Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Maria, Panagiotaki"'
Autor:
Olga Themeli, Maria Panagiotaki
Publikováno v:
European Journal of Counselling Psychology, Vol 3, Iss 1, Pp 1-19 (2014)
Although there is plenty of literature on the consequences of child sexual abuse, little research has been conducted regarding the risk of secondary victimization when a child victim testifies as a witness throughout the preliminary proceeding to the
Publikováno v:
European Journal of Organic Chemistry. 2005:3052-3059
Various alkyl-substituted phenols react readily with nitrogen dioxide (·NO2) in different solvents at room temperature. In all cases nitration is the major reaction and leads to the formation of mono- and dinitrophenols and 4-nitrocyclohexa-2,5-dien
Autor:
Julius Liobikas, Paola Costantini, Ove Eriksson, Maria Panagiotaki, Lucedio Greci, Milena Johans, Marina Franck, Paolo Bernardi, Giovanni Principato, Christoffer Johans, Eva Milanesi, Paavo K.J. Kinnunen
Publikováno v:
Journal of Biological Chemistry. 280:12130-12136
Methylglyoxal and synthetic glyoxal derivatives react covalently with arginine residue(s) on the mitochondrial permeability transition pore (PTP). In this study, we have investigated how the binding of a panel of synthetic phenylglyoxal derivatives i
Publikováno v:
Free Radical Research. 39:137-144
Spin trapping of nitrogen dioxide radical by several nitrones has been studied. The reaction results in the formation of persistent acyl nitroxides, after the oxidation of the intermediate spin adducts having an -ONO group on C-2 atom. The intermedia
Autor:
Milena, Johans, Eva, Milanesi, Marina, Franck, Christoffer, Johans, Julius, Liobikas, Maria, Panagiotaki, Lucedio, Greci, Giovanni, Principato, Paavo K J, Kinnunen, Paolo, Bernardi, Paola, Costantini, Ove, Eriksson
Publikováno v:
The Journal of biological chemistry. 280(13)
Methylglyoxal and synthetic glyoxal derivatives react covalently with arginine residue(s) on the mitochondrial permeability transition pore (PTP). In this study, we have investigated how the binding of a panel of synthetic phenylglyoxal derivatives i
Publikováno v:
Scopus-Elsevier
Chiral 4-alkyloxymethyl- and silyloxymethylpyrrolidin-2-ones, (10a-c), underwent alkylation to give the corresponding 3,4-trans-disubstituted pyrrolidin-2-ones, (lla-g), in good yield and total stereoselection, as shown by 'H NMR spectral data and n.
Publikováno v:
Molecular biotechnology 37 (2007): 19–25. doi:10.1007/s12033-007-0054-9
info:cnr-pdr/source/autori:Ferreri, Carla; Panagiotaki, Maria; Chatgilialoglu, Chryssostomos/titolo:Trans fatty acids in membranes: The free radical path/doi:10.1007%2Fs12033-007-0054-9/rivista:Molecular biotechnology/anno:2007/pagina_da:19/pagina_a:25/intervallo_pagine:19–25/volume:37
info:cnr-pdr/source/autori:Ferreri, Carla; Panagiotaki, Maria; Chatgilialoglu, Chryssostomos/titolo:Trans fatty acids in membranes: The free radical path/doi:10.1007%2Fs12033-007-0054-9/rivista:Molecular biotechnology/anno:2007/pagina_da:19/pagina_a:25/intervallo_pagine:19–25/volume:37
The double bond geometry of most of the naturally occurring unsaturated fatty acid residues is cis. Due to the relevance of fatty acids as structural components of cell membranes and as biologically active molecules, the change of the cis geometry me
Publikováno v:
Organic & Biomolecular Chemistry. 4:3282
The reaction of 2-phenyl- and 1-methyl-2-phenylindole with nitrogen dioxide or with nitrous acid (NaNO2-CH3COOH) in benzene leads mainly to the formation of the isonitroso and 3-nitroso indole derivatives, respectively. When reacted with nitrous acid
Autor:
Konstantinos Goumas, Athanasios J. Archimandritis, Androniki Poulou, Dimitrios Dandakis, Maria Panagiotaki, Dimitrios Soutos, Ioannis Tyrmpas, Androniki Georgouli
Publikováno v:
World Journal of Gastroenterology. 12:739
To investigate whether microproteinuria in patients with inflammatory bowel disease (IBD) is associated with the disease activity or the treatment with 5-aminosalicylic acid (5-ASA).We prospectively studied microproteinuria in 86 consecutive patients
Publikováno v:
European Journal of Organic Chemistry; Jul2005, Vol. 2005 Issue 14, p3052-3059, 8p