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Proceedings of the National Academy of Sciences of the United States of America|August 1, 1993
"Diversomers": an approach to nonpeptide, nonoligomeric chemical diversityS H DeWitt, J S Kiely, C J Stankovic, et al.Renal Failure|May 22, 2012
Influence of dialysis modality and membrane flux on quality of life in hemodialysis patientsMarinela Z Knezevic, Vladimir V Djordjevic, Radmila M Radovanovic-Velickovic, et al.Journal of Pharmaceutical Sciences|January 1, 2009
The development and validation of a computational model to predict rat liver microsomal clearanceCheng Chang, David B Duignan, Kjell D Johnson, et al.Drug Design and Discovery|April 1, 1996
Hydrophobic D-amino acids in the design of peptide ligands for the pp60src SH2 domainM S Plummer, E A Lunney, K S Para, et al.Bioorganic & Medicinal Chemistry Letters|October 10, 2001
Structure-based design of caspase-1 inhibitor containing a diphenyl ether sulfonamideA B Shahripour, M S Plummer, E A Lunney, et al.Bioorganic & Medicinal Chemistry Letters|April 16, 2013
Discovery of potent, selective, bioavailable phosphodiesterase 2 (PDE2) inhibitors active in an osteoarthritis pain model, part I: transformation of selective pyrazolodiazepinone phosphodiesterase 4 (PDE4) inhibitors into selective PDE2 inhibitorsMark S Plummer, Joseph Cornicelli, Howard Roark, et al.Bioorganic & Medicinal Chemistry Letters|April 20, 2013
Discovery of potent selective bioavailable phosphodiesterase 2 (PDE2) inhibitors active in an osteoarthritis pain model. Part II: optimization studies and demonstration of in vivo efficacyMark S Plummer, Joseph Cornicelli, Howard Roark, et al.Pageof 2