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M. Hammarson, Nilsson, J. R., Li, S., Beke-Somfai, T., and Andréasson, J., Characterization of the thermal and photoinduced reactions of photochromic spiropyrans in aqueous solution, Journal of Physical Chemistry B, vol. 117, no. 43, pp. 13561 - 13571, 2013.
P. Hari, Bikadi, Z., Hazai, E., Lockwood, S. F., and Zsila, F., Non-covalent binding of lycopene and lycophyll, in Lycopene: Nutritional, Medicinal and Therapeutic Properties, Science Publishers, 2010, pp. 65 - 81.
V. Harmat, Domokos, K., Menyhárd, D. K., Palló, A., Szeltner, Z., Szamosi, I., Beke-Somfai, T., Náray-Szabó, G., and Polgár, L., Structure and catalysis of acylaminoacyl peptidase: Closed and open subunits of a dimer oligopeptidase, Journal of Biological Chemistry, vol. 286, no. 3, pp. 1987 - 1998, 2011.
N. Harris, Koppel, J., Zsila, F., Juhas, S., Il'kova, G., Kogan, F. Yurgenzon, Lahmy, O., Wildbaum, G., Karin, N., Zhuk, R., and Gregor, P., Mechanism of action and efficacy of RX-111, a thieno[2,3-c]pyridine derivative and small molecule inhibitor of protein interaction with glycosaminoglycans (SMIGs), in delayed-type hypersensitivity, TNBS-induced colitis and experimental autoimmune encephalomyelitis., Inflamm Res, vol. 65, no. 4, pp. 285-294., 2016.
E. Hazai, Bikadi, Z., Zsila, F., and Lockwood, S. F., Non-covalent binding of disodium disuccinate astaxanthin to the catalytic site of phosphodiesterase 5A: A molecular modeling study, Letters in Drug Design & Discovery, vol. 4, no. 2, pp. 128 - 136, 2007.
E. Hazai, Bikadi, Z., Zsila, F., and Lockwood, S. F., Molecular modeling of the non-covalent binding of the dietary tomato carotenoids lycopene and lycophyll, and selected oxidative metabolites with 5-lipoxygenase., Bioorg Med Chem, vol. 14, no. 20, pp. 6859-67, 2006.
Z. Hegedüs, Makra, I., Imre, N., Hetényi, A., Mándity, I. M., Monostori, É., and Martinek, T. A., Foldameric probes for membrane interactions by induced β-sheet folding, Chemical Communications, vol. 52, pp. 1891–1894, 2016.
H. Hegedus, Gergely, A., Veress, T., and Zsila, F., Determination of the enantiomeric purity of amphetamine after derivatization with Sanger's reagent (2,4-dinitrofluorobenzene [DNFB]) by simultaneous dual circular dichroism and ultraviolet spectroscopy, Fresenius' Journal of Analytical Chemistry, vol. 364, no. 8, pp. 749 - 752, 1999.
A. Hetenyi, Mándity, I. M., Martinek, T., Toth, G. K., and Fülöp, F., TRUE FOLDING OF CONFORMATIONALLY CONSTRAINED beta-PEPTIDES: CHAIN LENGTH-DEPENDENT SECONDARY STRUCTURE, Journal of Peptide Science, vol. 10, p. 273, 2004.
A. Hetenyi, Szakonyi, Z., Mándity, I. M., Szolnoki, E., Toth, G. K., Martinek, T. A., and Fülöp, F., Sculpting the beta-peptide foldamer H12 helix via a designed side-chain shape, Chemical Communications, pp. 177–179, 2009.
A. Hetenyi, Mándity, I. M., A. T, M., K. G, T., and Fülöp, F., Chain-length-dependent helical motifs and self-association of beta-peptides with constrained side chains, Journal of the American Chemical Society, vol. 127, p. 547–RF, 2004, BIOCHEMISTRY-US, V43, P9527, DOI 10.1021/bi0494141.
K. Hill, Pénzes, C. B., Schnöller, D., Horváti, K., Bősze, S., Hudecz, F., Keszthelyi, T., and Kiss, É., Characterisation of the membrane affinity of an isoniazide peptide conjugate by tensiometry, atomic force microscopy and sum-frequency vibrational spectroscopy, using a phospholipid Langmuir monolayer model, Physical Chemistry Chemical Physics, vol. 12, pp. 11498–11506, 2010.
A. Hoell, Varga, Z., Raghuwanshi, V. Singh, Krumrey, M., Bocker, C., and Rüssel, C., ASAXS study of CaF2 nanoparticles embedded in a silicate glass matrix, Journal of Applied Crystallography, vol. 47, no. 1, pp. 60-66, 2014.
Á. Horváth, Menghis, A., Botz, B., Borbély, É., Kemény, Á., Tékus, V., Csepregi, J. Zsófia, Mócsai, A., Juhász, T., Zákány, R., Bogdan, D., Matyus, P., Keeble, J., Pintér, E., and Helyes, Z., Analgesic and Anti-Inflammatory Effects of the Novel Semicarbazide-Sensitive Amine-Oxidase Inhibitor SzV-1287 in Chronic Arthritis Models of the Mouse, Scientific reports, vol. 7, p. 39863, 2017.
D. B. Horváthy, Vácz, G., Szabó, T., Szigyártó, I. Cs., Torõ, I., Vámos, B., Hornyák, I., Renner, K., Klára, T., Szabó, B. T., Dobõ-Nagy, C., Doros, A., and Lacza, Z., Serum albumin coating of demineralized bone matrix results in stronger new bone formation, Journal of Biomedical Materials Research - Part B Applied Biomaterials, vol. 104, no. 1, pp. 126 - 132, 2016.
K. Horváti, Bacsa, B., Mlinkó, T., Szabó, N., Hudecz, F., Zsila, F., and Bősze, S., Comparative analysis of internalisation, haemolytic, cytotoxic and antibacterial effect of membrane-active cationic peptides: aspects of experimental setup, Amino Acids, vol. 49, pp. 1053–1067, 2017.
C. - T. Hsieh, Ötvös, S. B., Wu, Y. - C., Mándity, I. M., Chang, F. - R., and Fülöp, F., Highly Selective Continuous-Flow Synthesis of Potentially Bioactive Deuterated Chalcone Derivatives, ChemPlusChem, vol. 80, pp. 859–864, 2015.
A. Jakli, Taushanoff, S., Molnár, M., Bóta, A., Kalman, E., and Varga, Z., Method for preparing anisotropic particles and devices thereof. US Patent 8,263,029, 2012.
C. Jiang, Séquaris, J. - M., Wacha, A., Bóta, A., Vereecken, H., and Klumpp, E., Effect of metal oxide on surface area and pore size of water-dispersible colloids from three German silt loam topsoils, Geoderma, vol. 235-236, pp. 260 - 270, 2014.
J. R. Johansson, Hermansson, E., Nordén, B., Kann, N., and Beke-Somfai, T., δ-Peptides from RuAAC-derived 1,5-disubstituted triazole units, European Journal of Organic Chemistry, vol. 2014, no. 13, pp. 2703 - 2713, 2014.
J. R. Johansson, Beke-Somfai, T., Stålsmeden, A. Said, and Kann, N., Ruthenium-Catalyzed Azide Alkyne Cycloaddition Reaction: Scope, Mechanism, and Applications, Chemical reviews, vol. 116, pp. 14726–14768, 2016.
F. Jonsson, Beke-Somfai, T., Andréasson, J., and Nordén, B., Interactions of a photochromic spiropyran with liposome model membranes, Langmuir, vol. 29, no. 7, pp. 2099 - 2103, 2013.
S. Juhas, Harris, N., Il’kova, G., Rehák, P., Zsila, F., Kogan, F. Yurgenzon, Lahmy, O., Zhuk, R., Gregor, P., and Koppel, J., RX-207, a small molecule inhibitor of protein interaction with glycosaminoglycans (SMIGs), reduces experimentally induced inflammation and increases survival rate in cecal ligation and puncture (CLP)-induced sepsis, Inflammation, vol. 41, pp. 307–314, 2018.