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Refinado por: Nome da Publicação: Eur J Pharmacol remover Nome da Publicação: European Journal Of Pharmacology remover
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1
Urantide mimics urotensin-II induced calcium release in cells expressing recombinant UT receptors
Urantide mimics urotensin-II induced calcium release in cells expressing recombinant UT receptors
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Urantide mimics urotensin-II induced calcium release in cells expressing recombinant UT receptors

Camarda, Valeria ; Song, Wei ; Marzola, Erika ; Spagnol, Martina ; Guerrini, Remo ; Salvadori, Severo ; Regoli, Domenico ; Thompson, Jonathan P. ; Rowbotham, David J. ; Behm, David J. ; Douglas, Stephen A. ; Calo', Girolamo ; Lambert, David G.

European journal of pharmacology, 2004-09, Vol.498 (1), p.83-86 [Periódico revisado por pares]

Amsterdam: Elsevier B.V

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2
Nociceptin inhibits acquisition of amphetamine-induced place preference and sensitization to stereotypy in rats
Nociceptin inhibits acquisition of amphetamine-induced place preference and sensitization to stereotypy in rats
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Nociceptin inhibits acquisition of amphetamine-induced place preference and sensitization to stereotypy in rats

Kotlinska, Jolanta ; Rafalski, Piotr ; Biala, Grazyna ; Dylag, Tomasz ; Rolka, Krzysztof ; Silberring, Jerzy

European journal of pharmacology, 2003-08, Vol.474 (2), p.233-239 [Periódico revisado por pares]

Amsterdam: Elsevier B.V

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3
A Novel nonpeptidic caspase-3/7 inhibitor, ( S)-(+)-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin reduces myocardial ischemic injury
A Novel nonpeptidic caspase-3/7 inhibitor, ( S)-(+)-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin reduces myocardial ischemic injury
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A Novel nonpeptidic caspase-3/7 inhibitor, ( S)-(+)-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin reduces myocardial ischemic injury

Chapman, Justin G ; Magee, William P ; Stukenbrok, Hans A ; Beckius, Gretchen E ; Milici, Anthony J ; Tracey, W.Ross

European journal of pharmacology, 2002-12, Vol.456 (1), p.59-68 [Periódico revisado por pares]

Amsterdam: Elsevier B.V

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4
Activation of peripheral ATP-sensitive K + channels mediates the antinociceptive effect of Crotalus durissus terrificus snake venom
Activation of peripheral ATP-sensitive K + channels mediates the antinociceptive effect of Crotalus durissus terrificus snake venom
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Activation of peripheral ATP-sensitive K + channels mediates the antinociceptive effect of Crotalus durissus terrificus snake venom

Picolo, Gisele ; Cassola, Antônio Carlos ; Cury, Yara

European journal of pharmacology, 2003-05, Vol.469 (1), p.57-64 [Periódico revisado por pares]

Amsterdam: Elsevier B.V

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5
Antisecretory effect of somatostatin on gastric acid via inhibition of histamine release in isolated mouse stomach
Antisecretory effect of somatostatin on gastric acid via inhibition of histamine release in isolated mouse stomach
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Antisecretory effect of somatostatin on gastric acid via inhibition of histamine release in isolated mouse stomach

Komasaka, Midori ; Horie, Syunji ; Watanabe, Kazuo ; Murayama, Toshihiko

European journal of pharmacology, 2002-10, Vol.452 (2), p.235-243 [Periódico revisado por pares]

Amsterdam: Elsevier B.V

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6
Dopamine D1 receptors and adenosine A1 receptors in the rat nucleus accumbens regulate motor activity but not prepulse inhibition
Dopamine D1 receptors and adenosine A1 receptors in the rat nucleus accumbens regulate motor activity but not prepulse inhibition
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Dopamine D1 receptors and adenosine A1 receptors in the rat nucleus accumbens regulate motor activity but not prepulse inhibition

SCHWIENBACHER, Isabel ; FENDT, Markus ; HAUBER, Wolfgang ; KOCH, Michael

European journal of pharmacology, 2002-05, Vol.444 (3), p.161-169 [Periódico revisado por pares]

Amsterdam: Elsevier

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7
Effects of 5-HT1A receptor antagonists on hippocampal 5-hydroxytryptamine levels : (S)-WAY100135, but not WAY100635, has partial agonist properties
Effects of 5-HT1A receptor antagonists on hippocampal 5-hydroxytryptamine levels : (S)-WAY100135, but not WAY100635, has partial agonist properties
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Effects of 5-HT1A receptor antagonists on hippocampal 5-hydroxytryptamine levels : (S)-WAY100135, but not WAY100635, has partial agonist properties

ASSIE, M.-B ; KOEK, W

European journal of pharmacology, 1996-05, Vol.304 (1-3), p.15-22 [Periódico revisado por pares]

Amsterdam: Elsevier

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8
The γ-aminobutyric acid (GABA) uptake inhibitor, tiagabine, increases extracellular brain levels of GABA in awake rats
The γ-aminobutyric acid (GABA) uptake inhibitor, tiagabine, increases extracellular brain levels of GABA in awake rats
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The γ-aminobutyric acid (GABA) uptake inhibitor, tiagabine, increases extracellular brain levels of GABA in awake rats

Fink-Jensen, Anders ; Suzdak, P.D. ; Swedberg, M.D.B. ; Judge, M.E. ; Hansen, L. ; Nielsen, P.G.

European journal of pharmacology, 1992-09, Vol.220 (2), p.197-201 [Periódico revisado por pares]

AMSTERDAM: Elsevier B.V

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9
PNU-151774E protects against kainate-induced status epilepticus and hippocampal lesions in the rat
PNU-151774E protects against kainate-induced status epilepticus and hippocampal lesions in the rat
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PNU-151774E protects against kainate-induced status epilepticus and hippocampal lesions in the rat

Maj, Roberto ; Fariello, Ruggero G ; Ukmar, Giorgio ; Varasi, Mario ; Pevarello, Paolo ; McArthur, Robert A ; Salvati, Patricia

European journal of pharmacology, 1998-10, Vol.359 (1), p.27-32 [Periódico revisado por pares]

Amsterdam: Elsevier B.V

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10
NNC-711, a novel potent and selective γ-aminobutyric acid uptake inhibitor: pharmacological characterization
NNC-711, a novel potent and selective γ-aminobutyric acid uptake inhibitor: pharmacological characterization
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NNC-711, a novel potent and selective γ-aminobutyric acid uptake inhibitor: pharmacological characterization

Suzdak, Peter D. ; Frederiksen, Kristen ; Andersen, Knud Erik ; Sørensen, Per O. ; Knutsen, Lars J.S. ; Nielsen, Erik B.

European journal of pharmacology, 1992-12, Vol.224 (2), p.189-198 [Periódico revisado por pares]

AMSTERDAM: Elsevier B.V

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