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Distribution and functional properties of human KCNH8 (Elk1) potassium channels.
Zou A, Lin Z, Humble M, Creech CD, Wagoner PK, Krafte D, Jegla TJ, Wickenden AD. Zou A, et al. Among authors: wickenden ad. Am J Physiol Cell Physiol. 2003 Dec;285(6):C1356-66. doi: 10.1152/ajpcell.00179.2003. Epub 2003 Jul 30. Am J Physiol Cell Physiol. 2003. PMID: 12890647 Free article.
Aryl sulfonamido tetralin inhibitors of the Kv1.5 ion channel.
Gross MF, Castle NA, Zou A, Wickenden AD, Yu W, Spear KL. Gross MF, et al. Among authors: wickenden ad. Bioorg Med Chem Lett. 2009 Jun 1;19(11):3063-6. doi: 10.1016/j.bmcl.2009.04.002. Epub 2009 Apr 8. Bioorg Med Chem Lett. 2009. PMID: 19398199
K(+) channels as therapeutic drug targets.
Wickenden A. Wickenden A. Pharmacol Ther. 2002 Apr-May;94(1-2):157-82. doi: 10.1016/s0163-7258(02)00201-2. Pharmacol Ther. 2002. PMID: 12191600 Review.
In vivo profile of ICA-27243 [N-(6-chloro-pyridin-3-yl)-3,4-difluoro-benzamide], a potent and selective KCNQ2/Q3 (Kv7.2/Kv7.3) activator in rodent anticonvulsant models.
Roeloffs R, Wickenden AD, Crean C, Werness S, McNaughton-Smith G, Stables J, McNamara JO, Ghodadra N, Rigdon GC. Roeloffs R, et al. Among authors: wickenden ad. J Pharmacol Exp Ther. 2008 Sep;326(3):818-28. doi: 10.1124/jpet.108.137794. Epub 2008 Jun 24. J Pharmacol Exp Ther. 2008. PMID: 18577704
71 results