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Results: 1-25 | 26-43
Results: 1-25/43
Construction and analysis of function of G protein-coupled receptor-G protein fusion proteins
Authors: Milligan, G
Citation: G. Milligan, Construction and analysis of function of G protein-coupled receptor-G protein fusion proteins, METH ENZYM, 343, 2002, pp. 260-273
Protein-protein interactions at G-protein-coupled receptors
Authors: Milligan, G White, JH
Citation: G. Milligan et Jh. White, Protein-protein interactions at G-protein-coupled receptors, TRENDS PHAR, 22(10), 2001, pp. 513-518
Multiple pertussis toxin-sensitive G-proteins can couple receptors to GIRKchannels in rat sympathetic neurons when expressed heterologously, but only native G(i)-proteins do so in situ
Authors: Fernandez-Fernandez, JM Abogadie, FC Milligan, G Delmas, P Brown, DA
Citation: Jm. Fernandez-fernandez et al., Multiple pertussis toxin-sensitive G-proteins can couple receptors to GIRKchannels in rat sympathetic neurons when expressed heterologously, but only native G(i)-proteins do so in situ, EUR J NEURO, 14(2), 2001, pp. 283-292
German national identity after the Holocaust.
Authors: Milligan, G
Citation: G. Milligan, German national identity after the Holocaust., PATT PREJUD, 35(3), 2001, pp. 90-93
Control of the efficiency of agonist-induced information transfer and stability of the ternary complex containing the delta opioid receptor and the alpha subunit of G(i1) by mutation of a receptor/G protein contact interface
Authors: Moon, HE Bahia, DS Cavalli, A Hoffmann, M Milligan, G
Citation: He. Moon et al., Control of the efficiency of agonist-induced information transfer and stability of the ternary complex containing the delta opioid receptor and the alpha subunit of G(i1) by mutation of a receptor/G protein contact interface, NEUROPHARM, 41(3), 2001, pp. 321-330
S 14506: novel receptor coupling at 5-HT1A receptors
Authors: Milligan, G Kellett, E Dacquet, C Dubreuil, V Jacoby, E Millan, MJ Lavielle, G Spedding, M
Citation: G. Milligan et al., S 14506: novel receptor coupling at 5-HT1A receptors, NEUROPHARM, 40(3), 2001, pp. 334-344
Analysis of the C-terminal tail of the rat thyrotropin-releasing hormone receptor-1 in interactions and cointernalization with beta-arrestin 1-green fluorescent protein
Authors: Groarke, DA Drmota, T Bahia, DS Evans, NA Wilson, S Milligan, G
Citation: Da. Groarke et al., Analysis of the C-terminal tail of the rat thyrotropin-releasing hormone receptor-1 in interactions and cointernalization with beta-arrestin 1-green fluorescent protein, MOLEC PHARM, 59(2), 2001, pp. 375-385
Antiparkinsonian agent piribedil displays antagonist properties at native,rat, and cloned, human alpha(2)-adrenoceptors: Cellular and functional characterization
Authors: Millan, MJ Cussac, D Milligan, G Carr, C Audinot, V Gobert, A Lejeune, F Rivet, JM Brocco, M Duqueyroix, D Nicolas, JP Boutin, JA Newman-Tancredi, A
Citation: Mj. Millan et al., Antiparkinsonian agent piribedil displays antagonist properties at native,rat, and cloned, human alpha(2)-adrenoceptors: Cellular and functional characterization, J PHARM EXP, 297(3), 2001, pp. 876-887
Differential capacities of the RGS1, RGS16 and RGS-GAIP regulators of G protein signaling to enhance alpha(2A)-adrenoreceptor agonist-stimulated GTPase activity of G(o1)alpha
Authors: Hoffmann, M Ward, RJ Cavalli, A Carr, IC Milligan, G
Citation: M. Hoffmann et al., Differential capacities of the RGS1, RGS16 and RGS-GAIP regulators of G protein signaling to enhance alpha(2A)-adrenoreceptor agonist-stimulated GTPase activity of G(o1)alpha, J NEUROCHEM, 78(4), 2001, pp. 797-806
Visualizing differences in ligand-induced beta-arrestin-GFP interactions and trafficking between three recently characterized G protein-coupled receptors
Authors: Evans, NA Groarke, DA Warrack, J Greenwood, CJ Dodgson, K Milligan, G Wilson, S
Citation: Na. Evans et al., Visualizing differences in ligand-induced beta-arrestin-GFP interactions and trafficking between three recently characterized G protein-coupled receptors, J NEUROCHEM, 77(2), 2001, pp. 476-485
The human delta opioid receptor activates G(i1)alpha more efficiently thanG(o1)alpha
Authors: Moon, HE Cavalli, A Bahia, DS Hoffmann, M Massotte, D Milligan, G
Citation: He. Moon et al., The human delta opioid receptor activates G(i1)alpha more efficiently thanG(o1)alpha, J NEUROCHEM, 76(6), 2001, pp. 1805-1813
Oligomerisation of G-protein-coupled receptors
Authors: Milligan, G
Citation: G. Milligan, Oligomerisation of G-protein-coupled receptors, J CELL SCI, 114(7), 2001, pp. 1265-1271
Coordinated agonist regulation of receptor and G protein palmitoylation and functional rescue of palmitoylation-deficient mutants of the G protein G(11)alpha following fusion to the alpha(1b)-adrenoreceptor - Palmitoylation of G(11 alpha) is not required for interaction with beta-gamma complex
Authors: Stevens, PA Pediani, J Carrillo, JJ Milligan, G
Citation: Pa. Stevens et al., Coordinated agonist regulation of receptor and G protein palmitoylation and functional rescue of palmitoylation-deficient mutants of the G protein G(11)alpha following fusion to the alpha(1b)-adrenoreceptor - Palmitoylation of G(11 alpha) is not required for interaction with beta-gamma complex, J BIOL CHEM, 276(38), 2001, pp. 35883-35890
Monitoring receptor oligomerization using time-resolved fluorescence resonance energy transfer and bioluminescence resonance energy transfer - The human delta-opioid receptor displays constitutive oligomerization at the cellsurface, which is not regulated by receptor occupancy
Authors: McVey, M Ramsay, D Kellett, E Rees, S Wilson, S Pope, AJ Milligan, G
Citation: M. Mcvey et al., Monitoring receptor oligomerization using time-resolved fluorescence resonance energy transfer and bioluminescence resonance energy transfer - The human delta-opioid receptor displays constitutive oligomerization at the cellsurface, which is not regulated by receptor occupancy, J BIOL CHEM, 276(17), 2001, pp. 14092-14099
Detection of receptor ligands by monitoring selective stabilization of a Renilla luciferase-tagged, constitutively active mutant, G-protein-coupled receptor
Authors: Ramsay, D Bevan, N Rees, S Milligan, G
Citation: D. Ramsay et al., Detection of receptor ligands by monitoring selective stabilization of a Renilla luciferase-tagged, constitutively active mutant, G-protein-coupled receptor, BR J PHARM, 133(2), 2001, pp. 315-323
Insights into ligand pharmacology using receptor-G-protein fusion proteins
Authors: Milligan, G
Citation: G. Milligan, Insights into ligand pharmacology using receptor-G-protein fusion proteins, TRENDS PHAR, 21(1), 2000, pp. 24-28
Molecular manipulation of G-protein-coupled receptors: A new avenue into drug discovery
Authors: Sautel, M Milligan, G
Citation: M. Sautel et G. Milligan, Molecular manipulation of G-protein-coupled receptors: A new avenue into drug discovery, CURR MED CH, 7(9), 2000, pp. 889-896
Kinetic analysis of the internalization and recycling of [H-3]TRH and C-terminal truncations of the long isoform of the rat thyrotropin-releasing hormone receptor-1
Authors: Drmota, T Milligan, G
Citation: T. Drmota et G. Milligan, Kinetic analysis of the internalization and recycling of [H-3]TRH and C-terminal truncations of the long isoform of the rat thyrotropin-releasing hormone receptor-1, BIOCHEM J, 346, 2000, pp. 711-718
Oligomerisation of G protein-coupled receptors
Authors: Milligan, G Rees, S
Citation: G. Milligan et S. Rees, Oligomerisation of G protein-coupled receptors, ANNU REP M, 35, 2000, pp. 271-279
Neurobiology - Receptors as kissing cousins
Authors: Milligan, G
Citation: G. Milligan, Neurobiology - Receptors as kissing cousins, SCIENCE, 288(5463), 2000, pp. 65
Resolution of inverse agonist-induced up-regulation from constitutive activity of mutants of the alpha(1b)-adrenoceptor
Authors: Stevens, PA Bevan, N Rees, S Milligan, G
Citation: Pa. Stevens et al., Resolution of inverse agonist-induced up-regulation from constitutive activity of mutants of the alpha(1b)-adrenoceptor, MOLEC PHARM, 58(2), 2000, pp. 438-448
S18616, a highly potent, spiroimidazoline agonist at alpha(2)-adrenoceptors: I. Receptor profile, antinociceptive and hypothermic actions in comparison with dexmedetomidine and clonidine
Authors: Millan, MJ Dekeyne, A Newman-Tancredi, A Cussac, D Audinot, V Milligan, G Duqueyroix, D Girardon, S Mullot, J Boutin, JA Nicolas, JP Renouard-Try, A Lacoste, JM Cordi, A
Citation: Mj. Millan et al., S18616, a highly potent, spiroimidazoline agonist at alpha(2)-adrenoceptors: I. Receptor profile, antinociceptive and hypothermic actions in comparison with dexmedetomidine and clonidine, J PHARM EXP, 295(3), 2000, pp. 1192-1205
Receptor for the pain modulatory neuropeptides FF and AF is an orphan G protein-coupled receptor
Authors: Elshourbagy, NA Ames, RS Fitzgerald, LR Foley, JJ Chambers, JK Szekeres, PG Evans, NA Schmidt, DB Buckley, PT Dytko, GM Murdock, PR Milligan, G Groarke, DA Tan, KB Shabon, U Nuthulaganti, P Wang, DY Wilson, S Bergsma, DJ Sarau, HM
Citation: Na. Elshourbagy et al., Receptor for the pain modulatory neuropeptides FF and AF is an orphan G protein-coupled receptor, J BIOL CHEM, 275(34), 2000, pp. 25965-25971
The regulator of G protein signaling RGS4 selectively enhances alpha(2A)-adreoreceptor stimulation of the GTPase activity of G(o1)alpha and G(i2)alpha
Authors: Cavalli, A Druey, KM Milligan, G
Citation: A. Cavalli et al., The regulator of G protein signaling RGS4 selectively enhances alpha(2A)-adreoreceptor stimulation of the GTPase activity of G(o1)alpha and G(i2)alpha, J BIOL CHEM, 275(31), 2000, pp. 23693-23699
The G protein alpha subunit has a key role in determining the specificity of coupling to, but not the activation of, G protein-gated inwardly rectifying K+ channels
Authors: Leaney, JL Milligan, G Tinker, A
Citation: Jl. Leaney et al., The G protein alpha subunit has a key role in determining the specificity of coupling to, but not the activation of, G protein-gated inwardly rectifying K+ channels, J BIOL CHEM, 275(2), 2000, pp. 921-929
Risultati: 1-25 | 26-43