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Results: 1-18 |
Results: 18
NH2-TERMINAL PROCESSING OF CHEMOKINES (RANTES, SDF1-ALPHA) BY CD26 DIPEPTIDYLPEPTIDASE-IV GENERATES INHIBITORS OF CHEMOTAXIS AND HIV-1 INFECTION/
Authors: VANDAMME J PROOST P STRUYF S WUYTS A LAMBEIR AM DEMEESTER I SCHOLS D SCHARPE S DECLERCQ E
Citation: J. Vandamme et al., NH2-TERMINAL PROCESSING OF CHEMOKINES (RANTES, SDF1-ALPHA) BY CD26 DIPEPTIDYLPEPTIDASE-IV GENERATES INHIBITORS OF CHEMOTAXIS AND HIV-1 INFECTION/, European cytokine network, 9(3), 1998, pp. 323-323
ISOLATION AND IDENTIFICATION OF NATURALLY MODIFIED C-C CHEMOKINES MCP-1, MCP-2 AND RANTES - EFFECTS OF POSTTRANSLATIONAL MODIFICATIONS ON RECEPTOR USAGE, CHEMOTACTIC AND ANTI-HIV-1 ACTIVITY
Authors: PROOST P STRUYF S WUYTS A MENTEN P DEMEESTER I LAMBEIR AM SCHARPE S SCHOLS D DECLERCQ E VANDAMME J
Citation: P. Proost et al., ISOLATION AND IDENTIFICATION OF NATURALLY MODIFIED C-C CHEMOKINES MCP-1, MCP-2 AND RANTES - EFFECTS OF POSTTRANSLATIONAL MODIFICATIONS ON RECEPTOR USAGE, CHEMOTACTIC AND ANTI-HIV-1 ACTIVITY, European cytokine network, 9, 1998, pp. 73-75
AMINO-TERMINAL TRUNCATION OF CHEMOKINES BY CD26 DIPEPTIDYLPEPTIDASE-IV - CONVERSION OF RANTES INTO A POTENT INHIBITOR OF MONOCYTE CHEMOTAXIS AND HIV-1-INFECTION/
Authors: PROOST P DEMEESTER I SCHOLS D STRUYF S LAMBEIR AM WUYTS A OPDENAKKER G DECLERCQ E SCHARPE S VANDAMME J
Citation: P. Proost et al., AMINO-TERMINAL TRUNCATION OF CHEMOKINES BY CD26 DIPEPTIDYLPEPTIDASE-IV - CONVERSION OF RANTES INTO A POTENT INHIBITOR OF MONOCYTE CHEMOTAXIS AND HIV-1-INFECTION/, The Journal of biological chemistry, 273(13), 1998, pp. 7222-7227
PYRROLIDIDES - SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIP AS INHIBITORS OF DIPEPTIDYL PEPTIDASE-IV
Authors: AUGUSTYNS KJL LAMBEIR AM BORLOO M DEMEESTER I VEDERNIKOVA I VANHOOF G HENDRIKS D SCHARPE S HAEMERS A
Citation: Kjl. Augustyns et al., PYRROLIDIDES - SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIP AS INHIBITORS OF DIPEPTIDYL PEPTIDASE-IV, European journal of medicinal chemistry, 32(4), 1997, pp. 301-309
A PREDICTION OF DPP-IV CD26 DOMAIN-STRUCTURE FROM A PHYSICOCHEMICAL INVESTIGATION OF DIPEPTIDYL PEPTIDASE-IV (CD26) FROM HUMAN SEMINAL PLASMA/
Authors: LAMBEIR AM PEREIRA JFD CHACON P VERMEULEN G HEREMANS K DEVREESE B VANBEEUMEN J DEMEESTER I SCHARPE S
Citation: Am. Lambeir et al., A PREDICTION OF DPP-IV CD26 DOMAIN-STRUCTURE FROM A PHYSICOCHEMICAL INVESTIGATION OF DIPEPTIDYL PEPTIDASE-IV (CD26) FROM HUMAN SEMINAL PLASMA/, Biochimica et biophysica acta. Protein structure and molecular enzymology, 1340(2), 1997, pp. 215-226
THE EFFECTS OF CD26 DPP IV-TARGETED THERAPY ON ACUTE ALLOGRAFT-REJECTION/
Authors: KOROM S DEMEESTER I ONODERA K STADLBAUER THW BORLOO M LAMBEIR AM KUPIECWEGLINSKI JW
Citation: S. Korom et al., THE EFFECTS OF CD26 DPP IV-TARGETED THERAPY ON ACUTE ALLOGRAFT-REJECTION/, Transplantation proceedings, 29(1-2), 1997, pp. 1274-1275
VIVO INHIBITION OF DIPEPTIDYL PEPTIDASE-IV ACTIVITY BY PRO-PRO-DIPHENYL-PHOSPHONATE (PRODIPINE)
Authors: DEMEESTER I BELYAEV A LAMBEIR AM DEMEYER GRY VANOSSELAER N HAEMERS A SCHARPE S
Citation: I. Demeester et al., VIVO INHIBITION OF DIPEPTIDYL PEPTIDASE-IV ACTIVITY BY PRO-PRO-DIPHENYL-PHOSPHONATE (PRODIPINE), Biochemical pharmacology, 54(1), 1997, pp. 173-179
DIPEPTIDE-DERIVED DIPHENYL PHOSPHONATE ESTERS - MECHANISM-BASED INHIBITORS OF DIPEPTIDYL PEPTIDASE-IV
Authors: LAMBEIR AM BORLOO M DEMEESTER I BELYAEV A AUGUSTYNS K HENDRIKS D SCHARPE S HAEMERS A
Citation: Am. Lambeir et al., DIPEPTIDE-DERIVED DIPHENYL PHOSPHONATE ESTERS - MECHANISM-BASED INHIBITORS OF DIPEPTIDYL PEPTIDASE-IV, Biochimica et biophysica acta (G). General subjects, 1290(1), 1996, pp. 76-82
USE OF IMMOBILIZED ADENOSINE-DEAMINASE (EC-3.5.4.4) FOR THE RAPID PURIFICATION OF NATIVE HUMAN CD26 DIPEPTIDYL PEPTIDASE-IV (EC-3.4.14.5)
Authors: DEMEESTER I VANHOOF G LAMBEIR AM SCHARPE S
Citation: I. Demeester et al., USE OF IMMOBILIZED ADENOSINE-DEAMINASE (EC-3.5.4.4) FOR THE RAPID PURIFICATION OF NATIVE HUMAN CD26 DIPEPTIDYL PEPTIDASE-IV (EC-3.4.14.5), Journal of immunological methods, 189(1), 1996, pp. 99-105
CHARACTERIZATION OF A NOVEL SERIES OF APROTININ-DERIVED ANTICOAGULANTS .1. IN-VITRO AND PHARMACOLOGICAL PROPERTIES
Authors: STASSEN JM LAMBEIR AM MATTHYSSENS G RIPKA WC NYSTROM A SIXMA JJ VERMYLEN J
Citation: Jm. Stassen et al., CHARACTERIZATION OF A NOVEL SERIES OF APROTININ-DERIVED ANTICOAGULANTS .1. IN-VITRO AND PHARMACOLOGICAL PROPERTIES, Thrombosis and haemostasis, 74(2), 1995, pp. 646-654
CHARACTERIZATION OF A NOVEL SERIES OF APROTININ-DERIVED ANTICOAGULANTS .2. COMPARATIVE ANTITHROMBOTIC EFFECTS ON PRIMARY THROMBUS FORMATIONIN-VIVO
Authors: STASSEN JM LAMBEIR AM VREYS I DECKMYN H MATHYSSENS G NYSTROM A VERMYLEN J
Citation: Jm. Stassen et al., CHARACTERIZATION OF A NOVEL SERIES OF APROTININ-DERIVED ANTICOAGULANTS .2. COMPARATIVE ANTITHROMBOTIC EFFECTS ON PRIMARY THROMBUS FORMATIONIN-VIVO, Thrombosis and haemostasis, 74(2), 1995, pp. 655-659
WILD-TYPE AND MUTANT D-XYLOSE ISOMERASE FROM ACTINOPLANES-MISSOURIENSIS - METAL-ION DISSOCIATION-CONSTANTS, KINETIC-PARAMETERS OF DEUTERATED AND NON-DEUTERATED SUBSTRATES AND SOLVENT-ISOTOPE EFFECTS
Authors: VANBASTELAERE PBM KERSTERSHILDERSON HLM LAMBEIR AM
Citation: Pbm. Vanbastelaere et al., WILD-TYPE AND MUTANT D-XYLOSE ISOMERASE FROM ACTINOPLANES-MISSOURIENSIS - METAL-ION DISSOCIATION-CONSTANTS, KINETIC-PARAMETERS OF DEUTERATED AND NON-DEUTERATED SUBSTRATES AND SOLVENT-ISOTOPE EFFECTS, Biochemical journal, 307, 1995, pp. 135-142
STRATEGIES IN THE DESIGN OF INHIBITORS OF SERINE PROTEASES OF THE COAGULATION CASCADE - FACTOR XA
Authors: RIPKA W BRUNCK T STANSSENS P LAROCHE Y LAUWEREYS M LAMBEIR AM LASTERS I DEMAEYER M VLASUK G LEVY O MILLER T WEBB T TAMURA S PEARSON D
Citation: W. Ripka et al., STRATEGIES IN THE DESIGN OF INHIBITORS OF SERINE PROTEASES OF THE COAGULATION CASCADE - FACTOR XA, European journal of medicinal chemistry, 30, 1995, pp. 87-100
A NEW SYNTHETIC METHOD FOR PROLINE DIPHENYL PHOSPHONATES
Authors: BELYAEV A BORLOO M AUGUSTYNS K LAMBEIR AM DEMEESTER I SCHARPE S BLATON N PEETERS OM DERANTER C HAEMERS A
Citation: A. Belyaev et al., A NEW SYNTHETIC METHOD FOR PROLINE DIPHENYL PHOSPHONATES, Tetrahedron letters, 36(21), 1995, pp. 3755-3758
COMPARATIVE PROPERTIES OF A FACTOR-XA INHIBITOR, 4C2 (AN APROTONIN ANALOG), HEPARIN AND HIRUDIN IN A HAMSTER FEMORAL VEIN PLATELET-RICH MURAL THROMBOSIS MODEL
Authors: STASSEN JM DECKMYN H VREYS I LAMBEIR AM
Citation: Jm. Stassen et al., COMPARATIVE PROPERTIES OF A FACTOR-XA INHIBITOR, 4C2 (AN APROTONIN ANALOG), HEPARIN AND HIRUDIN IN A HAMSTER FEMORAL VEIN PLATELET-RICH MURAL THROMBOSIS MODEL, Thrombosis and haemostasis, 69(6), 1993, pp. 588-588
ECOTIN AS A POTENT FACTOR-XA INHIBITOR
Authors: LAUWEREYS M STANSSENS P LAMBEIR AM MESSENS J DEMPSEY E VLASUK GP
Citation: M. Lauwereys et al., ECOTIN AS A POTENT FACTOR-XA INHIBITOR, Thrombosis and haemostasis, 69(6), 1993, pp. 783-783
RECOMBINANT KUNITZ INHIBITORS OF COAGULATION PROTEASES .2. RANDOM MUTAGENESIS
Authors: DEMAEYER M LAMBEIR AM LAROCHE Y LASTERS I LAUWEREYS M MATTHYSSENS G STANSSENS P RIPKA W VLASUK G
Citation: M. Demaeyer et al., RECOMBINANT KUNITZ INHIBITORS OF COAGULATION PROTEASES .2. RANDOM MUTAGENESIS, Thrombosis and haemostasis, 69(6), 1993, pp. 888-888
RECOMBINANT KUNITZ INHIBITORS OF COAGULATION PROTEASES .1. SITE-SPECIFIC MUTAGENESIS
Authors: DEMAEYER M LAMBEIR AM LAROCHE Y LASTERS I LAUWEREYS M MATTHYSSENS G STANSSENS P RIPKA W VLASUK G
Citation: M. Demaeyer et al., RECOMBINANT KUNITZ INHIBITORS OF COAGULATION PROTEASES .1. SITE-SPECIFIC MUTAGENESIS, Thrombosis and haemostasis, 69(6), 1993, pp. 889-889
Risultati: 1-18 |