Priestley T - Search Results

1

Long-term potentiation is increased in the CA1 area of the hippocampus of APP(swe/ind) CRND8 mice.

Jolas T, Zhang XS, Zhang Q, Wong G, Del Vecchio R, Gold L, Priestley T. Jolas T, et al. Among authors: priestley t. Neurobiol Dis. 2002 Dec;11(3):394-409. doi: 10.1006/nbdi.2002.0557. Neurobiol Dis. 2002. PMID: 12586549

2

Characterization of a hERG screen using the IonWorks HT: comparison to a hERG rubidium efflux screen.

Sorota S, Zhang XS, Margulis M, Tucker K, Priestley T. Sorota S, et al. Among authors: priestley t. Assay Drug Dev Technol. 2005 Feb;3(1):47-57. doi: 10.1089/adt.2005.3.47. Assay Drug Dev Technol. 2005. PMID: 15798395

3

Structural determinants for histamine H(1) affinity, hERG affinity and QTc prolongation in a series of terfenadine analogs.

Aslanian R, Piwinski JJ, Zhu X, Priestley T, Sorota S, Du XY, Zhang XS, McLeod RL, West RE, Williams SM, Hey JA. Aslanian R, et al. Among authors: priestley t. Bioorg Med Chem Lett. 2009 Sep 1;19(17):5043-7. doi: 10.1016/j.bmcl.2009.07.047. Epub 2009 Aug 5. Bioorg Med Chem Lett. 2009. PMID: 19660947

4

Activation of spinal ORL-1 receptors prevents acute cutaneous neurogenic inflammation: role of nociceptin-induced suppression of primary afferent depolarization.

Dong XW, Williams PA, Jia YP, Priestley T. Dong XW, et al. Among authors: priestley t. Pain. 2002 Apr;96(3):309-318. doi: 10.1016/S0304-3959(01)00460-2. Pain. 2002. PMID: 11973003

5

Vinpocetine is a potent blocker of rat NaV1.8 tetrodotoxin-resistant sodium channels.

Zhou X, Dong XW, Crona J, Maguire M, Priestley T. Zhou X, et al. Among authors: priestley t. J Pharmacol Exp Ther. 2003 Aug;306(2):498-504. doi: 10.1124/jpet.103.051086. Epub 2003 May 1. J Pharmacol Exp Ther. 2003. PMID: 12730276

6

T-type calcium channel blockers: spiro-piperidine azetidines and azetidinones-optimization, design and synthesis.

Smith EM, Sorota S, Kim HM, McKittrick BA, Nechuta TL, Bennett C, Knutson C, Burnett DA, Kieselgof J, Tan Z, Rindgen D, Bridal T, Zhou X, Jia YP, Dong Z, Mullins D, Zhang X, Priestley T, Correll CC, Tulshian D, Czarniecki M, Greenlee WJ. Smith EM, et al. Among authors: priestley t. Bioorg Med Chem Lett. 2010 Aug 1;20(15):4602-6. doi: 10.1016/j.bmcl.2010.06.012. Epub 2010 Jun 8. Bioorg Med Chem Lett. 2010. PMID: 20580233

7

Nociceptin/orphanin FQ inhibits capsaicin-induced guinea-pig airway contraction through an inward-rectifier potassium channel.

Jia Y, Wang X, Aponte SI, Rivelli MA, Yang R, Rizzo CA, Corboz MR, Priestley T, Hey JA. Jia Y, et al. Among authors: priestley t. Br J Pharmacol. 2002 Feb;135(3):764-70. doi: 10.1038/sj.bjp.0704515. Br J Pharmacol. 2002. PMID: 11834624 Free PMC article.

8

Tetrahydroquinoline sulfonamides as vasopressin 1b receptor antagonists.

Scott JD, Miller MW, Li SW, Lin SI, Vaccaro HA, Hong L, Mullins DE, Guzzi M, Weinstein J, Hodgson RA, Varty GB, Stamford AW, Chan TY, McKittrick BA, Greenlee WJ, Priestley T, Parker EM. Scott JD, et al. Among authors: priestley t. Bioorg Med Chem Lett. 2009 Nov 1;19(21):6018-22. doi: 10.1016/j.bmcl.2009.09.050. Epub 2009 Sep 17. Bioorg Med Chem Lett. 2009. PMID: 19800231

9

Discovery and characterization of vicriviroc (SCH 417690), a CCR5 antagonist with potent activity against human immunodeficiency virus type 1.

Strizki JM, Tremblay C, Xu S, Wojcik L, Wagner N, Gonsiorek W, Hipkin RW, Chou CC, Pugliese-Sivo C, Xiao Y, Tagat JR, Cox K, Priestley T, Sorota S, Huang W, Hirsch M, Reyes GR, Baroudy BM. Strizki JM, et al. Among authors: priestley t. Antimicrob Agents Chemother. 2005 Dec;49(12):4911-9. doi: 10.1128/AAC.49.12.4911-4919.2005. Antimicrob Agents Chemother. 2005. PMID: 16304152 Free PMC article.

10

Protein binding-dependent decreases in hERG channel blocker potency assessed by whole-cell voltage clamp in serum.

Margulis M, Sorota S, Chu I, Soares A, Priestley T, Nomeir AA. Margulis M, et al. Among authors: priestley t. J Cardiovasc Pharmacol. 2010 Apr;55(4):368-76. doi: 10.1097/FJC.0b013e3181d2ce39. J Cardiovasc Pharmacol. 2010. PMID: 20125032

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