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Structure of the catalytic domain of human polo-like kinase 1.
Biochemistry. 2007 May 22;46(20):5960-71. doi: 10.1021/bi602474j. Epub 2007 Apr 27.
Biochemistry. 2007.
PMID: 17461553
Inhibition of IL-1beta-dependent prostaglandin E2 release by antisense microsomal prostaglandin E synthase 1 oligonucleotides in A549 cells.
Sweeney FJ, Wachtmann TS, Eskra JD, Verdries KA, Lambalot RH, Carty TJ, Perez JR, Audoly LP.
Sweeney FJ, et al. Among authors: verdries ka.
Mol Cell Endocrinol. 2003 Jul 31;205(1-2):151-7. doi: 10.1016/s0303-7207(03)00091-1.
Mol Cell Endocrinol. 2003.
PMID: 12890577
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A new class of selective and potent inhibitors of neuronal nitric oxide synthase.
Lowe JA 3rd, Qian W, Volkmann RA, Heck S, Nowakowski J, Nelson R, Nolan C, Liston D, Ward K, Zorn S, Johnson C, Vanase M, Faraci WS, Verdries KA, Baxter J, Doran S, Sanders M, Ashton M, Whittle P, Stefaniak M.
Lowe JA 3rd, et al. Among authors: verdries ka.
Bioorg Med Chem Lett. 1999 Sep 6;9(17):2569-72. doi: 10.1016/s0960-894x(99)00432-1.
Bioorg Med Chem Lett. 1999.
PMID: 10498210
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UK-78,282, a novel piperidine compound that potently blocks the Kv1.3 voltage-gated potassium channel and inhibits human T cell activation.
Hanson DC, Nguyen A, Mather RJ, Rauer H, Koch K, Burgess LE, Rizzi JP, Donovan CB, Bruns MJ, Canniff PC, Cunningham AC, Verdries KA, Mena E, Kath JC, Gutman GA, Cahalan MD, Grissmer S, Chandy KG.
Hanson DC, et al. Among authors: verdries ka.
Br J Pharmacol. 1999 Apr;126(8):1707-16. doi: 10.1038/sj.bjp.0702480.
Br J Pharmacol. 1999.
PMID: 10372812
Free PMC article.
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2-Amino-4-methylpyridine as a potent inhibitor of inducible NO synthase activity in vitro and in vivo.
Faraci WS, Nagel AA, Verdries KA, Vincent LA, Xu H, Nichols LE, Labasi JM, Salter ED, Pettipher ER.
Faraci WS, et al. Among authors: verdries ka.
Br J Pharmacol. 1996 Nov;119(6):1101-8. doi: 10.1111/j.1476-5381.1996.tb16010.x.
Br J Pharmacol. 1996.
PMID: 8937711
Free PMC article.
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