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2. The leukemia inhibitory factor regulates fibroblast growth factor receptor 4 transcription in gastric cancer

7. Bile acids serve as endogenous antagonists of the Leukemia inhibitory factor (LIF) receptor in oncogenesis

8. Activation of GPBAR1 attenuates vascular inflammation and atherosclerosis in a mouse model of NAFLD-related cardiovascular disease

10. Design, Synthesis, and Pharmacological Evaluation of Dual FXR-LIFR Modulators for the Treatment of Liver Fibrosis.

11. Bile Acids-Based Therapies for Primary Sclerosing Cholangitis: Current Landscape and Future Developments.

12. Current Landscape and Evolving Therapies for Primary Biliary Cholangitis.

14. The Pharmacology of Bile Acids and Their Receptors

15. Chenodeoxycholic Acid: An Update on Its Therapeutic Applications

16. Obeticholic Acid: An Update of Its Pharmacological Activities in Liver Disorders

17. A microbial derived bile acid acts as GPBAR1 agonist and RORγt inverse agonist and reverses inflammation in inflammatory bowel disease

22. BAR502/fibrate conjugates: synthesis, biological evaluation and metabolic profile.

24. Defective Bile Acid Signaling Promotes Vascular Dysfunction, Supporting a Role for G‐Protein Bile Acid Receptor 1/Farnesoid X Receptor Agonism and Statins in the Treatment of Nonalcoholic Fatty Liver Disease

27. Correction to “Discovery of a Novel Class of Dual GPBAR1 Agonists–RORγt Inverse Agonists for the Treatment of IL-17-Mediated Disorders”

28. The leukemia inhibitory factor regulates fibroblast growth factor receptor 4 transcription in gastric cancer

29. Bile Acids Serve As Endogenous Antagonists Of The Leukemia Inhibitory Factor (LIF) Receptor in Oncogenesis

43. Discovery of BAR502, as potent steroidal antagonist of leukemia inhibitory factor receptor for the treatment of pancreatic adenocarcinoma

47. Discovery of a Novel Class of Dual GPBAR1 Agonists–RORγt Inverse Agonists for the Treatment of IL-17-Mediated Disorders

48. The crosstalk between gut barrier impairment, mitochondrial dysfunction, and microbiota alterations in people living with HIV

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