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2. JNJ-77242113, a highly potent, selective peptide targeting the IL-23 receptor, provides robust IL-23 pathway inhibition upon oral dosing in rats and humans

3. Gene expression and metabolism in malignant hyperthermia susceptible and normal skeletal muscle

6. Efecto 2020 en la siniestralidad laboral de la República del Ecuador: un año atípico por COVID-19

8. Identification of highly selective SIK1/2 inhibitors that modulate innate immune activation and suppress intestinal inflammation

10. S1028 Characterization of a First-in-Class Oral Therapy Selectively Targeting the IL-23 Pathway

11. Adaptive Complex Contagions and Threshold Dynamical Systems

14. Identification of highly selective SIK1/2 inhibitors that modulate innate immune activation and suppress intestinal inflammation.

17. Discovery of JNJ-64264681: A Potent and Selective Covalent Inhibitor of Bruton’s Tyrosine Kinase

20. Mo1504: IN SILICO EVALUATION AND PRE-CLINICAL EFFICACY OF ANTI-TNF AND ANTI-IL-23 COMBINATION THERAPY IN INFLAMMATORY BOWEL DISEASE

22. Discovery of a Potent and Selective Covalent Inhibitor of Bruton’s Tyrosine Kinase with Oral Anti-Inflammatory Activity

32. Analysis of integrated inflammatory bowel disease mouse models to assess their disease driving pathways and relevance for Crohn’s disease and Ulcerative colitis

33. Incompressible Navier-Stokes Calculations in Pump Flows

34. Computation of incompressible viscous flows through turbopump components

35. Multigrid convergence of an implicit symmetric relaxation scheme

36. Incompressible Navier-Stokes computations of rotating flows

40. Stereotactic laser ablation as treatment for brain metastases that recur after stereotactic radiosurgery: a multiinstitutional experience

44. Preclinical Characterization of the FAAH Inhibitor JNJ-42165279

48. Aryl Piperazinyl Ureas as Inhibitors of Fatty Acid Amide Hydrolase (FAAH) in Rat, Dog, and Primate

49. Lessons learned from the institution of the Surgical Care Improvement Project at a teaching medical center

50. Biochemical and Biological Properties of 4-(3-phenyl-[1,2,4] thiadiazol-5-yl)-piperazine-1-carboxylic acid phenylamide, a Mechanism-Based Inhibitor of Fatty Acid Amide Hydrolase

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