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Results: 1-25 | 26-39
Results: 1-25/39
L-PRINTABLE SETS
Authors: FORTNOW L GOLDSMITH J LEVY MA MAHANEY S
Citation: L. Fortnow et al., L-PRINTABLE SETS, SIAM journal on computing (Print), 28(1), 1999, pp. 137-151
SELECTIVE ELEVATION OF GLUTATHIONE LEVELS IN TARGET TISSUES WITH L-2-OXOTHIAZOLIDINE-4-CARBOXYLATE (OTC) PROTECTS AGAINST HYPEROXIA-INDUCEDLUNG DAMAGE IN PROTEIN-ENERGY MALNOURISHED RATS - IMPLICATIONS FOR A NEW TREATMENT STRATEGY
Authors: LEVY MA SIKORSKI B BRAY TM
Citation: Ma. Levy et al., SELECTIVE ELEVATION OF GLUTATHIONE LEVELS IN TARGET TISSUES WITH L-2-OXOTHIAZOLIDINE-4-CARBOXYLATE (OTC) PROTECTS AGAINST HYPEROXIA-INDUCEDLUNG DAMAGE IN PROTEIN-ENERGY MALNOURISHED RATS - IMPLICATIONS FOR A NEW TREATMENT STRATEGY, The Journal of nutrition, 128(4), 1998, pp. 671-676
STRUCTURE-BASED DESIGN OF CATHEPSIN-K INHIBITORS CONTAINING A BENZYLOXY-SUBSTITUTED BENZOYL PEPTIDOMIMETIC
Authors: THOMPSON SK SMITH WW ZHAO BG HALBERT SM TOMASZEK TA TEW DG LEVY MA JANSON CA DALESSIO KJ MCQUENEY MS KURDYLA J JONES CS DESJARLAIS RL ABDELMEGUID SS VEBER DF
Citation: Sk. Thompson et al., STRUCTURE-BASED DESIGN OF CATHEPSIN-K INHIBITORS CONTAINING A BENZYLOXY-SUBSTITUTED BENZOYL PEPTIDOMIMETIC, Journal of medicinal chemistry, 41(21), 1998, pp. 3923-3927
CONFORMATIONALLY CONSTRAINED 1,3-DIAMINO KETONES - A SERIES OF POTENTINHIBITORS OF THE CYSTEINE PROTEASE CATHEPSIN-K
Authors: MARQUIS RW YAMASHITA DS RU Y LOCASTRO SM OH HJ ERHARD KF DESJARLAIS RL HEAD MS SMITH WW ZHAO BG JANSON CA ABDELMEGUID SS TOMASZEK TA LEVY MA VEBER DF
Citation: Rw. Marquis et al., CONFORMATIONALLY CONSTRAINED 1,3-DIAMINO KETONES - A SERIES OF POTENTINHIBITORS OF THE CYSTEINE PROTEASE CATHEPSIN-K, Journal of medicinal chemistry, 41(19), 1998, pp. 3563-3567
USE OF X-RAY CO-CRYSTAL STRUCTURES AND MOLECULAR MODELING TO DESIGN POTENT AND SELECTIVE NONPEPTIDE INHIBITORS OF CATHEPSIN-K
Authors: DESJARLAIS RL YAMASHITA DS OH HJ UZINSKAS IN ERHARD KF ALLEN AC HALTIWANGER RC ZHAO BG SMITH WW ABDELMEGUID SS DALESSIO K JANSON CA MCQUENEY MS TOMASZEK TA LEVY MA VEBER DF
Citation: Rl. Desjarlais et al., USE OF X-RAY CO-CRYSTAL STRUCTURES AND MOLECULAR MODELING TO DESIGN POTENT AND SELECTIVE NONPEPTIDE INHIBITORS OF CATHEPSIN-K, Journal of the American Chemical Society, 120(35), 1998, pp. 9114-9115
DIETARY SUPPLEMENTATION OF GLUTATHIONE (GSH) PRECURSOR, NOT PROTEIN PROTECTS AGAINST HYPEROXIA-INDUCED LUNG INJURY IN PROTEIN-ENERGY MALNOURISHED (PEM)
Authors: BRAY TM SIKORSKI B LEVY MA
Citation: Tm. Bray et al., DIETARY SUPPLEMENTATION OF GLUTATHIONE (GSH) PRECURSOR, NOT PROTEIN PROTECTS AGAINST HYPEROXIA-INDUCED LUNG INJURY IN PROTEIN-ENERGY MALNOURISHED (PEM), The FASEB journal, 11(3), 1997, pp. 3744-3744
PEPTIDE ALDEHYDE INHIBITORS OF CATHEPSIN-K INHIBIT BONE-RESORPTION BOTH IN-VITRO AND IN-VIVO
Authors: VOTTA BJ LEVY MA BADGER A BRADBEER J DODDS RA JAMES IE THOMPSON S BOSSARD MJ CARR T CONNOR JR TOMASZEK TA SZEWCZUK L DRAKE FH VEBER DF GOWEN M
Citation: Bj. Votta et al., PEPTIDE ALDEHYDE INHIBITORS OF CATHEPSIN-K INHIBIT BONE-RESORPTION BOTH IN-VITRO AND IN-VIVO, Journal of bone and mineral research, 12(9), 1997, pp. 1396-1406
PREPARATION AND BIOLOGICAL-ACTIVITY OF TRICYCLIC NONSTEROIDAL INHIBITORS OF HUMAN STEROID 5-ALPHA-REDUCTASE
Authors: ABELL AD BRANDT M LEVY MA HOLT DA
Citation: Ad. Abell et al., PREPARATION AND BIOLOGICAL-ACTIVITY OF TRICYCLIC NONSTEROIDAL INHIBITORS OF HUMAN STEROID 5-ALPHA-REDUCTASE, Journal of the Chemical Society. Perkin transactions. I, (11), 1997, pp. 1663-1667
DESIGN OF POTENT AND SELECTIVE HUMAN CATHEPSIN-K INHIBITORS THAT SPANTHE ACTIVE-SITE
Authors: THOMPSON SK HALBERT SM BOSSARD MJ TOMASZEK TA LEVY MA ZHAO BG SMITH WW ABDELMEGUID SS JANSON CA DALESSIO KJ MCQUENEY MS AMEGADZIE BY HANNING CR DESJARLAIS RL BRIAND J SARKAR SK HUDDLESTON MJ IJAMES CF CARR SA GARNES KT SHU A HEYS JR BRADBEER J ZEMBRYKI D LEERYKACZEWSKI L JAMES IE LARK MW DRAKE FH GOWEN M GLEASON JG VEBER DF
Citation: Sk. Thompson et al., DESIGN OF POTENT AND SELECTIVE HUMAN CATHEPSIN-K INHIBITORS THAT SPANTHE ACTIVE-SITE, Proceedings of the National Academy of Sciences of the United Statesof America, 94(26), 1997, pp. 14249-14254
NGOS AND ENVIRONMENTAL POLICIES - ASIA AND AFRICA - POTTER,D
Authors: LEVY MA
Citation: Ma. Levy, NGOS AND ENVIRONMENTAL POLICIES - ASIA AND AFRICA - POTTER,D, The Journal of developing areas, 32(1), 1997, pp. 141-143
STRUCTURE AND DESIGN OF POTENT AND SELECTIVE CATHEPSIN-K INHIBITORS
Authors: YAMASHITA DS SMITH WW ZHAO BG JANSON CA TOMASZEK TA BOSSARD MJ LEVY MA OH HJ CARR TJ THOMPSON SK IJAMES CF CARR SA MCQUENEY M DALESSIO KJ AMEGADZIE BY HANNING CR ABDELMEGUID S DESJARLAIS RL GLEASON JG VEBER DF
Citation: Ds. Yamashita et al., STRUCTURE AND DESIGN OF POTENT AND SELECTIVE CATHEPSIN-K INHIBITORS, Journal of the American Chemical Society, 119(46), 1997, pp. 11351-11352
THE PREPARATION AND EVALUATION OF (+ YL-1,2,3,4,4A-9,10,10A-OCTAHYDRO-PHENANTHREN-2-ONE AS AN INHIBITOR OF HUMAN TYPE-1 STEROID 5-ALPHA-REDUCTASE/
Authors: ABELL AD BRANDT M LEVY MA HOLT DA
Citation: Ad. Abell et al., THE PREPARATION AND EVALUATION OF (+ YL-1,2,3,4,4A-9,10,10A-OCTAHYDRO-PHENANTHREN-2-ONE AS AN INHIBITOR OF HUMAN TYPE-1 STEROID 5-ALPHA-REDUCTASE/, Bioorganic & medicinal chemistry letters, 6(7), 1996, pp. 883-884
A COMPARISON OF STEROIDAL AND NONSTEROIDAL INHIBITORS OF HUMAN STEROID 5-ALPHA-REDUCTASE - NEW TRICYCLIC ARYL ACID INHIBITORS OF THE TYPE-1ISOZYME
Authors: ABELL AD BRANDT M LEVY MA HOLT DA
Citation: Ad. Abell et al., A COMPARISON OF STEROIDAL AND NONSTEROIDAL INHIBITORS OF HUMAN STEROID 5-ALPHA-REDUCTASE - NEW TRICYCLIC ARYL ACID INHIBITORS OF THE TYPE-1ISOZYME, Bioorganic & medicinal chemistry letters, 6(4), 1996, pp. 481-484
PEPTIDE ALDEHYDE INHIBITORS OF CATHEPSIN-K INHIBIT BONE-RESORPTION BOTH IN-VITRO AND IN-VIVO
Authors: DRAKE F VOTTA BJ BADGER A DODDS RA JAMES I LEVY MA THOMPSON S BOSSARD MJ CARR T CONNOR JR TOMASZEK TA SZEWCZUK L VEBER D GOWEN M
Citation: F. Drake et al., PEPTIDE ALDEHYDE INHIBITORS OF CATHEPSIN-K INHIBIT BONE-RESORPTION BOTH IN-VITRO AND IN-VIVO, Journal of bone and mineral research, 11, 1996, pp. 246-246
ENVIRONMENT AND SECURITY - REPLY
Authors: LEVY MA
Citation: Ma. Levy, ENVIRONMENT AND SECURITY - REPLY, International security, 20(3), 1996, pp. 195-198
PROTEOLYTIC ACTIVITY OF HUMAN OSTEOCLAST CATHEPSIN-K - EXPRESSION, PURIFICATION, ACTIVATION, AND SUBSTRATE IDENTIFICATION
Authors: BOSSARD MJ TOMASZEK TA THOMPSON SK AMEGADZIE BY HANNING CR JONES C KURDYLA JT MCNULTY DE DRAKE FH GOWEN M LEVY MA
Citation: Mj. Bossard et al., PROTEOLYTIC ACTIVITY OF HUMAN OSTEOCLAST CATHEPSIN-K - EXPRESSION, PURIFICATION, ACTIVATION, AND SUBSTRATE IDENTIFICATION, The Journal of biological chemistry, 271(21), 1996, pp. 12517-12524
STRUCTURE-ACTIVITY STUDIES OF RAPAMYCIN ANALOGS - EVIDENCE THAT THE C-7 METHOXY GROUP IS PART OF THE EFFECTOR DOMAIN AND POSITIONED AT THE FKBP12-FRAP INTERFACE
Authors: LUENGO JI YAMASHITA DS DUNNINGTON D BECK AK ROZAMUS LW YEN HK BOSSARD MJ LEVY MA HAND A NEWMANTARR T BADGER A FAUCETTE L JOHNSON RK DALESSIO K PORTER T SHU AYL HEYS R CHOI JW KONGSAEREE P CLARDY J HOLT DA
Citation: Ji. Luengo et al., STRUCTURE-ACTIVITY STUDIES OF RAPAMYCIN ANALOGS - EVIDENCE THAT THE C-7 METHOXY GROUP IS PART OF THE EFFECTOR DOMAIN AND POSITIONED AT THE FKBP12-FRAP INTERFACE, Chemistry & biology, 2(7), 1995, pp. 471-481
CLONING, EXPRESSION AND FUNCTIONAL-CHARACTERIZATION OF TYPE-1 AND TYPE-2 STEROID 5-ALPHA-REDUCTASES FROM CYNOMOLGUS MONKEY - COMPARISONS WITH HUMAN AND RAT ISOENZYMES
Authors: LEVY MA BRANDT M SHEEDY KM HOLT DA HEASLIP JI TRILL JJ RYAN PJ MORRIS RA GARRISON LM BERGSMA DJ
Citation: Ma. Levy et al., CLONING, EXPRESSION AND FUNCTIONAL-CHARACTERIZATION OF TYPE-1 AND TYPE-2 STEROID 5-ALPHA-REDUCTASES FROM CYNOMOLGUS MONKEY - COMPARISONS WITH HUMAN AND RAT ISOENZYMES, Journal of steroid biochemistry and molecular biology, 52(4), 1995, pp. 307-319
IS THE ENVIRONMENT A NATIONAL-SECURITY ISSUE
Authors: LEVY MA
Citation: Ma. Levy, IS THE ENVIRONMENT A NATIONAL-SECURITY ISSUE, International security, 20(2), 1995, pp. 35-62
BENZOPHENONECARBOXYLIC AND INDOLECARBOXYLIC ACIDS - POTENT TYPE-2 SPECIFIC INHIBITORS OF HUMAN STEROID 5-ALPHA-REDUCTASE
Authors: HOLT DA YAMASHITA DS KONIALIANBECK AL LUENGO JI ABELL AD BERGSMA DJ BRANDT M LEVY MA
Citation: Da. Holt et al., BENZOPHENONECARBOXYLIC AND INDOLECARBOXYLIC ACIDS - POTENT TYPE-2 SPECIFIC INHIBITORS OF HUMAN STEROID 5-ALPHA-REDUCTASE, Journal of medicinal chemistry, 38(1), 1995, pp. 13-15
INSULIN-SENSITIVE TARGETING OF THE GLUT4 GLUCOSE-TRANSPORTER IN L6 MYOBLASTS IS CONFERRED BY ITS COOH-TERMINAL CYTOPLASMIC TAIL
Authors: HANEY PM LEVY MA STRUBE MS MUECKLER M
Citation: Pm. Haney et al., INSULIN-SENSITIVE TARGETING OF THE GLUT4 GLUCOSE-TRANSPORTER IN L6 MYOBLASTS IS CONFERRED BY ITS COOH-TERMINAL CYTOPLASMIC TAIL, The Journal of cell biology, 129(3), 1995, pp. 641-658
27-O-DEMETHYLRAPAMYCIN, AN IMMUNOSUPPRESSANT COMPOUND PRODUCED BY A NEW STRAIN OF STREPTOMYCES-HYGROSCOPICUS
Authors: BOX SJ SHELLEY PR TYLER JW VERRALL MS WARR SRC BADGER AM LEVY MA BANKS RM
Citation: Sj. Box et al., 27-O-DEMETHYLRAPAMYCIN, AN IMMUNOSUPPRESSANT COMPOUND PRODUCED BY A NEW STRAIN OF STREPTOMYCES-HYGROSCOPICUS, Journal of antibiotics, 48(11), 1995, pp. 1347-1349
GLOBAL ACCORD - ENVIRONMENTAL CHALLENGES AND INTERNATIONAL RESPONSES - CHOUCRI,N
Authors: LEVY MA
Citation: Ma. Levy, GLOBAL ACCORD - ENVIRONMENTAL CHALLENGES AND INTERNATIONAL RESPONSES - CHOUCRI,N, The American political science review, 89(3), 1995, pp. 797-798
STRUCTURE-ACTIVITY STUDIES OF SYNTHETIC FKBP LIGANDS AS PEPTIDYL-PROLYL ISOMERASE INHIBITORS
Authors: HOLT DA KONIALIANBECK AL OH HJ YEN HK ROZAMUS LW KROG AJ ERHARD KF ORTIZ E LEVY MA BRANDT M BOSSARD MJ LUENGO JI
Citation: Da. Holt et al., STRUCTURE-ACTIVITY STUDIES OF SYNTHETIC FKBP LIGANDS AS PEPTIDYL-PROLYL ISOMERASE INHIBITORS, Bioorganic & medicinal chemistry letters, 4(2), 1994, pp. 315-320
SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF MACROCYCLIC FKBP LIGANDS
Authors: LUENGO JI KONIALIANBECK A LEVY MA BRANDT M EGGLESTON DS HOLT DA
Citation: Ji. Luengo et al., SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF MACROCYCLIC FKBP LIGANDS, Bioorganic & medicinal chemistry letters, 4(2), 1994, pp. 321-324
Risultati: 1-25 | 26-39