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Results: 1-17 |
Results: 17

Authors: Zgodka, D Milewski, S Borowski, E
Citation: D. Zgodka et al., A diffusible analogue of N-3-(4-methoxyfumaroyl)-L-2,3-diaminopropanoic acid with antifungal activity, MICROBI-SGM, 147, 2001, pp. 1955-1959

Authors: Zgodka, D Jedrzejczak, R Milewski, S Borowski, E
Citation: D. Zgodka et al., Amide and ester derivatives of N-3-(4-methoxyumaroyl)-(S)-2,3-diaminopropanoic acid: The selective inhibitor of glucosamine-6-phosphate synthase, BIO MED CH, 9(4), 2001, pp. 931-938

Authors: Szlinder-Richert, J Mazerski, J Cybulska, B Grzybowska, J Borowski, E
Citation: J. Szlinder-richert et al., MFAME, N-methyl-N-D-fructosyl amphotericin B methyl ester, a new amphotericin B derivative of low toxicity: relationship between self-association andeffects on red blood cells, BBA-GEN SUB, 1528(1), 2001, pp. 15-24

Authors: Milewski, S Mignini, F Prasad, R Borowski, E
Citation: S. Milewski et al., Unusual susceptibility of a multidrug-resistant yeast strain to peptidic antifungals, ANTIM AG CH, 45(1), 2001, pp. 223-228

Authors: Tkaczyk-Gobis, K Tarasiuk, J Seksek, O Stefanska, B Borowski, E Garnier-Suillerot, A
Citation: K. Tkaczyk-gobis et al., Transport of new non-cross-resistant antitumor compounds of the benzoperimidine family in multidrug resistant cells, EUR J PHARM, 413(2-3), 2001, pp. 131-141

Authors: Andruszkiewicz, R Jedrzejczak, R Zieniawa, T Wojciechowski, M Borowski, E
Citation: R. Andruszkiewicz et al., N-3-oxoacyl derivatives of L-2,3-diaminopropanoic acid and their peptides;Novel inhibitors of glucosamine-6-phosphate synthase, J ENZ INHIB, 15(5), 2000, pp. 429

Authors: Sachadyn, P Jedrzejczak, R Milewski, S Kur, J Borowski, E
Citation: P. Sachadyn et al., Purification to homogeneity of Candida albicans glucosamine-6-phosphate synthase overexpressed in Escherichia coli, PROT EX PUR, 19(3), 2000, pp. 343-349

Authors: Resat, H Sungur, FA Baginski, M Borowski, E Aviyente, V
Citation: H. Resat et al., Conformational properties of amphotericin B amide derivatives - impact on selective toxicity, J COMPUT A, 14(7), 2000, pp. 689-703

Authors: Garcia-Chaumont, C Seksek, O Grzybowska, J Borowski, E Bolard, J
Citation: C. Garcia-chaumont et al., Delivery systems for antisense oligonucleotides, PHARM THERA, 87(2-3), 2000, pp. 255-277

Authors: Borowski, E Blamowski, ZK Michalek, W
Citation: E. Borowski et al., Effects of Tomatex (Triacontanol) on chlorophyll fluorescence and tomato (Lycopersicon esculentum Mill.) yields, ACT PHYS PL, 22(3), 2000, pp. 271-274

Authors: Borowski, E
Citation: E. Borowski, Novel approaches in the rational design of antifungal agents of low toxicity, FARMACO, 55(3), 2000, pp. 206-208

Authors: Shugar, D Rode, W Borowski, E
Citation: D. Shugar et al., Chemotherapy: molecular aspects - Preface, ACT BIOCH P, 47(1), 2000, pp. NIL_3-NIL_4

Authors: Cybulska, B Gadomska, I Mazerski, J Grzybowska, J Borowski, E Cheron, M Bolard, J
Citation: B. Cybulska et al., N-methyl-N-D-fructosyl amphotericin B methyl ester (MF-AME), a novel antifungal agent of low toxicity: Monomer/micelle control over selective toxicity, ACT BIOCH P, 47(1), 2000, pp. 121-131

Authors: Szlinder-Richert, J Cybulska, B Grzybowska, J Borowski, E Prasad, R
Citation: J. Szlinder-richert et al., Comparative studies on cell stimulatory, permeabilizing and toxic effects induced in sensitive and multidrug resistant fungal strains by amphotericinB (AMB) and N-methyl-N-D-fructosyl amphotericin B methyl ester (MFAME), ACT BIOCH P, 47(1), 2000, pp. 133-140

Authors: Pawlowska, J Tarasiuk, J Borowski, E Wasowska, M Oszczapowicz, I Wolf, CR
Citation: J. Pawlowska et al., The ability of new formamidine sugar-modified derivatives of daunorubicin to stimulate free radical formation in three enzymatic systems: NADH dehydrogenase, NADPH cytochrome P450 reductase and xanthine oxidase, ACT BIOCH P, 47(1), 2000, pp. 141-147

Authors: Stefanska, B Dzieduszycka, M Bontemps-Gracz, MM Borowski, E Martelli, S Supino, R Pratesi, G De Cesare, M Zunino, F Kusnierczyk, H Radzikowski, C
Citation: B. Stefanska et al., 8,11-dihydroxy-6-[(aminoalkyl)amino]-7H-benzo[e]perimidin-7-ones with activity in multidrug-resistant cell lines: Synthesis and antitumor evaluation, J MED CHEM, 42(18), 1999, pp. 3494-3501

Authors: Tarasiuk, J Tkaczyk-Gobis, K Stefanska, B Dzieduszycka, M Priebe, W Martelli, S Borowski, E
Citation: J. Tarasiuk et al., The role of structural factors of anthraquinone compounds and their quinone-modified analogues in NADH dehydrogenase-catalysed oxygen radical formation, ANTI-CAN DR, 13(8), 1998, pp. 923-939
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