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Acta Crystallographica. Section D, Biological Crystallography|October 27, 2004
RARbeta ligand-binding domain bound to an SRC-1 co-activator peptide: purification, crystallization and preliminary X-ray diffraction analysisSabrina Kammerer, Pierre Germain, Ralf Flaig, et al.Chemmedchem|September 17, 2016
Identification and Structure-Activity Relationship Studies of Small-Molecule Inhibitors of the Methyllysine Reader Protein Spindlin1Dina Robaa, Tobias Wagner, Chiara Luise, et al.The Journal of Biological Chemistry|April 29, 2008
Communication between the ERRalpha homodimer interface and the PGC-1alpha binding surface via the helix 8-9 loopHolger Greschik, Magnus Althage, Ralf Flaig, et al.Future Medicinal Chemistry|March 15, 2016
Substituted 2-(2-aminopyrimidin-4-yl)pyridine-4-carboxylates as potent inhibitors of JumonjiC domain-containing histone demethylasesMartin Roatsch, Dina Robaa, Martin Pippel, et al.Acta Crystallographica. Section D, Structural Biology|April 6, 2019
How best to use photonsGraeme Winter, Richard J Gildea, Neil G Paterson, et al.Nature Structural & Molecular Biology|January 12, 2016
Assembly of methylated KDM1A and CHD1 drives androgen receptor-dependent transcription and translocationEric Metzger, Dominica Willmann, Joel McMillan, et al.Methods in Molecular Biology (Clifton, N.J.)|December 16, 2014
Application of in situ diffraction in high-throughput structure determination platformsPierre Aller, Juan Sanchez-Weatherby, James Foadi, et al.Journal of Medicinal Chemistry|May 5, 2026
Development of High-Affinity CHD1 Chromodomain InhibitorsHolger Greschik, Florian Friedrich, Ludwig Seifert, et al.Pageof 2