Publications

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2019
K. Szilágyi, Hajdu, I., Blachner, B., Lorincz, Z., Balczer, J., Gal, P., Zavodszy, P., .Pirli, C., Balogh, B., Mandity, I. M., Cseh, S., and Dorman, G., Design and Selection of Novel C1s Inhibitors by In Silico and In Vitro Approaches, Molecules, vol. 24, no. 20, 2019.
K. Szilágyi, Hajdu, I., Blachner, B., Lorincz, Z., Balczer, J., Gal, P., Zavodszy, P., .Pirli, C., Balogh, B., Mandity, I. M., Cseh, S., and Dorman, G., Design and Selection of Novel C1s Inhibitors by In Silico and In Vitro Approaches, Molecules, vol. 24, no. 20, 2019.
K. Szilágyi, Hajdu, I., Blachner, B., Lorincz, Z., Balczer, J., Gal, P., Zavodszy, P., .Pirli, C., Balogh, B., Mandity, I. M., Cseh, S., and Dorman, G., Design and Selection of Novel C1s Inhibitors by In Silico and In Vitro Approaches, Molecules, vol. 24, no. 20, 2019.
F. Zsila, Kohut, G., and Beke-Somfai, T., Disorder-to-helix conformational conversion of the human immunomodulatory peptide LL-37 induced by antiinflammatory drugs, food dyes and some metabolites, International Journal of Biological Macromolecules, vol. 129, pp. 50-60, 2019.
T. Beke-Somfai, Felgyorsított evolúció – A 2018-as kémiai Nobel-díj, Magyar Tudomány, 2019.
I. Nekkaa, Bogdán, D., Gáti, T., Béni, S., Juhász, T., Palkó, M., Paragi, G., Tóth, G. K., Fülöp, F., and Mándity, I. M., Flow-chemistry enabled efficient synthesis of β-peptides: backbone topology vs. helix formation, Chemical communications, vol. 55, pp. 3061–3064, 2019.
I. Nekkaa, Bogdán, D., Gáti, T., Béni, S., Juhász, T., Palkó, M., Paragi, G., Tóth, G. K., Fülöp, F., and Mándity, I. M., Flow-chemistry enabled efficient synthesis of β-peptides: backbone topology vs. helix formation, Chemical communications, vol. 55, pp. 3061–3064, 2019.
B. Nizami, Bereczki-Szakál, D., Varro, N., Battioui, Kel, Nagaraj, V. U., Szigyártó, I. Cs., Mándity, I., and Somfai, T. - B., FoldamerDB: a database of peptidic foldamers, Nucleic Acids Research, 2019.
B. Nizami, Bereczki-Szakál, D., Varro, N., Battioui, Kel, Nagaraj, V. U., Szigyártó, I. Cs., Mándity, I., and Somfai, T. - B., FoldamerDB: a database of peptidic foldamers, Nucleic Acids Research, 2019.
L. Almásy, Putz, A. - M., Tian, Q., Kopitsa, G., Khamova, T., Barabás, R., Rigó, M., Bóta, A., Wacha, A., Mirica, M., Ţăranu, B., and Savii, C., Hybrid mesoporous silica with controlled drug release, Journal of the Serbian Chemical Society, vol. 84, pp. 1027–1039, 2019.
L. Almásy, Putz, A. - M., Tian, Q., Kopitsa, G., Khamova, T., Barabás, R., Rigó, M., Bóta, A., Wacha, A., Mirica, M., Ţăranu, B., and Savii, C., Hybrid mesoporous silica with controlled drug release, Journal of the Serbian Chemical Society, vol. 84, pp. 1027–1039, 2019.
T. Visnovitz, Osteikoetxea, X., Sódar, B. W., Mihály, J., Lőrincz, P., Vukman, K. V., Tóth, E. Ágnes, Koncz, A., Székács, I., Horváth, R., Varga, Z., and Buzás, E. I., An improved 96 well plate format lipid quantification assay for standardisation of experiments with extracellular vesicles, Journal of Extracellular Vesicles, vol. 8, p. 1565263, 2019.
A. Wacha, Beke-Somfai, T., and Nagy, T., Improved Modeling of Peptidic Foldamers Using a Quantum Chemical Parametrization Based on Torsional Minimum Energy Path Matching, ChemPlusChem, vol. 84, pp. 927–941, 2019.
F. Zsila, Bosze, S., and Beke-Somfai, T., Interaction of antitubercular drug candidates with α1-acid glycoprotein produced in pulmonary granulomas, International Journal of Biological Macromolecules, 2019.
F. Zsila, Bosze, S., and Beke-Somfai, T., Interaction of antitubercular drug candidates with α1-acid glycoprotein produced in pulmonary granulomas, International Journal of Biological Macromolecules, 2019.
F. Sauvage, Legrand, F. - X., Roux, M., Rajkovic, I., Weiss, T. M., Varga, Z., Augis, L., Nugue, G., Debouzy, J. - C., Vergnaud-Gauduchon, J., and Barratt, G., Interaction of dequalinium chloride with phosphatidylcholine bilayers: A biophysical study with consequences on the development of lipid-based mitochondrial nanomedicines, Journal of Colloid and Interface Science, vol. 537, pp. 704–715, 2019.
D. Krüzselyi, Vetter, J., Ott, P. G., Darcsi, A., Béni, S., Gömöry, Á., Drahos, L., Zsila, F., and Móricz, Á. M., Isolation and structural elucidation of a novel brunnein-type antioxidant β-carboline alkaloid from Cyclocybe cylindracea, Fitoterapia, vol. 137, p. 104180, 2019.
M. Quemé-Peña, Juhász, T., Mihály, J., Szigyártó, I. Csilla, Horváti, K., Bosze, S., Henczkó, J., Pályi, B., Németh, C., Varga, Z., Zsila, F., and Beke-Somfai, T., Manipulating Active Structure and Function of Cationic Antimicrobial Peptide CM15 by the Polysulfonated Drug Suramin: A Step Closer to in vivo Complexity, ChemBioChem, 2019.
M. Quemé-Peña, Juhász, T., Mihály, J., Szigyártó, I. Csilla, Horváti, K., Bosze, S., Henczkó, J., Pályi, B., Németh, C., Varga, Z., Zsila, F., and Beke-Somfai, T., Manipulating Active Structure and Function of Cationic Antimicrobial Peptide CM15 by the Polysulfonated Drug Suramin: A Step Closer to in vivo Complexity, ChemBioChem, 2019.
G. Kohut, Sieradzan, A., Zsila, F., Juhász, T., Bosze, S., Liwo, A., Samsonov, S. A., and Beke-Somfai, T., The molecular mechanism of structural changes in the antimicrobial peptide CM15 upon complex formation with drug molecule suramin: a computational analysis, Physical Chemistry Chemical Physics, vol. 21, pp. 10644–10659, 2019.
G. Kohut, Sieradzan, A., Zsila, F., Juhász, T., Bosze, S., Liwo, A., Samsonov, S. A., and Beke-Somfai, T., The molecular mechanism of structural changes in the antimicrobial peptide CM15 upon complex formation with drug molecule suramin: a computational analysis, Physical Chemistry Chemical Physics, vol. 21, pp. 10644–10659, 2019.
R. Deak, Mihály, J., Szigyártó, I. Cs., Beke-Somfai, T., Turiák, L., Drahos, L., Wacha, A., Bóta, A., and Varga, Z., Nanoerythrosomes tailoring: Lipid induced protein scaffolding in ghost membrane derived vesicles, Materials Science and Engineering: C, p. 110428, 2019.
R. Deak, Mihály, J., Szigyártó, I. Cs., Beke-Somfai, T., Turiák, L., Drahos, L., Wacha, A., Bóta, A., and Varga, Z., Nanoerythrosomes tailoring: Lipid induced protein scaffolding in ghost membrane derived vesicles, Materials Science and Engineering: C, p. 110428, 2019.

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