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Results: 1-13 |
Results: 13

Authors: Stoll, R Renner, C Zweckstetter, M Bruggert, M Ambrosius, D Palme, S Engh, RA Golob, M Breibach, I Buettner, R Voelter, W Holak, TA Bosserhoff, AK
Citation: R. Stoll et al., The extracellular human melanoma inhibitory activity (MIA) protein adopts an SH3 domain-like fold, EMBO J, 20(3), 2001, pp. 340-349

Authors: Zeslawski, W Beisel, HG Kamionka, M Kalus, W Engh, RA Huber, R Lang, K Holak, TA
Citation: W. Zeslawski et al., The interaction of insulin-like growth factor-I with the N-terminal domainof IGFBP-5, EMBO J, 20(14), 2001, pp. 3638-3644

Authors: Klein, C Georges, G Kunkele, AP Huber, R Engh, RA Hansen, S
Citation: C. Klein et al., High thermostability and lack of cooperative DNA binding distinguish the p63 core domain from the homologous tumor suppressor p53, J BIOL CHEM, 276(40), 2001, pp. 37390-37401

Authors: Brandstetter, H Grams, F Glitz, D Lang, A Haber, R Bode, W Krell, HW Engh, RA
Citation: H. Brandstetter et al., The 1.8-angstrom crystal structure of a matrix metalloproteinase 8-barbiturate inhibitor complex reveals a previously unobserved mechanism for collagenase substrate recognition (vol 276, 17405, 2001), J BIOL CHEM, 276(33), 2001, pp. 31474-31474

Authors: Brandstetter, H Grams, F Glitz, D Lang, A Huber, R Bode, W Krell, HW Engh, RA
Citation: H. Brandstetter et al., The 1.8-angstrom crystal structure of a matrix metallaproteinase 8-barbiturate inhibitor complex reveals a previously unobserved mechanism for collagenase substrate recognition, J BIOL CHEM, 276(20), 2001, pp. 17405-17412

Authors: Stoll, R Renner, C Hansen, S Palme, S Klein, C Belling, A Zeslawski, W Kamionka, M Rehm, T Muhlhahn, P Schumacher, R Hesse, F Kaluza, B Voelter, W Engh, RA Holak, TA
Citation: R. Stoll et al., Chalcone derivatives antagonize interactions between the human oncoproteinMDM2 and p53, BIOCHEM, 40(2), 2001, pp. 336-344

Authors: Stoll, R Renner, C Muhlhahn, P Hansen, S Schumacher, R Hesse, F Kaluza, B Engh, RA Voelter, W Holak, TA
Citation: R. Stoll et al., Sequence-specific H-1, N-15, and C-13 assignment of the N-terminal domain of the human oncoprotein MDM2 that binds to p53, J BIOM NMR, 17(1), 2000, pp. 91-92

Authors: Grams, F Brandstetter, H Engh, RA Glitz, D Krell, HW Livi, V Menta, E Moroder, L Constanze, J Muller, D von Roedern, EG Zimmermann, G
Citation: F. Grams et al., Research on MMP inhibitors with unusual scaffolds, CANC DRUG, 2000, pp. 223-243

Authors: Hopfner, KP Lang, A Karcher, A Sichler, K Kopetzki, E Brandstetter, H Huber, R Bode, W Engh, RA
Citation: Kp. Hopfner et al., Coagulation factor IXa: the relaxed conformation of Tyr99 blocks substratebinding, STRUCT F D, 7(8), 1999, pp. 989-996

Authors: Knegtel, RMA Bayada, DM Engh, RA von der Saal, W van Geerestein, VJ Grootenhuis, PDJ
Citation: Rma. Knegtel et al., Comparison of two implementations of the incremental construction algorithm in flexible docking of thrombin inhibitors, J COMPUT A, 13(2), 1999, pp. 167-183

Authors: Hopfner, KP Eichinger, A Engh, RA Laue, F Ankenbauer, W Huber, R Angerer, B
Citation: Kp. Hopfner et al., Crystal structure of a thermostable type B DNA polymerase from Thermococcus gorgonarius, P NAS US, 96(7), 1999, pp. 3600-3605

Authors: Adang, AEP Lucas, H de Man, APA Engh, RA Grootenhuis, PDJ
Citation: Aep. Adang et al., Novel acylguanidine containing thrombin inhibitors with reduced basicity at the P-1 moiety, BIOORG MED, 8(24), 1998, pp. 3603-3608

Authors: Kucznierz, R Grams, F Leinert, H Marzenell, K Engh, RA von der Saal, W
Citation: R. Kucznierz et al., Tetrahydro-isoquinoline-based factor Xa inhibitors, J MED CHEM, 41(25), 1998, pp. 4983-4994
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