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A self-inhibitory interaction within Nup155 and membrane binding are required for nuclear pore complex formation
Oxford University Press | 2018| -
Development of Accessible Peptidic Tool Compounds To Study the Phosphatase PTP1B in Intact Cells
American Chemical Society | 2014| -
Blocking Inflammasome Activation Caused by β‑Amyloid Peptide (Aβ) and Islet Amyloid Polypeptide (IAPP) through an IAPP Mimic
American Chemical Society | 2019| -
An amphipathic helix in Brl1 is required for nuclear pore complex biogenesis in S. cerevisiae
Free accessBASE | 2022| -
Exploiting Cross-Amyloid Interactions To Inhibit Protein Aggregation but not Function: Nanomolar Affinity Inhibition of Insulin Aggregation by an IAPP Mimic We are grateful to S. Stevanovic and C. Henkel for MALDI measurements, J. Bernhagen for help in establishing the insulin receptor assays, and L. M. Yan for helpful discussions and preliminary studies on insulin fibrillization. This work was supported by the Deutsche Forschungsgemeinschaft (DFG).
Online Contents | 2008|Contributors: Tatarek-Nossol, Marianna
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