Wee1
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- Chemogenetic Profiling Identifies RAD17 As Synthetically Lethal with Checkpoint Kinase Inhibition
- Exploring the Regulation and Function of Human Lats1 and Aurora a Kinases in Mitosis Thesis Advisor: Prof Nigg E.A., Dr
- The Roles of Cyclin-Dependent Kinases in Cell-Cycle Progression and Therapeutic Strategies in Human Breast Cancer
- Identification of Aurora Kinase B and Wee1-Like Protein Kinase As
- Targeted Therapies for Pancreatic Cancer: Overview of Current Treatments and New Opportunities for Personalized Oncology
- A Regimen Combining the Wee1 Inhibitor AZD1775 with HDAC Inhibitors Targets Human Acute Myeloid Leukemia Cells Harboring Various Genetic Mutations
- WEE1 Kinase Inhibition Enhances the Radiation Response of Diffuse Intrinsic Pontine Gliomas
- Inhibition of AAK1 Kinase As a Novel Therapeutic Approach to Treat Neuropathic Pain S
- Identification of Wee1 As a Novel Therapeutic Target for Mutant RAS
- Mob Family Proteins: Regulatory Partners in Hippo and Hippo-Like Intracellular Signaling Pathways
- Essential Role of the Histone Lysine Demethylase KDM4A in the Biology of Malignant Pleural Mesothelioma (MPM)
- Association of CHEK2 Polymorphisms with the Efficacy of Platinum-Based Chemotherapy for Advanced Non-Small-Cell Lung Cancer in Chinese Never-Smoking Women
- Chemogenetic Profiling Identifies RAD17 As Synthetically Lethal with Checkpoint Kinase Inhibition
- The Role of Hippo Pathway in Mitosis and Cancer
- Crosstalk Between the Mtor and DNA Damage Response Pathways in Fission Yeast
- 1. Introduction 6. Summary 4. Wee1 Selectivity Enhances
- Strong Antitumor Synergy Between DNA Crosslinking and HSP90 Inhibition Causes Massive Premitotic DNA Fragmentation in Ovarian Cancer Cells
- Wee1 Inhibitor MK1775 Sensitizes KRAS Mutated NSCLC Cells To