AAAAAA

   
Results: 1-3 |
Results: 3

Authors: Proudfoot, JR Betageri, R Cardozo, M Gilmore, TA Glynn, S Hickey, ER Jakes, S Kabcenell, A Kirrane, TM Tibolla, AK Lukas, S Patel, UR Sharma, R Yazdanian, M Moss, N Beaulieu, PL Cameron, DR Ferland, JM Gauthier, J Gillard, J Gorys, V Poirier, M Rancourt, J Wernic, D Llinas-Brunet, M
Citation: Jr. Proudfoot et al., Nonpeptidic, monocharged, cell permeable ligands for the p56lck SH2 domain, J MED CHEM, 44(15), 2001, pp. 2421-2431

Authors: Last-Barney, K Davidson, W Cardozo, M Frye, LL Grygon, CA Hopkins, JL Jeanfavre, DD Pav, S Qian, CG Stevenson, JM Tong, L Zindell, R Kelly, TA
Citation: K. Last-barney et al., Binding site elucidation of hydantoin-based antagonists of LFA-1 using multidisciplinary technologies: Evidence for the allosteric inhibition of a protein-protein interaction, J AM CHEM S, 123(24), 2001, pp. 5643-5650

Authors: Beaulieu, PL Cameron, DR Ferland, JM Gauthier, J Ghiro, E Gillard, J Gorys, V Poirier, M Rancourt, J Wernic, D Llinas-Brunet, M Betageri, R Cardozo, M Hickey, ER Ingraham, R Jakes, S Kabcenell, A Kirrane, T Lukas, S Patel, U Proudfoot, J Sharma, R Tong, L Moss, N
Citation: Pl. Beaulieu et al., Ligands for the tyrosine kinase p56(lck) SH2 domain: Discovery of potent dipeptide derivatives with monocharged, nonhydrolyzable phosphate replacements, J MED CHEM, 42(10), 1999, pp. 1757-1766
Risultati: 1-3 |