Zobrazeno 1 - 10 of 1 182 pro vyhledávání: '"SUNDELL, S"'
1
Akademický článek
Assessing the discharge instructing in the emergency department: Patient perspective
Autor: Mäkinen, M., Castrén, M., Huttunen, K., Sundell, S., Kaartinen, J., Ben-Meir, M., Renholm, M.
Publikováno v: In International Emergency Nursing March 2019 43:40-44
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2
Akademický článek
Surface coating of particles by nanospray process and CCVD in circulating fluidised bed.
Autor: Oljaca, M.1 moljaca@ngimat.com, Sundell, S.1, Smith, P.1, Hunt, A.1, Tellefsen, M.2
Publikováno v: Surface Engineering. Feb2005, Vol. 21 Issue 1, p47-52. 6p.
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3
Akademický článek
CLOSED LOOP CONTROLLED DEPOSITION OF Ba[subx]Sr[sub1-x]TiO[sub3] THIN FILMS IN SPRAY FLAMES.
Autor: Vukasinovic, B.1 moljaca@microcoating.com, Sundell, S.1, Oljaca, M.1
Publikováno v: Surface Engineering. Jun2003, Vol. 19 Issue 3, p179. 6p. 4 Black and White Photographs, 3 Diagrams, 1 Chart, 6 Graphs.
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5
Synthesis and pharmacological evaluation of thiopyran analogues of the dopamine D-3 receptor-selective agonist (4aR,10bR)-(+)-trans-3,4,4a,10b-tetrahydro-4-n-propyl-2H,5H-[1]benzopyrano[4,3-b]-1,4-oxazin-9-ol (PD 128907)
Autor: van Vliet, L.A, Rodenhuis, N, Dijkstra, D., Wikström, H.V, Pugsley, T.A, Serpa, K.A., Meltzer, L.Th, Heffner, T.G, Wise, L.D, Lajiness, M.E, Huff, R.M, Svensson, K, Sundell, S, Lundmark, M
Publikováno v: Journal of Medicinal Chemistry, 43(15), 2871-2882. AMER CHEMICAL SOC
Journal of Medicinal Chemistry, 15, 2871-2882. AMER CHEMICAL SOC
Benzopyranoxazine (+)-7 (PD 128907) is the most dopamine (DA) D-3 receptor-selective agonist presently known. The only structural feature which distinguishes 7 from the analogous nonselective naphthoxazines is an oxygen atom in the 6-position. To ext
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8c984a140aa299b41e94a910ae920fdf
https://research.rug.nl/en/publications/d0381fd2-4a22-475e-8ea3-0e4e800e76e7
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6
New selective and potent 5-HT 1B/1D antagonists: Chemistry and pharmacological evaluation of N-piperazinylphenyl biphenylcarboxamides and biphenylsulfonamides
Autor: Liao, Y, Bottcher, H, Harting, J, Greiner, H, van Amsterdam, C, Cremers, T, Sundell, S, Marz, J, Rautenberg, W, Wikstrom, H
Publikováno v: Journal of Medicinal Chemistry, 3, 517-525. AMER CHEMICAL SOC
Journal of Medicinal Chemistry, 43(3), 517-525. AMER CHEMICAL SOC
A series of new analogues of N-[4-methoxy-3-(4-methylpiperazin-1-yl)phenyl] 2'-methyl-4'-(5-methyl-1,2,4-oxadiazol-3-yl)biphenyl-4-carboxamide (1; GR127935) as potent and selective 5-HT1B/1D antagonists were synthesized and evaluated pharmacologicall
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a0758d1940210da470bfcedc4f67a1bf
https://research.rug.nl/en/publications/dc5369fd-3e31-4b11-9d4e-178ca50381e3
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8
Akademický článek
Orthodontic findings and treatment need in patients with amelogenesis imperfecta: a descriptive analysis.
Autor: Möhlhenrich, Stephan Christian1 (AUTHOR) stephan.moehlhenrich@uni-wh.de, Chhatwani, Sachin1 (AUTHOR), Schmidt, Peter2 (AUTHOR), Kniha, Kristian3 (AUTHOR), Postberg, Jan4 (AUTHOR), Schulte, Andreas G.2 (AUTHOR), Jackowski, Jochen5 (AUTHOR), Zimmer, Stefan6 (AUTHOR), Danesh, Gholamreza1 (AUTHOR)
Publikováno v: Head & Face Medicine. 6/14/2024, Vol. 20 Issue 1, p1-14. 14p.
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9
Akademický článek
Normal and Dysregulated Sphingolipid Metabolism: Contributions to Podocyte Injury and Beyond.
Autor: Tolerico, Matthew1 (AUTHOR) mxt1001@miami.edu, Merscher, Sandra1 (AUTHOR) smerscher@med.miami.edu, Fornoni, Alessia1 (AUTHOR) smerscher@med.miami.edu
Publikováno v: Cells (2073-4409). Jun2024, Vol. 13 Issue 11, p890. 17p.
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10
STRUCTURE-ACTIVITY-RELATIONSHIPS IN THE 8-AMINO-6,7,8,9-TETRAHYDRO-3H-BENZ[E]INDOLE RING-SYSTEM .1. EFFECTS OF SUBSTITUENTS IN THE AROMATIC SYSTEM ON SEROTONIN AND DOPAMINE-RECEPTOR SUBTYPES
Autor: STJERNLOF, P, ENNIS, MD, HANSSON, LO, HOFFMAN, RL, GHAZAL, NB, SUNDELL, S, SMITH, MW, SVENSSON, K, CARLSSON, A, WIKSTROM, H
Publikováno v: Journal of Medicinal Chemistry, 38(12), 2202-2216. AMER CHEMICAL SOC
A series of 1-, 3-, and 4-substituted analogs to the potent 5-HT1A agonist 8-(dipropylamino)-6,7,8,9-tetrahydro-3H-benz[e]indole-1-carbaldehyde (5) were prepared and tested in vitro at 5-HT1A, 5-HT1D alpha, 5-HT1D beta, D-2, and D-3 receptors and in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::70b683f306b10ac8a03dbf4a103fd387
https://research.rug.nl/en/publications/270db756-0ade-4f8f-b5d7-e9963d74156c
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