State-Dependent Compound Inhibition of Nav1.2 Sodium Channels Using the FLIPR Vm Dye: On-Target and Off-Target Effects of Diverse Pharmacological Agents

This publication has 39 references indexed in Scilit:

• V102862 (Co 102862): a potent, broad-spectrum state-dependent blocker of mammalian voltage-gated sodium channels
  British Journal of Pharmacology, 2005
• Phenoxyphenyl Pyridines as Novel State-Dependent, High-Potency Sodium Channel Inhibitors
  Journal of Medicinal Chemistry, 2004
• Comparison of the Pharmacological Properties of Rat NaV1.8 with Rat NaV1.2a and Human NaV1.5 Voltage-Gated Sodium Channel Subtypes Using a Membrane Potential Sensitive Dye and FLIPRR
  Receptors and Channels, 2004
• Sodium Channel β Subunits: Anything but Auxiliary
  The Neuroscientist, 2001
• From Ionic Currents to Molecular Mechanisms
  Published by Elsevier ,2000
• New class of potent ligands for the human peripheral cannabinoid receptor
  Bioorganic & Medicinal Chemistry Letters, 1996
• Identification of a mutation in the gene causing hyperkalemic periodic paralysis
  Cell, 1991
• Molecular Mechanisms of Local Anesthesia
  Anesthesiology, 1990
• [14C]Guanidinium ion influx into Na+ channel preparations from mouse cerebral cortex
  European Journal of Pharmacology: Molecular Pharmacology, 1990
• Antiarrhythmic Agents: The Modulated Receptor Mechanism of Action of Sodium and Calcium Channel-Blocking Drugs
  Annual Review of Pharmacology and Toxicology, 1984