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3. Secondary structure of the channel forming transmembrane segments from the nicotinic acetylcholine receptor

4. Trisubstituted ureas as potent and selective mPGES-1 inhibitors

6. Discovery of disubstituted phenanthrene imidazoles as potent, selective and orally active mPGES-1 inhibitors

9. MF63 [2-(6-Chloro-1H-phenanthro[9,10-d]imidazol-2-yl)-isophthalonitrile], a Selective Microsomal Prostaglandin E Synthase-1 Inhibitor, Relieves Pyresis and Pain in Preclinical Models of Inflammation

12. Inhibitors of the inducible microsomal prostaglandin E2 synthase (mPGES-1) derived from MK-886

14. Differential Efficacy of Caspase Inhibitors on Apoptosis Markers during Sepsis in Rats and Implication for Fractional Inhibition Requirements for Therapeutics

17. Characterization of Transgenic Mice with Targeted Disruption of the Catalytic Domain of the Double-stranded RNA-dependent Protein Kinase, PKR

26. An absolute requirement for Cubitus interruptus in Hedgehog signaling

27. Suppressor of Fused opposes Hedgehog signal transduction by impeding nuclear accumulation of the activator form of Cubitus interruptus

28. Inhibitors of the inducible microsomal prostaglandin E2 synthase (mPGES-1) derived from MK-886

29. Deletion of Microsomal Prostaglandin E2 (PGE2) Synthase-1 Reduces Inducible and Basal PGE2 Production and Alters the Gastric Prostanoid Profile.

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