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Browsing by Author "Goebel, C."

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Now showing 1 - 7 of 7
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    Formation of oxylipins by CYP74 enzymes for flavor production.
    (Amer Chemical Soc, 2004)
    Feussner, Ivo  
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    Goebel, C.
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    Stumpe, M.
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    Carsjens, J. G.
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    Identification of metabolic changes after wounding in Arabidopsis thaliana by an unbiased UPLC-MS approach
    (Elsevier Ireland Ltd, 2009)
    Goebel, C.
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    Feussner, Kristin
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    Kaever, Alexander  
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    Meinicke, Peter  
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    Morgenstern, Burkhard  
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    Feussner, Ivo  
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    Lipid metabolism in ectomycorrhizal fungi: Fatty acid patterns and in silico analysis of related enzymes
    (Bochumer Universitätsverlag, 2005)
    Reich, M.
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    Kilaru, S.
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    Goebel, C.
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    Kües, U.  
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    Feussner, I.
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    Martin, F.
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    Polle, A.
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    Metal directed one-pot syntheses: Mono-, di- and tetra-nuclear clusters [1]
    (Verlag Z Naturforsch, 2003)
    Saalfrank, Rolf W.
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    Reimann, U.
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    Hampel, F.
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    Goebel, C.
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    Herbst-Irmer, R.  
    Upon reaction of HL1 1 (picoline-tetrazolylamide) with cobalt(II) acetate under aerobic conditions or with copper(II) acetate, the mono-nuclear complex [Co-III(L-1)(3)] 3 and the di-nuclear complex [Cu-2(L-1)(4)] 4 were generated. In 3 and 4, (L-1)(-) exclusively coordinates across its nitrogen donors. However, when HL2 5 (picoline-tetrazolylthioamide) was reacted with copper- or nickel acetate, the di-nuclear cluster [Cu-2(L-2)(4)] 6 and the tetra-nuclear cluster [Ni-4(L-2)(8)] 7, respectively, were isolated. Contrary to 3 and 4, in 6 and 7, (L-2)- also coordinates across sulfur.
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    Quantitative risk assessment for contact allergens: a simplified approach for hair dye ingredients
    (Nature Publishing Group, 2013)
    Goebel, C.
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    Diepgen, Thomas Ludwig
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    Krasteva, Maya
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    Schlatter, Harald
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    Nicolas, J-F
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    Blomeke, B.
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    Coenraads, Pieter-Jan
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    Schnuch, Axel
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    Taylor, J. S.
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    Fautz, Rolf
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    Schuh, Werner
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    Gerberick, G. Frank
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    Kimber, Ian
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    Sertraline versus paroxetine in the treatment of panic disorder: A multinational randomized double-blind 15 week study
    (Elsevier Science Bv, 2002)
    Bandelow, Borwin  
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    Behnke, K.
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    Lenoir, S.
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    Hendriks, G. J.
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    Alkin, T.
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    Dombrowski, A.
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    Goebel, C.
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    Sertraline versus paroxetine in the treatment of panic disorder: An acute, double-blind noninferiority comparison
    (Physicians Postgraduate Press, 2004)
    Bandelow, Borwin  
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    Behnke, K.
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    Lenoir, S.
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    Hendriks, G. J.
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    Alkin, T.
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    Goebel, C.
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    Clary, C. M.
    Objective: Several classes of medications have demonstrated efficacy in panic disorder, but direct comparison of 2 proven treatments is still uncommon. The purpose of this study was to compare sertraline and paroxetine in the acute treatment of panic disorder. Method: Adult outpatients with panic disorder with or without agoraphobia (DSM-IV and ICD-10 criteria) were randomly assigned in double-blind fashion to 12 weeks of treatment with flexible doses of sertraline (titrated up to 50-150 mg/day; N = 112) or paroxetine (titrated up to 40-60 mg/day; N = 113). Patients were then tapered off medication over 3 weeks. The primary analysis was a noninferiority analysis of Panic and Agoraphobia Scale (PAS) scores. Secondary measures included panic attack frequency and the Clinical Global Impressions-Improvement scale (CGI-I) (with responders defined as those with a CGI-I score less than or equal to 2). Data were collected from January 2000 to June 2001. Results: Sertraline and paroxetine were associated with equivalent levels of improvement on the PAS total score, as well as on all secondary outcome measures. Eighty-two percent of patients taking sertraline versus 78% of those taking paroxetine were CGI-I responders at endpoint. Numerically more patients on paroxetine treatment compared with sertraline treatment discontinued due to adverse events (18% vs. 12%; NS), and a significantly higher proportion of paroxetine patients showed greater than or equal to 7% weight gain (7% vs. < 1%; p < .05). During the taper period, the proportion of panic-free patients increased by 4% with sertraline but decreased by 11% with paroxetine (p < .05). Conclusion: Sertraline and paroxetine had equivalent efficacy in panic disorder, but sertraline was significantly better tolerated and was associated with significantly less clinical worsening during taper than paroxetine.

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