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Publications by Yumi Ueda
Design, Synthesis, and Characterization of a Potent, Nonpeptide, Cell-Permeable, Bivalent Smac Mimetic That Concurrently Targets Both the BIR2 and BIR3 Domains in XIAP
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Altered GABAergic Neurotransmission Is Associated With Increased Kainate-Induced Seizure in Prostaglandin-Endoperoxide Synthase-2 Deficient Mice
Brain Research Bulletin
Neuroscience
Related publications
Design, Synthesis, and Evaluation of a Potent, Cell-Permeable, Conformationally Constrained Second Mitochondria Derived Activator of Caspase (Smac) Mimetic
Design and Synthesis of a Simplified Inhibitor for XIAP-BIR3 Domain
Bioorganic and Medicinal Chemistry Letters
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
SM-164: A Novel, Bivalent Smac Mimetic That Induces Apoptosis and Tumor Regression by Concurrent Removal of the Blockade of cIAP-1/2 and XIAP
Cancer Research
Cancer Research
Oncology
Structural Insight Into Inhibitor of Apoptosis Proteins Recognition by a Potent Divalent Smac-Mimetic
PLoS ONE
Multidisciplinary
Corrigendum: Chimeric Design, Synthesis, and Biological Assays of a New Nonpeptide Insulin-Mimetic Vanadium Compound to Inhibit Protein Tyrosine Phosphatase 1B
Drug Design, Development and Therapy
Drug Discovery
Pharmacology
Pharmaceutical Science
The BIR2/BIR3-interacting Phospholipase D Gamma 1 Negatively Regulates Immunity in Arabidopsis
Design, Synthesis, and Biological Characterization of a Peptide-Mimetic Antagonist for a Tethered-Ligand Receptor
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
XIAP Impairs Smac Release From the Mitochondria During Apoptosis
Cell Death and Disease
Molecular Neuroscience
Immunology
Cell Biology
Cancer Research
Cellular
Medicine
Structure-Based Design, Synthesis, Evaluation, and Crystallographic Studies of Conformationally Constrained Smac Mimetics as Inhibitors of the X-Linked Inhibitor of Apoptosis Protein (XIAP)†
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
