Search Results - "Aluisio, L"
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Histamine H3 receptor antagonists: from target identification to drug leads
Published in Biochemical pharmacology (15-04-2007)“…The successful cloning and functional expression of the histamine H(3) receptor in the late 1990 s has greatly facilitated our efforts to identify small…”
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Acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H 3 antagonist
Published in British journal of pharmacology (17-02-2009)“…1‐[4‐(3‐piperidin‐1‐yl‐propoxy)‐benzyl]‐piperidine (JNJ‐5207852) is a novel, non‐imidazole histamine H 3 receptor antagonist, with high affinity at the rat (p…”
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Image Gallery: A case of cutaneous giant angiosarcoma treated successfully with electrochemotherapy
Published in British journal of dermatology (1951) (01-08-2017)Get full text
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Acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H3 antagonist
Published in British journal of pharmacology (01-11-2004)“…1‐[4‐(3‐piperidin‐1‐yl‐propoxy)‐benzyl]‐piperidine (JNJ‐5207852) is a novel, non‐imidazole histamine H3 receptor antagonist, with high affinity at the rat…”
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P.033 Managing esketamine treatment frequency toward successful outcomes: Analysis of phase 3 data
Published in European neuropsychopharmacology (01-12-2019)Get full text
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P.327 Withdrawal symptom assessment in an esketamine safety study in patients with treatment-resistant depression
Published in European neuropsychopharmacology (01-12-2019)Get full text
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Histamine H 3 receptor antagonists: From target identification to drug leads
Published in Biochemical pharmacology (15-04-2007)“…The successful cloning and functional expression of the histamine H 3 receptor in the late 1990s has greatly facilitated our efforts to identify small…”
Get full text
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Pharmacokinetics and pharmacodynamics of norfluoxetine in rats: Increasing extracellular serotonin level in the frontal cortex
Published in Pharmacology, biochemistry and behavior (01-05-2009)“…Norfluoxetine is the most important active metabolite of the widely used antidepressant fluoxetine. Although the pharmacokinetics/pharmacodynamics (PK/PD)…”
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Corrigendum to acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H 3 antagonist
Published in British journal of pharmacology (29-01-2009)Get full text
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Corrigendum to acute wake‐promoting actions of JNJ‐5207852, a novel, diamine‐based H3 antagonist
Published in British journal of pharmacology (01-01-2005)Get full text
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Novel substituted 4-phenyl-[1,3]dioxanes: potent and selective orexin receptor 2 (OX 2R) antagonists
Published in Bioorganic & medicinal chemistry letters (16-08-2004)“…A series of novel, selective orexin receptor 2 antagonists consisting of substituted 4-phenyl-[1,3]dioxanes is reported (e.g. 9). Orexins, also termed…”
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