Results 131 to 140 of about 10,364 (172)
Expression Dynamics of Neurotransmitter System Genes in Early Sea Urchin Embryos: Insights from a Four-Species Comparative Transcriptome Analysis. [PDF]
Shmukler YB +3 more
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The relaxant effect of the extract of <i>Crocus sativus</i> petal on Wistar rats airway smooth muscle and its possible mechanisms. [PDF]
Behrouz S +4 more
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Diagnostic workup in paradoxical urticaria induced by H1-antihistamines. [PDF]
Xiang YK, Kocatürk E.
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Effects of Haloperidol on Cardiac Histamine H<sub>2</sub> Receptors and β-Adrenoceptors in Isolated Mouse and Human Atrial Preparations. [PDF]
Schlicht JMA +4 more
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TRPV4 Promotes Histamine Receptor Signaling in Lymphatic Endothelial Cells
Retamal JS +11 more
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Developments in histamine H1-receptor agonists
1995The story of histamine started in the early 1900’s with the fundamental investigations of Dale et al. [l–3], which recognized the remarkable physiological behavior of this biogenic amine. Scientific progress over the past decades has proved that histamine interacts with specific histamine receptors as a neurotransmitter and nearly all mammalian tissues
V, Zingel, C, Leschke, W, Schunack
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Domain Swapping in the Human Histamine H1 Receptor
The Journal of Pharmacology and Experimental Therapeutics, 2004G-protein-coupled receptors (GPCRs) represent the largest family of receptors involved in transmembrane signaling. Although these receptors were generally believed to be monomeric entities, accumulating evidence supports the presence of GPCRs in multimeric forms.
Bakker, R.A. +7 more
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Agents and Actions, 1985
We have shown that [3H]mepyramine labels histamine H1-receptor-binding sites in bovine aortic membranes. Further characterization of H1-receptors in this tissue was done by the interaction of an unlabelled histamine receptor agonist or antagonist, with the radioantagonist [3H]mepyramine-binding sites.
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We have shown that [3H]mepyramine labels histamine H1-receptor-binding sites in bovine aortic membranes. Further characterization of H1-receptors in this tissue was done by the interaction of an unlabelled histamine receptor agonist or antagonist, with the radioantagonist [3H]mepyramine-binding sites.
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