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                             13 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Characterization of cannabinoid receptors coupled to vasorelaxation by endothelium-derived hyperpolarizing factor Harris, David
1999
359 1 p. 48-52
artikel
2 Comparison of CGS 15943, ZM 241385 and SCH 58261 as antagonists at human adenosine receptors Ongini, E.
1999
359 1 p. 7-10
artikel
3 Comparisons of hallucinogenic phenylisopropylamine binding affinities at cloned human 5-HT2A, 5-HT2B and 5-HT2C receptors Nelson, D. L.
1999
359 1 p. 1-6
artikel
4 Defaecation, intestinal fluid accumulation and motility in rodents: implications of cannabinoid CB1 receptors Izzo, Angelo A.
1999
359 1 p. 65-70
artikel
5 Differences in agonist-independent activity of 5-HT2A and 5-HT2C receptors revealed by heterologous expression Grotewiel, M. S.
1999
359 1 p. 21-27
artikel
6 Different tachykinin receptors mediate chloride secretion in the distal colon through activation of submucosal neurones Frieling, T.
1999
359 1 p. 71-79
artikel
7 Effects of retigabine (D-23129) on different patterns of epileptiform activity induced by 4-aminopyridine in rat entorhinal cortex hippocampal slices Armand, V.
1999
359 1 p. 33-39
artikel
8 High blood levels of nitric oxide in rats subjected to prolonged respiratory arrest and their modulation during adrenocorticotropin-induced resuscitation Bazzani, C.
1999
359 1 p. 53-59
artikel
9 Histaprodifen, methylhistaprodifen, and dimethylhistaprodifen are potent H1-receptor agonists in the pithed and in the anaesthetized rat Malinowska, B.
1999
359 1 p. 11-16
artikel
10 5-HT1B receptors modulate release of [3H]dopamine from rat striatal synaptosomes Sarhan, Hala
1999
359 1 p. 40-47
artikel
11 Na+-channel modulating effect of the inotropic compound S(-)BDF 9196 in human myocardium Müller-Ehmsen, Jochen
1999
359 1 p. 60-64
artikel
12 Signaling via A2A adenosine receptor in four PC12 cell clones Arslan, G.
1999
359 1 p. 28-32
artikel
13 The stereoselective κ-opioid receptor antagonist Mr 2266 does not exhibit stereoselectivity as an antagonist at the orphan opioid (ORL1) receptor Bauer, U.
1999
359 1 p. 17-20
artikel
                             13 gevonden resultaten
 
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