Stefan Knapp

发表

DARPins detect the formation of hetero-tetramers of p63 and p73 in epithelial tissues and in squamous cell carcinoma

C. Osterburg, J. Gebel, M. Tuppi, 2023, Cell death & disease.

P116 from Mycoplasma is a self-sufficient lipid uptake and delivery machinery

A. Frangakis, Roberto Covino, Martin P. Schwalm, 2023, bioRxiv.

Targeting LC3/GABARAP for degrader development and autophagy modulation

E. Proschak, V. Rogov, D. Fearon, 2023, bioRxiv.

Development of Selective Pyrido[2,3-d]pyrimidin-7(8H)-one-Based Mammalian STE20-Like (MST3/4) Kinase Inhibitors.

A. Joerger, T. Kronenberger, Andreas Krämer, 2024, Journal of medicinal chemistry.

Expanding the ligand spaces for E3 ligases for the design of protein degraders.

Rahman Shah Zaib Saleem, Stefan Knapp, M. P. Schwalm, 2024, Bioorganic & medicinal chemistry.

Furo[3,2-b]pyridine: A Privileged Scaffold for Highly Selective Kinase Inhibitors and Effective Modulators of the Hedgehog Pathway.

S. Knapp, H. Waldmann, B. Berger, 2019, Angewandte Chemie.

Furo[3,2‐b]pyridine: A Privileged Scaffold for Highly Selective Kinase Inhibitors and Effective Modulators of the Hedgehog Pathway

B. Berger, K. Paruch, Slava Ziegler, 2018, Angewandte Chemie.

Copper is required for oncogenic BRAF signaling and tumorigenesis

Michelle L. Turski, Donita C. Brady, Matt Crowe, 2014, Nature.

Development of Highly Potent and Selective Covalent FGFR4 Inhibitors Based on SNAr Electrophiles.

Stefan A. Laufer, M. Gehringer, D. Dauch, 2024, Journal of medicinal chemistry.

Splice variants of CK1α and CK1α-like: Comparative analysis of subcellular localization, kinase activity, and function in the Wnt signaling pathway

B. Berger, V. Bryja, Tomáš Gybeľ, 2024, The Journal of biological chemistry.

Design of a "Two-in-One" Mutant-Selective Epidermal Growth Factor Receptor Inhibitor That Spans the Orthosteric and Allosteric Sites.

Anna M. Schmoker, S. Knapp, P. Jänne, 2021, Journal of medicinal chemistry.

Chemogenomics for NR1 nuclear hormone receptors

Alexandra Stolz, Laura Isigkeit, Espen Schallmayer, 2024, Nature communications.

Structure-Based Design of Dual Partial Peroxisome Proliferator-Activated Receptor γ Agonists/Soluble Epoxide Hydrolase Inhibitors.

S. Knapp, D. Steinhilber, E. Proschak, 2021, Journal of medicinal chemistry.

Inhibition of bromodomain and extra-terminal proteins targets constitutively active NFκB and STAT signaling in lymphoma and influences the expression of the antiapoptotic proteins BCL2A1 and c-MYC

D. Bruecher, Stefan Knapp, Nadja M. Pieper, 2024, Cell communication and signaling : CCS.

Novel Dihydropteridinone Derivatives As Potent Inhibitors of the Understudied Human Kinases Vaccinia-Related Kinase 1 and Casein Kinase 1δ/ε.

P. Z. Ramos, R. Couñago, K. Massirer, 2024, Journal of medicinal chemistry.

Elimination of mutant SWI/SNF complexes by protein quality control: new opportunities targeting aggressive rhabdoid tumours

Stefan Knapp, Andreas Krämer, 2024, Signal transduction and targeted therapy.