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Journal Article (2790)

Journal Article
Schneidewind, T.; Brause, A.; Schölermann, B.; Sievers, S.; Pahl, A.; Sankar, M. G.; Winzker, M.; Janning, P.; Kumar, K.; Ziegler, S. et al.; Waldmann, H.: Combined morphological and proteome profiling reveals target-independent impairment of cholesterol homeostasis. Cell Chemical Biology 28, pp. 1 - 21 (2021)
Journal Article
Pospich, S.; Sweeney, H. L.; Houdusse, A.; Raunser, S.: High-resolution structures of the actomyosin-V complex in three nucleotide states provide insights into the force generation mechanism. eLife 10, e73724, pp. 1 - 81 (2021)
Journal Article
Huis in´t Veld, P. J.; Wohlgemuth, S.; Koerner, C.; Müller, F.; Janning, P.; Musacchio, A.: Reconstitution and use of highly active human CDK1:Cyclin-B:CKS1 complexes. Protein Science, pp. 1 - 25 (2021)
Journal Article
Belyy, A.; Merino, F.; Mechold, U.; Raunser, S.: Mechanism of actin-dependent activation of nucleotidyl cyclase toxins from bacterial human pathogens. Nature Communications 12 (1), 6628, pp. 1 - 9 (2021)
Journal Article
Hui, C.; Brieger, L.; Strohmann, C.; Antonchick, A. P.: Stereoselective Synthesis of Cyclobutanes by Contraction of Pyrrolidines. Journal of the American Chemical Society, pp. 1 - 7 (2021)
Journal Article
Shaaban, S.; Merten, C.; Waldmann, H.: Catalytic Atroposelective C7-Functionalisation of Indolines and Indoles. Chemistry – A European Journal, pp. 1 - 7 (2021)
Journal Article
Schoppe, J.; Schubert, E.; Apelbaum, A.; Yavavli, E.; Birkholz, O.; Stephanowitz, H.; Han, Y.; Perz, A.; Hofnagel, O.; Liu, F. et al.; Piehler, J.; Raunser, S.; Ungermann, C.: Flexible open conformation of the AP-3 complex explains its role in cargo recruitment at the Golgi. The Journal of Biological Chemistry, 101334, pp. 1 - 48 (2021)
Journal Article
Gally, J.-M.; Pahl, A.; Czodrowski, P.; Waldmann, H.: Pseudonatural Products Occur Frequently in Biologically Relevant Compounds. Journal of Chemical Information and Modeling, pp. 1 - 11 (2021)
Journal Article
Raina, D.; Bahadori, A.; Stanoev, A.; Protzek, M.; Koseska, A.; Schröter, C.: Cell-cell communication through FGF4 generates and maintains robust proportions of differentiated cell types in embryonic stem cells. Development, pp. 1 - 53 (2021)
Journal Article
Ruiz, E. J.; Pinto-Fernandez, A.; Turnball, A. P.; Lan, L.; Charlton, T. M.; Scott, H. C.; Damianou, A.; Vere, G.; Riising, E. M.; Da Costa, C. et al.; Krajewski, W. W.; Guerin, D.; Kearns, J. D.; Ioannidis , S.; Katz, M.; McKinnon, C.; O´Connell, J.; Moncaut, N.; Rosewell, I.; Nye, E.; Jones, N.; Heride, C.; Gersch, M.; Wu, M.; Dinsmore, C. J.; Hammonds, T. R.; Kim, S.; Komander, D.; Urbe, S.; Clague, M. J.; Kessler, B. M.; Behrens, A.: USP28 deletion and small-molecule inhibition destabilizes c-MYC and elicits regression of squamous cell lung carcinoma. eLife, 10:e71596, pp. 1 - 23 (2021)
Journal Article
Silistre, H.; Raoux-Barbot, D.; Mancinelli, F.; Sangouard, F.; Dupin, A.; Belyy, A.; Deruelle, V.; Renault, L.; Ladant, D.; Touqui, L. et al.; Mechold, U.: Prevalence of ExoY Activity in Pseudomonas aeruginosa Reference Panel Strains and Impact on Cytotoxicity in Epithelial Cells. Frontiers in Microbiology 12, 666097, pp. 1 - 16 (2021)
Journal Article
Burhop, A.; Bag, S.; Grigalunas, M.; Woitalla, S.; Bodenbinder, P.-J.; Brieger, L.; Strohmann, C.; Pahl, A.; Sievers, S.; Waldmann, H.: Synthesis of Indofulvin Pseudo-Natural Products Yields a New Autophagy Inhibitor Chemotype. Advanced Science 8 (19), e2102042, pp. 1 - 10 (2021)
Journal Article
Loh, C. C. J.: Exploiting non-covalent interactions in selective carbohydrate synthesis. Nature Reviews Chemistry, pp. 1 - 24 (2021)
Journal Article
Liu, J.; Flegel, J.; Otte, F.; Pahl, A.; Sievers, S.; Strohmann, C.; Waldmann, H.: Combination of Pseudo-Natural Product Design and Formal Natural Product Ring Distortion Yields Stereochemically and Biologically Diverse Pseudo-Sesquiterpenoid Alkaloids. Angewandte Chemie International Edition 60 (39), pp. 21384 - 21395 (2021)
Journal Article
Liu, J.; Flegel, J.; Otte, F.; Pahl, A.; Sievers, S.; Strohmann, C.; Waldmann, H.: Combination of Pseudo-Natural Product Design and Formal Natural Product Ring Distortion Yields Stereochemically and Biologically Diverse Pseudo-Sesquiterpenoid Alkaloids. Angewandte Chemie 133 (39), pp. 21554 - 21565 (2021)
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