Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Szabolcs, Udvari"'
Autor:
Ferenc A. Antoni, Szabolcs Udvari, Katalin Megyeri, Ágnes Pataki, Istvan Gacsalyi, Balázs Mihalik, Krisztina Moricz, Gabor Gigler, Adrienn Pálvölgyi
Publikováno v:
Neuropharmacology. 128:408-415
Gamma-amino butyric acid (GABA) is an abundant neurotransmitter in the CNS. GABAergic interneurons orchestrate pyramidal neurons in the cerebral cortex, and thus control learning and memory. Ionotropic receptors for GABA (GABAAR) are heteropentameric
Autor:
Adrienn, Pálvölgyi, Krisztina, Móricz, Ágnes, Pataki, Balázs, Mihalik, Gábor, Gigler, Katalin, Megyeri, Szabolcs, Udvari, István, Gacsályi, Ferenc A, Antoni
Publikováno v:
Neuropharmacology. 128
Gamma-amino butyric acid (GABA) is an abundant neurotransmitter in the CNS. GABAergic interneurons orchestrate pyramidal neurons in the cerebral cortex, and thus control learning and memory. Ionotropic receptors for GABA (GABA
Autor:
Katalin Pallagi, György Lévay, Balázs Volk, József Barkóczy, Gyula Simig, Szabolcs Udvari, Kompagne Hajnalka, Andras Egyed, Michael Spedding, Laszlo G. Harsing, Istvan Gacsalyi, Tibor Mezei, Endre Hegedüs
Publikováno v:
Journal of Medicinal Chemistry. 51:2522-2532
A series of potent 5-hydroxytryptamine 7 (5-HT 7) ligands has been synthesized that contain a 1,3-dihydro-2 H-indol-2-one (oxindole) skeleton. The binding of these compounds to the 5-HT 7 and 5-HT 1A receptors was measured. Despite the structural sim
Autor:
Pál Tapolcsányi, Laszlo G. Harsing, Julia Timár, Katalin Nagy, Péter Mátyus, Marko Bernadett Martonne, Andrea Czompa, Szabolcs Udvari, Geza Szabo, Ákos Kocsis, Gabriella Zsilla
Publikováno v:
Current pharmaceutical design. 21(17)
We have synthesized a novel series of N-substituted sarcosines, analogues of NFPS ( N -[3-(biphenyl-4- yloxy)-3-(4-fluorophenyl)propyl]- N -methylglycine), as type-1 glycine transporter (GlyT-1) inhibitors. Several compounds incorporated a diazine ri
Autor:
Jean Paul Harpey, Seymour Packman, Bridget Wilcken, Peter Bross, I Knudsen, Nestor A. Chamoles, Stanislav Kmoch, Kimberly Hart, Jean-Marie Saudubray, Lars Bolund, Niels Gregersen, Brage S. Andresen, George Gray, Vibeke Winter, Jean M Kirk, Daniel E. Hale, Szabolcs Udvari, Steen Kølvraa, Ichiro Yokota
Publikováno v:
Andresen, B S, Bross, P, Udvari, S, Kirk, J, Gray, G, Kmoch, S, Chamoles, N, Knudsen, I, Winter, V, Wilcken, B, Yokota, I, Hart, K, Packman, S, Harpey, J P, Saudubray, J M, Hale, D E, Bolund, L, Kølvraa, S & Gregersen, N 1997, ' The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients : Is there correlation between genotype and phenotype? ', Human Molecular Genetics, vol. 6, no. 5, pp. 695-707 . https://doi.org/10.1093/hmg/6.5.695
Scopus-Elsevier
Scopus-Elsevier
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is the most commonly recognized defect of mitochondrial β-oxidation. It is potentially fatal, but shows a wide clinical spectrum. The aim of the present study was to investigate whether any corre
Publikováno v:
Brain research. 1492
We used isolated chicken retina to induce spreading depression by the glutamate receptor agonist N-methyl-d-aspartate. The N-methyl-d-aspartate-induced latency time of spreading depression was extended by the glycine(B) binding site competitive antag
Publikováno v:
Current Views of Fatty Acid Oxidation and Ketogenesis ISBN: 0306462001
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d372e1a12fa5c34c999b96c8be2609a2
https://doi.org/10.1007/0-306-46818-2_45
https://doi.org/10.1007/0-306-46818-2_45
Autor:
Peter Bross, Niels Gregersen, Brage S. Andresen, Joseph Muenzer, Szabolcs Udvari, Donald H. Chace, Shawn E. McCandless, Edwin W. Naylor, Rick Banas, Inga Knudsen, Linda P. O’Reilly, Paul C. Engel, Dianne M. Frazier, Steve F. Dobrowolski
Publikováno v:
American journal of human genetics. 68(6)
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is the most frequently diagnosed mitochondrial beta-oxidation defect, and it is potentially fatal. Eighty percent of patients are homozygous for a common mutation, 985A--G, and a further 18% have
Publikováno v:
Biochemical Society Transactions. 26:S65-S65
Autor:
Balázs Volk, József Barkóczy, Endre Hegedus, Szabolcs Udvari, István Gacsályi, Tibor Mezei, Katalin Pallagi, Hajnalka Kompagne, György Lévay, András Egyed, László G. Hársing Jr., Michael Spedding, Gyula Simig
Publikováno v:
Journal of Medicinal Chemistry; Mar2008, Vol. 51 Issue 8, p2522-2532, 11p