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2. Pharmacological characterization of seven human histamine H3 receptor isoforms
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3. The long duration of action of the second generation antihistamine bilastine coincides with its long residence time at the histamine H1 receptor
4. Selective histamine H3 and H4 receptor agonists exert opposite effects against the gastric lesions induced by HCl in the rat stomach
5. Agonist-dependent effects of mutations in the sphingosine-1-phosphate type 1 receptor
6. The collagen-breakdown product N-acetyl-Proline-Glycine-Proline ( N-α -PGP) does not interact directly with human CXCR1 and CXCR2
7. Cloning and pharmacological characterization of the dog histamine H 4 receptor
8. The histamine H 3 receptor antagonist clobenpropit enhances GABA release to protect against NMDA-induced excitotoxicity through the cAMP/protein kinase A pathway in cultured cortical neurons
9. A “locked-on,” constitutively active mutant of the adenosine A 1 receptor
10. Cloning and pharmacological characterization of the dog histamine H4 receptor
11. The histamine H3 receptor antagonist clobenpropit enhances GABA release to protect against NMDA-induced excitotoxicity through the cAMP/protein kinase A pathway in cultured cortical neurons
12. Antiinflammatory and antinociceptive effects of the selective histamine H4-receptor antagonists JNJ7777120 and VUF6002 in a rat model of carrageenan-induced acute inflammation
13. A “locked-on,” constitutively active mutant of the adenosine A1 receptor
14. Allosteric modulation and constitutive activity of fusion proteins between the adenosine A 1 receptor and different 351Cys-mutated G i α-subunits
15. Mutational analysis of the histamine H 1-receptor binding pocket of histaprodifens
16. Allosteric modulation and constitutive activity of fusion proteins between the adenosine A1 receptor and different 351Cys-mutated Gi α-subunits
17. Mutational analysis of the histamine H1-receptor binding pocket of histaprodifens
18. Effects of clobenpropit on pentylenetetrazole-kindled seizures in rats
19. The long duration of action of the second generation antihistamine bilastine coincides with its long residence time at the histamine H
20. Recombinant Semliki Forest virus for over-expression and pharmacological characterisation of the histamine H 2 receptor in mammalian cells
21. Selective histamine H3 and H4 receptor agonists exert opposite effects against the gastric lesions induced by HCl in the rat stomach
22. Agonist-dependent effects of mutations in the sphingosine-1-phosphate type 1 receptor
23. The collagen-breakdown product N-acetyl-Proline-Glycine-Proline (N-alpha-PGP) does not interact directly with human CXCR1 and CXCR2
24. The histamine H3 receptor antagonist clobenpropit enhances GABA release to protect against NMDA-induced excitotoxicity through the cAMP/protein kinase A pathway in cultured cortical neurons
25. Allosteric modulation and constitutive activity of fusion proteins between the adenosine A1 receptor and different 351Cys-mutated Gi α-subunits
26. Mutational analysis of the histamine H1-receptor binding pocket of histaprodifens
27. Effects of clobenpropit on pentylenetetrazole-kindled seizures in rats
28. Recombinant Semliki Forest virus for over-expression and pharmacological characterisation of the histamine H2 receptor in mammalian cells
29. Selective histamine H₃ and H₄ receptor agonists exert opposite effects against the gastric lesions induced by HCl in the rat stomach
30. Homologous histamine H1 receptor desensitization results in reduction of H1 receptor agonist efficacy
31. Ebselen inhibits contractile responses of guinea-pig parenchymal lung strips
32. Clobenpropit (VUF-9153), a new histamine H3 receptor antagonist, inhibits electrically induced convulsions in mice
33. Antiinflammatory and antinociceptive effects of the selective histamine H 4-receptor antagonists JNJ7777120 and VUF6002 in a rat model of carrageenan-induced acute inflammation
34. Recombinant Semliki Forest virus for over-expression and pharmacological characterisation of the histamine H2 receptor in mammalian cells
35. Constitutive activity of the histamine H1 receptor reveals inverse agonism of histamine H1 receptor antagonists
36. Homologous and heterologous desensitisation of histamine H1-receptor mediated contractions of guinea-pig jejunum
37. Purification of [3H]mepyramine receptor from rat liver and its amino acid sequence homology with debrisoquine 4-hydroxylase cytochrome P-450
38. Relaxations of the guinea-pig intestinal smooth muscle by histetmine H2-receptor agonists are not related to H2-receptor stimulation
39. Clobenpropit (VUF-9153), a new histamine H3 receptor antagonist, inhibits electrically induced convulsions in mice
40. Homologous histamine H1 receptor desensitization results in reduction of H1 receptor agonist efficacy
41. Desensitisation off histamine H1-receptor mediated cyclic-GMP production in guinea-pig lung slices
42. Constitutive activity of the histamine H 1 receptor reveals inverse agonism of histamine H 1 receptor antagonists
43. Purification of [3H]mepyramine receptor from rat liver and its amino acid sequence homology with debrisoquine 4-hydroxylase cytochrome P-450
44. Ebselen inhibits contractile responses of guinea-pig parenchymal lung strips
45. Clobenpropit (VUF-9153), a new histamine H 3 receptor antagonist, inhibits electrically induced convulsions in mice
46. Homologous histamine H 1 receptor desensitization results in reduction of H 1 receptor agonist efficacy
47. Selective histamine H3 and H4 receptor agonists exert opposite effects against the gastric lesions induced by HCl in the rat stomach
48. Cloning and pharmacological characterization of the dog histamine H4 receptor
49. Antiinflammatory and antinociceptive effects of the selective histamine H4-receptor antagonists JNJ7777120 and VUF6002 in a rat model of carrageenan-induced acute inflammation
50. The histamine H3 receptor antagonist clobenpropit enhances GABA release to protect against NMDA-induced excitotoxicity through the cAMP/protein kinase A pathway in cultured cortical neurons
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