Managing risks in drug discovery: reproducibility of published findingsCommon misconceptions about data analysis and statisticsGef10--the third member of a Rho-specific guanine nucleotide exchange factor subfamily with unusual protein architectureTransmembrane water influx via aquaporin-1 is inhibited by barbiturates and propofol in red blood cellsPharmacological characterization of mitogen-activated protein kinase activation by recombinant human 5-HT2C, 5-HT2A, and 5-HT2B receptorsPharmacological treatment options for mast cell activation diseaseTRPA1 as a drug target--promise and challengesUnderstanding protein kinase CK2 mis-regulation upon F508del CFTR expressionThe deamination of dopamine by human brain monoamine oxidase. Specificity for the two enzyme forms in seven brain regions.Cholecystokinin (CCK) increases GABA release in the rat anterior nucleus accumbens via CCK(B) receptors located on glutamatergic interneuronsAspirin, but not the more selective cyclooxygenase (COX)-2 inhibitors meloxicam and SC 58125, aggravates postischaemic cardiac dysfunction, independent of COX functionComparison of a cloned ANF-sensitive guanylate cyclase (GC-A) with particulate guanylate cyclase from adrenal cortexEvidence for a short form of RGS3 preferentially expressed in the human heartThe influences of temperature and naloxone on the antinociceptive activity of Corchorus olitorius L. in miceEffect of aspirin on prostanoids and nitric oxide production in streptozotocin-diabetic rats with ischemic retinopathyProtective effect of triflusal and its main metabolite HTB in an in vitro model of anoxia-reoxygenation in rat brain slices: comparison with acetylsalicylic and salicylic acidsNociceptin receptor antagonists display antidepressant-like properties in the mouse forced swimming testThe Frizzled-1/(beta(2))-adrenergic receptor chimera: pharmacological properties of a unique G protein-linked receptorA role for cyclooxygenase in aging-related changes of beta-adrenoceptor-mediated relaxation in rat aortasChlorophenylpiperazine: a central serotonin agonist causing powerful anorexia in rats[3H]LY334370, a novel radioligand for the 5-HT1F receptor. I. In vitro characterization of binding propertiesp63RhoGEF and GEFT are Rho-specific guanine nucleotide exchange factors encoded by the same geneNeurotoxicity of apamin and MCD peptide upon central applicationInhibition of voltage-gated calcium currents in type II vestibular hair cells by cinnarizinePharmacological modulation of transmitter release by inhibition of pressure-dependent potassium currents in vestibular hair cellsInvestigation of the influence of lithium upon the down-regulation of serotonin2 receptors in rat frontal cortex induced by long-term treatment with dibenzepin, an antidepressant without appreciable affinity to serotonin2 receptorsAntidepressant-like effects of the nociceptin/orphanin FQ receptor antagonist UFP-101: new evidence from rats and miceBIMT 17, a 5-HT2A receptor antagonist and 5-HT1A receptor full agonist in rat cerebral cortexStudy of a mechanism responsible for potential antidepressant activity of EMD 386088, a 5-HT6 partial agonist in ratsDirect labelling of myocardial beta 1-adrenoceptors. Comparison of binding affinity of 3H-(-)-bisoprolol with its blocking potencyStudies on lung N-methyltransferases, a pharmacological approachComparison of the effects of eleven histamine H1-receptor antagonists on monoamine turnover in the mouse brainEvidence for a displaceable non-specific [3H]neurotensin binding site in rat brainThe in vitro receptor profile of rotigotine: a new agent for the treatment of Parkinson's diseaseIvabradine in patients with inappropriate sinus tachycardiaBlock of wild-type and inactivation-deficient human ether-a-go-go-related gene K+ channels by halofantrine5-Methoxytryptamine and 2-methyl-5-hydroxytryptamine-induced desensitization as a discriminative tool for the 5-HT3 and putative 5-HT4 receptors in guinea pig ileumCannabidiol is an allosteric modulator at mu- and delta-opioid receptorsTianeptine, a selective enhancer of serotonin uptake in rat brainClass Ia anti-arrhythmic drug ajmaline blocks HERG potassium channels: mode of action
P1433
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P1433
description
Wissenschaftliche Fachzeitschrift
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revista científica
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revue scientifique
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rivista scientifica
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scientific journal
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vědecký časopis
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wetenschappelijk tijdschrift van Springer Science+Business Media
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науковий журнал
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مجلة
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वैज्ञानिक पत्रिका
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
@fi
Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
@it
Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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Naunyn-Schmiedeberg's Archives of Pharmacology
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1873-01-01T00:00:00Z