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Annals of Neurology|June 10, 2019
A functional substitution in the L-aromatic amino acid decarboxylase enzyme worsens somatic symptoms via a serotonergic pathwaySamar Khoury, Marjo H Piltonen, Anh-Tien Ton, et al.
Transfusion Medicine (Oxford, England)|September 6, 2000
Effect of premedication guidelines and leukoreduction on the rate of febrile nonhaemolytic platelet transfusion reactionsB J Patterson, J Freedman, V Blanchette, et al.
Bioorganic & Medicinal Chemistry Letters|November 1, 2003
N-arylaminonitriles as bioavailable peptidomimetic inhibitors of cathepsin BPaul D Greenspan, Kirk L Clark, Scott D Cowen, et al.
The Journal of Pain|November 27, 2013
Study protocol, sample characteristics, and loss to follow-up: the OPPERA prospective cohort studyEric Bair, Naomi C Brownstein, Richard Ohrbach, et al.
Journal of Medicinal Chemistry|January 15, 1999
Carboxy-substituted cinnamides: a novel series of potent, orally active LTB4 receptor antagonistsP D Greenspan, R A Fujimoto, P J Marshall, et al.
Pain|December 1, 2020
Phenotypic profile clustering pragmatically identifies diagnostically and mechanistically informative subgroups of chronic pain patientsSheila M Gaynor, Andrey Bortsov, Eric Bair, et al.
The Journal of Pain|November 15, 2011
Study methods, recruitment, sociodemographic findings, and demographic representativeness in the OPPERA studyGary D Slade, Eric Bair, Kunthel By, et al.
Pain|July 25, 2015
COMT gene locus: new functional variantsCarolina B Meloto, Samantha K Segall, Shad Smith, et al.
Bioorganic & Medicinal Chemistry Letters|January 26, 2016
Optimization of tetrahydronaphthalene inhibitors of Raf with selectivity over hERGShih-Chung Huang, Sharmila Adhikari, Roushan Afroze, et al.
Journal of Medicinal Chemistry|December 14, 2001
Identification of dipeptidyl nitriles as potent and selective inhibitors of cathepsin B through structure-based drug designP D Greenspan, K L Clark, R A Tommasi, et al.
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