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Results: 1-12 |
Results: 12

Authors: Soni, R O'Reilly, T Furet, P Muller, L Stephan, C Zumstein-Mecker, S Fretz, H Fabbro, D Chaudhuri, B
Citation: R. Soni et al., Selective in vivo and in vitro effects of a small molecule inhibitor of cyclin-dependent kinase 4, J NAT CANC, 93(6), 2001, pp. 436

Authors: Hormann, A Chaudhuri, B Fretz, H
Citation: A. Hormann et al., DNA binding properties of the marine sponge pigment fascaplysin, BIO MED CH, 9(4), 2001, pp. 917-921

Authors: Furet, P Meyer, T Mittl, P Fretz, H
Citation: P. Furet et al., Identification of cylin-dependent kinase 1 inhibitors of a new chemical type by structure-based design and database searching, J COMPUT A, 15(5), 2001, pp. 489-495

Authors: Fretz, H Ucci-Stoll, K Hug, P Schoepfer, J Lang, M
Citation: H. Fretz et al., Investigations on the reactivity of fascaplysin - Part II - General stability considerations and products formed with nucleophiles, HELV CHIM A, 84(4), 2001, pp. 867-873

Authors: Fretz, H Furet, P Garcia-Echeverria, C Rahuel, J Schoepfer, J
Citation: H. Fretz et al., Structure-based design of compounds inhibiting Grb2-SH2 mediated protein-protein interactions in signal transduction pathways, CUR PHARM D, 6(18), 2000, pp. 1777-1796

Authors: Furet, P Caravatti, G Denholm, AA Faessler, A Fretz, H Garcia-Echeverria, C Gay, B Irving, E Press, NJ Rahuel, J Schoepfer, J Walker, CV
Citation: P. Furet et al., Structure-based design and synthesis of phosphinate isosteres of phosphotyrosine for incorporation in Grb2-SH2 domain inhibitors. Part 1, BIOORG MED, 10(20), 2000, pp. 2337-2341

Authors: Fretz, H Gaugler, M Schneider, J
Citation: H. Fretz et al., 3-(arylamino)quinolin-2(1H)- and -4(1H)-ones: Reinvestigation of the reaction between ethyl 2-chloro-3-(phenylamino)but-2-enoate and arylamines, HELV CHIM A, 83(6), 2000, pp. 1145-1150

Authors: Fretz, H Ucci-Stoll, K Hug, P Schoepfer, J Lang, M
Citation: H. Fretz et al., Investigations on the reactivity of fascaplysin - Part I - Aromatic electrophilic substitutions occur at position 9, HELV CHIM A, 83(11), 2000, pp. 3064-3068

Authors: Soni, R Muller, L Furet, P Schoepfer, J Stephan, C Zumstein-Mecker, S Fretz, H Chaudhuri, B
Citation: R. Soni et al., Inhibition of cyclin-dependent kinase 4 (Cdk4) by fascaplysin, a marine natural product, BIOC BIOP R, 275(3), 2000, pp. 877-884

Authors: Soni, R Fretz, H Muller, L Schoepfer, J Chaudhuri, B
Citation: R. Soni et al., Novel Cdk inhibitors restore TGF-beta sensitivity in Cdk4 overexpressing epithelial cells, BIOC BIOP R, 272(3), 2000, pp. 794-800

Authors: Schoepfer, J Fretz, H Gay, B Furet, P Garcia-Echeverria, C End, N Caravatti, G
Citation: J. Schoepfer et al., Highly potent inhibitors of the Grb2-SH2 domain, BIOORG MED, 9(2), 1999, pp. 221-226

Authors: Nordmann, A Blommers, MJJ Fretz, H Arvinte, T Drake, AF
Citation: A. Nordmann et al., Aspects of the molecular structure and dynamics of neuropeptide Y, EUR J BIOCH, 261(1), 1999, pp. 216-226
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