Zobrazeno 1 - 10 of 97 pro vyhledávání: '"E Ronken"'
1
Short and long term plasticity after lesioning of the cell body or terminal field area of the dopaminergic mesocorticolimbic system in the rat
Autor: Harry W.M. Steinbusch, J.M. van Ree, E. Ronken, P.E. Vos
Publikováno v: Brain Research, 831, 1-2, pp. 237-247
Brain Research, 831, 237-247
To investigate within one study regenerative capacities of dopaminergic axons and cell bodies, short and long term recovery of behavioral and biochemical impairments following a bilateral 6-hydroxydopamine (6-OHDA) lesion of the ventral tegmental are
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1982feaac660ccc141f9fa4165b46965
https://doi.org/10.1016/s0006-8993(99)01453-5
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2
Mutational analysis of the potential phosphorylation sites for protein kinase C on the CCKAreceptor
Autor: E Ronken, S.E. van Emst-de Vries, M A. Fouraux, R.L.L. Smeets, J.J.H.H.M. De Pont, Peter H.G.M. Willems, W Pouwels
Publikováno v: British Journal of Pharmacology. 124:935-945
Many G protein-coupled receptors contain potential phosphorylation sites for protein kinase C (PKC), the exact role of which is poorly understood. In the present study, a mutant cholecystokininA (CCKA) receptor was generated in which the four consens
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bfaf972617b06946b790e007a44d1a9a
https://doi.org/10.1038/sj.bjp.0701913
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3
In vitro and in vivo characterization of newly developed iodinated 1-{2-[Bis(4-fluorophenyl)methoxy]ethyl}piperazine derivatives in rats: Limited value as dopamine transporter SPECT ligands
Autor: K. De Bruin, A. G. M. Janssen, Tamme Doornbos, G. J. Boer, E. A. Van Royen, L. J. M. Rijks, Jan Booij, E. Ronken, R. J. Vermeulen
Publikováno v: Synapse (New York, N.Y.), 23(3), 201-207. Wiley-Liss Inc.
A series of 1-{2-[bis(4-fluorophenyl)methoxy]ethyl}piperazines (CYD1, 2, 3, 5) with a 4-substituent incorporating a 1-hydroxy-3-iodo-2-propenyl moiety, except CYD2 which lacks the hydroxy, was synthesized as potential in vivo imaging ligands for the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dce194366176f0c8950ba7723b9e979d
https://doi.org/10.1002/(sici)1098-2396(199607)23:3<201::aid-syn9>3.0.co
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5
Mutational analysis of the potential phosphorylation sites for protein kinase C on the CCK(A) receptor
Autor: R L, Smeets, M A, Fouraux, W, Pouwels, S E, van Emst-de Vries, E, Ronken, J J, De Pont, P H, Willems
Publikováno v: British journal of pharmacology. 124(5)
1. Many G protein-coupled receptors contain potential phosphorylation sites for protein kinase C (PKC), the exact role of which is poorly understood. In the present study, a mutant cholecystokininA (CCK(A)) receptor was generated in which the four co
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b2a167fd93dcedd03be5048037a18c1c
https://pubmed.ncbi.nlm.nih.gov/9692779
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6
In vitro and in vivo characterization of newly developed iodinated 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]piperazine derivatives in rats: limited value as dopamine transporter SPECT ligands
Autor: L J, Rijks, J, Booij, T, Doornbos, G J, Boer, E, Ronken, K, de Bruin, R J, Vermeulen, A G, Janssen, E A, Van Royen
Publikováno v: Synapse (New York, N.Y.). 23(3)
A series of 1-{2-[bis(4-fluorophenyl)methoxy]ethyl}piperazines (CYD1, 2, 3, 5) with a 4-substituent incorporating a 1-hydroxy-3-iodo-2-propenyl moiety, except CYD2 which lacks the hydroxy, was synthesized as potential in vivo imaging ligands for the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::670b01f82cab0e69db2a52dde50d5a27
https://pubmed.ncbi.nlm.nih.gov/8807748
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7
Chronic activation of mu- and kappa-opioid receptors in cultured catecholaminergic neurons from rat brain causes neuronal supersensitivity without receptor desensitization
Autor: E, Ronken, A H, Mulder, A N, Schoffelmeer
Publikováno v: The Journal of pharmacology and experimental therapeutics. 268(2)
The effects of chronic activation of mu- and kappa-opioid receptors on the release of [3H]dopamine from cultured ventral mesencephalic neurons and that of [3H]noradrenaline from cultured locus ceruleus neurons were studied. It was found that a 4-day
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cb2da21d2e6262e59dedeed43cc9d995
https://pubmed.ncbi.nlm.nih.gov/8113970
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8
Topography and characteristics of specific binding sites for non-opioid gamma-type endorphins in the rat brain as studied by autoradiography with [35S]Met-desenkephalin-gamma-endorphin
Autor: Jeroen A.D.M. Tonnaer, C. J. J. Rust, H. W. Bruning, Frans M. Kaspersen, T. De Boer, E. Ronken, Victor M. Wiegant, J. W. Van Nispen
Publikováno v: Brain research. 615(1)
An in vitro autoradiographic study was performed to characterize specific rat brain binding sites for non-opioid neuroleptic-like gamma-type endorphins, using [35S]Met-des-enkephalin-gamma-endorphin ([35S]Met-DE gamma E; [35]S-beta-endorphins(5-17))
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9440a736274f9e8cbfb9a19bf0307dd
https://pubmed.ncbi.nlm.nih.gov/8395956
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