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Journal of Neurology, Neurosurgery, and Psychiatry|March 26, 2011
Dissecting the Gilles de la Tourette spectrum: a factor analytic study on 639 patientsAndrea E Cavanna, Hugo D Critchley, Michael Orth, et al.Journal of Prosthodontics : Official Journal of the American College of Prosthodontists|February 2, 2010
Reducing the incidence of denture stomatitis: are denture cleansers sufficient?Anto Jose, Brent J Coco, Steven Milligan, et al.Bioorganic & Medicinal Chemistry Letters|May 6, 2008
The discovery of fused pyrrole carboxylic acids as novel, potent D-amino acid oxidase (DAO) inhibitorsTim Sparey, Pravien Abeywickrema, Sarah Almond, et al.Bioorganic & Medicinal Chemistry Letters|August 28, 2003
Discovery and evaluation of 3-(5-thien-3-ylpyridin-3-yl)-1H-indoles as a novel class of KDR kinase inhibitorsMark E Fraley, Kenneth L Arrington, Scott R Hambaugh, et al.The Journal of Pharmacology and Experimental Therapeutics|December 18, 2008
The behavioral and neurochemical effects of a novel D-amino acid oxidase inhibitor compound 8 [4H-thieno [3,2-b]pyrrole-5-carboxylic acid] and D-serineSean M Smith, Jason M Uslaner, Lihang Yao, et al.Journal of Medicinal Chemistry|December 8, 2006
Discovery of oxadiazoyl tertiary carbinamine inhibitors of beta-secretase (BACE-1)Hemaka A Rajapakse, Philippe G Nantermet, Harold G Selnick, et al.Journal of Medicinal Chemistry|November 4, 2009
Biaryl ethers as novel non-nucleoside reverse transcriptase inhibitors with improved potency against key mutant virusesDai-Shi Su, John J Lim, Elizabeth Tinney, et al.Bioorganic & Medicinal Chemistry Letters|May 8, 2007
Design, synthesis, and SAR of macrocyclic tertiary carbinamine BACE-1 inhibitorsStacey R Lindsley, Keith P Moore, Hemaka A Rajapakse, et al.Bioorganic & Medicinal Chemistry Letters|July 28, 2009
Substituted tetrahydroquinolines as potent allosteric inhibitors of reverse transcriptase and its key mutantsDai-Shi Su, John J Lim, Elizabeth Tinney, et al.Bioorganic & Medicinal Chemistry Letters|July 9, 2010
Biaryl ethers as potent allosteric inhibitors of reverse transcriptase and its key mutant viruses: aryl substituted pyrazole as a surrogate for the pyrazolopyridine motifDai-Shi Su, John J Lim, Elizabeth Tinney, et al.Pageof 4