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British Journal of Pharmacology|January 29, 2005
SEA0400, a specific inhibitor of the Na+-Ca2+ exchanger, attenuates sodium nitroprusside-induced apoptosis in cultured rat microgliaTakayuki Nagano, Masakazu Osakada, Yukio Ago, et al.
British Journal of Pharmacology|January 29, 2005
Vasomotion: cellular background for the oscillator and for the synchronization of smooth muscle cellsChristian Aalkjaer, Holger Nilsson
British Journal of Pharmacology|January 29, 2005
Studies using isolated uterine and other preparations show bimatoprost and prostanoid FP agonists have different activity profilesJune Chen, Judith Senior, Kay Marshall, et al.
British Journal of Pharmacology|January 29, 2005
AT(2) receptors mediate tonic renal medullary vasoconstriction in renovascular hypertensionLisa M Duke, Robert E Widdop, Michelle M Kett, et al.
British Journal of Pharmacology|February 3, 2005
Antihyperalgesic activity of a novel nonpeptide bradykinin B1 receptor antagonist in transgenic mice expressing the human B1 receptorAlyson Fox, Satbir Kaur, Bifang Li, et al.
British Journal of Pharmacology|February 3, 2005
Pharmacological characterisation of the adenosine receptor mediating increased ion transport in the mouse isolated trachea and the effect of allergen challengeKristin N Kornerup, Clive P Page, James D Moffatt
British Journal of Pharmacology|February 3, 2005
Prenatal cocaine exposure increases apoptosis of neonatal rat heart and heart susceptibility to ischemia-reperfusion injury in 1-month-old ratSoochan Bae, Lubo Zhang
British Journal of Pharmacology|February 3, 2005
Cardioprotective effect of an endothelin receptor antagonist during ischaemia/reperfusion in the severely atherosclerotic mouse heartAdrian T Gonon, Alexander Bulhak, Anders Bröijersén, et al.
British Journal of Pharmacology|February 3, 2005
An electrophysiological study of excitatory purinergic neuromuscular transmission in longitudinal smooth muscle of chicken anterior mesenteric arteryMaisa Khalifa, AbuBakr El-Mahmoudy, Takahiko Shiina, et al.
British Journal of Pharmacology|February 3, 2005
Inhibition of the human two-pore domain potassium channel, TREK-1, by fluoxetine and its metabolite norfluoxetineLouise E Kennard, Justin R Chumbley, Kishani M Ranatunga, et al.
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