Works matching IS 00281298 AND DT 2008 AND VI 378 AND IP 5
Results: 9
Interactions of tiagabine with ethosuximide in the mouse pentylenetetrazole-induced seizure model: an isobolographic analysis for non-parallel dose-response relationship curves.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2008, v. 378, n. 5, p. 483, doi. 10.1007/s00210-008-0305-8
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Local effects and mechanisms of antiarrhythmic peptide AAP10 in acute regional myocardial ischemia: electrophysiological and molecular findings.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2008, v. 378, n. 5, p. 459, doi. 10.1007/s00210-008-0317-4
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Subnanomolar dopamine D<sub>3</sub> receptor antagonism coupled to moderate D<sub>2</sub> affinity results in favourable antipsychotic-like activity in rodent models: I. neurochemical characterisation of RG-15.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2008, v. 378, n. 5, p. 515, doi. 10.1007/s00210-008-0308-5
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CPU86017 and its isomers improve hypoxic pulmonary hypertension by attenuating increased ETA receptor expression and extracellular matrix accumulation.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2008, v. 378, n. 5, p. 541, doi. 10.1007/s00210-008-0309-4
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- Article
Subnanomolar dopamine D<sub>3</sub> receptor antagonism coupled to moderate D<sub>2</sub> affinity results in favourable antipsychotic-like activity in rodent models: II. behavioural characterisation of RG-15.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2008, v. 378, n. 5, p. 529, doi. 10.1007/s00210-008-0311-x
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Role of the soluble guanylyl cyclase α<sub>1</sub>/α<sub>2</sub> subunits in the relaxant effect of CO and CORM-2 in murine gastric fundus.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2008, v. 378, n. 5, p. 493, doi. 10.1007/s00210-008-0315-6
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Toxic-dose warfarin-induced apoptosis and its enhancement by gamma ionizing radiation in leukemia K562 and HL-60 cells is not mediated by induction of oxidative stress.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2008, v. 378, n. 5, p. 471, doi. 10.1007/s00210-008-0306-7
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A signaling-selective, nanomolar potent allosteric low molecular weight agonist for the human luteinizing hormone receptor.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2008, v. 378, n. 5, p. 503, doi. 10.1007/s00210-008-0318-3
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Denbinobin induces apoptosis by apoptosis-inducing factor releasing and DNA damage in human colorectal cancer HCT-116 cells.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2008, v. 378, n. 5, p. 447, doi. 10.1007/s00210-008-0324-5
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- Article