Publications of Peter `T Hart

Journal Article (9)

Journal Article
Chang, J.-Y.; Neugebauer, C.; Schmeing, S.; Amrahova, G.; `T Hart, P.: Macrocyclic peptides as inhibitors of WDR5 - lncRNA interactions. Chemical Communications (2023)
Journal Article
Scheming, S.; Amrahova, G.; Bigler, K.; Opney, J.; Pal, S.; Posada, L.; Gasper, R.; `T Hart, P.: Rationally designed stapled peptides allosterically inhibit PTBP1 RNA-binding. Chemical Science 14 (31) (2023)
Journal Article
Nowacki, J.; Malenica, M.; Schmeing, S.; Schiller, D.; Buchmuller, B.; Amrahova, G.; `T Hart, P.: A translational repression reporter assay for the analysis of RNA-binding protein consensus sites. RNA Biology (2023)
Journal Article
Krzyzanowski, A.; Esser, L. M.; Willaume, A.; Prudent, R.; `T Hart, P.; Waldmann, H.: Development of Macrocyclic PRMT5-Adaptor Protein Interaction Inhibitors. European Journal of Medicinal Chemistry (2022)
Journal Article
Openy, J.; Amrahova, G.; Chang, J.-Y.; Noisier, A.; `T Hart, P.: Solid-phase peptide modification via deaminative photochemical Csp3- Csp3 bond formation using Katritzky salts. Chemistry – A European Journal, pp. 1 - 9 (2022)
Journal Article
Krzyzanowski, A.; Gasper, R.; Adihou, H.; `T Hart, P.; Waldmann, H.: Biochemical Investigation of the Interaction of pICln, RioK1 and COPR5 with the PRMT5-MEP50 Complex. Chembiochem 22 (11), pp. 1908 - 1914 (2021)
Journal Article
`T Hart, P.; Hommen, P.; Noisier, A.; Krzyzanowski, A.; Schüler, D.; Porfetye, A. T.; Akbarzadeh, M.; Vetter, I. R.; Adihou, H.; Waldmann, H.: Structure based design of bicyclic peptide inhibitors of RbAp48. Angewandte Chemie International Edition 60 (4), pp. 1813 - 1820 (2020)
Journal Article
`T Hart, P.; Hommen, P.; Noisier, A.; Krzyzanowski, A.; Schüler, D.; Porfetye, A. T.; Akbarzadeh, M.; Vetter, I. R.; Adihou, H.; Waldmann, H.: Structure based design of bicyclic peptide inhibitors of RbAp48. Angewandte Chemie 133 (4), pp. 1841 - 1848 (2020)
Journal Article
`T Hart, P.; Openy, J.; Krzyzanowski, A.; Adihou, H.; Waldmann, H.: Hot-spot guided design of macrocyclic inhibitors of the LSD1-CoREST1 interaction. Tetrahedron 75 (48), 130685, pp. 1 - 11 (2019)
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