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Communications Biology|November 28, 2024
JmjC catalysed histone H2a N-methyl arginine demethylation and C4-arginine hydroxylation reveals importance of sequence-reactivity relationshipsJoanna Bonnici, Razanne Oueini, Eidarus Salah, et al.FEBS Letters|October 22, 2002
Human spermatid-specific thioredoxin-1 (Sptrx-1) is a two-domain protein with oxidizing activityAlberto Jiménez, Catrine Johansson, Johanna Ljung, et al.Cancer Research|August 29, 2020
Inhibition of Histone H3K27 Demethylases Inactivates Brachyury (TBXT) and Promotes Chordoma Cell DeathLucia Cottone, Adam P Cribbs, Garima Khandelwal, et al.Chemical Communications (Cambridge, England)|November 30, 2017
Investigating d-lysine stereochemistry for epigenetic methylation, demethylation and recognitionRoman Belle, Abbas H K Al Temimi, Kiran Kumar, et al.Journal of Medicinal Chemistry|March 27, 2024
Discovery of a Potent, Selective, and Cell-Active SPIN1 InhibitorYan Xiong, Holger Greschik, Catrine Johansson, et al.Nature Communications|August 25, 2022
Elucidating the path to Plasmodium prolyl-tRNA synthetase inhibitors that overcome halofuginone resistanceMark A Tye, N Connor Payne, Catrine Johansson, et al.Journal of Medicinal Chemistry|May 17, 2018
Discovery of Orally Bioavailable, Quinoline-Based Aldehyde Dehydrogenase 1A1 (ALDH1A1) Inhibitors with Potent Cellular ActivityShyh-Ming Yang, Natalia J Martinez, Adam Yasgar, et al.Nature Chemistry|April 15, 2026
KDM3A catalyses the oxidation of acetyl-lysine to hydroxyacetyl-lysine on histone H3K9Roman Belle, John-Paul Bukowski, Rachel Schiller, et al.Journal of Medicinal Chemistry|July 2, 2019
Discovery of a Potent and Selective Fragment-like Inhibitor of Methyllysine Reader Protein Spindlin 1 (SPIN1)Yan Xiong, Holger Greschik, Catrine Johansson, et al.Journal of Medicinal Chemistry|November 29, 2021
First-in-Class Inhibitors of the Ribosomal Oxygenase MINA53Radosław P Nowak, Anthony Tumber, Eline Hendrix, et al.Pageof 4