Pharmacogenetics of new analgesics
Pregnane X receptor- and CYP3A4 -humanized mouse models and their applications
Pharmacological modulation of connexin-formed channels in cardiac pathophysiology
T-type voltage-gated calcium channels as targets for the development of novel pain therapies
Cardiac ion channel modulation by the hypoglycaemic agent rosiglitazone
Effects of rosiglitazone on the configuration of action potentials and ion currents in canine ventricular cells
Rosiglitazone inhibits Kv4.3 potassium channels by open-channel block and acceleration of closed-state inactivation
Formoterol and salmeterol induce a similar degree of β2-adrenoceptor tolerance in human small airways but via different mechanisms
The Rho kinase inhibitor Fasudil up-regulates astrocytic glutamate transport subsequent to actin remodelling in murine cultured astrocytes
Double-transfected MDCK cells expressing human OCT1/MATE1 or OCT2/MATE1: determinants of uptake and transcellular translocation of organic cations
PPARδ agonists have opposing effects on insulin resistance in high fat-fed rats and mice due to different metabolic responses in muscle
The anti-tumour compound, RH1, causes mitochondria-mediated apoptosis by activating c-Jun N-terminal kinase
Honokiol ameliorates renal fibrosis by inhibiting extracellular matrix and pro-inflammatory factors in vivo and in vitro
Hesperedin promotes MyoD-induced myogenic differentiation in vitro and in vivo
PPARα mediates the anti-inflammatory effect of simvastatin in an experimental model of zymosan-induced multiple organ failure
δ-Opioid receptors stimulate GLUT1-mediated glucose uptake through Src- and IGF-1 receptor-dependent activation of PI3-kinase signalling in CHO cells
Contribution of Rho-kinase to membrane excitability of murine colonic smooth muscle
Cigarette smoke and α,β-unsaturated aldehydes elicit VEGF release through the p38 MAPK pathway in human airway smooth muscle cells and lung fibroblasts
Effect of verapamil on the action of methanethiosulfonate reagents on human voltage-gated Kv1.3 channels: implications for the C-type inactivated state