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Does bovine besnoitiosis affect the sexual function of chronically infected bulls?

Theriogenology, 2016-09, Vol.86 (5), p.1325-1332

2016

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No detection of Besnoitia besnoiti DNA in the semen of chronically infected bulls

Parasitology research (1987), 2014-06, Vol.113 (6), p.2355-2362

2014

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A new alternative mechanism in glioblastoma vascularization: tubular vasculogenic mimicry

Brain (London, England : 1878), 2010-04, Vol.133 (4), p.973-982

2010

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S33005, a novel ligand at both serotonin and norepinephrine transporters: I. Receptor binding, electrophysiological, and neurochemical profile in comparison with venlafaxine, reboxetine, citalopram, and clomipramine

The Journal of pharmacology and experimental therapeutics, 2001-08, Vol.298 (2), p.565

2001

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S33005, a novel ligand at both serotonin and norepinephrine transporters: II. Behavioral profile in comparison with venlafaxine, reboxetine, citalopram, and clomipramine

The Journal of pharmacology and experimental therapeutics, 2001-08, Vol.298 (2), p.581

2001

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5-HT2C receptors mediate penile erections in rats : actions of novel and selective agonists and antagonists

European journal of pharmacology, 1997-04, Vol.325 (1), p.9-12

1997

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A Short and Efficient Stereoselective Synthesis of the Octalactin Lactone Using Enantioselective Crotyltitanations and a Cross-Metathesis Reaction

Synlett, 2005-11, Vol.2005 (18), p.2851-2853

2005

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Functional correlates of dopamine D3 receptor activation in the rat in vivo and their modulation by the selective antagonist, (+)-S 14297: II. Both D2 and "silent" D3 autoreceptors control synthesis and release in mesolimbic, mesocortical and nigrostriatal pathways

The Journal of pharmacology and experimental therapeutics, 1995-11, Vol.275 (2), p.899

1995

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Improvement in the Selectivity and Metabolic Stability of the Serotonin 5-HT1A Ligand, S 15535: A Series of cis- and trans-2-(Arylcycloalkylamine) 1-Indanols

Journal of medicinal chemistry, 2002-01, Vol.45 (1), p.165-176

2002

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S18327 (1-[2-[4-(6-fluoro-1, 2-benzisoxazol-3-yl)piperid-1-yl]ethyl]3-phenyl imidazolin-2-one), a novel, potential antipsychotic displaying marked antagonist properties at alpha(1)- and alpha(2)-adrenergic receptors: II. Functional profile and a multiparametric comparison with haloperidol, clozapine, and 11 other antipsychotic agents

The Journal of pharmacology and experimental therapeutics, 2000-01, Vol.292 (1), p.54

2000

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Démarches qualité et pastoralisme en France

Revue de géographie alpine, 2014-09

2014

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Characterization of Potent and Selective Antagonists at Postsynaptic 5-HT1A Receptors in a Series of N4-Substituted Arylpiperazines

Journal of medicinal chemistry, 1995-09, Vol.38 (20), p.4044-4055

1995

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Modulation of mesolimbic dopamine release by the selective dopamine D3 receptor antagonist, (+)-S 14297

European journal of pharmacology, 1994-11, Vol.265 (3), p.175-177

1994

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S 18126 ([2-[4-(2,3-dihydrobenzo[1,4]dioxin-6-yl)piperazin-1-yl methyl]indan-2-yl]), a potent, selective and competitive antagonist at dopamine D4 receptors: an in vitro and in vivo comparison with L 745,870 (3-(4-[4-chlorophenyl]piperazin-1-yl)methyl-1H-pyrrolo[2, 3b]pyridine) and raclopride

The Journal of pharmacology and experimental therapeutics, 1998-10, Vol.287 (1), p.167

1998

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S 15535 : a highly selective benzodioxopiperazine 5-HT1A receptor ligand which acts as an agonist and an antagonist at presynaptic and postsynaptic sites respectively

European journal of pharmacology, 1993-01, Vol.230 (1), p.99-102

1993

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S 14297, a novel selective ligand at cloned human dopamine D3 receptors, blocks 7-OH-DPAT-induced hypothermia in rats

European journal of pharmacology, 1994-08, Vol.260 (2-3), p.R3-R5

1994

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Démarches qualité et pastoralisme en France: Synergies et paradoxes

Revue de géographie alpine, 2014, Vol.102 (2)

2014

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Tetracyclic analogues of [+]-S 14297 : Synthesis and determination of affinity and selectivity at cloned human dopamine D3 vs D2 receptors

Bioorganic & medicinal chemistry letters, 1997-04, Vol.7 (7), p.881-886

1997

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L’article L. 132-13 du Code des assurances et le droit des successions et des libéralités - Pour la réintégration dans la succession des primes d’assurances-vie

Revue de droit d'Assas, 2020-10 (20)

Péglion-Zika, Claire-Marie

2020

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S32504, a Novel Naphtoxazine Agonist at Dopamine D 3 /D 2 Receptors: III. Actions in Models of Potential Antidepressive and Anxiolytic Activity in Comparison with Ropinirole

The Journal of pharmacology and experimental therapeutics, 2004-06, Vol.309 (3), p.936-950

2004

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The calcium channel antagonist S 11568 causes endothelium-dependent relaxation in canine arteries

European journal of pharmacology, 1991-05, Vol.197 (1), p.41-48

1991

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S32504, a Novel Naphtoxazine Agonist at Dopamine D 3 /D 2 Receptors: I. Cellular, Electrophysiological, and Neurochemical Profile in Comparison with Ropinirole

The Journal of pharmacology and experimental therapeutics, 2004-06, Vol.309 (3), p.903-920

2004

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Modulation of mesolimbic dopamine release by the selective dopamine D 3 receptor antagonist, (+)-S 14297

European journal of pharmacology, 1994-11, Vol.265 (3), p.175-177

1994

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[3H](+)S 14297 : a novel, selective radioligand at cloned human dopamine D3 receptors

Neuropharmacology, 1995-12, Vol.34 (12), p.1693-1696

1995

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Novel benzodioxopiperazines acting as antagonists at postsynaptic 5-HT1A receptors and as agonists at 5-HT1A autoreceptors: a comparative pharmacological characterization with proposed 5-HT1A antagonists

The Journal of pharmacology and experimental therapeutics, 1994-01, Vol.268 (1), p.337

1994

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Does bovine besnoitiosis affect the sexual function of chronically infected bulls?

No detection of Besnoitia besnoiti DNA in the semen of chronically infected bulls

A new alternative mechanism in glioblastoma vascularization: tubular vasculogenic mimicry

S33005, a novel ligand at both serotonin and norepinephrine transporters: I. Receptor binding, electrophysiological, and neurochemical profile in comparison with venlafaxine, reboxetine, citalopram, and clomipramine

S33005, a novel ligand at both serotonin and norepinephrine transporters: II. Behavioral profile in comparison with venlafaxine, reboxetine, citalopram, and clomipramine

5-HT2C receptors mediate penile erections in rats : actions of novel and selective agonists and antagonists

A Short and Efficient Stereoselective Synthesis of the Octalactin Lactone Using Enantioselective Crotyltitanations and a Cross-Metathesis Reaction

Functional correlates of dopamine D3 receptor activation in the rat in vivo and their modulation by the selective antagonist, (+)-S 14297: II. Both D2 and "silent" D3 autoreceptors control synthesis and release in mesolimbic, mesocortical and nigrostriatal pathways

Improvement in the Selectivity and Metabolic Stability of the Serotonin 5-HT1A Ligand, S 15535: A Series of cis- and trans-2-(Arylcycloalkylamine) 1-Indanols

Démarches qualité et pastoralisme en France

Characterization of Potent and Selective Antagonists at Postsynaptic 5-HT1A Receptors in a Series of N4-Substituted Arylpiperazines

Modulation of mesolimbic dopamine release by the selective dopamine D3 receptor antagonist, (+)-S 14297

S 18126 ([2-[4-(2,3-dihydrobenzo[1,4]dioxin-6-yl)piperazin-1-yl methyl]indan-2-yl]), a potent, selective and competitive antagonist at dopamine D4 receptors: an in vitro and in vivo comparison with L 745,870 (3-(4-[4-chlorophenyl]piperazin-1-yl)methyl-1H-pyrrolo[2, 3b]pyridine) and raclopride

S 15535 : a highly selective benzodioxopiperazine 5-HT1A receptor ligand which acts as an agonist and an antagonist at presynaptic and postsynaptic sites respectively

S 14297, a novel selective ligand at cloned human dopamine D3 receptors, blocks 7-OH-DPAT-induced hypothermia in rats

Démarches qualité et pastoralisme en France: Synergies et paradoxes

Tetracyclic analogues of [+]-S 14297 : Synthesis and determination of affinity and selectivity at cloned human dopamine D3 vs D2 receptors

L’article L. 132-13 du Code des assurances et le droit des successions et des libéralités - Pour la réintégration dans la succession des primes d’assurances-vie

S32504, a Novel Naphtoxazine Agonist at Dopamine D 3 /D 2 Receptors: III. Actions in Models of Potential Antidepressive and Anxiolytic Activity in Comparison with Ropinirole

The calcium channel antagonist S 11568 causes endothelium-dependent relaxation in canine arteries

S32504, a Novel Naphtoxazine Agonist at Dopamine D 3 /D 2 Receptors: I. Cellular, Electrophysiological, and Neurochemical Profile in Comparison with Ropinirole

Modulation of mesolimbic dopamine release by the selective dopamine D 3 receptor antagonist, (+)-S 14297

[3H](+)S 14297 : a novel, selective radioligand at cloned human dopamine D3 receptors

Novel benzodioxopiperazines acting as antagonists at postsynaptic 5-HT1A receptors and as agonists at 5-HT1A autoreceptors: a comparative pharmacological characterization with proposed 5-HT1A antagonists

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