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J M Arrang

Showing results (61-70 of 96) with videos related to

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British Journal of Pharmacology|January 30, 2002
Histamine H3-receptor-mediated [35S]GTP gamma[S] binding: evidence for constitutive activity of the recombinant and native rat and human H3 receptorsA Rouleau, X Ligneau, J Tardivel-Lacombe, et al.
Agents and Actions. Supplements|January 1, 1991
The histamine H3-receptor: pharmacology, roles and clinical implications studied with agonistsJ M Arrang, M Garbarg, J C Schwartz, et al.
Bioorganic & Medicinal Chemistry Letters|October 31, 2000
Analogues and derivatives of ciproxifan, a novel prototype for generating potent histamine H3-receptor antagonistsH Stark, X Ligneau, B Sadek, et al.
Bioorganic & Medicinal Chemistry Letters|April 11, 2001
Different antagonist binding properties of human and rat histamine H3 receptorsH Stark, W Sippl, X Ligneau, et al.
Progress in Medicinal Chemistry|January 5, 2002
The histamine H3 receptor and its ligandsH Stark, J M Arrang, X Ligneau, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 1993
Molecular cloning, characterization, and localization of a high-affinity serotonin receptor (5-HT7) activating cAMP formationM Ruat, E Traiffort, R Leurs, et al.
Journal of Medicinal Chemistry|March 1, 1996
Novel carbamates as potent histamine H3 receptor antagonists with high in vitro and oral in vivo activityH Stark, K Purand, X Ligneau, et al.
Brain Research|July 23, 1990
Involvement of histaminergic neurons in arousal mechanisms demonstrated with H3-receptor ligands in the catJ S Lin, K Sakai, G Vanni-Mercier, et al.
Archiv Der Pharmazie|August 1, 1996
Novel histamine H3-receptor antagonists with benzyl ether structure or related moieties: synthesis and structure-activity relationshipsA Hüls, K Purand, H Stark, et al.
Archiv Der Pharmazie|August 26, 1998
Development of FUB 181, a selective histamine H3-receptor antagonist of high oral in vivo potency with 4-(omega-(arylalkyloxy)alkyl)-1H-imidazole structureH Stark, A Hüls, X Ligneau, et al.
Pageof 10

Showing results (61-70 of 96) with videos related to

Sort By:
Pageof 10
British Journal of Pharmacology|January 30, 2002
Histamine H3-receptor-mediated [35S]GTP gamma[S] binding: evidence for constitutive activity of the recombinant and native rat and human H3 receptorsA Rouleau, X Ligneau, J Tardivel-Lacombe, et al.
Agents and Actions. Supplements|January 1, 1991
The histamine H3-receptor: pharmacology, roles and clinical implications studied with agonistsJ M Arrang, M Garbarg, J C Schwartz, et al.
Bioorganic & Medicinal Chemistry Letters|October 31, 2000
Analogues and derivatives of ciproxifan, a novel prototype for generating potent histamine H3-receptor antagonistsH Stark, X Ligneau, B Sadek, et al.
Bioorganic & Medicinal Chemistry Letters|April 11, 2001
Different antagonist binding properties of human and rat histamine H3 receptorsH Stark, W Sippl, X Ligneau, et al.
Progress in Medicinal Chemistry|January 5, 2002
The histamine H3 receptor and its ligandsH Stark, J M Arrang, X Ligneau, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 1993
Molecular cloning, characterization, and localization of a high-affinity serotonin receptor (5-HT7) activating cAMP formationM Ruat, E Traiffort, R Leurs, et al.
Journal of Medicinal Chemistry|March 1, 1996
Novel carbamates as potent histamine H3 receptor antagonists with high in vitro and oral in vivo activityH Stark, K Purand, X Ligneau, et al.
Brain Research|July 23, 1990
Involvement of histaminergic neurons in arousal mechanisms demonstrated with H3-receptor ligands in the catJ S Lin, K Sakai, G Vanni-Mercier, et al.
Archiv Der Pharmazie|August 1, 1996
Novel histamine H3-receptor antagonists with benzyl ether structure or related moieties: synthesis and structure-activity relationshipsA Hüls, K Purand, H Stark, et al.
Archiv Der Pharmazie|August 26, 1998
Development of FUB 181, a selective histamine H3-receptor antagonist of high oral in vivo potency with 4-(omega-(arylalkyloxy)alkyl)-1H-imidazole structureH Stark, A Hüls, X Ligneau, et al.
Pageof 10