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Results: 1-9 |
Results: 9
SELECTIVE TIGHT-BINDING INHIBITORS OF TRYPANOSOMAL GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE VIA STRUCTURE-BASED DRUG DESIGN
Authors: ARONOV AM VERLINDE CLMJ HOL WGJ GELB MH
Citation: Am. Aronov et al., SELECTIVE TIGHT-BINDING INHIBITORS OF TRYPANOSOMAL GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE VIA STRUCTURE-BASED DRUG DESIGN, Journal of medicinal chemistry, 41(24), 1998, pp. 4790-4799
EFFICIENT TECHNIQUE FOR SCREENING DRUGS FOR ACTIVITY AGAINST TRYPANOSOMA-CRUZI USING PARASITES EXPRESSING BETA-GALACTOSIDASE
Authors: BUCKNER FS VERLINDE CLMJ LAFLAMME AC VANVOORHIS WC
Citation: Fs. Buckner et al., EFFICIENT TECHNIQUE FOR SCREENING DRUGS FOR ACTIVITY AGAINST TRYPANOSOMA-CRUZI USING PARASITES EXPRESSING BETA-GALACTOSIDASE, Antimicrobial agents and chemotherapy, 40(11), 1996, pp. 2592-2597
DRUG OR TOOL, DESIGN OR SERENDIPITY
Authors: VERLINDE CLMJ DIJKSTRA BW
Citation: Clmj. Verlinde et Bw. Dijkstra, DRUG OR TOOL, DESIGN OR SERENDIPITY, Nature structural biology, 2(6), 1995, pp. 429-432
3-DIMENSIONAL STRUCTURE OF THE DIPHTHERIA-TOXIN REPRESSOR IN COMPLEX WITH DIVALENT-CATION CO-REPRESSORS
Authors: QIU XY VERLINDE CLMJ ZHANG SP SCHMITT MP HOLMES RK HOL WGJ
Citation: Xy. Qiu et al., 3-DIMENSIONAL STRUCTURE OF THE DIPHTHERIA-TOXIN REPRESSOR IN COMPLEX WITH DIVALENT-CATION CO-REPRESSORS, Structure, 3(1), 1995, pp. 87-100
SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF ANALOGS OF 2'-DEOXY-2'-(3-METHOXYBENZAMIDO)ADENOSINE, A SELECTIVE INHIBITOR OF TRYPANOSOMAL GLYCOSOMAL GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE
Authors: VANCALENBERGH S VERLINDE CLMJ SOENENS J DEBRUYN A CALLENS M BLATON NM PEETERS OM ROZENSKI J HOL WGJ HERDEWIJN P
Citation: S. Vancalenbergh et al., SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF ANALOGS OF 2'-DEOXY-2'-(3-METHOXYBENZAMIDO)ADENOSINE, A SELECTIVE INHIBITOR OF TRYPANOSOMAL GLYCOSOMAL GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE, Journal of medicinal chemistry, 38(19), 1995, pp. 3838-3849
CRYSTAL-STRUCTURE OF GLYCOSOMAL GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE FROM LEISHMANIA-MEXICANA - IMPLICATIONS FOR STRUCTURE-BASED DRUG DESIGN AND A NEW POSITION FOR THE INORGANIC-PHOSPHATE BINDING-SITE
Authors: KIM HD FEIL IK VERLINDE CLMJ PETRA PH HOL WGJ
Citation: Hd. Kim et al., CRYSTAL-STRUCTURE OF GLYCOSOMAL GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE FROM LEISHMANIA-MEXICANA - IMPLICATIONS FOR STRUCTURE-BASED DRUG DESIGN AND A NEW POSITION FOR THE INORGANIC-PHOSPHATE BINDING-SITE, Biochemistry, 34(46), 1995, pp. 14975-14986
STRUCTURE-BASED DRUG DESIGN - PROGRESS, RESULTS AND CHALLENGES
Authors: VERLINDE CLMJ HOL WGJ
Citation: Clmj. Verlinde et Wgj. Hol, STRUCTURE-BASED DRUG DESIGN - PROGRESS, RESULTS AND CHALLENGES, Structure, 2(7), 1994, pp. 577-587
PROTEIN CRYSTALLOGRAPHY AND INFECTIOUS-DISEASES
Authors: VERLINDE CLMJ MERRITT EA VANDENAKKER F KIM HD FEIL I DELBONI LF MANDE SC SARFATY S PETRA PH HOL WGJ
Citation: Clmj. Verlinde et al., PROTEIN CRYSTALLOGRAPHY AND INFECTIOUS-DISEASES, Protein science, 3(10), 1994, pp. 1670-1686
SELECTIVE-INHIBITION OF TRYPANOSOMAL GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE BY PROTEIN STRUCTURE-BASED DESIGN - TOWARD NEW DRUGS FOR THE TREATMENT OF SLEEPING SICKNESS
Authors: VERLINDE CLMJ CALLENS M VANCALENBERGH S VANAERSCHOT A HERDEWIJN P HANNAERT V MICHELS PAM OPPERDOES FR HOL WGJ
Citation: Clmj. Verlinde et al., SELECTIVE-INHIBITION OF TRYPANOSOMAL GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE BY PROTEIN STRUCTURE-BASED DESIGN - TOWARD NEW DRUGS FOR THE TREATMENT OF SLEEPING SICKNESS, Journal of medicinal chemistry, 37(21), 1994, pp. 3605-3613
Risultati: 1-9 |