Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Theo B.A. Mulder"'
Autor:
Jan B. De Vries, Johann W. Wiechers, Theo B.A. Mulder, Cor J. Grol, Alan S. Horn, Durk Dijkstra
Publikováno v:
Naunyn-Schmiedebergs Archives of Pharmacology, 336(5), 494-501. SPRINGER
The in vitro binding of the putative dopamine autoreceptor agonist [3H]DP-7-ATN to rat striatal membrane homogenates was investigated. The maximum number of binding sites Bmax was 497.5 +/- 50.2 fmol/mg protein and the affinity constant KD was 8.3 +/
Autor:
J. Mooy, Margot J. H. de Reus, G. R. Mohn, Ch. M. Leijdekkers, J. Van Harten, H. J. M. Salden, J. G. Loeber, M. Raghoebar, R. J. M. ten Berge, Joop S. de Graaf, W. de Jong, E. M. van der Beek, C. A. M. Van Ginneken, P. W. Wester, J. B. M. van Driel, Peter M. Edelbroek, Hans Rollema, C. A. J. M. Vulders, D. J. Touw, J. J. Grote, Pramod R. Saxena, E. I. Krajnc, Frans P. Nijkamp, J. Kreukniet, Frederik A. de Wolff, H. Burbach, F. C. Hillen, W. Kruizinga, F. W. J. Gribnau, P. H. Hofman, M. J. A. M. Franssen, K. H. Rahn, Frans G. M. Russel, Hans J. Steenbergen, E. Laban, D.J. de Wildt, H. Wollersheim, Npe Vermeulen, H. M. E. Scheres, M. Van Der Graaff, L. R. Remeyer, E. Ronald de Kloet, M. C. M. Rijk, H. J. H. Salden, F. J. Jongeneelen, Theo Mulder, H. E. Sluiter, T. Bultsma, A. B. M. Klaassen, M. v. Baak, J. A. H. Raaijmakers, A. J. van Rozen, J. F. M. Nouws, R. A. P. Koene, N. Verbeke, H. L. G. H. Tiemessen, B. J. L. Kothuis, Cor J. de Vos, R.P. Bos, J. G. P. Peters, Frans W. H. M. Merkus, C. E. M. Zoetemelk, Mjmc Thoolen, M. R. Linschoten, P. T. A. Schellekens, W. Buijs, Th. Thien, H. Th. M. Folgering, L. Conings, D. K. F. Meijer, J. J. Cox van Put, J. De Gier, Ferdi Engels, W. Kateman, P. Lomax, F. Th. M. Huysmans, F. X. R. van Leeuwen, C. J. Van Boxtel, Y. Tan, M. J. Krielaart, G. A. Charbon, J. G. Vos, B. J. 't Hart, J. Jelinek, P. van Heuven-Nolsen, W. J. Wijnands, A. de Jonge, G. R. Bolt, U. R. Tjaden, K. U. Leuven, Durk Oijkstra, Lambert H.M. Janssen, C. M. M. Veldhoven, H. M. N. Nievelstein, E. J. AriËns, H. M. J. Roelofs, A. van 't Laar, L. H. van den Berg, H. N. Doods, F. Corstens, M. v. Hengstum, O. Driessen, R. Groothedde, G. B. van der Voet, W. Kuijpers, A. de Klerk, E. Schönbaum, D. D. Breimer, B. van Ommen, C. A. van der Heijden, M. v. Hooff, E. A. De Bruijn, Hendrik Timmerman, L. C. M. Baars, P van Brummelen, C. T. A. Evelo, A. J. Beld, H. H. W. Thljssen, G. Aué, R. van Doorn, H. A. M. G. Vaessen, J. Fennis, Theo B.A. Mulder, W. v. d. Broek, G. K. Terpstra, A. T. van Oosterom, Cor J. Grol, R. A. Lefebvre, P. A. Van Zwieten, A. C. Wouterse, Rob B. M. Anzion, J. F. Rodrigues De Miranda, C. Neef, R. S. Oosting, A. Van Der Gen, C. H. Kleinbloesem, Marian W. Tijhuis, Yechiel A. Hekster, H. A. J. Struyker Boudier, C. L. A. van Herwaarden, Bob Wilffert, Dora Mastebroex, E. A. van der Velde, A. S. P. M. Breed, H. L. M. Siero, Gerard van Aalst, J. L. G. Theuws, F. A. De Wolff, J. Rozing, E. I. Krajc, R. H. B. Meyboom, M. A. M. ten Broeke, J. Festen, P.J.L. van Gemert, A. P. I. Jzerman, Hans Wynberg, Alan Horn, H. J. E. Reeuwijk, B. O Osterhuis, R. Dorlas, P. A. M. Peeters, J. Willemsen, L. M. de Brauw, Jan B. de Vries, L. B. A. van de Putte, Alan S. Horn, J. H. Canton, H. J. E. M. Reeuwijk, M. Schols, J. A. M. Raaijmakers, Marcus Bogaert, J. van Noordwijk, Durk Dijkstra, P.Th. Henderson, Peter P. Koopmans, J. W. J. Lammers, T. B. Vree, C. J. H. van de Velde, C. J. Van Koppen, Bernard Hazelhoff, Jaap Wilting, H. M. Pinedo, W. Kuypers, C. M. Ruland, H. A. J. Struyker-Boudier, J. M. Neis, P. B. M. W. M. Timmermans, H. O. Kalkman, P. R. M. Kerklaan, P. A. F. Jansen, J. Peter, J. H. Koeman, H. J. Huidekoper, Mj Mathy, A.F. De Schaepdryver, R.A.M. van der Hoeven, Jos F.M. Smits, Tjeerd van den Berg, E. H. den Tonkelaar, J. W. M. Lenders, P. Sandor, C. A. v. d. Heijden, G. A. Wassink, O. Castelein, P. H. Th. J. Slee
Publikováno v:
Pharmaceutisch Weekblad. 6:163-184
Autor:
Hans Rollema, Theo B.A. Mulder, Matthijs G.P. Feenstra, Alan S. Horn, Jan Willem Homan, Ben H.C. Westerink, Durk Dijkstra
Publikováno v:
Journal of Chromatography A, 230(2), 271-287. ELSEVIER SCIENCE BV
The liquid chromatographic determination of N-alkylated analogues of dopamine is described. The retention and separation of these compounds, ranging from dopamine to N,N-dibutyl-dopamine, was studied on four bonded-phase columns, of which Nucleosil 5
Publikováno v:
Life Sciences, 32(5), 459-465
A sensitive and selective method of determination of N,N-dipropylamino-5, 6-dihydroxytetralin and its 6,7-dihydroxy isomer in rat plasma and brain tissue is described. The method is based on isolation of these dopamine receptor agonists from the biol
Autor:
Hans Rollema, Durk Dijkstra, Theo B.A. Mulder, Ben H.C. Westerink, Alan S. Horn, Matthijs G.P. Feenstra
Publikováno v:
European Journal of Pharmacology, 64(4), 313-323. ELSEVIER SCIENCE BV
After i.p. administration of the dibenzoylester of 2-amino-6,7-dihydroxytetralin (DB-6,7-ADTN) a metabolite was found in rat brain and serum, which was identified as 2-amino-6-hydroxy-7-methoxytetralin (7-O-MeADTN). By means of HPLC coupled with ampe
Autor:
Hans Rollema, Jan Van der Weide, Pieter G. Tepper, Alan S. Horn, Durk Dijkstra, Theo B.A. Mulder
Publikováno v:
Journal of Medicinal Chemistry, 31(11), 2178-2182. AMER CHEMICAL SOC
The 6-oxa analogues of potent dopamine agonists, hexahydronaphthoxazines (4a,4b), have been tested for dopamine receptor binding and stimulating activity and were found to be almost inactive. pKa value determinations indicated that these compounds ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64cf3476a3dff21e78283753b93d9504
https://research.rug.nl/en/publications/b6d151b7-9d8b-48fc-a843-b09914411318
https://research.rug.nl/en/publications/b6d151b7-9d8b-48fc-a843-b09914411318
Publikováno v:
European Journal of Pharmacology, 109(2), 229-240. ELSEVIER SCIENCE BV
A series of mono- (5 and 7) and dihydroxylated (5,6 and 6,7)N-methyl,N-propargyl-2-aminotetralins were studied with respect to their dopamine agonistic and monoamine oxidase inhibitory activities. MAO inhibition was found to be reduced by hydroxylati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef9d06448765ab110955c047967ee2af
https://research.rug.nl/en/publications/425f8754-9cee-4b32-b722-fdee0cea8479
https://research.rug.nl/en/publications/425f8754-9cee-4b32-b722-fdee0cea8479
Publikováno v:
European Journal of Pharmacology, 112(1), 73-79. ELSEVIER SCIENCE BV
The in vitro binding of the new tritiated dopaminergic ligand [3H]N,N-dipropyl-5,6-dihydroxy-2-aminotetralin to rat striatal membranes is described. Binding assays were performed in 50 mM Tris-HCl pH 7.5 containing 1 mM EDTA and 0.01% ascorbic acid a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f1341765a19095e1d3ba79820e3b28e
https://research.rug.nl/en/publications/09263f22-8695-439a-b150-56de7655cb93
https://research.rug.nl/en/publications/09263f22-8695-439a-b150-56de7655cb93