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Biochimica Et Biophysica Acta|May 8, 2007
E2F-1 regulates expression of FOXO1 and FOXO3aKatrin Nowak, Katrin Killmer, Christine Gessner, et al.American Journal of Primatology|September 10, 2004
Cross-species amplification of human microsatellite markers using noninvasive samples from white-handed gibbons (Hylobates lar)Karen E Chambers, Ulrich H Reichard, Asja Möller, et al.Journal of Neurochemistry|March 17, 2006
The transcription factor Yin Yang 1 is an activator of BACE1 expressionKatrin Nowak, Christine Lange-Dohna, Ulrike Zeitschel, et al.British Journal of Pharmacology|September 24, 2015
Characterization of 12 GnRH peptide agonists - a kinetic perspectiveIndira Nederpelt, Victoria Georgi, Felix Schiele, et al.Nucleic Acids Research|April 4, 2006
BMI1 is a target gene of E2F-1 and is strongly expressed in primary neuroblastomasKatrin Nowak, Kornelius Kerl, Daniel Fehr, et al.Molecular Pharmacology|June 22, 2023
Discovery and In Vitro Characterization of BAY 2686013, an Allosteric Small Molecule Antagonist of the Human Pituitary Adenylate Cyclase-Activating Polypeptide ReceptorGernot Langer, John Scott, Christoffer Lind, et al.Journal of Medicinal Chemistry|September 22, 2020
Discovery and Characterization of BAY 1214784, an Orally Available Spiroindoline Derivative Acting as a Potent and Selective Antagonist of the Human Gonadotropin-Releasing Hormone Receptor as Proven in a First-In-Human Study in Postmenopausal WomenOlaf Panknin, Andrea Wagenfeld, Wilhelm Bone, et al.Journal of Medicinal Chemistry|November 1, 2019
Discovery of BAY-298 and BAY-899: Tetrahydro-1,6-naphthyridine-Based, Potent, and Selective Antagonists of the Luteinizing Hormone Receptor Which Reduce Sex Hormone Levels in VivoLars Wortmann, Bernhard Lindenthal, Peter Muhn, et al.Journal of Medicinal Chemistry|October 28, 2024
Discovery of BAY 2413555, First Selective Positive Allosteric Modulator of the M2 Receptor to Restore Cardiac Autonomic BalanceAlexandros Vakalopoulos, Daniel Basting, Markus Brechmann, et al.Journal of Medicinal Chemistry|December 20, 2018
Discovery and Characterization of the Potent and Highly Selective (Piperidin-4-yl)pyrido[3,2- d]pyrimidine Based in Vitro Probe BAY-885 for the Kinase ERK5Duy Nguyen, Clara Lemos, Lars Wortmann, et al.Pageof 2