In Vitro and In Vivo Properties of Ro 63-9141, a Novel Broad-Spectrum Cephalosporin with Activity against Methicillin-Resistant Staphylococci von HEBEISEN, Paul, HEINZE-KRAUSS, Ingrid, ANGEHRN, Peter, HOHL, Peter, PAGE, Malcolm G. P, THEN, Rudolf L

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Antibacterial activities of epiroprim, a new dihydrofolate reductase inhibitor, alone and in combination with dapsone von LOCHER, H. H, SCHLUNEGGER, H, HARTMAN, P. G, ANGEHRN, P, THEN, R. L

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GyrB mutations in Staphylococcus aureus strains resistant to cyclothialidine, coumermycin, and novobiocin von STIEGER, M, ANGEHRN, P, WOHLGENSINGER, B, GMÜNDER, H

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New Antibacterial Agents Derived from the DNA Gyrase Inhibitor Cyclothialidine von Angehrn, Peter, Buchmann, Stefan, Funk, Christoph, Goetschi, Erwin, Gmuender, Hans, Hebeisen, Paul, Kostrewa, Dirk, Link, Helmut, Luebbers, Thomas, Masciadri, Raffaello, Nielsen, Joergen, Reindl, Peter, Ricklin, Fabienne, Schmitt-Hoffmann, Anne, Theil, Frank-Peter

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Trapping of nonhydrolyzable cephalosporins by cephalosporinases in Enterobacter cloacae and Pseudomonas aeruginosa as a possible resistance mechanism von Then, R L, Angehrn, P

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Design, synthesis, and structure-activity relationship studies of ATP analogues as DNA gyrase inhibitors von LÜBBERS, T, ANGEHRN, P, GMÜNDER, H, HERZIG, S, KULHANEK, J

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Cyclothialidine and its congeners: A new class of DNA gyrase inhibitors von Goetschi, E., Angehrn, P., Gmuender, H., Hebeisen, P., Link, H., Masciadri, R., Nielsen, J.

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Antibacterial properties of Ro 40-6890, a broad-spectrum cephalosporin, and its novel orally absorbable ester, Ro 41-3399 von ANGEHRN, P, HOHL, P, HUBSCHWERLEN, C, PAGE, M, THEN, R

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Novel ketolide antibiotics with a fused five-membered lactone ring––synthesis, physicochemical and antimicrobial properties von Hunziker, Daniel, Wyss, Pierre-C, Angehrn, Peter, Mueller, Aranka, Marty, Hans-Peter, Halm, Remy, Kellenberger, Laurenz, Bitsch, Veronique, Biringer, Gerard, Arnold, Wolf, Stämpfli, Andreas, Schmitt-Hoffmann, Anne, Cousot, Denis

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(6R)-6-(SUBSTITUTED METHYL)PENICILLANIC ACID SULFONES: NEW POTENT β-LACTAMASE INHIBITORS von ADAM, S., THEN, R., ANGEHRN, P.

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In vitro and in vivo evaluation of Ro 09-1428, a new parenteral cephalosporin with high antipseudomonal activity von ARISAWA, M, SEKINE, Y, SHIMIZU, S, TAKANO, H, ANGEHRN, P, THEN, R. L

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Multiply resistant mutants of Enterobacter cloacae selected by beta-lactam antibiotics von THEN, R. L, ANGEHRN, P

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Pyrimido[1,6-a]benzimidazoles: a new class of DNA gyrase inhibitors von Hubschwerlen, C, Pflieger, P, Specklin, J. L, Gubernator, K, Gmuender, H, Angehrn, P, Kompis, I

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Ro 13-9904, a long-acting broad-spectrum cephalosporin: in vitro and in vivo studies von Angehrn, P, Probst, P J, Reiner, R, Then, R L

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In vitro antibacterial properties of cefetamet and in vivo activity of its orally absorbable ester derivative, cefetamet pivoxil von Angehrn, P, Hohl, P, Then, R L

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Structure-Based Design of β-Lactamase Inhibitors. 1. Synthesis and Evaluation of Bridged Monobactams von Heinze-Krauss, Ingrid, Angehrn, Peter, Charnas, Robert L, Gubernator, Klaus, Gutknecht, Eva-Maria, Hubschwerlen, Christian, Kania, Malgosia, Oefner, Christian, Page, Malcolm G. P, Sogabe, Satoshi, Specklin, Jean-Luc, Winkler, Fritz

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METHYLENE (2S, 5R)-6-(3-FORMYLALLYLIDENE)PENICILLANATE PIVALATE, A PRODRUG OF A NEW β-LACTAMASE INHIBITOR von ADAM, S., THEN, R., ANGEHRN, P.

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Monocyclic and tricyclic analogs of quinolones: mechanism of action von GEORGOPARADAKOU, N. H, DIX, B. A, ANGEHRN, P, WICK, A, OLSON, G. L

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Design, Synthesis, and Evaluation of 2β-Alkenyl Penam Sulfone Acids as Inhibitors of β-Lactamases von Richter, Hans G. F, Angehrn, Peter, Hubschwerlen, Christian, Kania, Malgosia, Page, Malcolm G. P, Specklin, Jean-Luc, Winkler, Fritz K

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POTENTIAL PRODRUGS OF 6-ACETYLMETHYLENEPENICILLANIC ACID (Ro 15-1903) von ADAM, S., THEN, R., ANGEHRN, P.

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