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Archives of Biochemistry and Biophysics|April 20, 2006
Effect of construct design on MAPKAP kinase-2 activity, thermodynamic stability and ligand-binding affinityJukka Kervinen, Hongchang Ma, Shariff Bayoumy, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 2017
Methylprednisolone acetate induces, and Δ7-dafachronic acid suppresses, <i>Strongyloides stercoralis</i> hyperinfection in NSG miceJohn B Patton, Sandra Bonne-Année, Jessica Deckman, et al.
American Journal of Human Genetics|February 20, 2021
Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significanceMarcy E Richardson, Chunling Hu, Kun Y Lee, et al.
Biochemistry|April 26, 2006
Dihydroquinone ansamycins: toward resolving the conflict between low in vitro affinity and high cellular potency of geldanamycin derivativesAnna C Maroney, Juan J Marugan, Tara M Mezzasalma, et al.
Journal of Personality Assessment|June 10, 2015
The Brief Aggression Questionnaire: Structure, Validity, Reliability, and GeneralizabilityGregory D Webster, C Nathan DeWall, Richard S Pond, et al.
Bioorganic & Medicinal Chemistry Letters|May 30, 2001
Structure-based design, synthesis and SAR of a novel series of thiopheneamidine urokinase plasminogen activator inhibitorsN L Subasinghe, C Illig, J Hoffman, et al.
Aggressive Behavior|October 12, 2013
The brief aggression questionnaire: psychometric and behavioral evidence for an efficient measure of trait aggressionGregory D Webster, C Nathan Dewall, Richard S Pond, et al.
Bioorganic & Medicinal Chemistry Letters|October 21, 2005
Discovery, SAR, and X-ray structure of novel biaryl-based dipeptidyl peptidase IV inhibitorsLei Qiao, Christian A Baumann, Carl S Crysler, et al.
Bioorganic & Medicinal Chemistry Letters|January 30, 2002
Design and synthesis of 4,5-disubstituted-thiophene-2-amidines as potent urokinase inhibitorsM Jonathan Rudolph, Carl R Illig, Nalin L Subasinghe, et al.
Protein Science : a Publication of the Protein Society|February 11, 2011
Crystal structure of a soluble form of human monoglyceride lipase in complex with an inhibitor at 1.35 Å resolutionCéline Schalk-Hihi, Carsten Schubert, Richard Alexander, et al.
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