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The Journal of Biological Chemistry|July 11, 2024
An E3 ubiquitin ligase localization screen uncovers DTX2 as a novel ADP-ribosylation-dependent regulator of DNA double-strand break repairBillel Djerir, Isabelle Marois, Jean-Christophe Dubois, et al.
The Journal of Biological Chemistry|October 10, 2025
A short SUMOylation tag modulates transcription factor activityAntoine Y Bouchard, Anaïs J I Vivet, Valérie C Cabana, et al.
Iscience|May 1, 2026
A ZNF-nanobody fusion reveals SUMOylation-dependent changes in p53 protein localizationAntoine Y Bouchard, Valérie C Cabana, Julien Plamondon, et al.
Nucleic Acids Research|July 24, 2022
Zinc controls PML nuclear body formation through regulation of a paralog specific auto-inhibition in SUMO1Mathieu Lussier-Price, Haytham M Wahba, Xavier H Mascle, et al.
Biochemistry|January 29, 2016
Structural and Biochemical Characterization of a Copper-Binding Mutant of the Organomercurial Lyase MerB: Insight into the Key Role of the Active Site Aspartic Acid in Hg-Carbon Bond Cleavage and Metal Binding SpecificityHaytham M Wahba, Lauriane Lecoq, Michael Stevenson, et al.
Structure (London, England : 1993)|December 16, 2014
Structural and functional characterization of the phosphorylation-dependent interaction between PML and SUMO1Laurent Cappadocia, Xavier H Mascle, Véronique Bourdeau, et al.
Plos Biology|March 19, 2024
SMARCAL1 ubiquitylation controls its association with RPA-coated ssDNA and promotes replication fork stabilityMaïlyn Yates, Isabelle Marois, Edlie St-Hilaire, et al.
Research Square|February 24, 2025
Remodeling of extracellular matrix collagen IV by MIG-6/papilin regulates neuronal architectureMalika Nadour, Robert I Valette Reveno Leatis, Marie Biard, et al.
Biorxiv : the Preprint Server for Biology|February 24, 2025
Remodeling of extracellular matrix collagen IV by MIG-6/papilin regulates neuronal architectureMalika Nadour, Robert I Valette Reveno Leatis, Marie Biard, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Ultra-rare biallelic THAP12 variants cause loss of function and underlie severe epileptic encephalopathyKatarzyna Ochenkowska, Bryce Rampal, Antoine Légaré, et al.
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