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Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|October 22, 2016
A single-dose, randomized, cross-over, two-way, open-label study for comparing the absorption of boswellic acids and its lecithin formulationAntonella Riva, Paolo Morazzoni, Christian Artaria, et al.
Bioorganic & Medicinal Chemistry Letters|February 9, 2010
Acidic elements in histamine H(3) receptor antagonistsKerstin Sander, Yvonne von Coburg, Jean-Claude Camelin, et al.
Bioorganic & Medicinal Chemistry|November 5, 2013
Synthesis and pharmacological characterization of benzenesulfonamides as dual species inhibitors of human and murine mPGES-1Thomas Hanke, Florian Rörsch, Theresa M Thieme, et al.
The EMBO Journal|December 14, 2004
A Cdk5 inhibitory peptide reduces tau hyperphosphorylation and apoptosis in neuronsYa-Li Zheng, Sashi Kesavapany, Maneth Gravell, et al.
Cell Chemical Biology|May 14, 2021
Endogenous vitamin E metabolites mediate allosteric PPARγ activation with unprecedented co-regulatory interactionsSabine Willems, Leonie Gellrich, Apirat Chaikuad, et al.
Scientific Reports|May 3, 2018
Allosteric modulation of the farnesoid X receptor by a small moleculeMatthias Gabler, Jan Kramer, Jurema Schmidt, et al.
Experimental Dermatology|December 5, 2008
Lipophilic prodrugs of amino acids and vitamin E as osmolytes for the compensation of hyperosmotic stress in human keratinocytesRüdiger Graf, Michael Kock, Andreas Bock, et al.
Journal of Medicinal Chemistry|May 28, 2010
Design, synthesis, and biological evaluation of a novel class of gamma-secretase modulators with PPARgamma activityMartina Hieke, Julia Ness, Ramona Steri, et al.
Journal of Medicinal Chemistry|April 22, 2009
An innovative method to study target protein-drug interactions by mass spectrometryMathias Q Müller, Leo J de Koning, Andreas Schmidt, et al.
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