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Year | Number of Results |
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1999 | 2 |
2006 | 1 |
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2011 | 2 |
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Page 1
Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH Inhibitor.
ACS Med Chem Lett. 2011 Feb 10;2(2):91-96. doi: 10.1021/ml100190t.
ACS Med Chem Lett. 2011.
PMID: 21666860
Free PMC article.
Mechanistic and pharmacological characterization of PF-04457845: a highly potent and selective fatty acid amide hydrolase inhibitor that reduces inflammatory and noninflammatory pain.
Ahn K, Smith SE, Liimatta MB, Beidler D, Sadagopan N, Dudley DT, Young T, Wren P, Zhang Y, Swaney S, Van Becelaere K, Blankman JL, Nomura DK, Bhattachar SN, Stiff C, Nomanbhoy TK, Weerapana E, Johnson DS, Cravatt BF.
Ahn K, et al. Among authors: liimatta mb.
J Pharmacol Exp Ther. 2011 Jul;338(1):114-24. doi: 10.1124/jpet.111.180257. Epub 2011 Apr 19.
J Pharmacol Exp Ther. 2011.
PMID: 21505060
Free PMC article.
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Down-regulation of protein kinase C inhibits insulin-like growth factor I-induced vascular smooth muscle cell proliferation, migration, and gene expression.
Yano K, Bauchat JR, Liimatta MB, Clemmons DR, Duan C.
Yano K, et al. Among authors: liimatta mb.
Endocrinology. 1999 Oct;140(10):4622-32. doi: 10.1210/endo.140.10.7035.
Endocrinology. 1999.
PMID: 10499519
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Insulin-like growth factor (IGF)-I regulates IGF-binding protein-5 gene expression through the phosphatidylinositol 3-kinase, protein kinase B/Akt, and p70 S6 kinase signaling pathway.
Duan C, Liimatta MB, Bottum OL.
Duan C, et al. Among authors: liimatta mb.
J Biol Chem. 1999 Dec 24;274(52):37147-53. doi: 10.1074/jbc.274.52.37147.
J Biol Chem. 1999.
PMID: 10601276
Free article.
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Design and synthesis of phenethyl benzo[1,4]oxazine-3-ones as potent inhibitors of PI3Kinasegamma.
Lanni TB Jr, Greene KL, Kolz CN, Para KS, Visnick M, Mobley JL, Dudley DT, Baginski TJ, Liimatta MB.
Lanni TB Jr, et al. Among authors: liimatta mb.
Bioorg Med Chem Lett. 2007 Feb 1;17(3):756-60. doi: 10.1016/j.bmcl.2006.10.080. Epub 2006 Oct 28.
Bioorg Med Chem Lett. 2007.
PMID: 17095227
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