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Publikacje na liście filadelfijskiej

Wykaz publikacji opublikowanych na liście filadelfijskiej: SCOPUS

 

 

  1. Sławińska-Brych, A., et al., Xanthohumol inhibits the extracellular signal regulated kinase (ERK) signalling pathway and suppresses cell growth of lung adenocarcinoma cells. Toxicology, 2016. 357-358: p. 65-73.
  2. Mroczek-Zdyrska, M., et al., Stimulation with a 130-mT magnetic field improves growth and biochemical parameters in lupin (Lupinus angustifolius l.). Turkish Journal of Biology, 2016. 40(3): p. 699-705.
  3. Klimek, K., et al., In vitro evaluation of antifungal and cytotoxic activities as also the therapeutic safety of the oxidized form of amphotericin B. Chemico-Biological Interactions, 2016. 256: p. 47-54.
  4. Czernel, G., et al., Catalytic effect of free iron ions and heme-iron on chromophore oxidation of a polyene antibiotic amphotericin B. Journal of Molecular Structure, 2016. 1111: p. 69-75.
  5. Sławińska-Brych, A., et al., Xanthohumol inhibits cell cycle progression and proliferation of larynx cancer cells in vitro. Chemico-Biological Interactions, 2015. 240: p. 110-118.
  6. Pietrow, M., et al., Evidence for weakly bound electrons in non-irradiated alkane crystals: The electrons as a probe of structural differences in crystals. Journal of Chemical Physics, 2015. 142(6).
  7. Matwijczuk, A., et al., Spectroscopic Studies of Dual Fluorescence in 2-((4-Fluorophenyl)amino)-5-(2,4-dihydroxybenzeno)-1,3,4-thiadiazole. Journal of Physical Chemistry A, 2015. 119(44): p. 10791-10805.
  8. Matwijczuk, A., et al., Influence of Solvent Polarizability on the Keto-Enol Equilibrium in 4-[5-(naphthalen-1-ylmethyl)-1,3,4-thiadiazol-2-yl]benzene-1,3-diol. Journal of Fluorescence, 2015. 25(6): p. 1867-1874.
  9. Kamiński, D.M., et al., The influence of amphotericin B on the molecular organization and structural properties of DPPC lipid membranes modified by sterols. Journal of Molecular Structure, 2015. 1082: p. 7-11.
  10. Gola, J., et al., Expression profiles of genes related to melatonin and oxidative stress in human renal proximal tubule cells treated with antibiotic amphotericin B and its modified forms. Turkish Journal of Biology, 2015. 39(6): p. 856-864.
  11. Chudzik, B., et al., A new look at the antibiotic amphotericin B effect on Candida albicans plasma membrane permeability and cell viability functions. European Biophysics Journal, 2015. 44(1-2): p. 77-90.
  12. Kamiński, D.M., et al., Effect of cholesterol and ergosterol on the antibiotic amphotericin B interactions with dipalmitoylphosphatidylcholine monolayers: X-ray reflectivity study. Biochimica et Biophysica Acta – Biomembranes, 2014. 1838(11): p. 2947-2953.
  13. Kamiński, D.M., et al., Antibiotic amphotericin B-DPPC lipid complex: X-ray diffraction and FTIR studies. Journal of Molecular Structure, 2014. 1080: p. 57-62.
  14. Gagoś, M. and G. Czernel, Oxidized forms of polyene antibiotic amphotericin B. Chemical Physics Letters, 2014. 598: p. 5-9.
  15. Bartnika, M., et al., Single crystal X-ray diffraction, spectroscopicand mass spectrometric studies of furanocoumarin peucedanin. Natural Product Communications, 2014. 9(1): p. 71-74.
  16. Pietrow, M., M. Gagoś, and D. Kamiński, The influence of crystal morphology on the process of positronium formation in docosane. The accessibility of electrons for trapping. Radiation Physics and Chemistry, 2013. 88: p. 38-44.
  17. Hoser, A.A., et al., On polymorphism of 2-(4-fluorophenylamino)-5-(2,4-dihydroxybenzeno)-1,3,4- thiadiazole (FABT) DMSO solvates. CrystEngComm, 2013. 15(10): p. 1978-1988.
  18. Chudzik, B., et al., Amphotericin B-copper(II) complex as a potential agent with higher antifungal activity against Candida albicans. European Journal of Pharmaceutical Sciences, 2013. 49(5): p. 850-857.
  19. Arczewska, M., et al., The molecular organization of prenylated flavonoid xanthohumol in DPPC multibilayers: X-ray diffraction and FTIR spectroscopic studies. Biochimica et Biophysica Acta – Biomembranes, 2013. 1828(2): p. 213-222.
  20. Strachecka, A., et al., The effect of amphotericin B on the lifespan, body-surface protein concentrations, and DNA methylation levels of honey bees (Apis mellifera). Journal of Apicultural Science, 2012. 56(2): p. 107-113.
  21. Rój, E., M. Gagoś, and A. Dobrzyńska-Inger. Cost optimization of extract production in supercritical extraction process with the use of CO2 – A novel approach. in Procedia Engineering. 2012.
  22. Kamiński, D.M., et al., Effect of 2-(4-fluorophenylamino)-5-(2,4-dihydroxyphenyl)-1,3,4-thiadiazole on the molecular organisation and structural properties of the DPPC lipid multibilayers. Biochimica et Biophysica Acta – Biomembranes, 2012. 1818(11): p. 2850-2859.
  23. Jarzembska, K.N., et al., Controlled crystallization, structure, and molecular properties of iodoacetylamphotericin B. Crystal Growth and Design, 2012. 12(5): p. 2336-2345.
  24. Grzyb, J., et al., Cadmium inhibitory action leads to changes in structure of ferredoxin:NADP + oxidoreductase. Journal of Biological Physics, 2012. 38(3): p. 415-428.
  25. Gagoś, M., et al., Spectroscopic evidence for self-organization of N -iodoacetylamphotericin B in crystalline and amorphous phases. Journal of Physical Chemistry B, 2012. 116(42): p. 12706-12713.
  26. Gagoś, M. and M. Arczewska, FTIR spectroscopic study of molecular organization of the antibiotic amphotericin B in aqueous solution and in DPPC lipid monolayers containing the sterols cholesterol and ergosterol. European Biophysics Journal, 2012. 41(8): p. 663-673.
  27. Gagoś, M., et al., Spectroscopic studies of intramolecular proton transfer in 2-(4-fluorophenylamino)-5-(2,4-dihydroxybenzeno)-1,3,4-thiadiazole. Journal of Fluorescence, 2011. 21(1): p. 1-10.
  28. Gagoś, M., et al., Spectroscopic studies of amphotericin B-Cu 2+ complexes. BioMetals, 2011. 24(5): p. 915-922.
  29. Gagoś, M., M. Arczewska, and W.I. Gruszecki, Raman spectroscopic study of aggregation process of antibiotic amphotericin B induced by H+, Na+, and K+ ions. Journal of Physical Chemistry B, 2011. 115(17): p. 5032-5036.
  30. Gagoś, M. and M. Arczewska, Influence of K+ and Na+ ions on the aggregation processes of antibiotic amphotericin B: Electronic absorption and FTIR spectroscopic studies. Journal of Physical Chemistry B, 2011. 115(12): p. 3185-3192.
  31. Borsuk, G., et al., Microscopic image of honeybee drone spermatozoa in three diluents. Journal of Apicultural Science, 2011. 55(2): p. 5-13.
  32. Arczewska, M. and M. Gagoś, Molecular organization of antibiotic amphotericin B in dipalmitoylphosphatidylcholine monolayers induced by K+ and Na + ions: The Langmuir technique study. Biochimica et Biophysica Acta – Biomembranes, 2011. 1808(11): p. 2706-2713.
  33. Kamiński, D.M., et al., Solvatomorphism of 2-(4-fluorophenylamino)-5-(2,4-dihydroxybenzeno)-1,3,4- thiadiazole chloride. Crystal Growth and Design, 2010. 10(8): p. 3480-3488.
  34. Gagoś, M. and M. Arczewska, Spectroscopic studies of molecular organization of antibiotic amphotericin B in monolayers and dipalmitoylphosphatidylcholine lipid multibilayers. Biochimica et Biophysica Acta – Biomembranes, 2010. 1798(11): p. 2124-2130.
  35. Muszyński, S., M. Gagoś, and S. Pietruszewski, Short-term pre-Germination exposure to ELF magnetic field does not influence seedling growth in durum wheat (Triticum durum). Polish Journal of Environmental Studies, 2009. 18(6): p. 1065-1072.
  36. Gruszecki, W.I., et al., Molecular organization of antifungal antibiotic amphotericin B in lipid monolayers studied by means of Fluorescence Lifetime Imaging Microscopy. Biophysical Chemistry, 2009. 143(1-2): p. 95-101.
  37. Hereć, M., et al., Secondary structure and orientation of the pore-forming toxin lysenin in a sphingomyelin-containing membrane. Biochimica et Biophysica Acta – Biomembranes, 2008. 1778(4): p. 872-879.
  38. Grzyb, J., et al., Interaction of ferredoxin:NADP+ oxidoreductase with model membranes. Biochimica et Biophysica Acta – Biomembranes, 2008. 1778(1): p. 133-142.
  39. Gagoś, M., et al., Anomalously high aggregation level of the polyene antibiotic amphotericin B in acidic medium: Implications for the biological action. Biophysical Chemistry, 2008. 136(1): p. 44-49.
  40. Gagoś, M. and W.I. Gruszecki, Organization of polyene antibiotic amphotericin B at the argon-water interface. Biophysical Chemistry, 2008. 137(2-3): p. 110-115.
  41. Gagoś, M., Molecular organization of 2-(2,4-dihydroxylphenyl)-5,6-dichlor 1,3-benzothiazole in monomolecular layers formed with diphytanoylphosphatidylcholine: A linear dichroism-FTIR study. Biochimica et Biophysica Acta – Biomembranes, 2008. 1778(11): p. 2520-2525.
  42. Sujak, A., et al., Organization of two-component monomolecular layers formed with dipalmitoylphosphatidylcholine and the carotenoid pigment, canthaxanthin. Molecular Membrane Biology, 2007. 24(5-6): p. 431-441.
  43. Hereć, M., et al., Effect of antibiotic amphotericin B on structural and dynamic properties of lipid membranes formed with egg yolk phosphatidylcholine. Chemistry and Physics of Lipids, 2007. 147(2): p. 78-86.
  44. Gabrielska, J., et al., Binding of antibiotic amphotericin B to lipid membranes: A 1H NMR study. FEBS Letters, 2006. 580(11): p. 2677-2685.
  45. Gagoś, M., et al., Molecular organization of the antifungal and anticancer drug 2-(2,4-dihydroxyphenylo)-5,6-dichlorobenzothiazole in solution and in monolayers: An effect of pH. Journal of Photochemistry and Photobiology B: Biology, 2005. 80(2): p. 101-106.
  46. Gagoś, M., et al., Binding of antibiotic amphotericin B to lipid membranes: Monomolecular layer technique and linear dichroism-FTIR studies. Molecular Membrane Biology, 2005. 22(5): p. 433-442.
  47. Gagoś, M., A. Niewiadomy, and W.I. Gruszecki, Molecular organization of the antifungal and anticancer drug 2-(2,4-dihydroxyphenylo)-5,6-dichlorobenzothiazole (dHBBT) in solution and in lipid membranes studied by means of electronic absorption spectroscopy. Journal of Photochemistry and Photobiology B: Biology, 2004. 76(1-3): p. 33-40.
  48. Gruszecki, W.I., et al., Organization of antibiotic amphotericin B in model lipid membranes. A mini review. Cellular and Molecular Biology Letters, 2003. 8(1): p. 161-170.
  49. Gruszecki, W.I., M. Gagoś, and M. Hereć, Dimers of polyene antibiotic amphotericin B detected by means of fluorescence spectroscopy: Molecular organization in solution and in lipid membranes. Journal of Photochemistry and Photobiology B: Biology, 2003. 69(1): p. 49-57.
  50. Gruszecki, W.I., M. Gagos, and P. Kernen, Polyene antibiotic amphotericin B in monomolecular layers: Spectrophotometric and scanning force microscopic analysis. FEBS Letters, 2002. 524(1-3): p. 92-96.
  51. Gagoś, M., R. Koper, and W. Gruszecki, Spectrophotometric analysis of organisation of dipalmitoylphosphatidylcholine bilayers containing the polyene antibiotic amphotericin B. Biochimica et Biophysica Acta – Biomembranes, 2001. 1511(1): p. 90-98.
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