The WMI Rat of Premature Cognitive Aging Presents Intrinsic Vulnerability to Oxidative Stress in Primary Neurons and Astrocytes Compared to Its Nearly Isogenic WLI Control von Ferreira, Adriana, Harter, Aspen, Afreen, Sana, Kanai, Karoly, Batori, Sandor, Redei, Eva E

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I. Discovery of a novel series of CXCR3 antagonists. Multiparametric optimization of N,N-disubstituted benzylamines von Bata, Imre, Tömösközi, Zsuzsanna, Buzder-Lantos, Péter, Vasas, Attila, Szeleczky, Gábor, Bátori, Sándor, Barta-Bodor, Veronika, Balázs, László, Ferenczy, György G.

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Interaction of SSR161421, a novel specific adenosine A(3) receptor antagonist with adenosine A(3) receptor agonists both in vitro and in vivo von Mikus, Endre G, Boér, Kinga, Timári, Géza, Urbán-Szabó, Katalin, Kapui, Zoltán, Szeredi, Judit, Gerber, Katalin, Szabó, Tibor, Bátori, Sándor, Finet, Michel, Arányi, Péter, Galzin, Anne-Marie

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Reactivity of 1,2,3-triazole-substituted 1-azabutadienes (vinamidines) von Bátori, Sandor, Bokotey, Sándor, Messmer, András

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A novel orally active inhibitor of HLE von Varga, Márton, Kapui, Zoltán, Bátori, Sándor, Nagy, Lajos T., Vasvári-Debreczy, Lelle, Mikus, Endre, Urbán-Szabó, Katalin, Arányi, Péter

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Synthetic procedure to pyrido[2,1-f][1,2,4]triazinium salt and related compounds von Bátori, Sándor, Csányi, Dorottya, Takács, Daniella, Egyed, Orsolya, Riedl, Zsuzsanna, Hajós, György

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Prolyl Oligopeptidase Inhibition by N-Acyl-pro-pyrrolidine-type Molecules von Kánai, Károly, Arányi, Péter, Böcskei, Zsolt, Ferenczy, György, Harmat, Veronika, Simon, Kálmán, Bátori, Sándor, Náray-Szabó, Gábor, Hermecz, István

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PHARMACEUTICALLY EFFECTIVE COMPOUNDS INHIBITING SELECTIVELY THE MYOSIN 2 ISOFORMS von GYIMESI Mate, SZABO Andras, LORINCZ Istvan, BATORI Sandor, MALNASI-CSIZMADIA Andras, HORVATH Adam Istvan, HARI Peter, PENZES Mate, HORVATH Vajk, SZONYEGI Zoltan, KOVACS Mihaly, VEGNER Laszlo, KUMAR Suthar Sharad, REPASI Jozsef, SIMON Zoltan

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Compounds for selectively inhibiting myosin ii isoforms von Loerincz Istvan, Gyimesi Mate, Szoenyegi Zoltan, Kovacs Mihaly, Kumar Suthar Sarad, Repasi Jozsef, Penzes Mate, Hari Peter, Horvath Vajk, Batori Sandor, Simon Zoltan, Vegner Laszlo, Horvath Adam Istvan, Malnasi-Csizmadia Andras, Szabo Andras

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CYCLOALKANE CARBOXYLIC ACID DERIVATIVES AS CXCR3 RECEPTOR ANTAGONISTS von VASAS, Attila, BATORI, Sandor, BATA, Imre, TOMOSOZI, Zsuzsanna, PATEK, Marcel, S. THORPE, David, SZELECZKY, Gabor, FERENCZY, Gyorgy, SMRCINA, Martin, BARTANE BODOR, Veronika, BUZDER-LANTOS, Peter, WEICHSEL, Aleksandra

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PHARMACEUTICALLY EFFECTIVE COMPOUNDS INHIBITING SELECTIVELY THE MYOSIN 2 ISOFORMS von VEGNER, LASZLO, SZONYEGI, ZOLTAN, SIMON, ZOLTAN, GYIMESI, MATE, HORVATH, VAJK, KUMAR, SUTHAR SHARAD, REPASI, JOZSEF, MALNASI-CSIZMADIA, ANDRAS, SZABO, ANDRAS, PENZES, MATE, KOVACS, MIHALY, HARI, PETER, HORVATH, ADAM ISTVAN, LORINCZ, ISTVAN, BATORI, SANDOR

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PHARMACEUTICALLY EFFECTIVE COMPOUNDS INHIBITING SELECTIVELY MYOSIN 2 ISOFORMS von ADAM ISTVAN HORVATH, VAJIK HORVATH, MATE PENZES, ISTVAN LOERINCZ, ZOLTAN SZOENYEGI, ANDRAS SZABO, MATE GYIMESI, ANDRAS MALNASI-CSIZMADIA, MIHALY KOVACS, ZOLTAN SIMON, LASZLO VEGNER, SUTHAR SHARAD KUMAR, JOSEF REPASI, SANDOR BATORI, PETER HARI

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Cycloalkane carboxylic acid derivatives as CXCR3 receptor antagonists von Bartane Bodor, Veronika, Smrcina, Martin, S.Thorpe, David, Szeleczky, Gabor, Patek, Marcel, Vasas, Attila, Ferenczy, Gyorgy, Budzer-Lantos, Peter, Bata, Imre, Batori, Sandor, Tomoskozi, Zsuzsanna, Weichsel, Aleksandra

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Cycloalkane carboxylic acid derivatives as CXCR3 receptor antagonists von FERENCZY GYORGY, TOMOSKOZI ZSUZSANNA, SMRCINA MARTIN, VASAS ATTILA, BATA IMRE, SZELECZKY GABOR, WEICHSEL ALEKSANDRA, BUZDER-LANTOS PETER, BARTANE BODOR VERONIKA, PATEK MARCEL, THORPE DAVID SQUIRE, BATORI SANDOR

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Pyrrolidinyl-alkyl-amide derivatives their preparation and their therapeutic application as CCR3 receptor ligands von PAPPNE BEHR, AGNES, BARTANE BODOR, VERONIKA, URBAN SZABO, KATALIN, KAPUI, ZOLTAN, BATA, IMRE, MIKUS, ENDRE, SZLAVIK, ZOLTAN, BATORI, SANDOR

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Pyrrolidinyl-alkyl-amide derivatives their preparation and their therapeutic application as CCR3 receptor ligands von PAPPNE BEHR, AGNES, BARTANE BODOR, VERONIKA, URBAN SZABO, KATALIN, KAPUI, ZOLTAN, SZLAVIK, ZSOLT, BATA, IMRE, MIKUS, ENDRE, BATORI, SANDOR

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TRIAZOL[1,5-A]QUINOLINAS COMO LIGANTES DE RECEPTORES DE ADENOSINA A3 von KINGA BOER, JUDIT VARGANE SZEREDI, KATALIN URBAN SZABO, ZOLTAN SZLAVIK, ZOLTAN KAPUI, EDIT SUSAN, SANDOR BATORI, GEZA TIMARI, ENDRE MIKUS, TIBOR SZABO, MICHEL FINET

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미오신 2 이소형을 선택적으로 억제하는 약제학적으로 효과적인 화합물 von KUMAR SUTHAR SHARAD, VEGNER LASZLO, HARI PETER, PENZES MATE, SZONYEGI ZOLTAN, LORINCZ ISTVAN, MALNASI CSIZMADIA ANDRAS, KOVACS MIHALY, HORVATH ADAM ISTVAN, GYIMESI MATE, REPASI JOZSEF, SIMON ZOLTAN, SZABO ANDRAS, BATORI SANDOR, HORVATH VAJK

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CYCLOALKANE CARBOXYLIC ACID DERIVATIVES AS CXCR3 RECEPTOR ANTAGONISTS von FERENCZY GYORGY, TOMOSKOZI ZSUZSANNA, SMRCINA MARTIN, VASAS ATTILA, BATA IMRE, SZELECZKY GABOR, WEICHSEL ALEKSANDRA, BUZDER-LANTOS PETER, BARTANE BODOR VERONIKA, PATEK MARCEL, THORPE DAVID SQUIRE, BATORI SANDOR

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