degrader therapeutics)) options ))', query time: 0.81s Refine Results
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    Fig 4 - by Sinthia Kabir Mumu (17705902)

    Published 2023
    Subjects:
  3. 143

    Discovery of Oral Degraders of the ROS1 Fusion Protein with Potent Activity against Secondary Resistance Mutations by Xianyou Peng (2130313)

    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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    Development of Oral, Potent, and Selective CK1α Degraders for AML Therapy by Lu Huang (211625)

    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.…”
  14. 154

    Development of Oral, Potent, and Selective CK1α Degraders for AML Therapy by Lu Huang (211625)

    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.…”
  15. 155

    Development of Oral, Potent, and Selective CK1α Degraders for AML Therapy by Lu Huang (211625)

    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 by Morgan A. Alford (8799320)

    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. …”