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Pharmacological characterization of five cloned voltage-gated K+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably expressed in mammalian cell lines.
Molecular Pharmacology · 1994 · Vol. 45(6) · pp. 1227–1234
Stephan Grissmer✉(University of California, Irvine)A. N. Nguyen(University of California, Irvine)Jayashree Aiyar(University of California, Irvine)Douglas C. Hanson(University of California, Irvine)Robert J. Mather(University of California, Irvine)George A. Gutman(University of California, Irvine)Michael J. Karmilowicz(University of California, Irvine)D. D. Auperin(University of California, Irvine)K. George Chandy(University of California, Irvine)
Ion channel regulation and functionNicotinic Acetylcholine Receptors StudyCharybdotoxinCromakalimChemistryResiniferatoxinIon channelElectrophysiologyCell culturePotassium channelPharmacologyMembrane potential
MeSH terms
AnimalsBase SequenceBenzopyransCapsaicinCell LineCells, CulturedCloning, MolecularDiltiazemDiterpenesElapid VenomsFlecainideMolecular Sequence DataNifedipineOligodeoxyribonucleotidesPeptides
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