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Angiotensin II-mediated calcium signals and mitogenesis in human prostate stromal cell line hPCPs
Pharmacological characterization of ligand–receptor interactions at the zebrafish bradykinin receptor
Antimony-induced cardiomyopathy in guinea-pig and protection by L-carnitine
Substrate specificity and functional characterisation of the H+/amino acid transporter rat PAT2 (Slc36a2)
Falcarindiol impairs the expression of inducible nitric oxide synthase by abrogating the activation of IKK and JAK in rat primary astrocytes
Modulation of voltage-gated channel currents by harmaline and harmane
Contrasting anesthetic sensitivities of T-type Ca2+ channels of reticular thalamic neurons and recombinant Cav3.3 channels
Acute impairment of contractile responses by 17 β -estradiol is cAMP and protein kinase G dependent in vascular smooth muscle cells of the porcine coronary arteries
Pharmacodynamics and pharmacokinetics of SQ109, a new diamine-based antitubercular drug
The acetylcholinesterase inhibitor BW284c51 is a potent blocker of Torpedo nicotinic AchRs incorporated into the Xenopus oocyte membrane
Intravenous anaesthetics inhibit nicotinic acetylcholine receptor-mediated currents and Ca2+ transients in rat intracardiac ganglion neurons
Connexin-mimetic peptides dissociate electrotonic EDHF-type signalling via myoendothelial and smooth muscle gap junctions in the rabbit iliac artery
Positron emission tomography using 18F-labelled endothelin-1 reveals prevention of binding to cardiac receptors owing to tissue-specific clearance by ETB receptors in vivo
The noble gas xenon induces pharmacological preconditioning in the rat heart in vivo via induction of PKC- ε and p38 MAPK
Prevention of progressive joint destruction in collagen-induced arthritis in rats by a novel matrix metalloproteinase inhibitor, FR255031
Intravenous anaesthetics inhibit nicotinic acetylcholine receptor-mediated currents and Ca2+ transients in rat intracardiac ganglion neurons
Corrigendum to acute wake-promoting actions of JNJ-5207852, a novel, diamine-based H3 antagonist