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Drug Discovery Today|November 3, 2021
Selectivity aspects of activity-based (chemical) probesStephanie Heinzlmeir, Susanne MüllerProteome Science|July 29, 2014
Probing SH2-domains using Inhibitor Affinity Purification (IAP)Michael Höfener, Stephanie Heinzlmeir, Bernhard Kuster, et al.The Plant Cell|March 19, 2015
DENEDDYLASE1 deconjugates NEDD8 from non-cullin protein substrates in Arabidopsis thalianaJulia Mergner, Stephanie Heinzlmeir, Bernhard Kuster, et al.Journal of Proteomics|November 5, 2013
A new chemical probe for quantitative proteomic profiling of fibroblast growth factor receptor and its inhibitorsXin Ku, Stephanie Heinzlmeir, Xiaofeng Liu, et al.Journal of Proteome Research|April 10, 2014
New affinity probe targeting VEGF receptors for kinase inhibitor selectivity profiling by chemical proteomicsXin Ku, Stephanie Heinzlmeir, Dominic Helm, et al.ACS Chemical Biology|September 18, 2015
Evaluation of Kinase Activity Profiling Using Chemical ProteomicsBenjamin Ruprecht, Jana Zecha, Stephanie Heinzlmeir, et al.Journal of Proteome Research|February 26, 2019
CiRCus: A Framework to Enable Classification of Complex High-Throughput ExperimentsFlorian Seefried, Tobias Schmidt, Maria Reinecke, et al.Chemmedchem|June 22, 2018
NVP-BHG712: Effects of Regioisomers on the Affinity and Selectivity toward the EPHrin FamilyAlix Tröster, Stephanie Heinzlmeir, Benedict-Tilman Berger, et al.Oncotarget|February 22, 2020
Identification of molecular targets for the targeted treatment of gastric cancer using dasatinibRaquel Carvalho Montenegro, Alison Howarth, Alessandro Ceroni, et al.ACS Chemical Biology|March 23, 2019
Chemoproteomic Selectivity Profiling of PIKK and PI3K Kinase InhibitorsMaria Reinecke, Benjamin Ruprecht, Sandra Poser, et al.Pageof 29