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Results: 1-8 |
Results: 8
TRIPEPTIDE ALDEHYDE INHIBITORS OF HUMAN RHINOVIRUS 3C PROTEASE - DESIGN, SYNTHESIS, BIOLOGICAL EVALUATION, AND COCRYSTAL STRUCTURE SOLUTIONOF P-1 GLUTAMINE ISOSTERIC REPLACEMENTS
Authors: WEBBER SE OKANO K LITTLE TL REICH SH XIN Y FUHRMAN SA MATTHEWS DA LOVE RA HENDRICKSON TF PATICK AK MEADOR JW FERRE RA BROWN EL FORD CE BINFORD SL WORLAND ST
Citation: Se. Webber et al., TRIPEPTIDE ALDEHYDE INHIBITORS OF HUMAN RHINOVIRUS 3C PROTEASE - DESIGN, SYNTHESIS, BIOLOGICAL EVALUATION, AND COCRYSTAL STRUCTURE SOLUTIONOF P-1 GLUTAMINE ISOSTERIC REPLACEMENTS, Journal of medicinal chemistry, 41(15), 1998, pp. 2786-2805
STRUCTURE-BASED DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF IRREVERSIBLE HUMAN RHINOVIRUS 3C PROTEASE INHIBITORS - 1 - MICHAEL ACCEPTORSTRUCTURE-ACTIVITY STUDIES
Authors: DRAGOVICH PS WEBBER SE BABINE RE FUHRMAN SA PATICK AK MATTHEWS DA LEE CA REICH SH PRINS TJ MARAKOVITS JT LITTLEFIELD ES ZHOU R TIKHE J FORD CE WALLACE MB MEADOR JW FERRE RA BROWN EL BINFORD SL HARR JEV DELISLE DM WORLAND ST
Citation: Ps. Dragovich et al., STRUCTURE-BASED DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF IRREVERSIBLE HUMAN RHINOVIRUS 3C PROTEASE INHIBITORS - 1 - MICHAEL ACCEPTORSTRUCTURE-ACTIVITY STUDIES, Journal of medicinal chemistry, 41(15), 1998, pp. 2806-2818
STRUCTURE-BASED DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF IRREVERSIBLE HUMAN RHINOVIRUS 3C PROTEASE INHIBITORS - 2 - PEPTIDE STRUCTURE-ACTIVITY STUDIES
Authors: DRAGOVICH PS WEBBER SE BABINE RE FUHRMAN SA PATICK AK MATTHEWS DA REICH SH MARAKOVITS JT PRINS TJ ZHOU R TIKHE J LITTLEFIELD ES BLECKMAN TM WALLACE MB LITTLE TL FORD CE MEADOR JW FERRE RA BROWN EL BINFORD SL DELISLE DM WORLAND ST
Citation: Ps. Dragovich et al., STRUCTURE-BASED DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF IRREVERSIBLE HUMAN RHINOVIRUS 3C PROTEASE INHIBITORS - 2 - PEPTIDE STRUCTURE-ACTIVITY STUDIES, Journal of medicinal chemistry, 41(15), 1998, pp. 2819-2834
INTERACTION OF A NOVEL GDP EXCHANGE INHIBITOR WITH THE RAS PROTEIN
Authors: GANGULY AK WANG YS PRAMANIK BN DOLL RJ SNOW ME TAVERAS AG REMISZEWSKI S CESARZ D DELROSARIO J VIBULBHAN B BROWN JE KIRSCHMEIER P HUANG EC HEIMARK L TSARBOPOULOS A GIRIJAVALLABHAN VM AUST RM BROWN EL DELISLE DM FUHRMAN SA HENDRICKSON TF KISSINGER CR LOVE RA SISSON WA VILLAFRANCA JE WEBBER SE
Citation: Ak. Ganguly et al., INTERACTION OF A NOVEL GDP EXCHANGE INHIBITOR WITH THE RAS PROTEIN, Biochemistry (Easton), 37(45), 1998, pp. 15631-15637
DESIGN, SYNTHESIS, AND EVALUATION OF NONPEPTIDIC INHIBITORS OF HUMAN RHINOVIRUS 3C PROTEASE
Authors: WEBBER SE TIKHE J WORLAND ST FUHRMAN SA HENDRICKSON TF MATTHEWS DA LOVE RA PATICK AK MEADOR JW FERRE RA BROWN EL DELISLE DM FORD CE BINFORD SL
Citation: Se. Webber et al., DESIGN, SYNTHESIS, AND EVALUATION OF NONPEPTIDIC INHIBITORS OF HUMAN RHINOVIRUS 3C PROTEASE, Journal of medicinal chemistry, 39(26), 1996, pp. 5072-5082
DELIVERING CLINICAL LABORATORY SERVICES TO INTENSIVE-CARE UNITS
Authors: STEFFES MW GILLEN JL FUHRMAN SA
Citation: Mw. Steffes et al., DELIVERING CLINICAL LABORATORY SERVICES TO INTENSIVE-CARE UNITS, Clinical chemistry, 42(3), 1996, pp. 387-391
THE MOBILE LABORATORY IN ALTERNATIVE SITE TESTING
Authors: FUHRMAN SA TRAVERS EM HANDORF CR
Citation: Sa. Fuhrman et al., THE MOBILE LABORATORY IN ALTERNATIVE SITE TESTING, Archives of pathology and laboratory medicine, 119(10), 1995, pp. 939-942
MUTATIONS THAT ABOLISH THE ABILITY OF HA-RAS TO ASSOCIATE WITH RAF-1
Authors: SHIROUZU M KOIDE H FUJITAYOSHIGAKI J OSHIO H TOYAMA Y YAMASAKI K FUHRMAN SA VILLAFRANCA E YOKOYAMA S KAZIRO Y
Citation: M. Shirouzu et al., MUTATIONS THAT ABOLISH THE ABILITY OF HA-RAS TO ASSOCIATE WITH RAF-1, Oncogene, 9(8), 1994, pp. 2153-2157
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