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2. Computational design of peptides to target NaV1.7 channel with high potency and selectivity for the treatment of pain

16. Computational design of peptides to target NaV1.7 channel with high potency and selectivity for the treatment of pain

17. Author response: Computational design of peptides to target NaV1.7 channel with high potency and selectivity for the treatment of pain

18. Computational design of peptides to target NaV1.7 channel with high potency and selectivity for the treatment of pain

23. Human cells and networks of pain: Transforming pain target identification and therapeutic development

27. The μ-opioid receptor differentiates two distinct human nociceptive populations relevant to clinical pain

29. Discovery and characterization of ORM‐11372, a novel inhibitor of the sodium‐calcium exchanger with positive inotropic activity

32. Activation of pruritogenic TGR5, MrgprA3, and MrgprC11 on colon-innervating afferents induces visceral hypersensitivity

33. Human-based approaches to pharmacology and cardiology: an interdisciplinary and intersectorial workshop

34. Quantitative Comparison of Effects of Dofetilide, Sotalol, Quinidine, and Verapamil between Human Ex vivo Trabeculae and In silico Ventricular Models Incorporating Inter-Individual Action Potential Variability

35. Chronic linaclotide treatment reduces colitis-induced neuroplasticity and reverses persistent bladder dysfunction

38. New mechanism underlying IL-31–induced atopic dermatitis

45. Human-based approaches to pharmacology and cardiology: an interdisciplinary and intersectorial workshop

47. Label-free imaging of atherosclerotic plaques using third-harmonic generation microscopy

48. The Cancer Chemotherapeutic Paclitaxel Increases Human and Rodent Sensory Neuron Responses to TRPV1 by Activation of TLR4.

49. Activation of pruritogenic TGR5, MrgprA3, and MrgprC11 on colon-innervating afferents induces visceral hypersensitivity

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