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Nature Communications|October 21, 2016
Quantitative interaction mapping reveals an extended UBX domain in ASPL that disrupts functional p97 hexamersAnup Arumughan, Yvette Roske, Carolin Barth, et al.Proceedings of the National Academy of Sciences of the United States of America|March 14, 2018
Structural changes of TasA in biofilm formation of Bacillus subtilisAnne Diehl, Yvette Roske, Linda Ball, et al.Chemmedchem|June 14, 2026
Probing 3-Amino-2H-Azaindazoles as Allosteric Inhibitors of the Protein Tyrosine Phosphatase SHP2Machoud Amoussa, Nina-Louisa Efrém, Feng Li, et al.Proceedings of the National Academy of Sciences of the United States of America|November 13, 2020
Designed nanomolar small-molecule inhibitors of Ena/VASP EVH1 interaction impair invasion and extravasation of breast cancer cellsMatthias Barone, Matthias Müller, Slim Chiha, et al.Nature Chemical Biology|September 15, 2022
Development of selective inhibitors of phosphatidylinositol 3-kinase C2αWen-Ting Lo, Hassane Belabed, Murat Kücükdisli, et al.Journal of Medicinal Chemistry|November 19, 2020
From Pyrazolones to Azaindoles: Evolution of Active-Site SHP2 Inhibitors Based on Scaffold Hopping and Bioisosteric ReplacementYelena Mostinski, Guus J J E Heynen, Maria Pascual López-Alberca, et al.Pageof 5