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Results: 1-19 |
Results: 19
STUDIES ON THE C-TERMINAL OF HEXAPEPTIDE INHIBITORS OF THE HEPATITIS-C VIRUS SERINE-PROTEASE
Authors: LLINASBRUNET M BAILEY M DEZIEL R FAZAL G GORYS V GOULET S HALMOS T MAURICE R POIRIER M POUPART MA RANCOURT J THIBEAULT D WERNIC D LAMARRE D
Citation: M. Llinasbrunet et al., STUDIES ON THE C-TERMINAL OF HEXAPEPTIDE INHIBITORS OF THE HEPATITIS-C VIRUS SERINE-PROTEASE, Bioorganic & medicinal chemistry letters, 8(19), 1998, pp. 2719-2724
PEPTIDE-BASED INHIBITORS OF THE HEPATITIS-C VIRUS SERINE-PROTEASE
Authors: LLINASBRUNET M BAILEY M FAZAL G GOULET S HALMOS T LAPLANTE S MAURICE R POIRIER M POUPART MA THIBEAULT D WERNIC D LAMARRE D
Citation: M. Llinasbrunet et al., PEPTIDE-BASED INHIBITORS OF THE HEPATITIS-C VIRUS SERINE-PROTEASE, Bioorganic & medicinal chemistry letters, 8(13), 1998, pp. 1713-1718
NOVEL GAG-POL FRAMESHIFT SITE IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VARIANTS RESISTANT TO PROTEASE INHIBITORS
Authors: DOYON L PAYANT C BRAKIERGINGRAS L LAMARRE D
Citation: L. Doyon et al., NOVEL GAG-POL FRAMESHIFT SITE IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VARIANTS RESISTANT TO PROTEASE INHIBITORS, Journal of virology, 72(7), 1998, pp. 6146-6150
ANTIVIRAL PROPERTIES OF PALINAVIR, A POTENT INHIBITOR OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROTEASE
Authors: LAMARRE D CROTEAU G WARDROP E BOURGON L THIBEAULT D CLOUETTE C VAILLANCOURT M COHEN E PARGELLIS C YOAKIM C ANDERSON P
Citation: D. Lamarre et al., ANTIVIRAL PROPERTIES OF PALINAVIR, A POTENT INHIBITOR OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROTEASE, Antimicrobial agents and chemotherapy, 41(5), 1997, pp. 965-971
IMPAIRED FITNESS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VARIANTS WITHHIGH-LEVEL RESISTANCE TO PROTEASE INHIBITORS
Authors: CROTEAU G DOYON L THIBEAULT D MCKERCHER G PILOTE L LAMARRE D
Citation: G. Croteau et al., IMPAIRED FITNESS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VARIANTS WITHHIGH-LEVEL RESISTANCE TO PROTEASE INHIBITORS, Journal of virology, 71(2), 1997, pp. 1089-1096
POTENT HIV PROTEASE INHIBITORS CONTAINING A NOVEL (HYDROXYETHYL)AMIDEISOSTERE
Authors: BEAULIEU PL WERNIC D ABRAHAM A ANDERSON PC BOGRI T BOUSQUET Y CROTEAU G GUSE I LAMARRE D LIARD F PARIS W THIBEAULT D PAV S TONG L
Citation: Pl. Beaulieu et al., POTENT HIV PROTEASE INHIBITORS CONTAINING A NOVEL (HYDROXYETHYL)AMIDEISOSTERE, Journal of medicinal chemistry, 40(14), 1997, pp. 2164-2176
BIOLOGICAL NUTRIENT REMOVAL FROM A PHOSPHORUS-RICH PRE-FERMENTED INDUSTRIAL WASTE-WATER
Authors: COMEAU Y LAMARRE D ROBERGE F PERRIER M DESJARDINS G HADE C MAYER R
Citation: Y. Comeau et al., BIOLOGICAL NUTRIENT REMOVAL FROM A PHOSPHORUS-RICH PRE-FERMENTED INDUSTRIAL WASTE-WATER, Water science and technology, 34(1-2), 1996, pp. 169-177
2ND LOCUS INVOLVED IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 RESISTANCE TO PROTEASE INHIBITORS
Authors: DOYON L CROTEAU G THIBEAULT D POULIN F PILOTE L LAMARRE D
Citation: L. Doyon et al., 2ND LOCUS INVOLVED IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 RESISTANCE TO PROTEASE INHIBITORS, Journal of virology, 70(6), 1996, pp. 3763-3769
MOLECULAR-BASIS OF HIV-1 RESISTANCE TO PROTEASE INHIBITORS - STRUCTURAL FLEXIBILITY OF THE PROTEASE AND 2ND-SITE COMPENSATORY MUTATIONS IN CLEAVAGE SITES
Authors: LAMARRE D DOYON L CROTEAU G PILOTE L THIBEAULT D
Citation: D. Lamarre et al., MOLECULAR-BASIS OF HIV-1 RESISTANCE TO PROTEASE INHIBITORS - STRUCTURAL FLEXIBILITY OF THE PROTEASE AND 2ND-SITE COMPENSATORY MUTATIONS IN CLEAVAGE SITES, Journal of acquired immune deficiency syndromes and human retrovirology, 10, 1995, pp. 62-62
CRYSTAL-STRUCTURES OF HIV-2 PROTEASE IN COMPLEX WITH INHIBITORS CONTAINING THE HYDROXYETHYLAMINE DIPEPTIDE ISOSTERE
Authors: TONG L PAV S MUI S LAMARRE D YOAKIM C BEAULIEU P ANDERSON PC
Citation: L. Tong et al., CRYSTAL-STRUCTURES OF HIV-2 PROTEASE IN COMPLEX WITH INHIBITORS CONTAINING THE HYDROXYETHYLAMINE DIPEPTIDE ISOSTERE, Structure, 3(1), 1995, pp. 33-40
ENZYMATIC CHARACTERIZATION OF PURIFIED RECOMBINANT HUMAN RENIN
Authors: PILOTE L MCKERCHER G THIBEAULT D LAMARRE D
Citation: L. Pilote et al., ENZYMATIC CHARACTERIZATION OF PURIFIED RECOMBINANT HUMAN RENIN, Biochemistry and cell biology, 73(3-4), 1995, pp. 163-170
HIGH-RESOLUTION CRYSTAL-STRUCTURES OF RECOMBINANT HUMAN RENIN IN COMPLEX WITH POLYHYDROXYMONOAMIDE INHIBITORS
Authors: TONG L PAV S LAMARRE D PILOTE L LAPLANTE S ANDERSON PC JUNG G
Citation: L. Tong et al., HIGH-RESOLUTION CRYSTAL-STRUCTURES OF RECOMBINANT HUMAN RENIN IN COMPLEX WITH POLYHYDROXYMONOAMIDE INHIBITORS, Journal of Molecular Biology, 250(2), 1995, pp. 211-222
TIME-RESOLVED LIGAND-EXCHANGE REACTIONS - KINETIC-MODELS FOR COMPETITIVE INHIBITORS WITH RECOMBINANT HUMAN RENIN
Authors: MORELOCK MM PARGELLIS CA GRAHAM ET LAMARRE D JUNG G
Citation: Mm. Morelock et al., TIME-RESOLVED LIGAND-EXCHANGE REACTIONS - KINETIC-MODELS FOR COMPETITIVE INHIBITORS WITH RECOMBINANT HUMAN RENIN, Journal of medicinal chemistry, 38(10), 1995, pp. 1751-1761
CRYSTALLOGRAPHIC STUDIES ON THE BINDING MODES OF P-2-P-3 BUTANEDIAMIDE RENIN INHIBITORS
Authors: TONG LA PAV S LAMARRE D SIMONEAU B LAVALLEE P JUNG G
Citation: La. Tong et al., CRYSTALLOGRAPHIC STUDIES ON THE BINDING MODES OF P-2-P-3 BUTANEDIAMIDE RENIN INHIBITORS, The Journal of biological chemistry, 270(49), 1995, pp. 29520-29524
MICROTUBE BATCH PROTEIN CRYSTALLIZATION - APPLICATIONS TO HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-2 (HIV-2) PROTEASE AND HUMAN RENIN
Authors: PAV S LUBBE K DO F LAMARRE D PARGELLIS C TONG L
Citation: S. Pav et al., MICROTUBE BATCH PROTEIN CRYSTALLIZATION - APPLICATIONS TO HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-2 (HIV-2) PROTEASE AND HUMAN RENIN, Proteins, 20(1), 1994, pp. 98-102
MUTATIONAL ANALYSIS OF HUMAN RENIN - IDENTIFICATION OF A SURFACE LOOPINVOLVED IN BINDING OF HUMAN ANGIOTENSINOGEN
Authors: THIBEAULT D PILOTE L MCKERCHER G GAUDETTE Y LESSARD I LAMARRE D
Citation: D. Thibeault et al., MUTATIONAL ANALYSIS OF HUMAN RENIN - IDENTIFICATION OF A SURFACE LOOPINVOLVED IN BINDING OF HUMAN ANGIOTENSINOGEN, Journal of cellular biochemistry, 1994, pp. 162-162
DETERMINATION OF KINETIC RATE CONSTANTS FOR HIV-1 PROTEASE - BINDING OF INHIBITORS AND MONOMER-DIMER INTERCONVERSION
Authors: PARGELLIS CA MORELOCK MM GRAHAM ET KINKADE P PAV S LUBBE K LAMARRE D ANDERSON P
Citation: Ca. Pargellis et al., DETERMINATION OF KINETIC RATE CONSTANTS FOR HIV-1 PROTEASE - BINDING OF INHIBITORS AND MONOMER-DIMER INTERCONVERSION, Journal of cellular biochemistry, 1994, pp. 171-171
DETERMINATION OF KINETIC RATE CONSTANTS FOR THE BINDING OF INHIBITORSTO HIV-1 PROTEASE AND FOR THE ASSOCIATION AND DISSOCIATION OF ACTIVE HOMODIMER
Authors: PARGELLIS CA MORELOCK MM GRAHAM ET KINKADE P PAV S LUBBE K LAMARRE D ANDERSON PC
Citation: Ca. Pargellis et al., DETERMINATION OF KINETIC RATE CONSTANTS FOR THE BINDING OF INHIBITORSTO HIV-1 PROTEASE AND FOR THE ASSOCIATION AND DISSOCIATION OF ACTIVE HOMODIMER, Biochemistry, 33(41), 1994, pp. 12527-12534
CRYSTAL-STRUCTURE OF HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) TYPE-2 PROTEASE IN COMPLEX WITH A REDUCED AMIDE INHIBITOR AND COMPARISON WITH HIV-1PROTEASE STRUCTURES
Authors: TONG L PAV S PARGELLIS C DO F LAMARRE D ANDERSON PC
Citation: L. Tong et al., CRYSTAL-STRUCTURE OF HUMAN-IMMUNODEFICIENCY-VIRUS (HIV) TYPE-2 PROTEASE IN COMPLEX WITH A REDUCED AMIDE INHIBITOR AND COMPARISON WITH HIV-1PROTEASE STRUCTURES, Proceedings of the National Academy of Sciences of the United Statesof America, 90(18), 1993, pp. 8387-8391
Risultati: 1-19 |