Hamon M - Search Results

1

SR 57227A: a potent and selective agonist at central and peripheral 5-HT3 receptors in vitro and in vivo.

Bachy A, Héaulme M, Giudice A, Michaud JC, Lefevre IA, Souilhac J, Manara L, Emerit MB, Gozlan H, Hamon M, et al. Bachy A, et al. Among authors: hamon m. Eur J Pharmacol. 1993 Jun 24;237(2-3):299-309. doi: 10.1016/0014-2999(93)90282-m. Eur J Pharmacol. 1993. PMID: 7689975

2

The potent 5-HT3 receptor antagonist (R)-zacopride labels an additional high affinity site in the central nervous system.

Kidd E, Bouchelet de Vendegies I, Levy JC, Hamon M, Gozlan H. Kidd E, et al. Among authors: hamon m. Eur J Pharmacol. 1992 Jan 28;211(1):133-6. doi: 10.1016/0014-2999(92)90276-a. Eur J Pharmacol. 1992. PMID: 1618262

3

Determination of the molecular size of the 5-HT3 receptor binding site by radiation inactivation.

Gozlan H, Schechter LE, Bolanos F, Emerit MB, Miquel MC, Nielsen M, Hamon M. Gozlan H, et al. Among authors: hamon m. Eur J Pharmacol. 1989 Dec 5;172(6):497-500. doi: 10.1016/0922-4106(89)90033-3. Eur J Pharmacol. 1989. PMID: 2533081

4

Selective in vivo labelling of brain 5-HT1A receptors by [3H]WAY 100635 in the mouse.

Laporte AM, Lima L, Gozlan H, Hamon M. Laporte AM, et al. Among authors: hamon m. Eur J Pharmacol. 1994 Dec 27;271(2-3):505-14. doi: 10.1016/0014-2999(94)90812-5. Eur J Pharmacol. 1994. PMID: 7705451

5

Biochemical and electrophysiological properties of SR 57746A, a new, potent 5-HT1A receptor agonist.

Bachy A, Steinberg R, Santucci V, Fournier M, Landi M, Hamon M, Manara L, Keane PE, Soubrié P, Le Fur G. Bachy A, et al. Among authors: hamon m. Fundam Clin Pharmacol. 1993;7(9):487-97. doi: 10.1111/j.1472-8206.1993.tb00253.x. Fundam Clin Pharmacol. 1993. PMID: 8314196

6

Interaction of S 21007 with 5-HT3 receptors. In vitro and in vivo characterization.

Delagrange P, Emerit MB, Merahi N, Abraham C, Morain P, Rault S, Renard P, Pfeiffer B, Guardiola-Lemaître B, Hamon M. Delagrange P, et al. Among authors: hamon m. Eur J Pharmacol. 1996 Dec 5;316(2-3):195-203. doi: 10.1016/s0014-2999(96)00680-2. Eur J Pharmacol. 1996. PMID: 8982686

7

[3H]5-methyl-urapidil labels 5-HT1A receptors and alpha 1-adrenoceptors in the rat CNS. In vitro binding and autoradiographic studies.

Laporte AM, Schechter LE, Bolaños FJ, Vergé D, Hamon M, Gozlan H. Laporte AM, et al. Among authors: hamon m. Eur J Pharmacol. 1991 May 30;198(1):59-67. doi: 10.1016/0014-2999(91)90562-5. Eur J Pharmacol. 1991. PMID: 1680714

8

Involvement of tryptophan residue(s) in the specific binding of agonists/antagonists to 5-HT3 receptors in NG108-15 clonal cells.

Miquel MC, Emerit MB, Gozlan H, Hamon M. Miquel MC, et al. Among authors: hamon m. Biochem Pharmacol. 1991 Sep 12;42(7):1453-61. doi: 10.1016/0006-2952(91)90459-i. Biochem Pharmacol. 1991. PMID: 1930269

9

Common pharmacological and physico-chemical properties of 5-HT3 binding sites in the rat cerebral cortex and NG 108-15 clonal cells.

Bolaños FJ, Schechter LE, Miquel MC, Emerit MB, Rumigny JF, Hamon M, Gozlan H. Bolaños FJ, et al. Among authors: hamon m. Biochem Pharmacol. 1990 Oct 1;40(7):1541-50. doi: 10.1016/0006-2952(90)90452-q. Biochem Pharmacol. 1990. PMID: 2222509

10

The central 5-HT1A receptors: pharmacological, biochemical, functional, and regulatory properties.

Hamon M, Gozlan H, el Mestikawy S, Emerit MB, Bolaños F, Schechter L. Hamon M, et al. Ann N Y Acad Sci. 1990;600:114-29; discussion 129-31. doi: 10.1111/j.1749-6632.1990.tb16877.x. Ann N Y Acad Sci. 1990. PMID: 2252305 Review. No abstract available.

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