Search Results - "GULLY, DANIELLE" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]5-methyl-N-(2-propynyl)-1, 3-thiazol-2-amine Hydrochloride (SSR125543A), a Potent and Selective Corticotrophin-Releasing Factor1 Receptor Antagonist. II. Characterization in Rodent Models of Stress-Related Disorders

4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]5-methyl-N-(2-propynyl)-1, 3-thiazol-2-amine Hydrochloride (SSR125543A), a Potent and Selective Corticotrophin-Releasing Factor1 Receptor Antagonist. II. Characterization in Rodent Models of Stress-Related Disorders

by Guy Griebel, Jacques Simiand, RÃ©gis Steinberg, Mireille Jung, Danielle Gully, Pierre Roger, Michel Geslin, Bernard Scatton, Jean-Pierre Maffrand, Philippe SoubriÃ
Published in The Journal of pharmacology and experimental therapeutics (01.04.2002)

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The 100-kDa Neurotensin Receptor Is gp95/Sortilin, A Non-G-Protein-coupled Receptor

The 100-kDa Neurotensin Receptor Is gp95/Sortilin, A Non-G-Protein-coupled Receptor

by Mazella, Jean, Zsürger, Nicole, Navarro, Valérie, Chabry, Joëlle, Kaghad, Mourad, Caput, Daniel, Ferrara, Pascual, Vita, Natalio, Gully, Danielle, Maffrand, Jean-Pierre, Vincent, Jean-Pierre
Published in The Journal of biological chemistry (09.10.1998)

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4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]5-methyl-N-(2-propynyl)-1,3-thiazol-2-amine Hydrochloride (SSR125543A): A Potent and Selective Corticotrophin-Releasing Factor1 Receptor Antagonist. I. Biochemical and Pharmacological Characterization

4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]5-methyl-N-(2-propynyl)-1,3-thiazol-2-amine Hydrochloride (SSR125543A): A Potent and Selective Corticotrophin-Releasing Factor1 Receptor Antagonist. I. Biochemical and Pharmacological Characterization

by Danielle Gully, Michel Geslin, Laurence Serva, Evelyne Fontaine, Pierre Roger, Christine Lair, Valerie Darre, Claudine Marcy, Pierre-Eric Rouby, Jacques Simiand, Josette Guitard, Georgette Gout, Regis Steinberg, Daniel Rodier, Guy Griebel, Philippe Soubrie, Marc Pascal, Rebecca Pruss, Bernard Scatton, Jean-Pierre Maffrand, Gerard Le Fur
Published in The Journal of pharmacology and experimental therapeutics (01.04.2002)

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Biochemical and Pharmacological Activities of SR 142948A, a New Potent Neurotensin Receptor Antagonist

Biochemical and Pharmacological Activities of SR 142948A, a New Potent Neurotensin Receptor Antagonist

by Gully, D, Labeeuw, B, Boigegrain, R, Oury-Donat, F, Bachy, A, Poncelet, M, Steinberg, R, Suaud-Chagny, M F, Santucci, V, Vita, N, Pecceu, F, Labbé-Jullié, C, Kitabgi, P, Soubrié, P, Le Fur, G, Maffrand, J P
Published in The Journal of pharmacology and experimental therapeutics (01.02.1997)

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Arginine 336 and Asparagine 333 of the Human Cholecystokinin-A Receptor Binding Site Interact with the Penultimate Aspartic Acid and the C-terminal Amide of Cholecystokinin

Arginine 336 and Asparagine 333 of the Human Cholecystokinin-A Receptor Binding Site Interact with the Penultimate Aspartic Acid and the C-terminal Amide of Cholecystokinin

by Gigoux, V, Escrieut, C, Fehrentz, J A, Poirot, S, Maigret, B, Moroder, L, Gully, D, Martinez, J, Vaysse, N, Fourmy, D
Published in The Journal of biological chemistry (16.07.1999)

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Met-195 of the Cholecystokinin-A Receptor Interacts with the Sulfated Tyrosine of Cholecystokinin and Is Crucial for Receptor Transition to High Affinity State

Met-195 of the Cholecystokinin-A Receptor Interacts with the Sulfated Tyrosine of Cholecystokinin and Is Crucial for Receptor Transition to High Affinity State

by Gigoux, Véronique, Escrieut, Chantal, Silvente-Poirot, Sandrine, Maigret, Bernard, Gouilleux, Laurent, Fehrentz, Jean-Alain, Gully, Danielle, Moroder, Luis, Vaysse, Nicole, Fourmy, Daniel
Published in The Journal of biological chemistry (05.06.1998)

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Identification of Two Amino Acids of the Human Cholecystokinin-A Receptor That Interact with the N-terminal Moiety of Cholecystokinin

Identification of Two Amino Acids of the Human Cholecystokinin-A Receptor That Interact with the N-terminal Moiety of Cholecystokinin

by Kennedy, Karen, Gigoux, Véronique, Escrieut, Chantal, Maigret, Bernard, Martinez, Jean, Moroder, Luis, Fréhel, Daniel, Gully, Danielle, Vaysse, Nicole, Fourmy, Daniel
Published in The Journal of biological chemistry (31.01.1997)

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Dose-Dependent Pain-Facilitatory and -Inhibitory Actions of Neurotensin Are Revealed by SR 48692, a Nonpeptide Neurotensin Antagonist: Influence on the Antinociceptive Effect of Morphine

Dose-Dependent Pain-Facilitatory and -Inhibitory Actions of Neurotensin Are Revealed by SR 48692, a Nonpeptide Neurotensin Antagonist: Influence on the Antinociceptive Effect of Morphine

by Smith, D J, Hawranko, A A, Monroe, P J, Gully, D, Urban, M O, Craig, C R, Smith, J P, Smith, D L
Published in The Journal of pharmacology and experimental therapeutics (01.08.1997)

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SR146131: A New Potent, Orally Active, and Selective Nonpeptide Cholecystokinin Subtype 1 Receptor Agonist. I: In Vitro Studies

SR146131: A New Potent, Orally Active, and Selective Nonpeptide Cholecystokinin Subtype 1 Receptor Agonist. I: In Vitro Studies

by Bignon, E, Bachy, A, Boigegrain, R, Brodin, R, Cottineau, M, Gully, D, Herbert, J M, Keane, P, Labie, C, Molimard, J C, Olliero, D, Oury-Donat, F, Petereau, C, Prabonnaud, V, Rockstroh, M P, Schaeffer, P, Servant, O, Thurneyssen, O, Soubrié, P, Pascal, M, Maffrand, J P, Le Fur, G
Published in The Journal of pharmacology and experimental therapeutics (01.05.1999)

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Inhibition of neurotensin‐induced pancreatic carcinoma growth by a nonpeptide neurotensin receptor antagonist, SR48692

Inhibition of neurotensin‐induced pancreatic carcinoma growth by a nonpeptide neurotensin receptor antagonist, SR48692

by Iwase, Kazuhiro, Evers, B. Mark, Hellmich, Mark R., Kim, Hong Jin, Higashide, Shunichi, Gully, Danielle, Thompson, James C., Townsend, Courtney M.
Published in Cancer (01.05.1997)

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Peripheral biological activity of SR 27897 : a new potent non-peptide antagonist of CCKA receptors

Peripheral biological activity of SR 27897 : a new potent non-peptide antagonist of CCKA receptors

by GULLY, D, FREHEL, D, MARCY, C, SPINAZZE, A, LESPY, L, NELIAT, G, MAFFRAND, J.-P, LE FUR, G
Published in European journal of pharmacology (23.02.1993)

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Human Umbilical Vein Endothelial Cells Express High Affinity Neurotensin Receptors Coupled to Intracellular Calcium Release (∗)

Human Umbilical Vein Endothelial Cells Express High Affinity Neurotensin Receptors Coupled to Intracellular Calcium Release (∗)

by Schaeffer, Paul, Laplace, Marie-Claude, Savi, Pierre, Pflieger, Anne-Marie, Gully, Danielle, Herbert, Jean-Marc
Published in The Journal of biological chemistry (17.02.1995)

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Negative modulation of nitric oxide production by neurotensin as a putative mechanism of the diuretic action of SR 48692 in rats

Negative modulation of nitric oxide production by neurotensin as a putative mechanism of the diuretic action of SR 48692 in rats

by Croci, Tiziano, Landi, Marco, Gully, Danielle, Maffrand, Jean‐Pierre, Le Fur, Gérard, Manara, Luciano
Published in British journal of pharmacology (01.04.1997)

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4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]5-methyl-N-(2-propynyl)-1, 3-thiazol-2-amine hydrochloride (SSR125543A), a potent and selective corticotrophin-releasing factor(1) receptor antagonist. II. Characterization in rodent models of stress-related disorders

4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]5-methyl-N-(2-propynyl)-1, 3-thiazol-2-amine hydrochloride (SSR125543A), a potent and selective corticotrophin-releasing factor(1) receptor antagonist. II. Characterization in rodent models of stress-related disorders

by Griebel, Guy, Simiand, Jacques, Steinberg, Régis, Jung, Mireille, Gully, Danielle, Roger, Pierre, Geslin, Michel, Scatton, Bernard, Maffrand, Jean-Pierre, Soubrié, Philippe
Published in The Journal of pharmacology and experimental therapeutics (01.04.2002)

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4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]5-methyl-N-(2-propynyl)-1,3-thiazol-2-amine hydrochloride (SSR125543A): a potent and selective corticotrophin-releasing factor(1) receptor antagonist. I. Biochemical and pharmacological characterization

4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl)ethyl]5-methyl-N-(2-propynyl)-1,3-thiazol-2-amine hydrochloride (SSR125543A): a potent and selective corticotrophin-releasing factor(1) receptor antagonist. I. Biochemical and pharmacological characterization

by Gully, Danielle, Geslin, Michel, Serva, Laurence, Fontaine, Evelyne, Roger, Pierre, Lair, Christine, Darre, Valerie, Marcy, Claudine, Rouby, Pierre-Eric, Simiand, Jacques, Guitard, Josette, Gout, Georgette, Steinberg, Regis, Rodier, Daniel, Griebel, Guy, Soubrie, Philippe, Pascal, Marc, Pruss, Rebecca, Scatton, Bernard, Maffrand, Jean-Pierre, Le Fur, Gerard
Published in The Journal of pharmacology and experimental therapeutics (01.04.2002)

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Neurotensin and a non‐peptide neurotensin receptor antagonist control human colon cancer cell growth in cell culture and in cells xenografted into nude mice

Neurotensin and a non‐peptide neurotensin receptor antagonist control human colon cancer cell growth in cell culture and in cells xenografted into nude mice

by Maoret, Jean‐José, Anini, Younes, Rouyer‐Fessard, Christiane, Gully, Danielle, Laburthe, Marc
Published in International journal of cancer (29.01.1999)

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Biochemical and Pharmacological Profile of a Potent and Selective Nonpeptide Antagonist of the Neurotensin Receptor

by Gully, Danielle, Canton, Maryse, Boigegrain, Robert, Jeanjean, Francis, Molimard, Jean-Charles, Poncelet, Martine, Gueudet, Christiane, Heaulme, Michel, Leyris, Roger, Brouard, Aline, Pelaprat, Didier, Labbe-Jullie, Catherine, Mazella, Jean, Soubrie, Philippe, Maffrand, Jean-Pierre, Rostene, William, Kitabgi, Patrick, Le Fur, Gerard
Published in Proceedings of the National Academy of Sciences - PNAS (01.01.1993)

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Arginine 197 of the cholecystokinin-A receptor binding site interacts with the sulfate of the peptide agonist cholecystokinin

Arginine 197 of the cholecystokinin-A receptor binding site interacts with the sulfate of the peptide agonist cholecystokinin

by GIGOUX, VÉRONIQUE, MAIGRET, BERNARD, ESCRIEUT, CHANTAL, SILVENTE-POIROT, SANDRINE, BOUISSON, MICHÈLE, FEHRENTZ, JEAN-ALAIN, MORODER, LUIS, GULLY, DANIELLE, MARTINEZ, JEAN, VAYSSE, NICOLE, FOURMY, DANIEL
Published in Protein science (01.11.1999)

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Characterization of binding sites of a new neurotensin receptor antagonist, [ [formula omitted]]SR 142948A, in the rat brain

Characterization of binding sites of a new neurotensin receptor antagonist, [ [formula omitted]]SR 142948A, in the rat brain

by Betancur, Catalina, Canton, Maryse, Burgos, Alain, Labeeuw, Bernard, Gully, Danielle, Rostène, William, Pélaprat, Didier
Published in European journal of pharmacology (05.02.1998)

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Use of nonpeptide antagonists to explore the physiological roles of neurotensin. Focus on brain neurotensin/dopamine interactions

Use of nonpeptide antagonists to explore the physiological roles of neurotensin. Focus on brain neurotensin/dopamine interactions

by Rostene, W, Azzi, M, Boudin, H, Lepee, I, Souaze, F, Mendez-Ubach, M, Betancur, C, Gully, D
Published in Annals of the New York Academy of Sciences (24.04.1997)

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