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Abstract

Screening for Discovery of Novel Peroxisome Proliferator-Activated Receptor-alpha and -gamma Agonists and Nuclear Factor-κB Inhibitors by Luciferase Reporter Gene Assays

Department of Pharmacognosy, University of Vienna, Althanstraße 14, 1090, Vienna, Austria
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2009, 77(7), 240; https://doi.org/10.3797/scipharm.oephg.21.PO-41
Submission received: 16 April 2009 / Accepted: 16 April 2009 / Published: 16 April 2009

Excerpt

Note: In lieu of an abstract, this is an excerpt from the first page.

Peroxisome proliferator-activated receptors (PPARs) are transcription factors that belong to the nuclear receptor super family and represent promising therapeutic targets for several inflammatory and metabolic disorders. Nuclear factor-κB (NF-κB) is also a well-known transcription factor that regulates genes involved in inflammation.[...]

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MDPI and ACS Style

FAKHRUDIN, N.; VOGL, S.; PICKER, P.; HEISS, E.H.; SAUKEL, J.; REZNICEK, G.; KOPP, B.; ATANASOV, A.G.; DIRSCH, V.M. Screening for Discovery of Novel Peroxisome Proliferator-Activated Receptor-alpha and -gamma Agonists and Nuclear Factor-κB Inhibitors by Luciferase Reporter Gene Assays. Sci. Pharm. 2009, 77, 240. https://doi.org/10.3797/scipharm.oephg.21.PO-41

AMA Style

FAKHRUDIN N, VOGL S, PICKER P, HEISS EH, SAUKEL J, REZNICEK G, KOPP B, ATANASOV AG, DIRSCH VM. Screening for Discovery of Novel Peroxisome Proliferator-Activated Receptor-alpha and -gamma Agonists and Nuclear Factor-κB Inhibitors by Luciferase Reporter Gene Assays. Scientia Pharmaceutica. 2009; 77(Posters (PO)):240. https://doi.org/10.3797/scipharm.oephg.21.PO-41

Chicago/Turabian Style

FAKHRUDIN, N., S. VOGL, P. PICKER, E. H. HEISS, J. SAUKEL, G. REZNICEK, B. KOPP, A. G. ATANASOV, and V. M. DIRSCH. 2009. "Screening for Discovery of Novel Peroxisome Proliferator-Activated Receptor-alpha and -gamma Agonists and Nuclear Factor-κB Inhibitors by Luciferase Reporter Gene Assays" Scientia Pharmaceutica 77, Posters (PO): 240. https://doi.org/10.3797/scipharm.oephg.21.PO-41

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