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Results: 1-10 |
Results: 10
Glycolysis as a target for the design of new anti-trypanosome drugs
Authors: Verlinde, CLM Hannaert, V Blonski, C Willson, M Perie, JJ Fothergill-Gilmore, LA Opperdoes, FR Gelb, MH Hol, WGJ Michels, PAM
Citation: Clm. Verlinde et al., Glycolysis as a target for the design of new anti-trypanosome drugs, DRUG RESIST, 4(1), 2001, pp. 50-65
Selective phosphorylation on primary alcohols of unprotected polyols
Authors: Ladame, S Claustre, S Willson, M
Citation: S. Ladame et al., Selective phosphorylation on primary alcohols of unprotected polyols, PHOSPHOR SU, 174, 2001, pp. 37-47
Selective inhibition of Trypanosoma brucei GAPDH by 1,3-bisphospho-D-glyceric acid (1,3-diPG) analogues
Authors: Ladame, S Bardet, M Perie, J Willson, M
Citation: S. Ladame et al., Selective inhibition of Trypanosoma brucei GAPDH by 1,3-bisphospho-D-glyceric acid (1,3-diPG) analogues, BIO MED CH, 9(3), 2001, pp. 773-783
Indazolylamino quinazolines and pyridopyrimidines as inhibitors of the EGFr and C-erbB-2
Authors: Cockerill, S Stubberfield, C Stables, J Carter, M Guntrip, S Smith, K McKeown, S Shaw, R Topley, P Thomsen, L Affleck, K Jowett, A Hayes, D Willson, M Woollard, P Spalding, D
Citation: S. Cockerill et al., Indazolylamino quinazolines and pyridopyrimidines as inhibitors of the EGFr and C-erbB-2, BIOORG MED, 11(11), 2001, pp. 1401-1405
Involvement of deacylation in activation of substrate hydrolysis by Drosophila acetylcholinesterase
Authors: Brochier, L Pontie, Y Willson, M Estrada-Mondaca, S Czaplicki, J Klaebe, A Fournier, D
Citation: L. Brochier et al., Involvement of deacylation in activation of substrate hydrolysis by Drosophila acetylcholinesterase, J BIOL CHEM, 276(21), 2001, pp. 18296-18302
Analysis of the kinetics of reversible enzyme inhibition by a general algebraic method. Application to multisite inhibition of the phosphoglycerate kinase from Trypanosoma brucei (vol 14, pg 27, 1998)
Authors: Puech, J Callens, M Willson, M
Citation: J. Puech et al., Analysis of the kinetics of reversible enzyme inhibition by a general algebraic method. Application to multisite inhibition of the phosphoglycerate kinase from Trypanosoma brucei (vol 14, pg 27, 1998), J ENZ INHIB, 14(5), 1999, pp. I-V
ECCO 10: Quality-of-life issues bumped into the spotlight
Authors: Willson, M
Citation: M. Willson, ECCO 10: Quality-of-life issues bumped into the spotlight, J NAT CANC, 91(20), 1999, pp. 1711-1712
Inhibition of yeast hexokinase: a kinetic and phosphorus nuclear magnetic resonance study
Authors: Willson, M Perie, J
Citation: M. Willson et J. Perie, Inhibition of yeast hexokinase: a kinetic and phosphorus nuclear magnetic resonance study, SPECT ACT A, 55(4), 1999, pp. 911-917
An easy stereospecific synthesis of 1-amino-2,5-anhydro-1-deoxy-D-mannitoland arylamino derivatives
Authors: Claustre, S Bringaud, F Azema, L Baron, R Perie, J Willson, M
Citation: S. Claustre et al., An easy stereospecific synthesis of 1-amino-2,5-anhydro-1-deoxy-D-mannitoland arylamino derivatives, CARBOHY RES, 315(3-4), 1999, pp. 339-344
Analysis of the kinetics of reversible enzyme inhibition by a general algebraic method. Application to multisite inhibition of the phosphoglycerate kinase from Trypanosoma brucei
Authors: Puech, J Callens, M Willson, M
Citation: J. Puech et al., Analysis of the kinetics of reversible enzyme inhibition by a general algebraic method. Application to multisite inhibition of the phosphoglycerate kinase from Trypanosoma brucei, J ENZ INHIB, 14(1), 1998, pp. 27-47
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