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European Journal of Biochemistry|December 16, 1998
Corticotropin-releasing factor receptor type 1 from Tupaia belangeri--cloning, functional expression and tissue distributionM R Palchaudhuri, S Wille, G Mevenkamp, et al.Behavioural Brain Research|November 16, 2010
Contribution of melanin-concentrating hormone (MCH1) receptor to thermoregulation and sleep stabilization: evidence from MCH1 (-/-) miceA Ahnaou, F M Dautzenberg, H Huysmans, et al.Biochemical and Biophysical Research Communications|February 19, 2000
Rapid agonist-induced phosphorylation of the human CRF receptor, type 1: a potential mechanism for homologous desensitizationR L Hauger, R D Smith, S Braun, et al.Bioorganic & Medicinal Chemistry Letters|September 7, 1999
8-acenaphthen-1-yl-1-phenyl-1,3,8-triaza-spiro[4.5]decan-4-one derivatives as orphanin FQ receptor agonistsJ Wichmann, G Adam, S Röver, et al.Neuropharmacology|November 15, 2000
125I-Antisauvagine-30: a novel and specific high-affinity radioligand for the characterization of corticotropin-releasing factor type 2 receptorsJ Higelin, G Py-Lang, C Paternoster, et al.The Journal of Pharmacology and Experimental Therapeutics|December 21, 2000
Different binding modes of amphibian and human corticotropin-releasing factor type 1 and type 2 receptors: evidence for evolutionary differencesF M Dautzenberg, G Py-Lang, J Higelin, et al.Trends in Endocrinology and Metabolism: TEM|April 15, 2008
Molecular Properties of the CRF ReceptorJ Spiess, F M Dautzenberg, S Sydow, et al.European Journal of Medicinal Chemistry|September 28, 2000
Synthesis of (1S,3aS)-8-(2,3,3a,4,5, 6-hexahydro-1H-phenalen-1-yl)-1-phenyl-1,3,8-triaza-spiro[4. 5]decan-4-one, a potent and selective orphanin FQ (OFQ) receptor agonist with anxiolytic-like propertiesJ Wichmann, G Adam, S Röver, et al.The Journal of Pharmacology and Experimental Therapeutics|July 17, 2001
Pharmacological characterization of the novel nonpeptide orphanin FQ/nociceptin receptor agonist Ro 64-6198: rapid and reversible desensitization of the ORL1 receptor in vitro and lack of tolerance in vivoF M Dautzenberg, J Wichmann, J Higelin, et al.Journal of Medicinal Chemistry|February 7, 2001
High-affinity, non-peptide agonists for the ORL1 (orphanin FQ/nociceptin) receptorS Röver, G Adam, A M Cesura, et al.Pageof 4