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Publications by Jürgen M. Lehmann
An Antidiabetic Thiazolidinedione Is a High Affinity Ligand for Peroxisome Proliferator-Activated Receptor Γ (PPARγ)
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Peroxisome Proliferator-Activated Receptors Α and Γ Are Activated by Indomethacin and Other Non-Steroidal Anti-Inflammatory Drugs
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Related publications
Peroxisome Proliferator-Activated Receptor-Γ (PPARG; PPARγ)
Science-Business eXchange
A Functional Peroxisome Proliferator-Activated Receptor-Γ Ligand-Binding Domain Is Not Required for Adipogenesis
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Peroxisome Proliferator-Activated Receptor Γ-Mediated Differentiation
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Nitrolinoleic Acid: An Endogenous Peroxisome Proliferator-Activated Receptor Ligand
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Peroxisome Proliferator-Activated Receptor Γ (PPARγ)-Independent Specific Cytotoxicity Against Immature Adipocytes Induced by PPARγ Antagonist T0070907
Biological and Pharmaceutical Bulletin
Medicine
Pharmacology
Pharmaceutical Science
Does Peroxisome Proliferator-Activated Receptor-Γ (PPARγ) Protect From Hypertension Directly Through Effects in the Vasculature?
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Peroxisome Proliferator-Activated Receptor-Γ-Independent Inhibition of Macrophage Activation by the Non-Thiazolidinedione Agonist L-796,449
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
The Antidiabetic Agent LG100754 Sensitizes Cells to Low Concentrations of Peroxisome Proliferator-Activated Receptor Γ Ligands
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Peroxisome Proliferator-Activated Receptor